| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39038007-39038343 | Common:1; Rare:83 | ||||
| chr13:39038346-39038429 | Rare:27 | ||||
| chr13:39655633-39655755 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40771129-40771299 | Common:2; Rare:53 | ||||
| chr13:41061161-41061586 | Common:4; Rare:144 | ||||
| chr13:41132707-41132945 | Rare:58 | ||||
| chr13:41194460-41194659 | Common:2; Rare:48 | ||||
| chr13:41311179-41311309 | Rare:59 | ||||
| chr13:42271702-42272041 | Common:2; Rare:94 | ||||
| chr13:43023553-43023667 | Common:1; Rare:56 | ||||
| chr13:43879492-43879599 | Rare:31 | ||||
| chr13:43879697-43879910 | Common:18; Rare:62 | ||||
| chr13:44435170-44435454 | Common:3; Rare:81 | ||||
| chr13:44989428-44989621 | Rare:74 | ||||
| chr13:45120358-45120597 | Common:2; Rare:73 |