| ID: 127885637 | H3K27ac hESC enhancer GRCh37_chr17:7145477-7146028 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7242158..7242709) | | |
| ID: 127885636 | H3K27ac hESC enhancer GRCh37_chr17:7144925-7145476 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7241606..7242157) | | |
| ID: 127885635 | H3K27ac hESC enhancer GRCh37_chr17:7142377-7143026 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7239058..7239724) | | |
| ID: 127885634 | H3K4me1 hESC enhancer GRCh37_chr17:7128275-7128774 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7224956..7225455) | | |
| ID: 127885633 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7123549-7124156 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7220230..7220837) | | |
| ID: 127885632 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7118298-7119276 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7214979..7215957) | | |
| ID: 127885631 | H3K4me1 hESC enhancer GRCh37_chr17:7114863-7115377 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7211544..7212058) | | |
| ID: 127885630 | H3K4me1 hESC enhancer GRCh37_chr17:7114348-7114862 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7211029..7211543) | | |
| ID: 127885629 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7077401-7078117 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7174082..7174798) | | |
| ID: 127885628 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7034277-7034814 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7130958..7131495) | | |
| ID: 127885627 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:7018293-7019079 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7114974..7115760) | | |
| ID: 127885626 | H3K4me1 hESC enhancer GRCh37_chr17:7015987-7016487 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7112668..7113168) | | |
| ID: 126862480 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:7132793-7133992 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7229474..7230673) | | |
| ID: 126862479 | MED14-independent group 3 enhancer GRCh37_chr17:7099412-7100611 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7196093..7197292) | | |
| ID: 124903911 | uncharacterized LOC124903911 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7169069..7173673) | | |
| ID: 124903910 | uncharacterized LOC124903910 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7142249..7142624, complement) | | |
| ID: 121587573 | Sharpr-MPRA regulatory region 12633 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7214310..7214604) | | |
| ID: 121587572 | Sharpr-MPRA regulatory region 10830 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7156330..7156624) | | |
| ID: 105371512 | uncharacterized LOC105371512 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7131247..7140763) | | |
| ID: 728486 | ribosomal protein L7a pseudogene 64 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7140945..7141592) | RPL7A_29_1509 | |