Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:121185472-121185668 | Rare:10 | ||||
chr1:144461548-144461974 | Common:5; Rare:142 | ||||
chr1:145823922-145824327 | Rare:134 | ||||
chr1:145845348-145845638 | Common:4; Rare:68 | ||||
chr1:145858996-145859175 | Rare:51 | ||||
chr1:145859750-145859935 | Common:2; Rare:64 | ||||
chr1:145918676-145919042 | Common:2; Rare:84; Clinvar:1 | ||||
chr1:145927364-145927653 | Common:1; Rare:75; Clinvar (pathogenic):1 | ||||
chr1:145957983-145958223 | Rare:57 | ||||
chr1:145964542-145964767 | Rare:55 | ||||
chr1:145996534-145996742 | Rare:83 | ||||
chr1:146228961-146229190 | Common:2; Rare:48 | ||||
chr1:146938247-146938343 | Rare:36 | ||||
chr1:147172427-147172843 | Common:2; Rare:105 | ||||
chr1:147242516-147242792 | Common:5; Rare:114 |