| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29666479-29666622 | Common:16; Rare:76 | ||||
| chr16:29666663-29667106 | Common:1; Rare:89 | ||||
| chr16:29676145-29676365 | Common:1; Rare:48 | ||||
| chr16:29804624-29805024 | Common:2; Rare:208; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:29812828-29813886 | Common:2; Rare:413; Clinvar:31; Clinvar (benign):36; Clinvar (pathogenic):12 | ||||
| chr16:29814941-29815341 | Common:2; Rare:110 | ||||
| chr16:30335314-30335539 | Common:2; Rare:82 | ||||
| chr16:30393963-30394363 | Common:2; Rare:111 | ||||
| chr16:30400172-30400464 | Rare:72 | ||||
| chr16:30400550-30400861 | Rare:73 | ||||
| chr16:30634228-30634612 | Common:2; Rare:95 | ||||
| chr16:30659033-30659149 | Rare:39 | ||||
| chr16:30775364-30775622 | Common:2; Rare:75 | ||||
| chr16:30778663-30779063 | Rare:104 | ||||
| chr16:30805455-30805636 | Rare:51 |