| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:98650695-98650841 | Rare:43 | ||||
| chr15:98722525-98722835 | Common:1; Rare:43 | ||||
| chr15:98899613-98899938 | Common:2; Rare:93; Clinvar:1 | ||||
| chr15:101057852-101058076 | Common:1; Rare:56 | ||||
| chr15:101167897-101168107 | Common:3; Rare:49 | ||||
| chr15:101201805-101201994 | Rare:26 | ||||
| chr15:101300889-101301008 | Common:1; Rare:18 | ||||
| chr15:101331649-101331954 | Common:6; Rare:75 | ||||
| chr15:101488225-101488502 | Common:3; Rare:60 | ||||
| chr15:101961526-101961630 | Rare:3 | ||||
| chr16:89791-90090 | Rare:89; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:374041-374293 | Common:2; Rare:111 | ||||
| chr16:871291-871598 | Common:2; Rare:112 | ||||
| chr16:1361688-1361931 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:1362060-1362251 | Rare:84; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 |