Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:53109655-53109963 | Common:1; Rare:141; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr5:53480730-53480766 | Rare:12 | ||||
| chr5:53560544-53560719 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:53560846-53561037 | Common:2; Rare:44 | ||||
| chr5:53561046-53561133 | Common:1; Rare:22 | ||||
| chr5:54310067-54310133 | Rare:20 | ||||
| chr5:54310405-54310823 | Common:3; Rare:136 | ||||
| chr5:54517669-54517877 | Common:1; Rare:87 | ||||
| chr5:55160044-55160263 | Rare:63 | ||||
| chr5:55173172-55173445 | Common:1; Rare:73 | ||||
| chr5:55226699-55226822 | Rare:25 | ||||
| chr5:55226861-55226956 | Rare:24; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:55227028-55227534 | Common:1; Rare:122; Clinvar (benign):1 | ||||
| chr5:55227593-55227662 | Rare:19 | ||||
| chr5:55232637-55233119 | Common:2; Rare:130 |
- 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