Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154234360-154235264 | Common:3; Rare:266 | ||||
chr1:154972604-154972863 | Rare:48 | ||||
chr1:155003820-155004360 | Common:2; Rare:130 | ||||
chr1:155124564-155124964 | Common:2; Rare:163 | ||||
chr1:155125783-155126706 | Common:1; Rare:258 | ||||
chr1:155193870-155194120 | Rare:68 | ||||
chr1:155194720-155195114 | Common:2; Rare:175 | ||||
chr1:155218986-155219298 | Common:1; Rare:76 | ||||
chr1:155226780-155227119 | Common:3; Rare:77 | ||||
chr1:155227392-155227786 | Common:7; Rare:217 | ||||
chr1:155983407-155983732 | Rare:78 | ||||
chr1:156105116-156105490 | Common:2; Rare:108 | ||||
chr1:156130280-156130730 | Common:5; Rare:195; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
chr1:156312040-156312360 | Rare:90 | ||||
chr1:156456430-156456850 | Common:4; Rare:154 |