| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013891-43014305 | Common:2; Rare:92 | ||||
| chr6:43053797-43054071 | Common:1; Rare:73; Clinvar:5 | ||||
| chr6:43181983-43182209 | Common:1; Rare:61 | ||||
| chr6:43516876-43517112 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575969-43576186 | Rare:81; Clinvar:4 | ||||
| chr6:43770070-43770230 | Common:2; Rare:48 | ||||
| chr6:44127351-44127665 | Common:4; Rare:91 | ||||
| chr6:44219512-44219645 | Rare:33 | ||||
| chr6:44387445-44387747 | Common:4; Rare:79 | ||||
| chr6:45377855-45378184 | Common:2; Rare:111 | ||||
| chr6:46921904-46922048 | Rare:40 | ||||
| chr6:49463137-49463412 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52284756-52285091 | Common:2; Rare:99 | ||||
| chr6:52420150-52420349 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995276-52995822 | Common:4; Rare:226 |