| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:47477680-47477981 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:49463178-49463376 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420041-52420314 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576950-52577307 | Common:7; Rare:124 | ||||
| chr6:52671049-52671163 | Rare:32 | ||||
| chr6:52995273-52995823 | Common:4; Rare:226 | ||||
| chr6:56542744-56543131 | Common:2; Rare:68 | ||||
| chr6:57172542-57172783 | Common:1; Rare:79 | ||||
| chr6:63572312-63572540 | Rare:89 | ||||
| chr6:63635680-63635906 | Rare:91 | ||||
| chr6:68634970-68635361 | Common:2; Rare:108 | ||||
| chr6:69796877-69797182 | Common:1; Rare:88; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:71288306-71288466 | Common:2; Rare:32 | ||||
| chr6:73263158-73263273 | Common:3; Rare:28 | ||||
| chr6:73452273-73452411 | Common:1; Rare:21 |