Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236795249-236795507 | Common:2; Rare:119; Clinvar:5; Clinvar (benign):1 | ||||
chr1:236795658-236795722 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:239386403-239386483 | Common:1; Rare:11 | ||||
chr1:239386499-239386717 | Rare:35 | ||||
chr1:239719102-239719143 | Rare:2 | ||||
chr1:240611961-240612292 | Rare:81 | ||||
chr1:241848116-241848257 | Common:1; Rare:24 | ||||
chr1:241998616-241998708 | Rare:24 | ||||
chr1:243255040-243255386 | Common:1; Rare:79 | ||||
chr1:243255431-243255700 | Rare:60 | ||||
chr1:243255772-243256182 | Common:1; Rare:125; Clinvar:5; Clinvar (benign):1 | ||||
chr1:243487466-243487869 | Common:5; Rare:93 | ||||
chr1:244048236-244048557 | Rare:98 | ||||
chr1:244451596-244451732 | Rare:41 | ||||
chr1:244451745-244452230 | Common:1; Rare:160 |