Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:148020693-148021106 | Common:2; Rare:94; Clinvar (benign):2 | ||||
chr2:148021493-148021632 | Rare:33 | ||||
chr2:149587310-149587365 | Rare:10 | ||||
chr2:149587685-149587823 | Common:1; Rare:39; Clinvar:1 | ||||
chr2:151261799-151261975 | Common:2; Rare:40 | ||||
chr2:151409793-151409920 | Common:1; Rare:28 | ||||
chr2:152717867-152718050 | Rare:67 | ||||
chr2:152718473-152718904 | Common:1; Rare:215; Clinvar:1 | ||||
chr2:159712404-159712546 | Common:2; Rare:62 | ||||
chr2:162073245-162073468 | Common:2; Rare:51 | ||||
chr2:162073481-162073542 | Rare:24 | ||||
chr2:162073550-162073690 | Rare:34 | ||||
chr2:162074000-162074271 | Common:1; Rare:68 | ||||
chr2:162318650-162318804 | Rare:29 | ||||
chr2:169584709-169584817 | Rare:29 |