| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:170816510-170817030 | Common:10; Rare:252; Clinvar:20; Clinvar (benign):6 | ||||
| chr2:170817050-170817450 | Common:13; Rare:121 | ||||
| chr2:170928070-170928400 | Common:1; Rare:51 | ||||
| chr2:170928808-170929404 | Common:16; Rare:448 | ||||
| chr2:171159769-171160141 | Rare:138 | ||||
| chr2:171160251-171161282 | Common:23; Rare:876 | ||||
| chr2:171433870-171434370 | Common:9; Rare:346 | ||||
| chr2:171434494-171434880 | Common:1; Rare:233; Clinvar:2 | ||||
| chr2:171522274-171522537 | Common:3; Rare:64 | ||||
| chr2:171523326-171523576 | Common:1; Rare:55 | ||||
| chr2:171687151-171687951 | Common:4; Rare:367 | ||||
| chr2:171894203-171894542 | Common:2; Rare:291; Clinvar:5 | ||||
| chr2:171922224-171922581 | Rare:303 | ||||
| chr2:171999320-171999720 | Common:2; Rare:107 | ||||
| chr2:171999751-172000122 | Common:6; Rare:281 |