| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:170714320-170715050 | Common:6; Rare:300 | ||||
| chr2:170715040-170715590 | Common:9; Rare:472 | ||||
| chr2:170816420-170817622 | Common:51; Rare:830; Clinvar:39; Clinvar (benign):9 | ||||
| chr2:170928032-170928484 | Common:2; Rare:133 | ||||
| chr2:170928834-170929382 | Common:33; Rare:911 | ||||
| chr2:170929463-170930141 | Common:10; Rare:359 | ||||
| chr2:171159137-171159557 | Rare:158 | ||||
| chr2:171159577-171159986 | Rare:693 | ||||
| chr2:171159910-171161690 | Common:68; Rare:2297 | ||||
| chr2:171432071-171433037 | Common:2; Rare:238 | ||||
| chr2:171433232-171433632 | Common:1; Rare:137 | ||||
| chr2:171433780-171434396 | Common:24; Rare:921; Clinvar:8 | ||||
| chr2:171434395-171435050 | Common:6; Rare:419; Clinvar:4 | ||||
| chr2:171521556-171521926 | Common:3; Rare:80 | ||||
| chr2:171521880-171523442 | Common:40; Rare:1282 |