Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113102990-113103510 | Common:10; Rare:78 | ||||
chr1:113389923-113390600 | Common:6; Rare:383 | ||||
chr1:113391040-113391188 | Rare:50 | ||||
chr1:113391487-113392060 | Common:3; Rare:140 | ||||
chr1:113758687-113759044 | Common:3; Rare:128 | ||||
chr1:113759339-113759686 | Common:9; Rare:205 | ||||
chr1:113759813-113760168 | Rare:75 | ||||
chr1:113812150-113812909 | Common:9; Rare:644 | ||||
chr1:113899536-113900260 | Common:7; Rare:419; Clinvar:15; Clinvar (benign):4 | ||||
chr1:113901261-113902192 | Common:5; Rare:427; Clinvar:4; Clinvar (benign):4 | ||||
chr1:113904592-113905578 | Common:21; Rare:721; Clinvar:1; Clinvar (benign):6 | ||||
chr1:113905629-113905913 | Common:1; Rare:121; Clinvar:4 | ||||
chr1:113929229-113929366 | Common:1; Rare:32 | ||||
chr1:113929380-113929939 | Common:10; Rare:348 | ||||
chr1:113930006-113930406 | Common:2; Rare:274 |