| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:162727752-162727974 | Rare:59; Clinvar:1 | ||||
| chr6:163414644-163414815 | Rare:71 | ||||
| chr6:166342526-166342690 | Common:3; Rare:67 | ||||
| chr6:169701970-169702356 | Common:5; Rare:165 | ||||
| chr6:169751503-169751654 | Rare:60; Clinvar (benign):2 | ||||
| chr6:170306554-170306805 | Common:1; Rare:86 | ||||
| chr6:170553218-170553364 | Common:1; Rare:67 | ||||
| chr6:170584587-170584782 | Common:1; Rare:64 | ||||
| chr7:727236-727314 | Rare:26; Clinvar:1 | ||||
| chr7:876277-876657 | Common:8; Rare:166 | ||||
| chr7:1055314-1055360 | Rare:20 | ||||
| chr7:1138198-1138461 | Common:2; Rare:82 | ||||
| chr7:1504317-1504484 | Common:2; Rare:78 | ||||
| chr7:1569955-1570082 | Common:1; Rare:48 | ||||
| chr7:2242171-2242266 | Common:2; Rare:56 |