Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:135531181-135531481 | Common:1; Rare:55 | ||||
chr2:137964132-137964315 | Rare:25 | ||||
chr2:148020678-148021097 | Common:2; Rare:98; Clinvar (benign):2 | ||||
chr2:148021493-148021673 | Rare:39 | ||||
chr2:152717831-152717958 | Rare:52 | ||||
chr2:152717982-152718012 | Rare:9 | ||||
chr2:159712308-159712534 | Common:3; Rare:85 | ||||
chr2:162073380-162073419 | Common:1; Rare:8 | ||||
chr2:162073550-162073690 | Rare:34 | ||||
chr2:162074032-162074238 | Common:1; Rare:51 | ||||
chr2:162318644-162318804 | Rare:30 | ||||
chr2:171433982-171434234 | Common:2; Rare:65 | ||||
chr2:171687597-171687799 | Rare:54 | ||||
chr2:171688104-171688136 | Rare:9 | ||||
chr2:174395617-174395810 | Common:2; Rare:60 |