| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066769-120066917 | Common:2; Rare:44 | ||||
| chr4:122922945-122923118 | Common:2; Rare:50 | ||||
| chr4:127880765-127880934 | Rare:61 | ||||
| chr4:128061002-128061320 | Common:1; Rare:115 | ||||
| chr4:129093494-129093712 | Rare:69 | ||||
| chr4:139453954-139454101 | Common:2; Rare:41; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:139665753-139666027 | Common:2; Rare:62 | ||||
| chr4:140373358-140373649 | Common:1; Rare:102 | ||||
| chr4:142405410-142405520 | Rare:20 | ||||
| chr4:145098156-145098335 | Rare:64 | ||||
| chr4:147684133-147684284 | Rare:60 | ||||
| chr4:151015220-151015357 | Rare:39 | ||||
| chr4:151099444-151099706 | Common:3; Rare:103 | ||||
| chr4:152779730-152780016 | Common:1; Rare:81 | ||||
| chr4:153204367-153204463 | Rare:20 |