| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169701958-169702174 | Common:2; Rare:102 | ||||
| chr6:169751526-169751660 | Rare:51; Clinvar (benign):2 | ||||
| chr6:170306548-170306820 | Common:2; Rare:88 | ||||
| chr6:170554211-170554416 | Common:1; Rare:65 | ||||
| chr7:519135-519312 | Rare:46 | ||||
| chr7:727261-727281 | Rare:5; Clinvar:1 | ||||
| chr7:945790-945825 | Rare:6 | ||||
| chr7:1028307-1028474 | Rare:59 | ||||
| chr7:1044354-1044611 | Common:6; Rare:95 | ||||
| chr7:1055106-1055382 | Common:1; Rare:94 | ||||
| chr7:1138216-1138461 | Common:2; Rare:74 | ||||
| chr7:1537309-1537483 | Rare:59 | ||||
| chr7:1570018-1570146 | Common:1; Rare:43 | ||||
| chr7:2242168-2242270 | Common:2; Rare:61 | ||||
| chr7:4775383-4775652 | Common:7; Rare:120; Clinvar:1 |