| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:148383777-148384022 | Rare:73 | ||||
| chr5:149345339-149345559 | Common:1; Rare:78 | ||||
| chr5:149550845-149551104 | Rare:66 | ||||
| chr5:149551277-149551663 | Common:2; Rare:87 | ||||
| chr5:149960569-149960984 | Rare:139; Clinvar:8; Clinvar (pathogenic):1 | ||||
| chr5:150166557-150166827 | Common:1; Rare:76 | ||||
| chr5:150166971-150167315 | Common:4; Rare:87; Clinvar:1 | ||||
| chr5:150449662-150449803 | Common:4; Rare:49 | ||||
| chr5:150485606-150485971 | Common:4; Rare:79 | ||||
| chr5:150486020-150486313 | Common:3; Rare:60 | ||||
| chr5:150700969-150701111 | Common:2; Rare:62 | ||||
| chr5:150904818-150904833 | Rare:6 | ||||
| chr5:151020335-151020737 | Common:2; Rare:100 | ||||
| chr5:151025105-151025491 | Common:1; Rare:80 | ||||
| chr5:151026017-151026313 | Common:2; Rare:55 |