Proximal
keratinocyte(Human) | 10483 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:182980482-182980755 | Rare:90 | ||||
| chr3:183099433-183099608 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183253039-183253362 | Common:3; Rare:88 | ||||
| chr3:183635397-183635697 | Common:4; Rare:87 | ||||
| chr3:183884822-183885204 | Common:3; Rare:117 | ||||
| chr3:184134985-184135021 | Common:1; Rare:6 | ||||
| chr3:184135215-184135413 | Common:2; Rare:60; Clinvar:5 | ||||
| chr3:184142821-184143098 | Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:184155061-184155500 | Rare:107 | ||||
| chr3:184174480-184174962 | Common:4; Rare:106 | ||||
| chr3:184181691-184182011 | Rare:67 | ||||
| chr3:184185880-184186233 | Common:4; Rare:133 | ||||
| chr3:184189632-184189932 | Rare:108; Clinvar:1 | ||||
| chr3:184245190-184245522 | Common:2; Rare:99; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr3:184248874-184249021 | Rare:77; Clinvar:5; Clinvar (benign):2 |
- 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