Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44387300-44387838 | Common:28; Rare:654 | ||||
| chr6:44387780-44388380 | Common:21; Rare:278 | ||||
| chr6:45377012-45377121 | Common:2; Rare:19 | ||||
| chr6:45377028-45377760 | Common:26; Rare:749 | ||||
| chr6:45377790-45378330 | Common:12; Rare:826 | ||||
| chr6:45378239-45378843 | Common:4; Rare:131 | ||||
| chr6:45421746-45422922 | Common:21; Rare:1107; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr6:46687655-46688055 | Common:3; Rare:162 | ||||
| chr6:47309368-47309951 | Common:10; Rare:316 | ||||
| chr6:47476717-47477331 | Common:4; Rare:112 | ||||
| chr6:47477563-47478073 | Common:9; Rare:568; Clinvar:12; Clinvar (benign):11 | ||||
| chr6:47478049-47478600 | Common:14; Rare:619; Clinvar:12; Clinvar (benign):22 | ||||
| chr6:49463082-49464051 | Common:8; Rare:704; Clinvar:8; Clinvar (benign):6 | ||||
| chr6:49636037-49636437 | Common:1; Rare:78 | ||||
| chr6:49636367-49636490 | Rare:23 |
- 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