| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30616981-30617146 | Rare:31 | ||||
| chr13:30617565-30618034 | Common:1; Rare:145 | ||||
| chr13:33285710-33285990 | Common:1; Rare:60 | ||||
| chr13:35476647-35476822 | Common:1; Rare:29 | ||||
| chr13:36346269-36346453 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36999278-36999459 | Rare:73 | ||||
| chr13:39038113-39038429 | Common:1; Rare:79 | ||||
| chr13:39655357-39655750 | Common:6; Rare:149; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:40771138-40771226 | Rare:38 | ||||
| chr13:41060868-41061068 | Common:16; Rare:115 | ||||
| chr13:41061356-41061575 | Common:2; Rare:64 | ||||
| chr13:43879509-43879885 | Common:19; Rare:107 | ||||
| chr13:44435170-44435447 | Common:3; Rare:79 | ||||
| chr13:44989449-44989621 | Rare:63 | ||||
| chr13:45120396-45120612 | Common:1; Rare:72 |