Proximal
MCF-7(Human) | 20727 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80654860-80655234 | Common:38; Rare:438; Clinvar:3; Clinvar (benign):9 | ||||
| chr5:81301402-81301747 | Common:15; Rare:257 | ||||
| chr5:81513376-81513783 | Common:1; Rare:156 | ||||
| chr5:81750974-81751772 | Common:8; Rare:551 | ||||
| chr5:81751707-81751925 | Common:2; Rare:96 | ||||
| chr5:81971863-81972452 | Common:8; Rare:410 | ||||
| chr5:82278255-82278748 | Common:13; Rare:432 | ||||
| chr5:83077279-83077646 | Common:3; Rare:308 | ||||
| chr5:83721885-83722147 | Common:3; Rare:50 | ||||
| chr5:84384556-84384740 | Rare:84 | ||||
| chr5:86617715-86618066 | Common:4; Rare:215 | ||||
| chr5:86618151-86618551 | Common:4; Rare:129 | ||||
| chr5:87267561-87268071 | Common:9; Rare:392 | ||||
| chr5:87268080-87268390 | Common:4; Rare:151; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:87268730-87269020 | Common:2; Rare:260; Clinvar:13; Clinvar (benign):10; 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