Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74553054-74553173 | Common:1; Rare:25 | ||||
chr2:74833915-74834148 | Rare:68 | ||||
chr2:74835131-74835324 | Rare:49 | ||||
chr2:74958821-74959079 | Rare:92 | ||||
chr2:75710675-75710775 | Common:1; Rare:39 | ||||
chr2:84459184-84459587 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:84905527-84905738 | Common:1; Rare:61 | ||||
chr2:85354524-85354784 | Common:1; Rare:84 | ||||
chr2:85538971-85539365 | Common:3; Rare:184; Clinvar (benign):7 | ||||
chr2:85561424-85561590 | Rare:62; Clinvar:4 | ||||
chr2:85595565-85595769 | Common:1; Rare:66 | ||||
chr2:85602620-85602909 | Rare:75 | ||||
chr2:85612030-85612103 | Rare:19 | ||||
chr2:86105790-86106244 | Common:2; Rare:133 | ||||
chr2:86195360-86195627 | Common:5; Rare:90 |