Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156601407-156601538 | Common:1; Rare:52 | ||||
chr1:156728388-156728485 | Common:1; Rare:18 | ||||
chr1:156741051-156741413 | Common:1; Rare:97 | ||||
chr1:156767393-156767574 | Rare:60 | ||||
chr1:157138342-157138632 | Common:3; Rare:85 | ||||
chr1:159925452-159925617 | Common:1; Rare:43 | ||||
chr1:159945582-159945703 | Common:1; Rare:35 | ||||
chr1:160031837-160032130 | Common:3; Rare:81 | ||||
chr1:160343129-160343405 | Rare:102 | ||||
chr1:161038894-161039027 | Common:1; Rare:47 | ||||
chr1:161045860-161046066 | Common:1; Rare:54 | ||||
chr1:161118022-161118141 | Rare:59 | ||||
chr1:161132417-161132700 | Common:1; Rare:94 | ||||
chr1:161166257-161166511 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161225768-161226072 | Common:10; Rare:44 |