Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:132687322-132687467 | Rare:57; Clinvar:2; Clinvar (benign):8 | ||||
chr12:132710722-132711042 | Common:4; Rare:109 | ||||
chr12:132829064-132829211 | Rare:74 | ||||
chr12:132887551-132887798 | Rare:74 | ||||
chr12:132956252-132956431 | Common:1; Rare:38 | ||||
chr12:132986278-132986421 | Rare:30 | ||||
chr12:133130238-133130659 | Common:7; Rare:142 | ||||
chr13:19633403-19633811 | Common:3; Rare:154 | ||||
chr13:19863441-19863944 | Common:6; Rare:180 | ||||
chr13:20525766-20525936 | Common:1; Rare:68 | ||||
chr13:20567044-20567202 | Common:1; Rare:52 | ||||
chr13:21061507-21061682 | Common:1; Rare:57 | ||||
chr13:21140304-21140651 | Rare:145 | ||||
chr13:21176557-21176711 | Rare:80 | ||||
chr13:21670975-21671162 | Rare:72; Clinvar:1; Clinvar (benign):1 |