| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:65749870-65750066 | Common:2; Rare:41 | ||||
| chr18:65750349-65750557 | Rare:42 | ||||
| chr18:65750629-65750816 | Rare:55 | ||||
| chr18:67516714-67517035 | Common:5; Rare:83 | ||||
| chr18:68714401-68714801 | Common:1; Rare:182 | ||||
| chr18:68715009-68715348 | Common:6; Rare:138 | ||||
| chr18:69400560-69400990 | Common:6; Rare:128 | ||||
| chr18:69401360-69401930 | Common:3; Rare:173 | ||||
| chr18:70205645-70205877 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr18:70205996-70206196 | Rare:61 | ||||
| chr18:70288901-70289093 | Common:3; Rare:64 | ||||
| chr18:72866553-72867814 | Common:10; Rare:484 | ||||
| chr18:72867961-72868094 | Common:3; Rare:44 | ||||
| chr18:74147734-74147952 | Common:11; Rare:133 | ||||
| chr18:74148352-74148601 | Common:1; Rare:75 |