| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72375951-72376137 | Common:2; Rare:77; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:72474201-72474667 | Rare:161 | ||||
| chr15:72475135-72475366 | Common:1; Rare:61 | ||||
| chr15:72686154-72686220 | Common:2; Rare:25; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72755605-72755776 | Rare:39 | ||||
| chr15:72758520-72758674 | Rare:26 | ||||
| chr15:72783467-72783816 | Common:2; Rare:137 | ||||
| chr15:73926288-73926501 | Rare:56 | ||||
| chr15:73994551-73994806 | Common:1; Rare:56 | ||||
| chr15:74173711-74173906 | Common:3; Rare:46 | ||||
| chr15:74208974-74209192 | Common:1; Rare:37 | ||||
| chr15:74461106-74461392 | Rare:82 | ||||
| chr15:74540960-74541303 | Common:6; Rare:121 | ||||
| chr15:74598283-74598535 | Common:1; Rare:111 | ||||
| chr15:74615559-74615912 | Common:5; Rare:112 |