Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:8390048-8390416 | Common:1; Rare:105 | ||||
chr19:11197524-11197616 | Rare:24 | ||||
chr19:18919349-18919739 | Common:2; Rare:137 | ||||
chr19:39391125-39391416 | Common:1; Rare:120 | ||||
chr19:43670151-43670369 | Common:2; Rare:51 | ||||
chr19:54115655-54115787 | Common:1; Rare:27; Clinvar:4 | ||||
chr19:58098216-58098432 | Common:8; Rare:79 | ||||
chr2:9423481-9423663 | Rare:55 | ||||
chr2:27370330-27370632 | Common:1; Rare:118 | ||||
chr2:38076149-38076255 | Rare:26 | ||||
chr2:43226604-43226816 | Common:1; Rare:78 | ||||
chr2:74529659-74530044 | Rare:116; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74958878-74959073 | Rare:68 | ||||
chr2:96265958-96266270 | Common:2; Rare:91; Clinvar:1 | ||||
chr2:98608453-98608589 | Common:1; Rare:59 |