| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:128811128-128811321 | Rare:41 | ||||
| chr4:129093378-129093748 | Common:2; Rare:102 | ||||
| chr4:133149087-133149295 | Common:2; Rare:61 | ||||
| chr4:137532392-137532623 | Common:1; Rare:37 | ||||
| chr4:139084170-139084563 | Common:4; Rare:171 | ||||
| chr4:139177175-139177415 | Rare:68 | ||||
| chr4:139301184-139301789 | Common:7; Rare:176 | ||||
| chr4:139302463-139302636 | Common:2; Rare:35 | ||||
| chr4:139453653-139453805 | Common:2; Rare:52 | ||||
| chr4:139453909-139454210 | Common:3; Rare:87; Clinvar:6; Clinvar (benign):4 | ||||
| chr4:139556100-139556357 | Rare:66 | ||||
| chr4:139556388-139556534 | Rare:18 | ||||
| chr4:139556742-139556976 | Rare:45 | ||||
| chr4:139665628-139666022 | Common:2; Rare:83 | ||||
| chr4:140153052-140153101 | Rare:14 |