| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174829220-174829412 | Common:1; Rare:39 | ||||
| chr4:175812369-175812820 | Rare:89 | ||||
| chr4:175813156-175813370 | Common:2; Rare:37 | ||||
| chr4:176002315-176002524 | Rare:56 | ||||
| chr4:176002533-176002582 | Rare:21 | ||||
| chr4:176065729-176066028 | Common:7; Rare:96 | ||||
| chr4:176319760-176320074 | Common:4; Rare:110 | ||||
| chr4:177442377-177442514 | Rare:82; Clinvar:2 | ||||
| chr4:183659122-183659396 | Common:1; Rare:90 | ||||
| chr4:184649406-184649775 | Common:4; Rare:122 | ||||
| chr4:184734066-184734376 | Common:5; Rare:110 | ||||
| chr4:185143163-185143353 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185203871-185204241 | Common:3; Rare:116 | ||||
| chr4:185425864-185426265 | Common:4; Rare:126 | ||||
| chr4:185535421-185535640 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):4 |