Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236541317-236541372 | Rare:13 | ||||
chr1:236541393-236541711 | Common:13; Rare:78 | ||||
chr1:236604426-236604626 | Common:4; Rare:66 | ||||
chr1:236893920-236893997 | Rare:15 | ||||
chr1:240091703-240092088 | Common:4; Rare:130 | ||||
chr1:240245022-240245380 | Common:2; Rare:62 | ||||
chr1:241519667-241519982 | Common:2; Rare:101; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:241639900-241639948 | Rare:14 | ||||
chr1:241639971-241639988 | Rare:5 | ||||
chr1:241847814-241848004 | Common:1; Rare:46 | ||||
chr1:241848136-241848269 | Common:1; Rare:21 | ||||
chr1:243254650-243254954 | Common:2; Rare:92 | ||||
chr1:243255041-243255467 | Common:1; Rare:100 | ||||
chr1:243255721-243256243 | Common:1; Rare:170; Clinvar:5; Clinvar (benign):1 | ||||
chr1:243850047-243850123 | Rare:32 |