| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:143404449-143404604 | Common:2; Rare:32 | ||||
| chr5:143405345-143405468 | Rare:38 | ||||
| chr5:144170537-144170886 | Common:2; Rare:110 | ||||
| chr5:144205088-144205187 | Rare:17 | ||||
| chr5:144205192-144205498 | Rare:67 | ||||
| chr5:145835245-145835504 | Common:2; Rare:65 | ||||
| chr5:146182501-146182925 | Common:4; Rare:129 | ||||
| chr5:146203259-146203772 | Common:4; Rare:160 | ||||
| chr5:146446913-146447150 | Common:1; Rare:37 | ||||
| chr5:146878687-146878813 | Common:2; Rare:32; Clinvar (benign):1 | ||||
| chr5:147453621-147454052 | Common:8; Rare:114 | ||||
| chr5:147509937-147510180 | Common:1; Rare:48 | ||||
| chr5:147782475-147782934 | Common:5; Rare:102 | ||||
| chr5:148383694-148384033 | Rare:90 | ||||
| chr5:149345322-149345542 | Common:1; Rare:72 |