ID: 127888362 | H3K4me1 hESC enhancer GRCh37_chr17:78398753-78399254 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80424953..80425454) | | |
ID: 127888361 | H3K4me1 hESC enhancer GRCh37_chr17:78371724-78372230 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80397924..80398430) | | |
ID: 127888360 | H3K4me1 hESC enhancer GRCh37_chr17:78371216-78371723 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80397416..80397923) | | |
ID: 127888359 | H3K4me1 hESC enhancer GRCh37_chr17:78369069-78369570 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80395269..80395770) | | |
ID: 127888358 | H3K4me1 hESC enhancer GRCh37_chr17:78354122-78354622 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80380322..80380822) | | |
ID: 127888357 | H3K4me1 hESC enhancer GRCh37_chr17:78258533-78259093 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80284734..80285294) | | |
ID: 127888356 | H3K4me1 hESC enhancer GRCh37_chr17:78251821-78252439 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80278022..80278640) | | |
ID: 127888355 | H3K4me1 hESC enhancer GRCh37_chr17:78247837-78248435 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80274038..80274636) | | |
ID: 127888354 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78237270-78237826 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80263304..80264027) | | |
ID: 127888352 | H3K4me1 hESC enhancer GRCh37_chr17:78210639-78211426 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80236840..80237627) | | |
ID: 126862664 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:78359110-78360309 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80385310..80386509) | | |
ID: 126862663 | BRD4-independent group 4 enhancer GRCh37_chr17:78345568-78346767 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80371768..80372967) | | |
ID: 116276483 | CRISPRi-validated cis-regulatory element chr17.5742 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80257264..80257484) | | |
ID: 108281162 | SLC26A11-RNF213 intergenic CAGE-defined mid-level expression enhancer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80254661..80255234) | | |
ID: 100616359 | microRNA 4730 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80419418..80419493) | | |
ID: 100294362 | RNF213 antisense RNA 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80351830..80415168, complement) | | |
ID: 284131 | endonuclease V [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80415167..80438086) | | 619821 |
ID: 284129 | solute carrier family 26 member 11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80220427..80253500) | | 610117 |
ID: 57674 | ring finger protein 213 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80260852..80398794) | ALO17, C17orf27, KIAA1618, MYMY2, MYSTR, NET57 | 613768 |