Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154405221-154405473 | Common:2; Rare:94 | ||||
chr1:154558594-154559063 | Common:4; Rare:253 | ||||
chr1:154608137-154608354 | Common:1; Rare:63 | ||||
chr1:154627862-154628046 | Common:6; Rare:177 | ||||
chr1:154936828-154937294 | Common:1; Rare:122 | ||||
chr1:154956073-154956215 | Rare:40 | ||||
chr1:154961230-154961640 | Rare:194 | ||||
chr1:154961701-154961856 | Common:2; Rare:125 | ||||
chr1:154970601-154970934 | Common:1; Rare:94 | ||||
chr1:154973593-154973993 | Common:1; Rare:147 | ||||
chr1:154974314-154974727 | Rare:186 | ||||
chr1:154974863-154975086 | Common:2; Rare:86 | ||||
chr1:154983085-154983396 | Common:4; Rare:119; Clinvar (benign):1 | ||||
chr1:155002099-155002378 | Common:2; Rare:155 | ||||
chr1:155002451-155002857 | Common:3; Rare:79 |