| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:193554819-193555036 | Common:1; Rare:46 | ||||
| chr3:193593095-193593372 | Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486994-194487172 | Common:3; Rare:78 | ||||
| chr3:194632809-194632943 | Rare:19 | ||||
| chr3:194633564-194633704 | Rare:30 | ||||
| chr3:194633710-194633782 | Common:2; Rare:15 | ||||
| chr3:194652947-194653277 | Common:3; Rare:85 | ||||
| chr3:195543127-195543485 | Common:4; Rare:122 | ||||
| chr3:195720718-195721011 | Common:5; Rare:32 | ||||
| chr3:195753452-195753583 | Common:1; Rare:22 | ||||
| chr3:195754274-195754632 | Common:1; Rare:85 | ||||
| chr3:195811611-195811694 | Common:1; Rare:17 | ||||
| chr3:195811711-195812066 | Common:6; Rare:98 | ||||
| chr3:195876708-195876956 | Common:3; Rare:86 | ||||
| chr3:196082043-196082226 | Common:1; Rare:82 |