Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32816595-32816995 | Common:6; Rare:186 | ||||
chr1:32817200-32817837 | Common:4; Rare:890; Clinvar:35; Clinvar (benign):11 | ||||
chr1:32817840-32818860 | Common:12; Rare:609; Clinvar:6; Clinvar (benign):6 | ||||
chr1:32870840-32871230 | Common:1; Rare:102 | ||||
chr1:32901250-32901721 | Common:5; Rare:225 | ||||
chr1:32964387-32965161 | Common:15; Rare:719 | ||||
chr1:33013230-33013600 | Common:9; Rare:105; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:33021580-33021880 | Rare:76; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:33035961-33036361 | Common:3; Rare:63 | ||||
chr1:33036430-33036830 | Common:4; Rare:106; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:33036777-33037248 | Rare:566; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:33080910-33081280 | Common:13; Rare:308 | ||||
chr1:33181942-33182342 | Common:1; Rare:163 | ||||
chr1:33256201-33256624 | Common:2; Rare:178 | ||||
chr1:33349490-33350166 | Common:11; Rare:984 |