Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113580631-113581002 | Common:13; Rare:178 | ||||
| chr9:113876166-113876404 | Rare:131 | ||||
| chr9:113876586-113876986 | Common:3; Rare:100 | ||||
| chr9:114077960-114078270 | Common:1; Rare:93 | ||||
| chr9:114078390-114078993 | Common:6; Rare:133 | ||||
| chr9:114098310-114098930 | Common:22; Rare:268 | ||||
| chr9:114099183-114099462 | Common:3; Rare:161 | ||||
| chr9:114155260-114155570 | Rare:132 | ||||
| chr9:114504240-114504801 | Common:1; Rare:224; Clinvar:10; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr9:114505367-114505714 | Common:6; Rare:246; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:114587307-114587955 | Common:13; Rare:535 | ||||
| chr9:114610702-114611117 | Common:2; Rare:120 | ||||
| chr9:114611146-114611670 | Common:11; Rare:417 | ||||
| chr9:114611690-114612200 | Common:4; Rare:121 | ||||
| chr9:116687126-116687410 | Common:12; Rare:251; Clinvar:6; Clinvar (benign):5 |
- 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