| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57797931-57798215 | Rare:100 | ||||
| chr16:57803010-57803264 | Common:1; Rare:40 | ||||
| chr16:57999552-57999603 | Rare:8 | ||||
| chr16:58000596-58000785 | Common:2; Rare:47 | ||||
| chr16:58001318-58001466 | Rare:44 | ||||
| chr16:58025461-58025833 | Rare:118 | ||||
| chr16:58129160-58129230 | Common:3; Rare:16 | ||||
| chr16:58129268-58129576 | Common:4; Rare:99 | ||||
| chr16:58198086-58198149 | Rare:35 | ||||
| chr16:58514781-58514984 | Common:1; Rare:25 | ||||
| chr16:58515150-58515543 | Common:5; Rare:103 | ||||
| chr16:58733646-58733931 | Common:4; Rare:56 | ||||
| chr16:66549807-66550015 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66550327-66550656 | Common:1; Rare:55 | ||||
| chr16:66552480-66552656 | Rare:73 |