| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:10940683-10940744 | Common:1; Rare:15 | ||||
| chr16:30634303-30634553 | Common:1; Rare:67 | ||||
| chr16:30875331-30875465 | Rare:43 | ||||
| chr16:72665001-72665145 | Rare:37 | ||||
| chr16:74368127-74368376 | Common:1; Rare:69 | ||||
| chr16:79770544-79770758 | Common:5; Rare:93 | ||||
| chr16:88896862-88897043 | Common:4; Rare:54 | ||||
| chr17:7006321-7006510 | Rare:53 | ||||
| chr17:10406017-10406394 | Common:1; Rare:102; Clinvar (benign):2 | ||||
| chr17:10406688-10406976 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:10415118-10415350 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr17:10533363-10533603 | Rare:66; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:10631606-10632018 | Common:2; Rare:140; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:10638871-10639192 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:10641086-10641329 | Common:2; Rare:59; Clinvar (benign):3 |