| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25376955-25377295 | Common:4; Rare:102 | ||||
| chr4:25914022-25914308 | Common:3; Rare:125 | ||||
| chr4:26320590-26320859 | Common:1; Rare:111 | ||||
| chr4:26860607-26860807 | Common:1; Rare:66 | ||||
| chr4:37826418-37826735 | Common:8; Rare:106 | ||||
| chr4:39182204-39182548 | Rare:74; Clinvar:2 | ||||
| chr4:39458849-39459112 | Common:3; Rare:149; Clinvar (benign):5 | ||||
| chr4:39527313-39527755 | Common:6; Rare:110 | ||||
| chr4:39638829-39639209 | Common:1; Rare:146 | ||||
| chr4:39697946-39698183 | Common:2; Rare:102 | ||||
| chr4:40056655-40056930 | Common:4; Rare:89 | ||||
| chr4:41256733-41256976 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41990401-41990572 | Common:1; Rare:62 | ||||
| chr4:44678401-44678496 | Rare:35 | ||||
| chr4:44678605-44678737 | Rare:62 |