Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144462807-144463150 | Common:2; Rare:705 | ||||
| chr8:144464654-144466132 | Common:61; Rare:1550 | ||||
| chr8:144466132-144466532 | Rare:167 | ||||
| chr8:144466710-144467110 | Common:16; Rare:398 | ||||
| chr8:144475050-144476050 | Common:16; Rare:815; Clinvar:14; Clinvar (benign):9 | ||||
| chr8:144476031-144477269 | Common:10; Rare:503; Clinvar:3; Clinvar (benign):2 | ||||
| chr8:144477650-144478150 | Common:42; Rare:741 | ||||
| chr8:144500801-144501238 | Rare:406 | ||||
| chr8:144508389-144509145 | Common:17; Rare:845 | ||||
| chr8:144509160-144509614 | Common:2; Rare:302 | ||||
| chr8:144509658-144510058 | Rare:354 | ||||
| chr8:144510063-144510509 | Common:3; Rare:443 | ||||
| chr8:144510558-144511470 | Common:9; Rare:586; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:144516817-144517326 | Common:7; Rare:342; Clinvar:34; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr8:144517333-144518200 | Common:17; Rare:1411; Clinvar:98; Clinvar (benign):49 |
- 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