Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:144517317-144517669 | Common:5; Rare:105; Clinvar:3; Clinvar (benign):5 | ||||
chr2:144518134-144518203 | Common:1; Rare:14 | ||||
chr2:144518394-144518505 | Rare:27 | ||||
chr2:144519952-144520561 | Common:4; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
chr2:148020681-148021096 | Common:2; Rare:97; Clinvar (benign):2 | ||||
chr2:148021335-148021407 | Rare:12 | ||||
chr2:148021571-148021652 | Rare:17 | ||||
chr2:148875579-148875611 | Rare:15; Clinvar (benign):1 | ||||
chr2:149330344-149330696 | Common:2; Rare:138 | ||||
chr2:149587321-149587414 | Common:1; Rare:20 | ||||
chr2:149587685-149587830 | Common:1; Rare:42; Clinvar:1 | ||||
chr2:151289611-151289667 | Rare:18 | ||||
chr2:152717824-152717964 | Rare:57 | ||||
chr2:152717995-152718161 | Common:1; Rare:47 | ||||
chr2:152718481-152718654 | Rare:71 |