Proximal
MCF 10A(Human) | 31434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104545-49104603 | Rare:16; Clinvar (benign):1 | ||||
| chr3:49104610-49105027 | Common:1; Rare:158; Clinvar:5; Clinvar (benign):7 | ||||
| chr3:49119416-49119714 | Rare:57 | ||||
| chr3:49120697-49121035 | Rare:93 | ||||
| chr3:49132270-49132579 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:49132976-49133163 | Rare:39; Clinvar:2 | ||||
| chr3:49165675-49166010 | Rare:77 | ||||
| chr3:49166214-49166541 | Common:1; Rare:73 | ||||
| chr3:49171128-49171312 | Rare:41 | ||||
| chr3:49171404-49171621 | Common:1; Rare:48 | ||||
| chr3:49277232-49277303 | Rare:32 | ||||
| chr3:49339961-49340355 | Common:3; Rare:138 | ||||
| chr3:49357847-49358013 | Common:3; Rare:73 | ||||
| chr3:49358208-49358582 | Common:4; Rare:180 | ||||
| chr3:49358669-49358880 | Common:1; Rare:48 |
- 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