| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:146878702-146878832 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr5:147234876-147235090 | Common:2; Rare:59 | ||||
| chr5:147509917-147510074 | Rare:40 | ||||
| chr5:147510083-147510207 | Common:1; Rare:17 | ||||
| chr5:148383781-148384021 | Rare:72 | ||||
| chr5:149345344-149345536 | Common:1; Rare:65 | ||||
| chr5:149551335-149551631 | Rare:69 | ||||
| chr5:150449672-150449797 | Common:4; Rare:45 | ||||
| chr5:150700989-150701169 | Common:2; Rare:75 | ||||
| chr5:150758989-150759074 | Common:2; Rare:37 | ||||
| chr5:150904801-150904889 | Common:1; Rare:24 | ||||
| chr5:150904961-150905252 | Common:2; Rare:70 | ||||
| chr5:151080981-151081192 | Common:1; Rare:69 | ||||
| chr5:151157715-151158021 | Common:2; Rare:67 | ||||
| chr5:154038882-154039010 | Common:1; Rare:45 |