| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29745930-29746117 | Rare:40 | ||||
| chr16:29790498-29790813 | Common:1; Rare:120; Clinvar (benign):2 | ||||
| chr16:29805482-29805710 | Common:2; Rare:108 | ||||
| chr16:29807744-29808144 | Common:2; Rare:212 | ||||
| chr16:29816018-29816366 | Common:2; Rare:100 | ||||
| chr16:29863180-29863549 | Common:1; Rare:98 | ||||
| chr16:29926004-29926316 | Common:2; Rare:116 | ||||
| chr16:29961989-29962165 | Common:1; Rare:57 | ||||
| chr16:29963229-29963466 | Common:2; Rare:86 | ||||
| chr16:29973610-29973931 | Common:5; Rare:110 | ||||
| chr16:29974365-29974632 | Common:2; Rare:49 | ||||
| chr16:29995445-29995713 | Common:1; Rare:122 | ||||
| chr16:29996070-29996394 | Common:2; Rare:124 | ||||
| chr16:30053019-30053197 | Common:1; Rare:66 | ||||
| chr16:30065560-30065921 | Rare:124 |