Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23778224-23778530 | Common:9; Rare:144 | ||||
chr1:23790998-23791258 | Rare:75 | ||||
chr1:23800651-23801056 | Common:1; Rare:134 | ||||
chr1:23825333-23825605 | Common:3; Rare:87; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:23868240-23868586 | Common:6; Rare:87; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959026-23959374 | Common:4; Rare:74 | ||||
chr1:23959385-23959425 | Rare:9 | ||||
chr1:23959519-23959980 | Common:5; Rare:109 | ||||
chr1:23959984-23960117 | Rare:47 | ||||
chr1:23960142-23960466 | Common:4; Rare:75 | ||||
chr1:23979843-23979960 | Common:3; Rare:37 | ||||
chr1:23980010-23980131 | Common:2; Rare:17 | ||||
chr1:23980191-23980663 | Common:1; Rare:116 | ||||
chr1:24187246-24187444 | Common:6; Rare:56 | ||||
chr1:24413328-24413392 | Common:1; Rare:11 |