Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150876544-150876869 | Common:5; Rare:124 | ||||
chr1:150926342-150926448 | Rare:33 | ||||
chr1:150974618-150974902 | Common:2; Rare:82 | ||||
chr1:151006859-151006941 | Rare:20 | ||||
chr1:151008196-151008541 | Common:2; Rare:89 | ||||
chr1:151060246-151060496 | Rare:46 | ||||
chr1:151070492-151070802 | Common:3; Rare:93 | ||||
chr1:151165819-151166171 | Common:3; Rare:103 | ||||
chr1:151190125-151190248 | Rare:38 | ||||
chr1:151198357-151198633 | Common:2; Rare:100 | ||||
chr1:151254687-151254798 | Rare:30 | ||||
chr1:151281933-151282352 | Rare:123 | ||||
chr1:151346852-151347008 | Rare:45 | ||||
chr1:151347201-151347527 | Rare:76 | ||||
chr1:151399388-151399597 | Common:1; Rare:62; Clinvar (pathogenic):1 |