Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117929632-117929808 | Common:3; Rare:46 | ||||
chr1:119140623-119140767 | Rare:49 | ||||
chr1:120914107-120914251 | Rare:17 | ||||
chr1:145823967-145824238 | Rare:93 | ||||
chr1:145858991-145859137 | Rare:43 | ||||
chr1:145918665-145919057 | Common:2; Rare:93; Clinvar:1 | ||||
chr1:145927477-145927644 | Rare:41 | ||||
chr1:145964571-145964737 | Rare:43 | ||||
chr1:145996017-145996371 | Rare:148 | ||||
chr1:147172460-147172730 | Common:1; Rare:71 | ||||
chr1:148458726-148459023 | Common:2; Rare:85 | ||||
chr1:149812358-149812611 | Common:1; Rare:70 | ||||
chr1:149886626-149886955 | Common:1; Rare:121 | ||||
chr1:149887961-149888215 | Rare:50 | ||||
chr1:149927760-149927910 | Common:1; Rare:60; Clinvar (benign):4 |