| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58000591-58000872 | Common:2; Rare:70 | ||||
| chr16:58001169-58001633 | Common:2; Rare:131; Clinvar (benign):1 | ||||
| chr16:58001645-58001765 | Common:1; Rare:28 | ||||
| chr16:58128734-58128926 | Common:1; Rare:41 | ||||
| chr16:58129198-58129789 | Common:8; Rare:190 | ||||
| chr16:58198026-58198396 | Common:3; Rare:120 | ||||
| chr16:58249713-58250037 | Rare:83 | ||||
| chr16:58392305-58392595 | Common:3; Rare:86 | ||||
| chr16:58392706-58392914 | Common:2; Rare:65 | ||||
| chr16:58499896-58500147 | Common:2; Rare:40 | ||||
| chr16:58515347-58515735 | Common:5; Rare:150 | ||||
| chr16:58516047-58516258 | Common:9; Rare:105; Clinvar:1 | ||||
| chr16:58518111-58518344 | Common:1; Rare:89 | ||||
| chr16:58629497-58629607 | Rare:20 | ||||
| chr16:58629751-58630241 | Common:3; Rare:136 |