Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:115620556-115620774 | Rare:51 | ||||
chr5:127858374-127858698 | Common:2; Rare:51 | ||||
chr5:137808630-137808930 | Common:2; Rare:57 | ||||
chr5:137808976-137809581 | Rare:108 | ||||
chr5:138933617-138934009 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
chr5:139395074-139395196 | Rare:27 | ||||
chr5:146068284-146068534 | Common:2; Rare:45 | ||||
chr5:148826402-148826637 | Common:3; Rare:63 | ||||
chr5:149380812-149381026 | Rare:41 | ||||
chr5:149382017-149382246 | Common:1; Rare:49 | ||||
chr5:149423912-149424156 | Common:2; Rare:37 | ||||
chr5:150405087-150405256 | Common:1; Rare:43 | ||||
chr5:150614194-150614388 | Common:1; Rare:32 | ||||
chr5:150626937-150626969 | Rare:5 | ||||
chr5:150778651-150778871 | Common:1; Rare:89 |