Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231422655-231423056 | Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
chr1:233657659-233657765 | Common:1; Rare:36 | ||||
chr1:234097402-234097511 | Common:1; Rare:17 | ||||
chr1:234356893-234357034 | Common:1; Rare:48 | ||||
chr1:234604134-234604314 | Rare:44 | ||||
chr1:234610136-234610286 | Common:1; Rare:66 | ||||
chr1:234610875-234611112 | Common:1; Rare:78 | ||||
chr1:234962131-234962261 | Common:1; Rare:28 | ||||
chr1:234963980-234964080 | Rare:21 | ||||
chr1:234980765-234980894 | Rare:20 | ||||
chr1:234997311-234997576 | Common:1; Rare:44 | ||||
chr1:235073560-235073845 | Common:2; Rare:53 | ||||
chr1:235075488-235075651 | Rare:21 | ||||
chr1:235137921-235138140 | Rare:51 | ||||
chr1:235148412-235148614 | Common:2; Rare:51 |