| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34684290-34684810 | Rare:85 | ||||
| chr5:34685931-34686129 | Common:2; Rare:23 | ||||
| chr5:34839082-34839448 | Common:3; Rare:119 | ||||
| chr5:34915438-34915758 | Common:1; Rare:85 | ||||
| chr5:34929214-34929541 | Common:2; Rare:69 | ||||
| chr5:34929730-34930150 | Common:3; Rare:126 | ||||
| chr5:35229750-35230526 | Common:15; Rare:192 | ||||
| chr5:35617680-35617950 | Common:1; Rare:56 | ||||
| chr5:36151874-36152146 | Rare:77 | ||||
| chr5:36240912-36241100 | Rare:47 | ||||
| chr5:36241111-36241353 | Common:2; Rare:54 | ||||
| chr5:36241629-36242458 | Common:8; Rare:252; Clinvar:1; Clinvar (benign):6 | ||||
| chr5:36606380-36606650 | Rare:45; Clinvar (benign):1 | ||||
| chr5:36606859-36607004 | Rare:19 | ||||
| chr5:36607256-36607972 | Common:8; Rare:148 |