Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129752970-129753237 | Common:1; Rare:141 | ||||
| chr9:129802986-129803253 | Common:6; Rare:239 | ||||
| chr9:129803361-129804257 | Common:18; Rare:458 | ||||
| chr9:129823978-129824297 | Common:10; Rare:248; Clinvar:7; Clinvar (benign):9 | ||||
| chr9:129835145-129835580 | Common:13; Rare:443 | ||||
| chr9:129835891-129836777 | Common:7; Rare:256 | ||||
| chr9:130042964-130043487 | Common:9; Rare:363 | ||||
| chr9:130053420-130053720 | Common:1; Rare:64 | ||||
| chr9:130053682-130054051 | Common:3; Rare:294 | ||||
| chr9:130172208-130172669 | Common:4; Rare:220 | ||||
| chr9:130444726-130445104 | Common:5; Rare:222; Clinvar:20; Clinvar (benign):1 | ||||
| chr9:130578907-130579120 | Common:2; Rare:39 | ||||
| chr9:130579344-130579741 | Common:21; Rare:367 | ||||
| chr9:130579869-130580867 | Common:2; Rare:279 | ||||
| chr9:130693509-130693882 | Common:3; Rare:327; 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