Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39639611-39639855 | Rare:92 | ||||
chr1:39691392-39691531 | Common:1; Rare:26 | ||||
chr1:39738726-39739044 | Common:3; Rare:81 | ||||
chr1:39739298-39739324 | Rare:5 | ||||
chr1:39882808-39883158 | Common:3; Rare:63 | ||||
chr1:39883440-39883689 | Common:3; Rare:82; Clinvar (pathogenic):1 | ||||
chr1:39901843-39902049 | Common:6; Rare:69 | ||||
chr1:39954913-39955236 | Common:1; Rare:79 | ||||
chr1:40039642-40039771 | Rare:35 | ||||
chr1:40039785-40040231 | Common:3; Rare:97 | ||||
chr1:40040374-40040874 | Common:4; Rare:158 | ||||
chr1:40096859-40097007 | Rare:14 | ||||
chr1:40097018-40097366 | Common:3; Rare:130; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):6 | ||||
chr1:40097451-40097484 | Rare:3 | ||||
chr1:40161154-40161460 | Common:1; Rare:102 |