| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112232127-112232185 | Rare:27 | ||||
| chr4:112285734-112286037 | Rare:91 | ||||
| chr4:112636893-112637204 | Common:2; Rare:82 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:118685349-118685465 | Common:2; Rare:40 | ||||
| chr4:119212355-119212761 | Common:4; Rare:125 | ||||
| chr4:120066807-120066977 | Common:4; Rare:48 | ||||
| chr4:121801233-121801396 | Common:2; Rare:54 | ||||
| chr4:122922992-122923101 | Common:1; Rare:29 | ||||
| chr4:129093428-129093748 | Common:2; Rare:90 | ||||
| chr4:139301276-139301559 | Common:4; Rare:86 | ||||
| chr4:139453954-139454229 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4 | ||||
| chr4:139556177-139556409 | Rare:54 | ||||
| chr4:139556719-139556935 | Rare:38 | ||||
| chr4:140373371-140373692 | Common:2; Rare:126 |