Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:21002098-21002158 | Common:3; Rare:16 | ||||
chr22:24270660-24270950 | Common:3; Rare:109 | ||||
chr22:24555843-24556066 | Rare:68 | ||||
chr22:26483772-26484002 | Common:6; Rare:96; Clinvar:5; Clinvar (benign):1 | ||||
chr22:26512408-26512550 | Common:1; Rare:61 | ||||
chr22:27919195-27919520 | Common:5; Rare:145 | ||||
chr22:28741798-28742068 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr22:28800395-28800702 | Common:5; Rare:111 | ||||
chr22:29267919-29268339 | Common:2; Rare:121 | ||||
chr22:29767053-29767408 | Common:4; Rare:111 | ||||
chr22:30356844-30356985 | Common:1; Rare:51 | ||||
chr22:30606988-30607236 | Common:3; Rare:75; Clinvar:3; Clinvar (benign):3 | ||||
chr22:31081057-31081351 | Common:1; Rare:77 | ||||
chr22:31093180-31093415 | Common:1; Rare:46 | ||||
chr22:31107497-31107661 | Common:2; Rare:55 |