| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44111229-44111406 | Rare:52 | ||||
| chr17:44123599-44123883 | Common:3; Rare:80 | ||||
| chr17:44186658-44187002 | Common:1; Rare:127 | ||||
| chr17:44187171-44187301 | Rare:35 | ||||
| chr17:44221200-44221361 | Rare:46 | ||||
| chr17:44222077-44222269 | Rare:41 | ||||
| chr17:44308401-44308598 | Common:1; Rare:63 | ||||
| chr17:44324748-44324997 | Common:3; Rare:92 | ||||
| chr17:44345072-44345334 | Rare:57; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44352016-44352571 | Common:1; Rare:183; Clinvar:16; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr17:44503366-44503714 | Rare:134 | ||||
| chr17:44899368-44899799 | Common:3; Rare:131; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44911473-44911587 | Common:2; Rare:39; Clinvar:1 | ||||
| chr17:45051409-45051696 | Common:1; Rare:93 | ||||
| chr17:45060912-45061353 | Common:3; Rare:118 |