Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:237280113-237280531 | Common:2; Rare:84 | ||||
chr2:237324878-237325096 | Common:2; Rare:44 | ||||
chr2:237327861-237327899 | Rare:6 | ||||
chr2:237328943-237328992 | Rare:9 | ||||
chr2:237329137-237329314 | Common:2; Rare:32 | ||||
chr2:237331751-237331858 | Rare:7 | ||||
chr2:237335870-237336562 | Common:9; Rare:188; Clinvar:17; Clinvar (benign):16; Clinvar (pathogenic):1 | ||||
chr2:237341857-237342192 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:237350120-237350229 | Common:1; Rare:40; Clinvar:8; Clinvar (benign):3 | ||||
chr2:237360045-237360190 | Rare:37; Clinvar:5; Clinvar (benign):3 | ||||
chr2:237382809-237382947 | Rare:25 | ||||
chr2:237384747-237385066 | Common:3; Rare:56 | ||||
chr2:237385511-237385557 | Rare:7 | ||||
chr2:237386375-237386522 | Common:2; Rare:25 | ||||
chr2:237392352-237392580 | Common:2; Rare:40 |