Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154501580-154501853 | Common:1; Rare:93 | ||||
chr1:154502406-154502498 | Common:1; Rare:23 | ||||
chr1:154627889-154628011 | Common:3; Rare:65 | ||||
chr1:154936618-154936773 | Common:2; Rare:55 | ||||
chr1:154936842-154937022 | Rare:36 | ||||
chr1:154956076-154956232 | Common:1; Rare:44 | ||||
chr1:154961476-154961584 | Rare:33 | ||||
chr1:154961712-154962066 | Common:1; Rare:124 | ||||
chr1:154968779-154969128 | Common:1; Rare:80 | ||||
chr1:154970129-154970338 | Common:1; Rare:64 | ||||
chr1:154970628-154970952 | Common:1; Rare:59 | ||||
chr1:154974314-154974742 | Rare:113 | ||||
chr1:154983124-154983393 | Common:2; Rare:53; Clinvar (benign):1 | ||||
chr1:155002105-155002376 | Common:1; Rare:76 | ||||
chr1:155002482-155002874 | Common:2; Rare:65 |