ID: 127885611 | H3K4me1 hESC enhancer GRCh37_chr17:6540081-6540863 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6636761..6637543) | | |
ID: 127885610 | H3K4me1 hESC enhancer GRCh37_chr17:6471007-6471507 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6567687..6568187) | | |
ID: 127885609 | H3K4me1 hESC enhancer GRCh37_chr17:6458140-6458786 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6554820..6555466) | | |
ID: 127885608 | H3K4me1 hESC enhancer GRCh37_chr17:6452242-6452960 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6548922..6549640) | | |
ID: 122526780 | uncharacterized LOC122526780 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6636780..6640316, complement) | | |
ID: 106479013 | RNA, 5S ribosomal pseudogene 435 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6600944..6601051, complement) | RN5S435 | |
ID: 83394 | PITPNM family member 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6451263..6556555, complement) | ACKR6, CORD5, NIR1, RDGBA3 | 608921 |
ID: 9851 | KIAA0753 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (6578147..6640711, complement) | JBTS38, MNR, OFIP, SRTD21 | 617112 |