Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49020536-49020597 | Rare:19 | ||||
| chr3:49020692-49021085 | Common:1; Rare:108 | ||||
| chr3:49021222-49021788 | Common:2; Rare:138; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:49021855-49022228 | Rare:110; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:49022312-49022391 | Rare:36; Clinvar (benign):2 | ||||
| chr3:49022472-49022578 | Rare:42; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:49028303-49028349 | Rare:15 | ||||
| chr3:49028884-49028929 | Rare:19 | ||||
| chr3:49029267-49029519 | Common:2; Rare:150 | ||||
| chr3:49092970-49093153 | Rare:50 | ||||
| chr3:49093414-49093835 | Common:1; Rare:118 | ||||
| chr3:49093891-49094237 | Rare:92 | ||||
| chr3:49094240-49094436 | Rare:44 | ||||
| chr3:49094532-49094629 | Rare:22 | ||||
| chr3:49094667-49094728 | Common:1; Rare:18 |
- 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