Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147172403-147172823 | Common:1; Rare:111 | ||||
chr1:147172893-147172993 | Common:2; Rare:24 | ||||
chr1:147242538-147242770 | Common:4; Rare:98 | ||||
chr1:148458890-148459001 | Common:1; Rare:38 | ||||
chr1:148952020-148952169 | Common:3; Rare:40 | ||||
chr1:148952271-148952635 | Common:5; Rare:102 | ||||
chr1:149812349-149812717 | Common:2; Rare:101 | ||||
chr1:149886619-149887256 | Common:3; Rare:236 | ||||
chr1:149887894-149888215 | Rare:99 | ||||
chr1:149927756-149927901 | Common:1; Rare:60; Clinvar (benign):5 | ||||
chr1:150010598-150010906 | Common:2; Rare:79 | ||||
chr1:150067610-150067886 | Common:1; Rare:76 | ||||
chr1:150150169-150150286 | Common:2; Rare:44 | ||||
chr1:150234669-150234709 | Rare:5 | ||||
chr1:150268362-150268463 | Rare:20 |