Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23865460-23865930 | Common:3; Rare:112; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:23902765-23903165 | Common:5; Rare:125 | ||||
chr1:23916760-23917260 | Common:4; Rare:96 | ||||
chr1:24018780-24019100 | Common:2; Rare:57 | ||||
chr1:24046332-24046509 | Common:1; Rare:32 | ||||
chr1:24047120-24047650 | Common:3; Rare:79 | ||||
chr1:24070830-24071170 | Common:2; Rare:85 | ||||
chr1:24108953-24109222 | Common:1; Rare:50 | ||||
chr1:24150548-24150780 | Common:1; Rare:46 | ||||
chr1:24201991-24202115 | Common:1; Rare:16 | ||||
chr1:24254783-24255201 | Common:9; Rare:203 | ||||
chr1:24321893-24322006 | Common:1; Rare:22 | ||||
chr1:24683743-24684049 | Common:1; Rare:55 | ||||
chr1:24705319-24705601 | Rare:71 | ||||
chr1:24720090-24720490 | Common:5; Rare:72 |