| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50527351-50527429 | Common:2; Rare:17 | ||||
| chr13:102394423-102394634 | Common:1; Rare:87 | ||||
| chr13:110449512-110449714 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:110870269-110870579 | Common:3; Rare:45 | ||||
| chr13:113409787-113410149 | Common:3; Rare:78 | ||||
| chr13:113410306-113410316 | Rare:2 | ||||
| chr13:113410500-113410715 | Common:1; Rare:54 | ||||
| chr13:113410865-113411016 | Common:1; Rare:35 | ||||
| chr13:113411045-113411249 | Common:2; Rare:51 | ||||
| chr13:113411365-113411602 | Common:2; Rare:43 | ||||
| chr13:113413575-113413978 | Common:4; Rare:91 | ||||
| chr14:22770572-22770863 | Common:2; Rare:67 | ||||
| chr14:23387527-23387876 | Common:2; Rare:126; Clinvar:10; Clinvar (benign):11 | ||||
| chr14:23393418-23393909 | Common:3; Rare:126; Clinvar:12; Clinvar (benign):9 | ||||
| chr14:23396692-23397018 | Common:3; Rare:97; Clinvar:7; Clinvar (benign):6 |