Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:93226897-93227100 | Rare:38; Clinvar:1 | ||||
chr13:93227139-93227539 | Common:1; Rare:101; Clinvar:7; Clinvar (benign):1 | ||||
chr13:94596121-94596334 | Common:2; Rare:75 | ||||
chr13:94601581-94601930 | Common:4; Rare:105 | ||||
chr13:95433457-95433823 | Common:3; Rare:65 | ||||
chr13:95676828-95677242 | Common:4; Rare:161 | ||||
chr13:96053209-96053510 | Common:2; Rare:123 | ||||
chr13:97222154-97222407 | Rare:43 | ||||
chr13:99200668-99200921 | Common:6; Rare:119 | ||||
chr13:99307374-99307420 | Rare:6 | ||||
chr13:100088844-100089134 | Rare:114; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674787-100675018 | Common:3; Rare:91 | ||||
chr13:102596788-102597039 | Common:1; Rare:118 | ||||
chr13:102773728-102773842 | Rare:54 | ||||
chr13:102798962-102799130 | Rare:35 |