| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:106567633-106568183 | Rare:164 | ||||
| chr13:108218313-108218520 | Rare:80 | ||||
| chr13:110307010-110307500 | Common:6; Rare:158; Clinvar:3; Clinvar (benign):9 | ||||
| chr13:110307614-110307889 | Common:3; Rare:78 | ||||
| chr13:110561664-110561889 | Common:5; Rare:81 | ||||
| chr13:110615268-110615677 | Common:3; Rare:130 | ||||
| chr13:110914928-110915199 | Common:3; Rare:118 | ||||
| chr13:111153599-111153714 | Common:2; Rare:53 | ||||
| chr13:113208625-113208775 | Rare:86 | ||||
| chr13:113490699-113491145 | Common:4; Rare:169 | ||||
| chr13:113491184-113491258 | Rare:21 | ||||
| chr13:113545958-113545970 | Rare:2 | ||||
| chr13:113759140-113759267 | Rare:38 | ||||
| chr13:113863853-113864191 | Common:2; Rare:83 | ||||
| chr13:114281519-114281674 | Common:2; Rare:91 |