| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144373781-144374076 | Common:3; Rare:96 | ||||
| chr8:144395499-144395673 | Common:1; Rare:49 | ||||
| chr8:144428487-144428683 | Common:2; Rare:77 | ||||
| chr8:144465356-144465512 | Common:3; Rare:57 | ||||
| chr8:144477887-144478082 | Common:4; Rare:78 | ||||
| chr8:144501050-144501569 | Rare:228 | ||||
| chr8:144502880-144503097 | Common:2; Rare:55 | ||||
| chr8:144503996-144504261 | Rare:64 | ||||
| chr8:144509022-144509125 | Rare:34 | ||||
| chr8:144517684-144518014 | Common:1; Rare:111; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144528913-144529187 | Common:2; Rare:116 | ||||
| chr8:144792273-144792562 | Common:3; Rare:101 | ||||
| chr8:144798652-144798924 | Common:3; Rare:84 | ||||
| chr8:144901416-144901734 | Common:1; Rare:90 | ||||
| chr8:144950610-144950906 | Common:4; Rare:96 |