Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:202341894-202342193 | Common:1; Rare:79 | ||||
chr1:202539315-202539516 | Rare:31 | ||||
chr1:202967214-202967430 | Common:5; Rare:39 | ||||
chr1:203305313-203305561 | Common:3; Rare:67 | ||||
chr1:203626512-203626896 | Common:1; Rare:82 | ||||
chr1:203861555-203861687 | Rare:66 | ||||
chr1:206003414-206003513 | Common:1; Rare:17 | ||||
chr1:207032644-207032926 | Common:3; Rare:50 | ||||
chr1:207053109-207053295 | Common:1; Rare:49 | ||||
chr1:207751844-207752201 | Common:2; Rare:118 | ||||
chr1:209652413-209652651 | Common:2; Rare:51; Clinvar:1 | ||||
chr1:209675264-209675557 | Common:2; Rare:76 | ||||
chr1:209768393-209768605 | Rare:32 | ||||
chr1:209806103-209806309 | Common:5; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
chr1:211675589-211675756 | Rare:33 |