| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29790442-29790794 | Common:2; Rare:127; Clinvar (benign):2 | ||||
| chr16:29805479-29805702 | Common:2; Rare:104 | ||||
| chr16:29807928-29808165 | Rare:137 | ||||
| chr16:29816018-29816311 | Common:1; Rare:85 | ||||
| chr16:29816377-29816597 | Rare:79 | ||||
| chr16:29926216-29926321 | Common:2; Rare:37 | ||||
| chr16:29961942-29962165 | Common:1; Rare:73 | ||||
| chr16:29973685-29973931 | Common:3; Rare:95 | ||||
| chr16:29985118-29985298 | Rare:40 | ||||
| chr16:29995601-29995735 | Rare:59 | ||||
| chr16:29996069-29996317 | Common:2; Rare:91 | ||||
| chr16:30053038-30053163 | Common:1; Rare:44 | ||||
| chr16:30063887-30064502 | Common:1; Rare:118; Clinvar (benign):1 | ||||
| chr16:30065524-30065946 | Rare:144 | ||||
| chr16:30075894-30076049 | Rare:53 |