Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:98045004-98045798 | Common:25; Rare:685 | ||||
| chr8:98045885-98046397 | Common:12; Rare:161 | ||||
| chr8:98116522-98116922 | Common:5; Rare:83 | ||||
| chr8:98117020-98117540 | Common:27; Rare:729 | ||||
| chr8:98117589-98117989 | Common:4; Rare:64 | ||||
| chr8:98117995-98118395 | Common:2; Rare:65 | ||||
| chr8:98825020-98825540 | Rare:180 | ||||
| chr8:98825496-98826169 | Common:48; Rare:1003 | ||||
| chr8:98943200-98943600 | Common:2; Rare:65 | ||||
| chr8:98944163-98944940 | Common:10; Rare:481 | ||||
| chr8:99012570-99012910 | Rare:111 | ||||
| chr8:99012931-99013590 | Rare:675; Clinvar:7 | ||||
| chr8:99013528-99013680 | Rare:32 | ||||
| chr8:99013609-99014009 | Common:1; Rare:160; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:99893051-99893483 | Common:1; Rare:274 |
- 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