Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128204413-128204531 | Common:1; Rare:20 | ||||
| chr9:128217578-128217978 | Common:1; Rare:75 | ||||
| chr9:128218647-128218748 | Common:2; Rare:24; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:128218670-128219150 | Common:13; Rare:369; Clinvar:6; Clinvar (benign):17 | ||||
| chr9:128222187-128222587 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):5 | ||||
| chr9:128250365-128250765 | Rare:396; Clinvar (benign):5 | ||||
| chr9:128274498-128275914 | Common:7; Rare:554 | ||||
| chr9:128275860-128276400 | Common:36; Rare:1329 | ||||
| chr9:128276429-128276839 | Common:2; Rare:252 | ||||
| chr9:128321896-128322694 | Common:9; Rare:902 | ||||
| chr9:128322660-128323020 | Common:17; Rare:601; Clinvar:7; Clinvar (benign):41; Clinvar (pathogenic):5 | ||||
| chr9:128322999-128323536 | Common:4; Rare:291; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr9:128339800-128340790 | Common:27; Rare:1059 | ||||
| chr9:128370921-128371032 | Rare:18 | ||||
| chr9:128371066-128371480 | Common:4; Rare:692 |
- 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