Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:80340812-80341065 | Common:1; Rare:70 | ||||
chr13:80341310-80341484 | Rare:53 | ||||
chr13:93226969-93227354 | Common:1; Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
chr13:94596130-94596334 | Common:2; Rare:69 | ||||
chr13:95301376-95301566 | Rare:52 | ||||
chr13:95676877-95677246 | Common:4; Rare:142 | ||||
chr13:96053269-96053510 | Common:2; Rare:106 | ||||
chr13:97222190-97222402 | Rare:35 | ||||
chr13:97433917-97434157 | Common:1; Rare:89 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:99307387-99307452 | Rare:7 | ||||
chr13:99606467-99606727 | Common:6; Rare:87 | ||||
chr13:100088907-100089167 | Rare:100; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr13:100674765-100675018 | Common:3; Rare:101 | ||||
chr13:102596773-102597145 | Common:1; Rare:147; Clinvar:2; Clinvar (benign):1 |