| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30650234-30650270 | Rare:4 | ||||
| chr16:30650436-30650786 | Rare:65 | ||||
| chr16:30650932-30651071 | Rare:47 | ||||
| chr16:30651322-30651683 | Rare:90 | ||||
| chr16:30657814-30658019 | Common:2; Rare:50 | ||||
| chr16:30658121-30658478 | Rare:77 | ||||
| chr16:30658560-30658866 | Common:1; Rare:93 | ||||
| chr16:30660050-30660374 | Common:3; Rare:84 | ||||
| chr16:30697964-30698301 | Common:1; Rare:147 | ||||
| chr16:30698373-30698678 | Common:1; Rare:121 | ||||
| chr16:30698900-30699186 | Rare:111; Clinvar (benign):1 | ||||
| chr16:30748062-30748516 | Common:2; Rare:124; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:30748766-30748823 | Rare:23 | ||||
| chr16:30761373-30761645 | Rare:105 | ||||
| chr16:30762014-30762387 | Common:3; Rare:120 |