| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44941786-44941855 | Common:1; Rare:21 | ||||
| chr2:44941880-44941936 | Rare:10 | ||||
| chr2:44942121-44942410 | Common:1; Rare:101; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:46297168-46297431 | Common:4; Rare:101 | ||||
| chr2:46616978-46617281 | Common:7; Rare:129 | ||||
| chr2:46698749-46698921 | Rare:50 | ||||
| chr2:46915721-46915964 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916024-46916175 | Common:2; Rare:51 | ||||
| chr2:46941717-46941806 | Common:2; Rare:29 | ||||
| chr2:47176430-47176952 | Common:7; Rare:240; Clinvar (benign):5 | ||||
| chr2:47344993-47345203 | Common:1; Rare:58 | ||||
| chr2:47402935-47403224 | Common:1; Rare:137; Clinvar:48; Clinvar (benign):33; Clinvar (pathogenic):1 | ||||
| chr2:47782956-47783189 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:47905489-47905828 | Common:3; Rare:165 | ||||
| chr2:48314158-48314783 | Common:1; Rare:214 |