Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147225303-147225480 | Common:3; Rare:39 | ||||
chr1:148458680-148458967 | Common:2; Rare:76 | ||||
chr1:148952031-148952642 | Common:8; Rare:157 | ||||
chr1:149842747-149842964 | Rare:3 | ||||
chr1:149886612-149887182 | Common:3; Rare:224 | ||||
chr1:149887902-149887986 | Rare:53 | ||||
chr1:149888001-149888082 | Rare:20 | ||||
chr1:149927760-149927901 | Common:1; Rare:58; Clinvar (benign):4 | ||||
chr1:150067138-150067369 | Common:4; Rare:44 | ||||
chr1:150067566-150067873 | Common:1; Rare:86 | ||||
chr1:150149382-150149717 | Common:1; Rare:73 | ||||
chr1:150234676-150234756 | Rare:15 | ||||
chr1:150272374-150272835 | Common:1; Rare:84 | ||||
chr1:150282158-150282288 | Rare:33 | ||||
chr1:150282299-150282591 | Common:3; Rare:57 |