Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31703161-31703579 | Common:6; Rare:483 | ||||
| chr6:31706579-31707330 | Common:5; Rare:134 | ||||
| chr6:31723190-31723440 | Common:2; Rare:112 | ||||
| chr6:31728838-31729455 | Common:2; Rare:192 | ||||
| chr6:31729620-31730650 | Common:17; Rare:657 | ||||
| chr6:31736029-31736766 | Common:17; Rare:565 | ||||
| chr6:31737371-31737888 | Common:3; Rare:160 | ||||
| chr6:31738901-31739631 | Common:11; Rare:94 | ||||
| chr6:31739633-31740169 | Common:26; Rare:752 | ||||
| chr6:31740140-31741299 | Common:19; Rare:730; Clinvar (benign):8 | ||||
| chr6:31772804-31773204 | Common:5; Rare:170 | ||||
| chr6:31776964-31777457 | Common:16; Rare:325 | ||||
| chr6:31777818-31778218 | Common:2; Rare:59 | ||||
| chr6:31794704-31796310 | Common:21; Rare:1179; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr6:31806490-31807200 | Common:18; Rare:998 |
- 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