| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:101681004-101681156 | Common:2; Rare:35 | ||||
| chr3:107240606-107240729 | Rare:53 | ||||
| chr3:112640384-112640429 | Rare:7 | ||||
| chr3:150408864-150408992 | Rare:38 | ||||
| chr3:157174923-157175225 | Common:3; Rare:131 | ||||
| chr3:169765038-169765222 | Rare:77; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:183447477-183447674 | Common:1; Rare:50 | ||||
| chr3:194583790-194584026 | Common:11; Rare:79 | ||||
| chr3:195657937-195658102 | Common:9; Rare:28 | ||||
| chr3:195990254-195990434 | Rare:23 | ||||
| chr3:197627843-197628011 | Common:6; Rare:61 | ||||
| chr4:6673869-6673946 | Common:6; Rare:42 | ||||
| chr4:52712223-52712510 | Common:4; Rare:74 | ||||
| chr4:54231870-54231985 | Common:1; Rare:26 | ||||
| chr4:76306533-76306655 | Rare:32 |