| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141618882-141619253 | Common:1; Rare:116; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636785-141637011 | Common:2; Rare:106 | ||||
| chr5:141651362-141651464 | Rare:35 | ||||
| chr5:141923721-141923946 | Common:1; Rare:70 | ||||
| chr5:141968959-141969275 | Common:3; Rare:99 | ||||
| chr5:142012979-142013116 | Rare:43 | ||||
| chr5:142108676-142108967 | Common:2; Rare:99 | ||||
| chr5:142324979-142325317 | Rare:105 | ||||
| chr5:142874687-142874890 | Common:1; Rare:40 | ||||
| chr5:143404425-143404623 | Common:2; Rare:46 | ||||
| chr5:144170540-144170880 | Common:2; Rare:109 | ||||
| chr5:144205216-144205436 | Rare:47 | ||||
| chr5:145835238-145835499 | Common:2; Rare:67 | ||||
| chr5:145936461-145936745 | Common:1; Rare:64 | ||||
| chr5:145937638-145937755 | Rare:29 |