Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75993733-75994133 | Common:8; Rare:87 | ||||
| chr7:75994477-75994998 | Common:27; Rare:906 | ||||
| chr7:76047768-76048228 | Common:16; Rare:796 | ||||
| chr7:76048279-76048804 | Common:5; Rare:168 | ||||
| chr7:76235122-76235776 | Common:13; Rare:469 | ||||
| chr7:76282251-76282850 | Common:3; Rare:193 | ||||
| chr7:76302380-76302730 | Common:12; Rare:434; Clinvar:13; Clinvar (benign):14 | ||||
| chr7:76302750-76303073 | Rare:336; Clinvar:32; Clinvar (benign):17; Clinvar (pathogenic):12 | ||||
| chr7:76303410-76303859 | Common:11; Rare:739; Clinvar:16; Clinvar (benign):10; Clinvar (pathogenic):17 | ||||
| chr7:76358223-76359257 | Common:17; Rare:807 | ||||
| chr7:76359180-76359665 | Common:41; Rare:560 | ||||
| chr7:76393030-76393487 | Common:14; Rare:781 | ||||
| chr7:76393511-76394008 | Common:26; Rare:299 | ||||
| chr7:76397280-76397700 | Common:2; Rare:560 | ||||
| chr7:76409576-76410005 | Common:8; Rare:272 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box