Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147172450-147172744 | Common:1; Rare:76 | ||||
chr1:147242608-147242722 | Common:1; Rare:54 | ||||
chr1:147928338-147928428 | Common:1; Rare:33 | ||||
chr1:148679740-148679907 | Rare:17 | ||||
chr1:148844407-148844428 | Rare:2 | ||||
chr1:148952230-148952402 | Common:1; Rare:47 | ||||
chr1:149812358-149812560 | Rare:62 | ||||
chr1:149842745-149842984 | Rare:3 | ||||
chr1:149850874-149851064 | |||||
chr1:149886425-149886563 | Rare:47 | ||||
chr1:149886619-149886987 | Common:2; Rare:143 | ||||
chr1:149887116-149887175 | Rare:26 | ||||
chr1:149887933-149888215 | Rare:71 | ||||
chr1:149927748-149927900 | Common:1; Rare:62; Clinvar (benign):5 | ||||
chr1:150010662-150010837 | Common:2; Rare:42 |