| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102773736-102773842 | Rare:52 | ||||
| chr13:102845681-102845936 | Common:6; Rare:73; Clinvar (benign):3 | ||||
| chr13:106567594-106567759 | Rare:56 | ||||
| chr13:106567919-106568267 | Rare:94 | ||||
| chr13:108218313-108218583 | Rare:103 | ||||
| chr13:110307010-110307514 | Common:6; Rare:158; Clinvar:3; Clinvar (benign):9 | ||||
| chr13:110561664-110561893 | Common:5; Rare:81 | ||||
| chr13:110713023-110713261 | Common:2; Rare:102 | ||||
| chr13:110713487-110713657 | Common:2; Rare:73 | ||||
| chr13:110715800-110715889 | Rare:64 | ||||
| chr13:111153619-111153724 | Common:2; Rare:46 | ||||
| chr13:112969116-112969228 | Common:2; Rare:36 | ||||
| chr13:113208620-113208751 | Rare:78 | ||||
| chr13:113490681-113491145 | Common:4; Rare:175 | ||||
| chr13:114132507-114132790 | Common:1; Rare:90 |