Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149812358-149812560 | Rare:62 | ||||
chr1:149842744-149842965 | Rare:3 | ||||
chr1:149850826-149851064 | Rare:1 | ||||
chr1:149886594-149887151 | Common:3; Rare:220 | ||||
chr1:149887890-149888217 | Rare:101 | ||||
chr1:149927755-149927872 | Rare:51; Clinvar (benign):4 | ||||
chr1:150067671-150067864 | Rare:62 | ||||
chr1:150293805-150293914 | Rare:37 | ||||
chr1:150321421-150321582 | Rare:53; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150364550-150364730 | Common:1; Rare:60 | ||||
chr1:150579157-150579312 | Rare:66 | ||||
chr1:150579585-150579893 | Common:10; Rare:99 | ||||
chr1:150629119-150629314 | Rare:55 | ||||
chr1:150629522-150629825 | Rare:60 | ||||
chr1:150876553-150876843 | Common:5; Rare:110 |