| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44373544-44373704 | Rare:36 | ||||
| chr13:44435311-44435447 | Common:1; Rare:38 | ||||
| chr13:44573756-44574009 | Common:1; Rare:101 | ||||
| chr13:44576313-44576362 | Rare:12 | ||||
| chr13:44577123-44577274 | Rare:33 | ||||
| chr13:44989443-44989607 | Rare:62 | ||||
| chr13:45120330-45120570 | Common:2; Rare:71 | ||||
| chr13:45341040-45341617 | Common:4; Rare:259 | ||||
| chr13:45418340-45418475 | Rare:42 | ||||
| chr13:45464728-45465018 | Common:1; Rare:71 | ||||
| chr13:46052561-46052830 | Common:2; Rare:67 | ||||
| chr13:46211786-46212002 | Common:2; Rare:66 | ||||
| chr13:48001265-48001430 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:48037920-48038007 | Common:2; Rare:35 | ||||
| chr13:48233060-48233475 | Common:3; Rare:144 |