| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:144170557-144170874 | Common:2; Rare:103 | ||||
| chr5:146182501-146182866 | Common:4; Rare:105 | ||||
| chr5:146203358-146203639 | Common:2; Rare:82 | ||||
| chr5:148383777-148384018 | Rare:70 | ||||
| chr5:149345441-149345541 | Common:1; Rare:44 | ||||
| chr5:149551364-149551656 | Rare:70 | ||||
| chr5:149960569-149960790 | Rare:73; Clinvar:4 | ||||
| chr5:150357426-150357803 | Rare:114; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150412628-150413123 | Common:2; Rare:102 | ||||
| chr5:150449675-150449795 | Common:4; Rare:42 | ||||
| chr5:150700981-150701131 | Common:2; Rare:67 | ||||
| chr5:150758997-150759077 | Common:2; Rare:36 | ||||
| chr5:151080974-151081210 | Common:2; Rare:80 | ||||
| chr5:151141639-151141800 | Rare:42 | ||||
| chr5:151157757-151157892 | Common:1; Rare:33 |