| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15747568-15747866 | Rare:72; Clinvar:7; Clinvar (benign):2 | ||||
| chr16:15748048-15748261 | Common:2; Rare:48; Clinvar:7; Clinvar (benign):6 | ||||
| chr16:15750289-15750416 | Rare:32; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:15759586-15759834 | Common:1; Rare:64; Clinvar:5; Clinvar (benign):6 | ||||
| chr16:17134639-17134899 | Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:17383117-17383223 | Common:1; Rare:14 | ||||
| chr16:21501894-21502112 | Common:2; Rare:41 | ||||
| chr16:21502116-21502122 | |||||
| chr16:21520385-21520563 | Common:1; Rare:18 | ||||
| chr16:21600526-21600641 | Rare:17 | ||||
| chr16:21820388-21820488 | Rare:24 | ||||
| chr16:22195794-22195917 | Common:4; Rare:63 | ||||
| chr16:23665427-23665718 | Common:2; Rare:65 | ||||
| chr16:23950627-23950840 | Rare:36 | ||||
| chr16:24968391-24968729 | Rare:84 |