Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75738940-75739480 | Common:7; Rare:278 | ||||
| chr7:75842966-75843181 | Common:2; Rare:33 | ||||
| chr7:75878761-75879181 | Common:36; Rare:352 | ||||
| chr7:75914807-75915294 | Common:12; Rare:379; Clinvar:9; Clinvar (benign):3 | ||||
| chr7:75983331-75983812 | Common:13; Rare:405; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:75994436-75994835 | Common:17; Rare:499 | ||||
| chr7:76047741-76048260 | Common:12; Rare:420; Clinvar (benign):1 | ||||
| chr7:76201318-76202012 | Common:5; Rare:191 | ||||
| chr7:76235118-76235510 | Common:5; Rare:221 | ||||
| chr7:76282485-76282767 | Common:2; Rare:130 | ||||
| chr7:76282780-76283400 | Common:9; Rare:187 | ||||
| chr7:76302305-76303182 | Common:15; Rare:837; Clinvar:47; Clinvar (benign):36; Clinvar (pathogenic):11 | ||||
| chr7:76303513-76304014 | Common:8; Rare:495; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):17 | ||||
| chr7:76358863-76359171 | Common:3; Rare:293 | ||||
| chr7:76359180-76359590 | Common:23; Rare:344 |
- 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