Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:96053353-96053588 | Common:2; Rare:95 | ||||
chr13:97222154-97222491 | Rare:61 | ||||
chr13:98576203-98576302 | Common:1; Rare:31 | ||||
chr13:99200662-99200896 | Common:6; Rare:106 | ||||
chr13:99307364-99307456 | Rare:10 | ||||
chr13:100088894-100089139 | Rare:90; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674777-100675060 | Common:3; Rare:115 | ||||
chr13:102596794-102597045 | Common:1; Rare:119; Clinvar (benign):1 | ||||
chr13:102773758-102773865 | Rare:42 | ||||
chr13:102798962-102799165 | Rare:43 | ||||
chr13:102845496-102845926 | Common:11; Rare:108; Clinvar (benign):3 | ||||
chr13:106567633-106568004 | Rare:108 | ||||
chr13:106568010-106568267 | Rare:70 | ||||
chr13:108218313-108218538 | Rare:84 | ||||
chr13:110306990-110307526 | Common:7; Rare:163; Clinvar:3; Clinvar (benign):10 |