Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593109-63593457 | Rare:111; Clinvar (benign):1 | ||||
chr1:63593469-63593689 | Rare:102; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:64841297-64841529 | Rare:53; Clinvar:1 | ||||
chr1:66924835-66925046 | Rare:86 | ||||
chr1:66925194-66925503 | Common:2; Rare:97 | ||||
chr1:67054083-67054432 | Common:5; Rare:69 | ||||
chr1:67429989-67430472 | Rare:184 | ||||
chr1:67684994-67685177 | Rare:42 | ||||
chr1:67833335-67833508 | Common:2; Rare:70 | ||||
chr1:70205518-70205770 | Rare:89 | ||||
chr1:70221311-70221614 | Rare:119 | ||||
chr1:70354634-70354862 | Rare:75 | ||||
chr1:70411069-70411279 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080945-71081387 | Rare:120 | ||||
chr1:74198139-74198338 | Common:2; Rare:112 |