Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100132674-100132813 | Common:1; Rare:40 | ||||
chr1:100132823-100133249 | Common:3; Rare:171 | ||||
chr1:100249555-100249610 | Common:1; Rare:15 | ||||
chr1:100249613-100250022 | Common:4; Rare:123; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:100265657-100265839 | Common:2; Rare:33 | ||||
chr1:100266083-100266344 | Common:3; Rare:95 | ||||
chr1:100266624-100266633 | Rare:3 | ||||
chr1:100266690-100266771 | Rare:11 | ||||
chr1:100351300-100351446 | Rare:32 | ||||
chr1:100351501-100351828 | Common:3; Rare:100 | ||||
chr1:100352154-100352731 | Common:3; Rare:124 | ||||
chr1:100352832-100352962 | Common:1; Rare:43; Clinvar (benign):2 | ||||
chr1:100894629-100895027 | Common:2; Rare:91 | ||||
chr1:100895113-100895466 | Common:2; Rare:68 | ||||
chr1:100895682-100895760 | Rare:16 |