| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88663083-88663374 | Common:8; Rare:119 | ||||
| chr16:88706240-88706533 | Common:4; Rare:138 | ||||
| chr16:88811895-88812096 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr16:88856932-88857163 | Common:4; Rare:103; Clinvar (benign):2 | ||||
| chr16:89217619-89217772 | Common:1; Rare:78 | ||||
| chr16:89508290-89508485 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560520-89560764 | Rare:111 | ||||
| chr16:89657654-89658111 | Common:3; Rare:239 | ||||
| chr16:89686522-89686713 | Common:7; Rare:82 | ||||
| chr16:89686898-89686999 | Rare:45 | ||||
| chr16:89816607-89816739 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:89873490-89873662 | Common:1; Rare:83 | ||||
| chr16:89923171-89923348 | Rare:64 | ||||
| chr16:89948560-89948806 | Common:3; Rare:74 | ||||
| chr16:89972485-89972635 | Common:1; Rare:58 |