| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144413548-144413704 | Rare:48; Clinvar:1 | ||||
| chr8:144428497-144428638 | Common:2; Rare:51 | ||||
| chr8:144475768-144476029 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:144477902-144478057 | Common:4; Rare:59 | ||||
| chr8:144792342-144792562 | Common:3; Rare:82 | ||||
| chr8:144901397-144901730 | Common:1; Rare:95 | ||||
| chr9:2844043-2844352 | Common:5; Rare:119 | ||||
| chr9:4679437-4679721 | Common:1; Rare:124 | ||||
| chr9:6015604-6015696 | Rare:40 | ||||
| chr9:6645704-6645921 | Common:1; Rare:73 | ||||
| chr9:13279616-13279811 | Common:2; Rare:61 | ||||
| chr9:16870719-16870836 | Rare:55 | ||||
| chr9:19102865-19103051 | Common:2; Rare:78 | ||||
| chr9:19127458-19127592 | Common:1; Rare:41 | ||||
| chr9:19380191-19380373 | Common:4; Rare:88 |