Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53946253-53946422 | Rare:68 | ||||
chr1:54053172-54053638 | Common:6; Rare:154 | ||||
chr1:54199993-54200204 | Rare:43 | ||||
chr1:54887168-54887442 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
chr1:63523186-63523552 | Common:3; Rare:91 | ||||
chr1:66924858-66925008 | Rare:62 | ||||
chr1:70205542-70205745 | Rare:63 | ||||
chr1:70354699-70354812 | Rare:40 | ||||
chr1:74198148-74198270 | Common:1; Rare:63 | ||||
chr1:74732994-74733238 | Common:4; Rare:76 | ||||
chr1:77219407-77219476 | Rare:33 | ||||
chr1:77979026-77979175 | Common:2; Rare:51 | ||||
chr1:84077894-84078124 | Common:1; Rare:85 | ||||
chr1:86704697-86704853 | Common:2; Rare:54 | ||||
chr1:93180355-93180694 | Common:1; Rare:142 |