Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95317535-95317915 | Common:4; Rare:272; Clinvar:7 | ||||
| chr9:95505820-95506216 | Common:3; Rare:227 | ||||
| chr9:95506440-95506840 | Common:4; Rare:192; Clinvar:16; Clinvar (benign):16; Clinvar (pathogenic):1 | ||||
| chr9:95507397-95507777 | Rare:250 | ||||
| chr9:95507976-95508258 | Common:8; Rare:135; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr9:95509117-95509480 | Rare:92 | ||||
| chr9:95875373-95875757 | Common:3; Rare:344 | ||||
| chr9:95875850-95876183 | Common:18; Rare:250; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:96383179-96383580 | Common:4; Rare:170 | ||||
| chr9:96383611-96383829 | Common:4; Rare:128 | ||||
| chr9:96418255-96419011 | Common:15; Rare:510 | ||||
| chr9:96449934-96450244 | Common:6; Rare:211 | ||||
| chr9:96566794-96567210 | Common:3; Rare:236 | ||||
| chr9:96567330-96567730 | Common:2; Rare:77 | ||||
| chr9:96619370-96619730 | Rare:133 |
- 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