| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159726911-159727162 | Common:1; Rare:97 | ||||
| chr6:159761834-159762111 | Common:4; Rare:139 | ||||
| chr6:159762316-159762584 | Common:2; Rare:73 | ||||
| chr6:159789528-159790006 | Common:4; Rare:159 | ||||
| chr6:166342519-166342665 | Common:3; Rare:55 | ||||
| chr6:166956544-166956678 | Common:2; Rare:46; Clinvar:3 | ||||
| chr6:166999074-166999409 | Common:1; Rare:114 | ||||
| chr6:169702023-169702340 | Common:5; Rare:134 | ||||
| chr6:169751520-169751645 | Rare:46; Clinvar (benign):1 | ||||
| chr6:170306603-170306799 | Common:1; Rare:58 | ||||
| chr6:170554211-170554409 | Common:1; Rare:64 | ||||
| chr7:727227-727285 | Rare:22; Clinvar:1 | ||||
| chr7:975502-975660 | Common:1; Rare:72 | ||||
| chr7:1028307-1028540 | Common:1; Rare:81 | ||||
| chr7:1504329-1504544 | Common:4; Rare:99 |