| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:135353880-135354113 | Common:1; Rare:30 | ||||
| chr5:135358423-135358768 | Common:4; Rare:51 | ||||
| chr5:148826377-148826639 | Common:3; Rare:66 | ||||
| chr5:148829960-148830173 | Common:1; Rare:48 | ||||
| chr5:150056312-150056365 | Rare:11; Clinvar (pathogenic):1 | ||||
| chr5:150778633-150778932 | Common:3; Rare:107 | ||||
| chr5:150779646-150779927 | Common:7; Rare:38 | ||||
| chr5:150779949-150780041 | Rare:16 | ||||
| chr5:150780252-150780491 | Rare:35 | ||||
| chr5:150946524-150946629 | Rare:24 | ||||
| chr5:151005770-151005780 | Rare:2 | ||||
| chr5:151022510-151022585 | Rare:12 | ||||
| chr5:151022699-151023037 | Common:7; Rare:47 | ||||
| chr5:154799732-154800036 | Common:2; Rare:81 | ||||
| chr5:154899241-154899440 | Common:1; Rare:44; Clinvar:1 |