| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46698590-46699001 | Common:4; Rare:114 | ||||
| chr2:46699235-46699445 | Common:2; Rare:57 | ||||
| chr2:46915759-46916193 | Common:4; Rare:138; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:46941060-46941377 | Common:1; Rare:116 | ||||
| chr2:46941469-46941908 | Common:5; Rare:148; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:46942220-46942574 | Common:4; Rare:84 | ||||
| chr2:46977987-46978230 | Common:1; Rare:39 | ||||
| chr2:47175542-47176089 | Common:7; Rare:196 | ||||
| chr2:47176354-47176607 | Rare:161; Clinvar (benign):5 | ||||
| chr2:47176761-47177093 | Common:4; Rare:122 | ||||
| chr2:47402794-47403230 | Common:1; Rare:197; Clinvar:59; Clinvar (benign):34; Clinvar (pathogenic):1 | ||||
| chr2:47403358-47403532 | Common:2; Rare:76; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr2:47782678-47783249 | Common:4; Rare:230; Clinvar:9; Clinvar (benign):22; Clinvar (pathogenic):2 | ||||
| chr2:47905284-47905528 | Common:2; Rare:96 | ||||
| chr2:47905665-47906185 | Common:1; Rare:205 |