Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:93226796-93227403 | Common:2; Rare:126; Clinvar:6; Clinvar (benign):2 | ||||
chr13:95301369-95301543 | Rare:52 | ||||
chr13:95676937-95677218 | Common:3; Rare:94 | ||||
chr13:96053311-96053574 | Common:2; Rare:117 | ||||
chr13:97222175-97222511 | Rare:60 | ||||
chr13:97976375-97976699 | Common:1; Rare:119 | ||||
chr13:98977785-98978209 | Common:3; Rare:100 | ||||
chr13:99200667-99200894 | Common:6; Rare:104 | ||||
chr13:99307366-99307562 | Common:2; Rare:26 | ||||
chr13:100088914-100089123 | Rare:77; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674777-100675018 | Common:3; Rare:96 | ||||
chr13:102596769-102597102 | Common:1; Rare:135; Clinvar (benign):1 | ||||
chr13:102798962-102799130 | Rare:35 | ||||
chr13:102845743-102846084 | Common:8; Rare:88; Clinvar:2; Clinvar (benign):4 | ||||
chr13:106567627-106568078 | Rare:124 |