Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:5046210-5046790 | Rare:245 | ||||
| chr7:5190006-5190343 | Common:4; Rare:356 | ||||
| chr7:5190442-5190975 | Common:8; Rare:333 | ||||
| chr7:5282428-5283124 | Common:12; Rare:96 | ||||
| chr7:5423449-5424403 | Common:19; Rare:636 | ||||
| chr7:5425105-5426270 | Common:1; Rare:613 | ||||
| chr7:5512652-5513650 | Common:8; Rare:408 | ||||
| chr7:5513667-5514395 | Common:13; Rare:534 | ||||
| chr7:5527327-5528290 | Common:18; Rare:641; Clinvar:2; Clinvar (benign):22; Clinvar (pathogenic):4 | ||||
| chr7:5529497-5530175 | Common:7; Rare:733; Clinvar:2; Clinvar (benign):19 | ||||
| chr7:5530393-5530928 | Common:7; Rare:464; Clinvar (benign):13 | ||||
| chr7:5562540-5563070 | Common:2; Rare:238 | ||||
| chr7:5781494-5781767 | Common:1; Rare:258 | ||||
| chr7:6008947-6009387 | Common:12; Rare:558; Clinvar:64; Clinvar (benign):72; Clinvar (pathogenic):9 | ||||
| chr7:6009380-6009640 | Common:9; Rare:329; Clinvar (pathogenic):3 |
- 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