| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139453988-139454185 | Common:3; Rare:52; Clinvar:5; Clinvar (benign):4 | ||||
| chr4:139556160-139556332 | Rare:40 | ||||
| chr4:139556388-139556463 | Rare:10 | ||||
| chr4:139665720-139666017 | Common:2; Rare:63 | ||||
| chr4:140154071-140154288 | Common:1; Rare:85 | ||||
| chr4:140373333-140373709 | Common:3; Rare:149 | ||||
| chr4:140523810-140524113 | Common:2; Rare:82 | ||||
| chr4:141220780-141220998 | Rare:76 | ||||
| chr4:142846258-142846358 | Rare:19 | ||||
| chr4:143184622-143185022 | Common:9; Rare:155 | ||||
| chr4:143336535-143336953 | Rare:96 | ||||
| chr4:143337111-143337206 | Rare:41 | ||||
| chr4:143337235-143337296 | Rare:27 | ||||
| chr4:143513349-143514101 | Common:4; Rare:276 | ||||
| chr4:145098134-145098379 | Rare:81 |