| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139561131-139561387 | Common:1; Rare:104 | ||||
| chr5:139561733-139561805 | Rare:29 | ||||
| chr5:139648168-139648368 | Rare:56 | ||||
| chr5:139904462-139904577 | Common:1; Rare:34 | ||||
| chr5:140303065-140303164 | Common:1; Rare:29 | ||||
| chr5:140564326-140564462 | Common:1; Rare:41 | ||||
| chr5:140564599-140564838 | Rare:64 | ||||
| chr5:140647569-140647889 | Common:5; Rare:130; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664673-140664910 | Common:4; Rare:56 | ||||
| chr5:140691313-140691620 | Common:1; Rare:108; Clinvar:8; Clinvar (benign):1 | ||||
| chr5:141320742-141320890 | Common:1; Rare:46 | ||||
| chr5:141636821-141636957 | Common:1; Rare:59 | ||||
| chr5:141682173-141682328 | Common:1; Rare:48 | ||||
| chr5:141923721-141923933 | Common:1; Rare:66 | ||||
| chr5:141958167-141958300 | Rare:29 |