| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29663173-29663265 | Rare:14 | ||||
| chr16:29790550-29790804 | Common:1; Rare:104; Clinvar (benign):2 | ||||
| chr16:29807896-29808289 | Rare:207 | ||||
| chr16:29816018-29816230 | Common:1; Rare:58 | ||||
| chr16:29863211-29863578 | Common:1; Rare:96 | ||||
| chr16:29926216-29926339 | Common:3; Rare:44 | ||||
| chr16:29962775-29962869 | Common:1; Rare:17 | ||||
| chr16:29973790-29973918 | Common:1; Rare:56 | ||||
| chr16:29995596-29995719 | Rare:56 | ||||
| chr16:29996070-29996317 | Common:2; Rare:91 | ||||
| chr16:30064339-30064480 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr16:30065581-30065923 | Rare:115 | ||||
| chr16:30069474-30070166 | Common:3; Rare:262; Clinvar:6; Clinvar (benign):13 | ||||
| chr16:30075894-30076091 | Common:1; Rare:66 | ||||
| chr16:30091908-30092108 | Common:1; Rare:47 |