Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26787887-26788217 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26862837-26863050 | Rare:46 | ||||
chr1:26863069-26863933 | Common:2; Rare:249 | ||||
chr1:26890224-26890368 | Common:1; Rare:57 | ||||
chr1:26900428-26900511 | Rare:33 | ||||
chr1:26960349-26960537 | Common:1; Rare:42 | ||||
chr1:27322200-27322338 | Common:1; Rare:60 | ||||
chr1:27341816-27342139 | Common:1; Rare:69 | ||||
chr1:27343033-27343267 | Common:3; Rare:43 | ||||
chr1:27366871-27367122 | Common:1; Rare:50 | ||||
chr1:28088528-28088801 | Common:3; Rare:89 | ||||
chr1:28232921-28233092 | Common:1; Rare:66 | ||||
chr1:28328914-28329073 | Common:1; Rare:47 | ||||
chr1:28505815-28506056 | Common:2; Rare:95 | ||||
chr1:28552862-28553120 | Common:2; Rare:99 |