Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234610145-234610313 | Common:2; Rare:70 | ||||
chr1:234610877-234611175 | Common:2; Rare:104 | ||||
chr1:234980759-234980885 | Rare:18 | ||||
chr1:244451073-244451248 | Common:2; Rare:43 | ||||
chr1:244863706-244863799 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
chr1:246569745-246569919 | Common:1; Rare:31 | ||||
chr1:247210792-247211053 | Common:3; Rare:69 | ||||
chr10:252159-252411 | Rare:53 | ||||
chr10:628307-628603 | Common:3; Rare:63 | ||||
chr10:3424561-3424755 | Common:1; Rare:44 | ||||
chr10:3435703-3435892 | Rare:35 | ||||
chr10:3469171-3469341 | Rare:35 | ||||
chr10:3783015-3783144 | Rare:31 | ||||
chr10:3783995-3784086 | Rare:20 | ||||
chr10:4943807-4944130 | Common:2; Rare:80 |