Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:135851468-135851806 | Rare:53 | ||||
| chr6:136249984-136250040 | Rare:10 | ||||
| chr6:136250190-136250622 | Common:5; Rare:123 | ||||
| chr6:136289305-136289556 | Rare:107 | ||||
| chr6:136289625-136290213 | Common:2; Rare:210 | ||||
| chr6:136290216-136290317 | Rare:17 | ||||
| chr6:136550353-136550787 | Common:2; Rare:121 | ||||
| chr6:136791893-136792107 | Common:1; Rare:63 | ||||
| chr6:136822203-136822296 | Rare:15 | ||||
| chr6:136822397-136822699 | Common:5; Rare:108; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr6:136822723-136823098 | Common:3; Rare:124; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr6:137044091-137044377 | Common:2; Rare:63 | ||||
| chr6:137044414-137044587 | Common:3; Rare:38 | ||||
| chr6:137218951-137219234 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:137219314-137219556 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |
- 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