Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:79405785-79405909 | Rare:43 | ||||
chr13:79406217-79406339 | Common:3; Rare:38 | ||||
chr13:93226624-93227099 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
chr13:93227263-93227576 | Common:1; Rare:92; Clinvar:6; Clinvar (benign):1 | ||||
chr13:94596133-94596334 | Common:2; Rare:67 | ||||
chr13:95301381-95301580 | Rare:55 | ||||
chr13:95676918-95677256 | Common:4; Rare:124 | ||||
chr13:96053269-96053515 | Common:2; Rare:110 | ||||
chr13:97222214-97222407 | Rare:32 | ||||
chr13:97433895-97434157 | Common:1; Rare:105 | ||||
chr13:97976416-97976731 | Common:1; Rare:118 | ||||
chr13:99200668-99200900 | Common:6; Rare:109 | ||||
chr13:99307362-99307706 | Common:3; Rare:50 | ||||
chr13:99312540-99312825 | Rare:43 | ||||
chr13:99606497-99606706 | Common:5; Rare:66 |