| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:147831531-147831873 | Common:5; Rare:80; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:148383819-148384022 | Rare:60 | ||||
| chr5:149345332-149345531 | Common:1; Rare:64 | ||||
| chr5:149551344-149551635 | Rare:69 | ||||
| chr5:149960599-149960917 | Rare:106; Clinvar:7 | ||||
| chr5:150289736-150289931 | Common:2; Rare:42 | ||||
| chr5:150412728-150413061 | Common:2; Rare:62 | ||||
| chr5:150449646-150449795 | Common:4; Rare:50 | ||||
| chr5:150700981-150701131 | Common:2; Rare:67 | ||||
| chr5:150758975-150759150 | Common:3; Rare:74 | ||||
| chr5:150904884-150905225 | Common:2; Rare:79 | ||||
| chr5:151080976-151081183 | Common:1; Rare:65 | ||||
| chr5:154038891-154039030 | Rare:48 | ||||
| chr5:154858461-154858722 | Common:1; Rare:83 | ||||
| chr5:154938180-154938276 | Rare:28 |