Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:60163821-60164088 | Common:2; Rare:64 | ||||
chr13:67230316-67230666 | Common:2; Rare:114 | ||||
chr13:72727591-72727934 | Common:4; Rare:124 | ||||
chr13:72781843-72782198 | Common:1; Rare:137 | ||||
chr13:75549482-75549808 | Common:6; Rare:76 | ||||
chr13:75636015-75636366 | Common:2; Rare:85 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:100088961-100089128 | Rare:63; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102596785-102597028 | Common:1; Rare:113 | ||||
chr13:102798883-102799180 | Common:1; Rare:61 | ||||
chr13:106568097-106568274 | Rare:53 | ||||
chr13:108215502-108215618 | Common:1; Rare:32 | ||||
chr13:108218270-108218520 | Common:1; Rare:92 | ||||
chr13:110307061-110307492 | Common:6; Rare:142; Clinvar:1; Clinvar (benign):8 | ||||
chr13:113208625-113208756 | Rare:76 |