| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158818226-158818356 | Common:3; Rare:51 | ||||
| chr6:158819322-158819450 | Common:2; Rare:47 | ||||
| chr6:158999746-158999938 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:159000172-159000244 | Rare:18 | ||||
| chr6:159693226-159693594 | Common:6; Rare:103 | ||||
| chr6:159726914-159727162 | Common:1; Rare:96 | ||||
| chr6:159789557-159789993 | Common:4; Rare:150 | ||||
| chr6:162727756-162728097 | Common:3; Rare:92; Clinvar:1 | ||||
| chr6:166342513-166342653 | Common:3; Rare:55 | ||||
| chr6:166627970-166628236 | Common:1; Rare:57 | ||||
| chr6:166999074-166999436 | Common:2; Rare:125 | ||||
| chr6:169253838-169254076 | Rare:38 | ||||
| chr6:169702023-169702138 | Common:1; Rare:44 | ||||
| chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
| chr6:170554211-170554404 | Common:1; Rare:63 |