Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106975193-106975600 | Common:5; Rare:439 | ||||
| chr6:107027945-107028425 | Common:9; Rare:342 | ||||
| chr6:107028430-107029020 | Common:7; Rare:158 | ||||
| chr6:107114113-107114660 | Common:3; Rare:346 | ||||
| chr6:107114919-107115045 | Rare:38 | ||||
| chr6:107115064-107116024 | Common:4; Rare:624 | ||||
| chr6:107458671-107459827 | Common:21; Rare:1027; Clinvar:14; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr6:107957112-107957543 | Common:4; Rare:176 | ||||
| chr6:107957574-107957974 | Common:2; Rare:181 | ||||
| chr6:107957988-107958909 | Common:23; Rare:991; Clinvar:14; Clinvar (benign):19 | ||||
| chr6:108074587-108075095 | Common:10; Rare:616; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr6:108260523-108261534 | Common:13; Rare:1469 | ||||
| chr6:108261459-108261859 | Common:1; Rare:75 | ||||
| chr6:108294470-108295266 | Common:11; Rare:928 | ||||
| chr6:108295213-108295870 | Common:4; Rare:307 |
- 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