Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9423398-9423697 | Rare:92 | ||||
chr2:9474493-9474642 | Common:6; Rare:71 | ||||
chr2:9555730-9555992 | Common:2; Rare:86 | ||||
chr2:9630950-9631316 | Common:3; Rare:118 | ||||
chr2:10689919-10690024 | Common:2; Rare:35 | ||||
chr2:17753711-17754168 | Common:4; Rare:143; Clinvar (benign):1 | ||||
chr2:19990058-19990211 | Rare:38 | ||||
chr2:20446887-20447074 | Common:2; Rare:62 | ||||
chr2:24076205-24076523 | Rare:91 | ||||
chr2:24123272-24123506 | Common:1; Rare:62 | ||||
chr2:24972042-24972138 | Common:1; Rare:26 | ||||
chr2:26033778-26034141 | Common:3; Rare:128 | ||||
chr2:26244592-26244975 | Common:2; Rare:140; Clinvar:5; Clinvar (benign):8 | ||||
chr2:26345812-26346165 | Common:1; Rare:106 | ||||
chr2:26764188-26764337 | Common:1; Rare:61 |