Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149927756-149927907 | Common:1; Rare:62; Clinvar (benign):5 | ||||
chr1:150067649-150067878 | Rare:66 | ||||
chr1:150234654-150234748 | Rare:18 | ||||
chr1:150235950-150236368 | Common:1; Rare:94 | ||||
chr1:150268062-150268227 | Rare:33 | ||||
chr1:150268360-150268516 | Rare:33 | ||||
chr1:150272368-150272728 | Common:1; Rare:60 | ||||
chr1:150321390-150321620 | Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363951-150364206 | Common:3; Rare:92 | ||||
chr1:150364562-150364724 | Common:1; Rare:53 | ||||
chr1:150487231-150487462 | Common:4; Rare:60; Clinvar (benign):3 | ||||
chr1:150549192-150549409 | Rare:55 | ||||
chr1:150552500-150552581 | Rare:24 | ||||
chr1:150578396-150578735 | Common:2; Rare:99 | ||||
chr1:150578823-150579318 | Common:3; Rare:201 |