Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159781230-159781690 | Rare:165 | ||||
chr1:159854632-159855032 | Rare:289 | ||||
chr1:159880040-159880494 | Common:5; Rare:166 | ||||
chr1:159899978-159900378 | Rare:226 | ||||
chr1:159923280-159924840 | Common:12; Rare:1017 | ||||
chr1:159924859-159925259 | Common:3; Rare:68 | ||||
chr1:159925400-159925840 | Common:7; Rare:384 | ||||
chr1:159945560-159945830 | Common:4; Rare:128 | ||||
chr1:159945834-159946340 | Common:2; Rare:209 | ||||
chr1:160031257-160032220 | Common:14; Rare:640; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:160098438-160099200 | Common:22; Rare:580 | ||||
chr1:160128095-160128495 | Common:5; Rare:160 | ||||
chr1:160205136-160205835 | Common:8; Rare:330 | ||||
chr1:160261313-160262850 | Common:13; Rare:1214 | ||||
chr1:160284310-160284710 | Common:6; Rare:160 |