| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99866815-99867003 | Rare:40 | ||||
| chr13:99971738-99972002 | Common:2; Rare:59 | ||||
| chr13:100088844-100089167 | Rare:129; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100674778-100675161 | Common:4; Rare:158 | ||||
| chr13:102401708-102401763 | Rare:13 | ||||
| chr13:102596782-102597089 | Common:1; Rare:130; Clinvar (benign):1 | ||||
| chr13:102773701-102773842 | Rare:63 | ||||
| chr13:102798961-102799207 | Rare:51 | ||||
| chr13:102845725-102846157 | Common:8; Rare:111; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567841-106568258 | Rare:115 | ||||
| chr13:107866946-107867015 | Rare:14 | ||||
| chr13:108215502-108215660 | Common:1; Rare:47 | ||||
| chr13:108218313-108218520 | Rare:80 | ||||
| chr13:110561656-110561889 | Common:5; Rare:82 | ||||
| chr13:110615509-110615610 | Rare:37 |