Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3889060-3889497 | Common:4; Rare:249; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr20:3889610-3889645 | Rare:16; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:3889744-3889849 | Common:6; Rare:52; Clinvar (benign):1 | ||||
| chr20:3890237-3890331 | Common:2; Rare:24 | ||||
| chr20:3929106-3929461 | Common:2; Rare:103 | ||||
| chr20:4015471-4015792 | Common:4; Rare:113 | ||||
| chr20:4148549-4148645 | Rare:18 | ||||
| chr20:4148681-4148919 | Rare:73 | ||||
| chr20:4172183-4172224 | Rare:11 | ||||
| chr20:4686137-4686712 | Common:3; Rare:139; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:5000769-5001050 | Common:2; Rare:61 | ||||
| chr20:5001389-5001649 | Common:1; Rare:69 | ||||
| chr20:5112696-5112778 | Rare:23 | ||||
| chr20:5112831-5113286 | Common:2; Rare:148 | ||||
| chr20:5119427-5119639 | Common:2; Rare:82 |
- 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