Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117929605-117929787 | Rare:47 | ||||
chr1:119140626-119140767 | Rare:46 | ||||
chr1:120176385-120176614 | Common:1; Rare:51 | ||||
chr1:145823922-145824238 | Rare:109 | ||||
chr1:145918689-145919021 | Common:2; Rare:73 | ||||
chr1:145927421-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964583-145964726 | Rare:31 | ||||
chr1:147172457-147172762 | Common:1; Rare:81 | ||||
chr1:148952043-148952141 | Common:3; Rare:22 | ||||
chr1:149886668-149886981 | Common:1; Rare:111 | ||||
chr1:149887952-149888215 | Rare:57 | ||||
chr1:150067606-150067817 | Common:1; Rare:52 | ||||
chr1:150293570-150293909 | Rare:90 | ||||
chr1:150579147-150579271 | Rare:52 | ||||
chr1:150579595-150579893 | Common:10; Rare:93 |