Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:144517337-144517585 | Rare:73; Clinvar:3; Clinvar (benign):4 | ||||
chr2:144518420-144518499 | Rare:18 | ||||
chr2:148020681-148021109 | Common:2; Rare:99; Clinvar (benign):2 | ||||
chr2:149587681-149587904 | Common:1; Rare:66; Clinvar:1 | ||||
chr2:152175699-152176043 | Common:1; Rare:93 | ||||
chr2:152717829-152717964 | Rare:56 | ||||
chr2:152718478-152718660 | Rare:74 | ||||
chr2:159712382-159712574 | Common:2; Rare:79 | ||||
chr2:161136785-161136981 | Rare:26 | ||||
chr2:161308376-161308539 | Common:2; Rare:41 | ||||
chr2:169584716-169584809 | Rare:24 | ||||
chr2:169694376-169694517 | Common:4; Rare:42 | ||||
chr2:169824846-169825022 | Common:2; Rare:55 | ||||
chr2:170928902-170929239 | Common:5; Rare:80 | ||||
chr2:171433940-171434234 | Common:3; Rare:77 |