Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52698334-52698450 | Common:2; Rare:37 | ||||
chr1:52927221-52927327 | Common:2; Rare:35 | ||||
chr1:53061911-53062215 | Common:6; Rare:65 | ||||
chr1:53220313-53220370 | Rare:28 | ||||
chr1:53220558-53220696 | Common:1; Rare:69 | ||||
chr1:53238464-53238598 | Rare:60 | ||||
chr1:53889749-53889886 | Common:1; Rare:44 | ||||
chr1:53945649-53946061 | Common:8; Rare:109 | ||||
chr1:53946260-53946486 | Rare:82 | ||||
chr1:54053161-54053658 | Common:6; Rare:170 | ||||
chr1:54199982-54200204 | Rare:44 | ||||
chr1:54715735-54715894 | Common:2; Rare:49 | ||||
chr1:54887154-54887440 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
chr1:58783973-58784388 | Common:1; Rare:112 | ||||
chr1:61725101-61725198 | Rare:52 |