Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244451946-244452032 | Rare:19 | ||||
chr1:244835142-244835333 | Rare:77 | ||||
chr1:244835562-244835736 | Common:2; Rare:74; Clinvar (benign):4 | ||||
chr1:244856475-244856884 | Common:1; Rare:81; Clinvar (benign):2 | ||||
chr1:244864356-244864677 | Rare:119 | ||||
chr1:244970044-244970420 | Common:5; Rare:160 | ||||
chr1:246566189-246566593 | Common:2; Rare:129 | ||||
chr1:247104324-247104570 | Common:2; Rare:70 | ||||
chr1:247331736-247331844 | Rare:36 | ||||
chr1:248825852-248825953 | Common:2; Rare:21 | ||||
chr1:248838052-248838469 | Common:3; Rare:133 | ||||
chr1:248838764-248839045 | Common:2; Rare:58 | ||||
chr1:248858924-248858959 | Rare:7 | ||||
chr10:650091-650126 | Rare:9 | ||||
chr10:931698-931994 | Rare:95 |