| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:100893803-100894090 | Common:1; Rare:58 | ||||
| chr15:100910104-100910408 | Common:3; Rare:35 | ||||
| chr15:100911827-100912200 | Common:2; Rare:51 | ||||
| chr15:100913556-100913745 | Rare:37 | ||||
| chr15:101359659-101359888 | Common:1; Rare:49 | ||||
| chr16:192323-192494 | Common:1; Rare:41 | ||||
| chr16:399437-399662 | Common:4; Rare:84 | ||||
| chr16:634744-635021 | Rare:106 | ||||
| chr16:1362870-1363172 | Rare:146; Clinvar:8; Clinvar (pathogenic):1 | ||||
| chr16:1939102-1939349 | Common:1; Rare:78 | ||||
| chr16:1978350-1978657 | Common:1; Rare:144 | ||||
| chr16:2515060-2515096 | Rare:5 | ||||
| chr16:2516125-2516402 | Common:1; Rare:62 | ||||
| chr16:2746842-2746941 | Common:1; Rare:21 | ||||
| chr16:2755227-2755534 | Common:1; Rare:93 |