| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43879467-43879913 | Common:19; Rare:119 | ||||
| chr13:44989463-44989602 | Rare:50 | ||||
| chr13:45120402-45120570 | Common:1; Rare:57 | ||||
| chr13:45341037-45341515 | Common:4; Rare:230 | ||||
| chr13:48001262-48001408 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:49247844-49247941 | Rare:26 | ||||
| chr13:50081980-50082256 | Common:1; Rare:77 | ||||
| chr13:51804113-51804219 | Common:2; Rare:36 | ||||
| chr13:52012116-52012418 | Common:2; Rare:98; Clinvar:1 | ||||
| chr13:52455240-52455503 | Common:3; Rare:81 | ||||
| chr13:72727598-72727915 | Common:4; Rare:108 | ||||
| chr13:72781865-72782182 | Common:1; Rare:121 | ||||
| chr13:79405818-79405882 | Rare:24 | ||||
| chr13:94596139-94596297 | Common:1; Rare:57 | ||||
| chr13:95676937-95677177 | Common:3; Rare:77 |