Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262520-160262658 | Common:1; Rare:41 | ||||
chr1:160343169-160343409 | Rare:95 | ||||
chr1:161021078-161021507 | Common:6; Rare:114 | ||||
chr1:161038913-161039027 | Common:1; Rare:41 | ||||
chr1:161045884-161046042 | Common:1; Rare:40 | ||||
chr1:161118022-161118141 | Rare:59 | ||||
chr1:161132605-161132700 | Common:1; Rare:31 | ||||
chr1:161225783-161226072 | Common:9; Rare:42 | ||||
chr1:161314262-161314405 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161766147-161766363 | Common:3; Rare:64 | ||||
chr1:162790516-162790781 | Common:4; Rare:76 | ||||
chr1:163321723-163322007 | Common:1; Rare:76 | ||||
chr1:165768826-165768933 | Common:1; Rare:49 | ||||
chr1:166839289-166839522 | Rare:70 | ||||
chr1:167935939-167936257 | Common:1; Rare:96 |