| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:25111480-25111758 | Common:2; Rare:65 | ||||
| chr16:27268724-27268850 | Common:1; Rare:39 | ||||
| chr16:27549897-27550158 | Common:2; Rare:91 | ||||
| chr16:29961955-29962122 | Common:1; Rare:49 | ||||
| chr16:29995608-29995735 | Rare:56 | ||||
| chr16:29996081-29996289 | Common:2; Rare:73 | ||||
| chr16:30065475-30065850 | Rare:127 | ||||
| chr16:30075900-30076042 | Rare:49 | ||||
| chr16:30762088-30762325 | Common:3; Rare:85 | ||||
| chr16:31033273-31033581 | Common:2; Rare:99 | ||||
| chr16:31180041-31180141 | Common:1; Rare:54 | ||||
| chr16:31472133-31472181 | Rare:12 | ||||
| chr16:46689141-46689416 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:47461043-47461343 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr16:53703828-53704167 | Rare:96; Clinvar:3 |