Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:216498749-216498845 | Rare:32 | ||||
chr2:219543794-219544034 | Common:3; Rare:76 | ||||
chr2:241315670-241315931 | Common:3; Rare:99 | ||||
chr20:1118485-1118648 | Common:2; Rare:52 | ||||
chr20:17968789-17969090 | Common:2; Rare:113 | ||||
chr20:37178947-37179094 | Rare:45 | ||||
chr20:46364388-46364523 | Rare:52 | ||||
chr21:44873672-44874012 | Common:7; Rare:142 | ||||
chr22:37019445-37019767 | Common:5; Rare:90 | ||||
chr3:139389596-139389857 | Common:1; Rare:81 | ||||
chr3:197949909-197950237 | Common:3; Rare:98; Clinvar (benign):1 | ||||
chr4:10116751-10117062 | Common:5; Rare:148 | ||||
chr5:443126-443257 | Common:5; Rare:52 | ||||
chr5:60945056-60945229 | Common:4; Rare:60; Clinvar:2; Clinvar (benign):4 | ||||
chr6:33271840-33272079 | Rare:80 |