| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166999088-166999405 | Common:1; Rare:110 | ||||
| chr6:169702027-169702138 | Common:1; Rare:42 | ||||
| chr6:169751520-169751645 | Rare:46; Clinvar (benign):1 | ||||
| chr6:170554221-170554420 | Common:1; Rare:64 | ||||
| chr6:170584586-170584773 | Common:1; Rare:63 | ||||
| chr7:519154-519287 | Rare:32 | ||||
| chr7:727243-727308 | Rare:21; Clinvar:1 | ||||
| chr7:975513-975650 | Common:1; Rare:58 | ||||
| chr7:1028307-1028466 | Rare:57 | ||||
| chr7:1138194-1138400 | Common:2; Rare:63 | ||||
| chr7:1448473-1448623 | Rare:46 | ||||
| chr7:1560799-1560933 | Common:2; Rare:32 | ||||
| chr7:1570012-1570117 | Common:1; Rare:32 | ||||
| chr7:2242168-2242283 | Common:2; Rare:62 | ||||
| chr7:2555489-2555850 | Common:5; Rare:101 |