| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69416279-69416422 | Common:1; Rare:40 | ||||
| chr10:69416765-69417083 | Common:5; Rare:81 | ||||
| chr10:69451232-69451611 | Common:2; Rare:102 | ||||
| chr10:69801575-69801953 | Common:2; Rare:92 | ||||
| chr10:70052607-70052908 | Rare:64 | ||||
| chr10:70132686-70132906 | Rare:62 | ||||
| chr10:70146180-70146511 | Common:4; Rare:110 | ||||
| chr10:70146616-70146869 | Common:1; Rare:73 | ||||
| chr10:70170425-70170737 | Common:4; Rare:98 | ||||
| chr10:70233319-70233563 | Common:6; Rare:87; Clinvar (benign):1 | ||||
| chr10:70403869-70404191 | Common:1; Rare:111 | ||||
| chr10:70404238-70404261 | Rare:4 | ||||
| chr10:70602702-70602846 | Common:1; Rare:18; Clinvar:1 | ||||
| chr10:71773447-71773751 | Common:4; Rare:93 | ||||
| chr10:71819441-71819902 | Common:2; Rare:186; Clinvar:5; Clinvar (benign):5 |