| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58000562-58000903 | Common:2; Rare:78 | ||||
| chr16:58001167-58001633 | Common:2; Rare:131; Clinvar (benign):1 | ||||
| chr16:58001645-58001813 | Common:3; Rare:36 | ||||
| chr16:58025431-58025800 | Rare:113 | ||||
| chr16:58128765-58128904 | Common:1; Rare:29 | ||||
| chr16:58129218-58129796 | Common:8; Rare:188 | ||||
| chr16:58198061-58198399 | Common:3; Rare:110 | ||||
| chr16:58249830-58250084 | Rare:71 | ||||
| chr16:58392309-58392551 | Common:3; Rare:67 | ||||
| chr16:58392684-58392941 | Common:2; Rare:81 | ||||
| chr16:58515342-58515590 | Common:4; Rare:104 | ||||
| chr16:58516033-58516242 | Common:9; Rare:104; Clinvar:1 | ||||
| chr16:58629039-58629379 | Common:2; Rare:90 | ||||
| chr16:58684644-58684853 | Common:1; Rare:53 | ||||
| chr16:58733593-58733870 | Common:4; Rare:57 |