| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:72093587-72093934 | Rare:86 | ||||
| chr16:74296460-74296909 | Common:1; Rare:149 | ||||
| chr16:74607070-74607206 | Rare:72 | ||||
| chr16:74666868-74667088 | Common:1; Rare:72 | ||||
| chr16:75433413-75433806 | Common:4; Rare:119 | ||||
| chr16:75556214-75556369 | Common:1; Rare:56; Clinvar (benign):3 | ||||
| chr16:75623222-75623370 | Common:3; Rare:53 | ||||
| chr16:75647614-75647822 | Common:2; Rare:102; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648622-75648650 | Rare:13 | ||||
| chr16:77190696-77191010 | Common:10; Rare:103 | ||||
| chr16:77191151-77191224 | Common:1; Rare:34 | ||||
| chr16:79600723-79600958 | Common:1; Rare:66 | ||||
| chr16:80540947-80541051 | Common:2; Rare:44 | ||||
| chr16:81006798-81007264 | Common:5; Rare:158 | ||||
| chr16:81077226-81077345 | Common:1; Rare:58 |