Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2412445-2412858 | Common:4; Rare:456; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
chr1:2413035-2414022 | Common:2; Rare:362 | ||||
chr1:2524988-2525743 | Common:6; Rare:258 | ||||
chr1:2526100-2526500 | Common:3; Rare:252 | ||||
chr1:2586310-2586918 | Common:9; Rare:378 | ||||
chr1:2592808-2593088 | Common:6; Rare:262 | ||||
chr1:3068810-3069280 | Common:7; Rare:242; Clinvar (benign):4 | ||||
chr1:3069376-3070090 | Common:5; Rare:345 | ||||
chr1:3454400-3454759 | Common:2; Rare:245 | ||||
chr1:3494710-3495050 | Common:8; Rare:76 | ||||
chr1:3531270-3531684 | Common:8; Rare:272 | ||||
chr1:3611440-3611783 | Common:5; Rare:72 | ||||
chr1:3624668-3625118 | Common:3; Rare:359 | ||||
chr1:3649929-3650241 | Common:14; Rare:223 | ||||
chr1:3652010-3652613 | Common:3; Rare:285 |