Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:220880086-220880225 | Common:1; Rare:47 | ||||
chr1:221845972-221846080 | Common:1; Rare:19 | ||||
chr1:222814982-222815133 | Common:1; Rare:56 | ||||
chr1:223992559-223992789 | Common:4; Rare:84 | ||||
chr1:226765182-226765372 | Rare:30 | ||||
chr1:228121285-228121582 | Rare:51 | ||||
chr1:234610176-234610313 | Common:2; Rare:53 | ||||
chr1:234611406-234611494 | Common:1; Rare:30 | ||||
chr1:234612770-234612942 | Rare:23 | ||||
chr1:234655552-234655787 | Common:2; Rare:28 | ||||
chr1:234657054-234657484 | Common:2; Rare:77 | ||||
chr1:243101689-243101920 | Common:11; Rare:140 | ||||
chr1:244599935-244600149 | Common:1; Rare:35 | ||||
chr1:244863870-244863887 | Rare:4; Clinvar (benign):1 | ||||
chr1:248731078-248731222 | Common:1; Rare:47 |