| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:162727009-162727166 | Common:1; Rare:36 | ||||
| chr6:162727737-162727974 | Rare:66; Clinvar:1 | ||||
| chr6:163415297-163415328 | Rare:7 | ||||
| chr6:166342513-166342659 | Common:3; Rare:58 | ||||
| chr6:166956220-166956367 | Rare:27; Clinvar:5 | ||||
| chr6:166999074-166999436 | Common:2; Rare:125 | ||||
| chr6:167826816-167827123 | Common:2; Rare:173 | ||||
| chr6:169751526-169751645 | Rare:42; Clinvar (benign):1 | ||||
| chr6:170554211-170554416 | Common:1; Rare:65 | ||||
| chr7:727246-727281 | Rare:13; Clinvar:1 | ||||
| chr7:1055312-1055372 | Rare:24 | ||||
| chr7:1537156-1537490 | Rare:108 | ||||
| chr7:1560800-1560890 | Common:2; Rare:26 | ||||
| chr7:1570012-1570151 | Common:1; Rare:45 | ||||
| chr7:2242174-2242268 | Common:2; Rare:55 |