Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124748767-124749075 | Common:3; Rare:73 | ||||
| chr5:124749262-124749381 | Rare:17 | ||||
| chr5:126423024-126423651 | Common:1; Rare:150 | ||||
| chr5:126423690-126423804 | Common:1; Rare:28 | ||||
| chr5:126472304-126472463 | Rare:35 | ||||
| chr5:126594934-126595129 | Rare:66; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:126595133-126595293 | Common:2; Rare:78; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr5:126595325-126595444 | Common:2; Rare:27; Clinvar (benign):2 | ||||
| chr5:126600838-126601022 | Common:1; Rare:88 | ||||
| chr5:126601241-126601418 | Rare:65 | ||||
| chr5:126776292-126776470 | Common:3; Rare:31 | ||||
| chr5:126776530-126776682 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr5:126776699-126777227 | Common:4; Rare:177; Clinvar:6; Clinvar (benign):7 | ||||
| chr5:126777376-126777704 | Rare:86; Clinvar (benign):1 | ||||
| chr5:126777732-126777899 | Common:2; Rare:47; Clinvar (benign):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