Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:197201269-197201517 | Common:1; Rare:85 | ||||
chr1:201562954-201563166 | Common:3; Rare:36 | ||||
chr1:211365970-211366190 | Rare:31 | ||||
chr1:211367526-211367701 | Common:3; Rare:24 | ||||
chr1:222711465-222711623 | Rare:33 | ||||
chr1:231421002-231421118 | Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
chr1:235137921-235138128 | Rare:46 | ||||
chr1:240093125-240093263 | Rare:29; Clinvar (benign):1 | ||||
chr1:244451115-244451261 | Common:2; Rare:41 | ||||
chr1:244863616-244863782 | Rare:60; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:4246941-4247262 | Common:3; Rare:66 | ||||
chr10:5596088-5596271 | Common:1; Rare:32 | ||||
chr10:22437781-22438122 | Common:3; Rare:61 | ||||
chr10:27744655-27744894 | Common:2; Rare:57 | ||||
chr10:27820331-27820485 | Common:2; Rare:27 |