| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388578-176388758 | Common:1; Rare:54 | ||||
| chr5:177022631-177022741 | Rare:42 | ||||
| chr5:177303667-177303843 | Common:4; Rare:88 | ||||
| chr5:177460489-177460653 | Rare:46 | ||||
| chr5:177516925-177517055 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr5:179806848-179807063 | Common:3; Rare:82 | ||||
| chr5:180810102-180810289 | Common:5; Rare:56 | ||||
| chr6:693083-693159 | Rare:30 | ||||
| chr6:3456046-3456181 | Rare:45 | ||||
| chr6:5003609-5003825 | Common:6; Rare:63 | ||||
| chr6:5260700-5261032 | Common:5; Rare:110; Clinvar (benign):3 | ||||
| chr6:5261250-5261603 | Common:9; Rare:100 | ||||
| chr6:8435411-8435632 | Common:3; Rare:78 | ||||
| chr6:11094107-11094260 | Rare:45 | ||||
| chr6:13615160-13615497 | Common:3; Rare:138 |