Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31836324-31836376 | Rare:10 | ||||
| chr6:31837061-31837081 | Rare:4 | ||||
| chr6:31862565-31862673 | Rare:30; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:31862735-31863267 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:31896766-31896888 | Common:1; Rare:49 | ||||
| chr6:31897193-31897293 | Rare:21 | ||||
| chr6:31897398-31897822 | Common:1; Rare:84 | ||||
| chr6:31898191-31898355 | Rare:29 | ||||
| chr6:31901659-31901692 | Rare:7 | ||||
| chr6:31902032-31902500 | Common:3; Rare:127 | ||||
| chr6:31945527-31946132 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:31948834-31948965 | Common:2; Rare:39; Clinvar (benign):2 | ||||
| chr6:31958841-31959225 | Rare:124; Clinvar:8 | ||||
| chr6:31970995-31971194 | Rare:68 | ||||
| chr6:31971491-31971590 | Common:1; Rare:30 |
- 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