| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46073692-46073873 | Rare:33 | ||||
| chr2:46297049-46297353 | Common:6; Rare:127 | ||||
| chr2:46355987-46356290 | Common:14; Rare:101; Clinvar:2; Clinvar (benign):7 | ||||
| chr2:46375464-46375775 | Common:2; Rare:82 | ||||
| chr2:46379997-46380281 | Common:1; Rare:75; Clinvar (pathogenic):1 | ||||
| chr2:46543113-46543185 | Rare:17 | ||||
| chr2:46543285-46543438 | Rare:34 | ||||
| chr2:46544043-46544248 | Rare:63 | ||||
| chr2:46617012-46617262 | Common:7; Rare:109 | ||||
| chr2:46915722-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916025-46916189 | Common:2; Rare:51 | ||||
| chr2:46941652-46941792 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:47176416-47176888 | Common:4; Rare:218; Clinvar (benign):5 | ||||
| chr2:47402951-47403183 | Common:1; Rare:103; Clinvar:30; Clinvar (benign):24 | ||||
| chr2:47782859-47783189 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):5 |