Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:239386480-239386598 | Rare:19 | ||||
chr1:240611918-240612295 | Rare:87 | ||||
chr1:241519637-241519977 | Common:3; Rare:109; Clinvar:13; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
chr1:241639858-241639929 | Rare:21 | ||||
chr1:241640762-241640874 | Common:2; Rare:24 | ||||
chr1:241847846-241848477 | Common:5; Rare:150 | ||||
chr1:241850163-241850437 | Common:2; Rare:66 | ||||
chr1:243255045-243255438 | Common:1; Rare:96 | ||||
chr1:243255442-243255457 | Rare:2 | ||||
chr1:243255472-243255523 | Rare:6 | ||||
chr1:243255752-243256135 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
chr1:243269563-243269741 | Common:2; Rare:26 | ||||
chr1:244451813-244452230 | Common:1; Rare:139 | ||||
chr1:244461244-244461325 | Common:1; Rare:23 | ||||
chr1:244652501-244652699 | Common:3; Rare:48 |