Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:220089690-220090191 | Common:4; Rare:99 | ||||
chr1:220093867-220094251 | Common:12; Rare:120; Clinvar (benign):2 | ||||
chr1:220094502-220094611 | Rare:34 | ||||
chr1:220272155-220272268 | Rare:37 | ||||
chr1:220272280-220272700 | Rare:118; Clinvar:6; Clinvar (benign):1 | ||||
chr1:220690178-220690448 | Rare:102 | ||||
chr1:220748152-220748352 | Common:1; Rare:40 | ||||
chr1:221741987-221742626 | Common:5; Rare:153 | ||||
chr1:222589713-222590082 | Common:2; Rare:101 | ||||
chr1:222617745-222618173 | Common:3; Rare:114 | ||||
chr1:222643872-222644462 | Common:6; Rare:164 | ||||
chr1:222711973-222712082 | Rare:27 | ||||
chr1:222712444-222712926 | Common:3; Rare:159 | ||||
chr1:222713130-222713547 | Common:1; Rare:117 | ||||
chr1:223143221-223143397 | Common:3; Rare:48 |