Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44219380-44219709 | Common:6; Rare:295 | ||||
| chr6:44219700-44219940 | Rare:179 | ||||
| chr6:44223300-44223700 | Common:5; Rare:280 | ||||
| chr6:44223768-44224617 | Common:8; Rare:252 | ||||
| chr6:44226041-44227011 | Common:4; Rare:202 | ||||
| chr6:44245935-44246595 | Common:9; Rare:497 | ||||
| chr6:44246810-44247665 | Common:29; Rare:921 | ||||
| chr6:44247578-44247698 | Common:1; Rare:35 | ||||
| chr6:44247738-44248525 | Common:11; Rare:409 | ||||
| chr6:44256550-44257190 | Common:9; Rare:396 | ||||
| chr6:44257105-44257837 | Common:3; Rare:725 | ||||
| chr6:44265339-44265725 | Common:6; Rare:256 | ||||
| chr6:44297570-44297970 | Common:1; Rare:115 | ||||
| chr6:44312777-44313190 | Common:8; Rare:197; Clinvar (benign):6 | ||||
| chr6:44313202-44313602 | Common:2; Rare:217; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 |
- 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