Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149927743-149927906 | Common:1; Rare:64; Clinvar (benign):5 | ||||
chr1:149928235-149928361 | Rare:25 | ||||
chr1:149931530-149931650 | Rare:20 | ||||
chr1:149936845-149936940 | Rare:19 | ||||
chr1:150010598-150010908 | Common:2; Rare:79 | ||||
chr1:150067105-150067466 | Common:4; Rare:66 | ||||
chr1:150067606-150067866 | Common:1; Rare:75 | ||||
chr1:150234632-150234766 | Rare:26 | ||||
chr1:150235731-150236374 | Common:3; Rare:138 | ||||
chr1:150268709-150268860 | Common:2; Rare:42 | ||||
chr1:150272368-150272742 | Common:1; Rare:63 | ||||
chr1:150282162-150282238 | Rare:19 | ||||
chr1:150282291-150282551 | Common:2; Rare:43 | ||||
chr1:150293803-150293927 | Common:1; Rare:44 | ||||
chr1:150321406-150321608 | Rare:63; Clinvar:3; Clinvar (benign):1 |