| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39038087-39038484 | Common:1; Rare:98 | ||||
| chr13:39603105-39603439 | Common:2; Rare:121 | ||||
| chr13:39655572-39655843 | Common:5; Rare:131; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr13:40771098-40771234 | Rare:58 | ||||
| chr13:40789377-40789609 | Common:2; Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:40982868-40983029 | Common:3; Rare:26 | ||||
| chr13:41060897-41061656 | Common:20; Rare:295 | ||||
| chr13:41132732-41132978 | Rare:68 | ||||
| chr13:41457289-41457547 | Common:2; Rare:76 | ||||
| chr13:42271804-42272054 | Common:2; Rare:70 | ||||
| chr13:43879492-43879600 | Rare:32 | ||||
| chr13:43879691-43879910 | Common:18; Rare:62 | ||||
| chr13:44435170-44435448 | Common:3; Rare:79 | ||||
| chr13:44989437-44989650 | Rare:84 | ||||
| chr13:45120392-45120586 | Common:1; Rare:62 |