Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20649187-20649218 | Rare:6; Clinvar (pathogenic):1 | ||||
chr1:20696888-20696943 | Rare:9 | ||||
chr1:20696950-20697170 | Common:1; Rare:50 | ||||
chr1:20883857-20883966 | Rare:24 | ||||
chr1:21022398-21022550 | Rare:27 | ||||
chr1:21149848-21150168 | Rare:53 | ||||
chr1:21150211-21150238 | Rare:7 | ||||
chr1:21175266-21175565 | Common:3; Rare:42 | ||||
chr1:21175566-21175612 | Rare:3 | ||||
chr1:21175778-21176054 | Common:3; Rare:69 | ||||
chr1:21252261-21252486 | Common:1; Rare:36 | ||||
chr1:21261683-21261736 | Rare:14 | ||||
chr1:21261875-21262172 | Common:3; Rare:62 | ||||
chr1:21324769-21325158 | Common:5; Rare:63 | ||||
chr1:21627222-21627281 | Rare:10 |