| ID: 127888354 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78237270-78237826 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80263304..80264027) | | |
| ID: 127888353 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78227308-78228024 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80253509..80254225) | | |
| ID: 127888352 | H3K4me1 hESC enhancer GRCh37_chr17:78210639-78211426 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80236840..80237627) | | |
| ID: 127888351 | H3K4me1 hESC enhancer GRCh37_chr17:78209849-78210638 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80236050..80236839) | | |
| ID: 127888350 | H3K4me1 hESC enhancer GRCh37_chr17:78200105-78200606 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80226306..80226807) | | |
| ID: 127888349 | H3K4me1 hESC enhancer GRCh37_chr17:78196789-78197626 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80222990..80223827) | | |
| ID: 127888348 | H3K4me1 hESC enhancer GRCh37_chr17:78195951-78196788 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80222152..80222989) | | |
| ID: 127888347 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78163065-78163581 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80189266..80189782) | | |
| ID: 126862662 | MED14-independent group 3 enhancer GRCh37_chr17:78178385-78179584 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80204586..80205785) | | |
| ID: 108281162 | SLC26A11-RNF213 intergenic CAGE-defined mid-level expression enhancer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80254661..80255234) | | |
| ID: 284129 | solute carrier family 26 member 11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80220427..80253500) | | 610117 |
| ID: 79092 | caspase recruitment domain family member 14 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80170030..80209331) | BIMP2, CARMA2, PRP, PSORS2, PSS1 | 607211 |
| ID: 57674 | ring finger protein 213 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80260852..80398794) | ALO17, C17orf27, KIAA1618, MYMY2, MYSTR, NET57 | 613768 |
| ID: 6448 | N-sulfoglucosamine sulfohydrolase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80200673..80220333, complement) | HSS, MPS3A, SFMD | 605270 |