Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66930302-66930397 | Rare:31 | ||||
chr1:67053643-67053846 | Common:4; Rare:97; Clinvar (pathogenic):1 | ||||
chr1:67053909-67054092 | Rare:86 | ||||
chr1:67054146-67054453 | Common:4; Rare:63 | ||||
chr1:67430131-67430605 | Rare:175 | ||||
chr1:68232402-68232643 | Common:1; Rare:53 | ||||
chr1:68497013-68497320 | Common:3; Rare:102 | ||||
chr1:70205538-70205770 | Rare:74 | ||||
chr1:70221276-70221573 | Rare:126 | ||||
chr1:70354654-70354925 | Rare:85 | ||||
chr1:70411063-70411325 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080974-71081379 | Rare:109 | ||||
chr1:72282989-72283371 | Common:3; Rare:109 | ||||
chr1:74198113-74198348 | Common:3; Rare:127 | ||||
chr1:74732980-74733353 | Common:6; Rare:131 |