| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159693195-159693609 | Common:6; Rare:125 | ||||
| chr6:159726917-159727155 | Common:1; Rare:92 | ||||
| chr6:159789538-159789993 | Common:4; Rare:152 | ||||
| chr6:159790252-159790514 | Common:7; Rare:84 | ||||
| chr6:166342513-166342648 | Common:3; Rare:52 | ||||
| chr6:166999074-166999406 | Common:1; Rare:113 | ||||
| chr6:169751526-169751644 | Rare:41; Clinvar (benign):1 | ||||
| chr6:170554221-170554432 | Common:1; Rare:68 | ||||
| chr7:727243-727291 | Rare:16; Clinvar:1 | ||||
| chr7:975511-975668 | Common:1; Rare:65 | ||||
| chr7:1138198-1138461 | Common:2; Rare:82 | ||||
| chr7:1570018-1570094 | Common:1; Rare:25 | ||||
| chr7:2242168-2242292 | Common:2; Rare:69 | ||||
| chr7:2558915-2559079 | Common:1; Rare:70 | ||||
| chr7:4775490-4775634 | Common:6; Rare:58 |