Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135497144-135498034 | Common:30; Rare:966; Clinvar:11; Clinvar (benign):15 | ||||
| chr6:136249436-136250982 | Common:24; Rare:922 | ||||
| chr6:136289166-136290120 | Common:12; Rare:1425 | ||||
| chr6:136290215-136290632 | Common:2; Rare:144 | ||||
| chr6:136466711-136467124 | Common:3; Rare:171 | ||||
| chr6:136550310-136550710 | Common:8; Rare:340 | ||||
| chr6:136550672-136550880 | Common:1; Rare:46 | ||||
| chr6:136792334-136793306 | Common:23; Rare:735 | ||||
| chr6:136821991-136823249 | Common:29; Rare:800; Clinvar:34; Clinvar (benign):16; Clinvar (pathogenic):11 | ||||
| chr6:137219255-137219655 | Common:20; Rare:428; Clinvar:4; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr6:137866658-137866798 | Rare:35 | ||||
| chr6:137866880-137867313 | Common:1; Rare:521 | ||||
| chr6:137867633-137868090 | Common:2; Rare:218 | ||||
| chr6:137868067-137868467 | Common:2; Rare:73 | ||||
| chr6:137870749-137871330 | Common:7; Rare:321 |
- 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