Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45687050-45687351 | Common:1; Rare:79 | ||||
chr1:45688061-45688232 | Common:1; Rare:51 | ||||
chr1:46303147-46303769 | Common:3; Rare:187 | ||||
chr1:47333705-47333984 | Common:3; Rare:91 | ||||
chr1:50969969-50970271 | Rare:55 | ||||
chr1:51878650-51878997 | Common:1; Rare:100 | ||||
chr1:52056136-52056338 | Rare:63 | ||||
chr1:52404436-52404623 | Common:1; Rare:55 | ||||
chr1:53220590-53220677 | Common:1; Rare:37 | ||||
chr1:53238469-53238687 | Common:2; Rare:80 | ||||
chr1:53946260-53946398 | Rare:55 | ||||
chr1:54053184-54053584 | Common:4; Rare:131 | ||||
chr1:54199995-54200215 | Rare:54 | ||||
chr1:54887158-54887366 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr1:58577253-58577499 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 |