Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:78360023-78360469 | Common:3; Rare:123 | ||||
chr17:78378516-78378734 | Common:1; Rare:80 | ||||
chr17:78736610-78736991 | Common:1; Rare:86 | ||||
chr17:78782177-78782731 | Common:10; Rare:162 | ||||
chr17:78840521-78840604 | Rare:28 | ||||
chr17:78840731-78841237 | Common:2; Rare:181 | ||||
chr17:78841395-78841547 | Rare:32 | ||||
chr17:78979919-78980094 | Common:2; Rare:37 | ||||
chr17:79009678-79009982 | Common:10; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr17:79074585-79075018 | Common:6; Rare:116 | ||||
chr17:79777991-79778226 | Common:1; Rare:91 | ||||
chr17:79796815-79796912 | Rare:31 | ||||
chr17:79796967-79797097 | Rare:46 | ||||
chr17:79797110-79797516 | Common:1; Rare:137 | ||||
chr17:79837441-79837553 | Rare:17 |