| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159789557-159789958 | Common:4; Rare:135 | ||||
| chr6:166342513-166342656 | Common:3; Rare:56 | ||||
| chr6:166999074-166999405 | Common:1; Rare:113 | ||||
| chr6:169702009-169702138 | Common:1; Rare:52 | ||||
| chr6:169751464-169751645 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr6:170554265-170554388 | Common:1; Rare:40 | ||||
| chr7:727247-727293 | Rare:15; Clinvar:1 | ||||
| chr7:2242177-2242270 | Common:2; Rare:53 | ||||
| chr7:5513746-5513876 | Common:1; Rare:55 | ||||
| chr7:6009030-6009323 | Common:3; Rare:122; Clinvar:3; Clinvar (benign):13 | ||||
| chr7:10940121-10940200 | Rare:34 | ||||
| chr7:20331739-20331778 | Common:1; Rare:13 | ||||
| chr7:22822769-22822969 | Common:3; Rare:76 | ||||
| chr7:23105685-23105809 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:23531962-23532085 | Rare:49 |