Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75748920-75749320 | Common:23; Rare:414; Clinvar:11 | ||||
| chr6:78866536-78867173 | Common:29; Rare:271 | ||||
| chr6:78867150-78867700 | Common:1; Rare:532 | ||||
| chr6:78867720-78868180 | Common:6; Rare:244 | ||||
| chr6:79077404-79077804 | Common:1; Rare:103 | ||||
| chr6:79077864-79078022 | Common:4; Rare:133 | ||||
| chr6:79078001-79078848 | Common:8; Rare:1546 | ||||
| chr6:79233696-79234920 | Common:24; Rare:730 | ||||
| chr6:79536870-79537281 | Common:5; Rare:430; Clinvar:17 | ||||
| chr6:79537301-79537769 | Common:11; Rare:693; Clinvar:22 | ||||
| chr6:79537877-79538277 | Common:2; Rare:91 | ||||
| chr6:79631031-79631431 | Common:11; Rare:346 | ||||
| chr6:79631565-79631965 | Common:3; Rare:76 | ||||
| chr6:80004372-80005126 | Common:33; Rare:473 | ||||
| chr6:80106359-80106759 | Common:9; Rare:503; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 |
- 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