| ID: 127457610 | NANOG hESC enhancer GRCh37_chr7:128622104-128622662 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128982050..128982608) | | |
| ID: 127457609 | H3K4me1 hESC enhancer GRCh37_chr7:128578271-128578854 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128937794..128938800) | | |
| ID: 127457608 | H3K4me1 hESC enhancer GRCh37_chr7:128569307-128569807 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128929253..128929753) | | |
| ID: 127457607 | H3K4me1 hESC enhancer GRCh37_chr7:128544412-128544916 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128904359..128904863) | | |
| ID: 127457606 | H3K4me1 hESC enhancer GRCh37_chr7:128543906-128544411 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128903853..128904358) | | |
| ID: 127457605 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:128531177-128531767 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128891123..128891713) | | |
| ID: 127457604 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:128530587-128531176 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128890533..128891122) | | |
| ID: 127457603 | H3K4me1 hESC enhancer GRCh37_chr7:128529996-128530586 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128889942..128890532) | | |
| ID: 127457602 | H3K4me1 hESC enhancer GRCh37_chr7:128524773-128525372 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128884719..128885318) | | |
| ID: 127457601 | H3K4me1 hESC enhancer GRCh37_chr7:128498247-128498747 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128858193..128858693) | | |
| ID: 127457600 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:128482493-128482997 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128842439..128842943) | | |
| ID: 127457599 | H3K4me1 hESC enhancer GRCh37_chr7:128473526-128474169 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128833472..128834115) | | |
| ID: 126860173 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:128532717-128533916 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128892663..128893863) | | |
| ID: 123956219 | Sharpr-MPRA regulatory region 1680 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128883635..128883929) | | |
| ID: 121175365 | Sharpr-MPRA regulatory region 2205 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128936255..128936549) | | |
| ID: 110806300 | FLNC antisense RNA 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128850162..128862626, complement) | | |
| ID: 106481006 | RNA, 7SL, cytoplasmic 306, pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128970734..128971029) | | |
| ID: 105375497 | uncharacterized LOC105375497 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128891229..128900925) | | |
| ID: 100130705 | sperm microtubule inner protein 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128866330..128872047) | ATP6V1FNB | |
| ID: 392787 | filamin C pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128912460..128914064, complement) | | |