| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:87671085-87671407 | Common:1; Rare:85 | ||||
| chr13:97432965-97433245 | Common:3; Rare:86 | ||||
| chr13:99087944-99087971 | Rare:8 | ||||
| chr13:99498731-99498852 | Common:1; Rare:34 | ||||
| chr13:102394509-102394668 | Common:1; Rare:62 | ||||
| chr13:110205351-110205530 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:110242690-110242846 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr13:110271395-110271672 | Common:2; Rare:48 | ||||
| chr13:110307861-110308120 | Common:1; Rare:99 | ||||
| chr13:110308493-110308622 | Common:2; Rare:25 | ||||
| chr13:110424731-110424971 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110503889-110504275 | Common:4; Rare:127; Clinvar:1; Clinvar (benign):3 | ||||
| chr13:112725687-112725813 | Rare:23 | ||||
| chr13:112730260-112730589 | Common:5; Rare:53 | ||||
| chr13:113489589-113489880 | Common:1; Rare:56 |