| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:10940683-10940744 | Not yet | Common:1; Rare:15 | 109 | ||
| chr16:30634303-30634553 | Not yet | Common:1; Rare:67 | 313 | ||
| chr16:30875331-30875465 | Not yet | Rare:43 | 179 | ||
| chr16:72665001-72665145 | Not yet | Rare:37 | 201 | ||
| chr16:74368127-74368376 | Not yet | Common:1; Rare:69 | 257 | ||
| chr16:79770544-79770758 | Not yet | Common:5; Rare:93 | 216 | ||
| chr16:88896862-88897043 | Not yet | Common:4; Rare:54 | 239 | ||
| chr17:7006321-7006510 | Not yet | Rare:53 | 251 | ||
| chr17:10406017-10406394 | Not yet | Common:1; Rare:102; Clinvar (benign):2 | 411 | ||
| chr17:10406688-10406976 | Not yet | Common:2; Rare:91; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | 414 | ||
| chr17:10415118-10415350 | Not yet | Common:1; Rare:45; Clinvar (benign):1 | 346 | ||
| chr17:10533363-10533603 | Not yet | Rare:66; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | 295 | ||
| chr17:10631606-10632018 | Not yet | Common:2; Rare:140; Clinvar:3; Clinvar (benign):4 | 324 | ||
| chr17:10638871-10639192 | Not yet | Common:1; Rare:75; Clinvar:3; Clinvar (benign):1 | 326 | ||
| chr17:10641086-10641329 | Not yet | Common:2; Rare:59; Clinvar (benign):3 | 356 |