| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564556-140564849 | Rare:77 | ||||
| chr5:140639293-140639478 | Common:3; Rare:45 | ||||
| chr5:140647579-140647923 | Common:5; Rare:140; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664713-140664926 | Common:3; Rare:59 | ||||
| chr5:140691309-140691653 | Common:1; Rare:123; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320725-141320914 | Common:2; Rare:66 | ||||
| chr5:141636803-141637011 | Common:2; Rare:93 | ||||
| chr5:141923741-141923872 | Common:1; Rare:27 | ||||
| chr5:142108707-142108942 | Common:2; Rare:79 | ||||
| chr5:142324973-142325296 | Rare:107 | ||||
| chr5:143404419-143404617 | Common:2; Rare:46 | ||||
| chr5:144170540-144170863 | Common:2; Rare:101 | ||||
| chr5:145835280-145835493 | Common:1; Rare:51 | ||||
| chr5:146182500-146182866 | Common:4; Rare:105 | ||||
| chr5:148383872-148384022 | Rare:49 |