| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158819322-158819450 | Common:2; Rare:47 | ||||
| chr6:158999752-158999870 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159000172-159000202 | Rare:8 | ||||
| chr6:159726911-159727162 | Common:1; Rare:97 | ||||
| chr6:159761800-159762077 | Common:5; Rare:133 | ||||
| chr6:159789528-159789993 | Common:4; Rare:156 | ||||
| chr6:166342519-166342657 | Common:3; Rare:52 | ||||
| chr6:166999074-166999404 | Common:1; Rare:112 | ||||
| chr6:169702027-169702347 | Common:5; Rare:134 | ||||
| chr6:169751534-169751645 | Rare:40; Clinvar (benign):1 | ||||
| chr6:170306548-170306808 | Common:1; Rare:87 | ||||
| chr6:170554195-170554412 | Common:1; Rare:69 | ||||
| chr7:727236-727325 | Rare:28; Clinvar:1 | ||||
| chr7:1138196-1138511 | Common:2; Rare:90 | ||||
| chr7:1570013-1570094 | Common:1; Rare:25 |