| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28985016-28985235 | Common:1; Rare:60 | ||||
| chr16:29454159-29454567 | |||||
| chr16:29745955-29746059 | Rare:27 | ||||
| chr16:29790550-29790796 | Common:1; Rare:104; Clinvar (benign):2 | ||||
| chr16:29805494-29805700 | Common:2; Rare:92 | ||||
| chr16:29807928-29808165 | Rare:137 | ||||
| chr16:29815993-29816230 | Common:1; Rare:68 | ||||
| chr16:29816301-29816539 | Common:1; Rare:75 | ||||
| chr16:29961971-29962141 | Common:1; Rare:49 | ||||
| chr16:29995601-29995708 | Rare:47 | ||||
| chr16:29996072-29996313 | Common:2; Rare:88 | ||||
| chr16:30065298-30065897 | Rare:184 | ||||
| chr16:30069502-30069993 | Common:1; Rare:185; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:30075883-30076059 | Common:1; Rare:59 | ||||
| chr16:30091908-30092149 | Common:1; Rare:57 |