Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:30607213-30607328 | Rare:29 | ||||
chr3:30608351-30608492 | Common:1; Rare:23 | ||||
chr3:30644544-30644856 | Rare:74; Clinvar:3; Clinvar (benign):5 | ||||
chr3:30681738-30681761 | Common:1; Rare:3 | ||||
chr3:37016451-37016687 | Common:1; Rare:40 | ||||
chr3:37065878-37066048 | Common:2; Rare:45 | ||||
chr3:37302083-37302235 | Rare:34 | ||||
chr3:39143911-39144217 | Rare:83 | ||||
chr3:40453155-40453428 | Common:6; Rare:61 | ||||
chr3:41202884-41203040 | Rare:27 | ||||
chr3:42654386-42654609 | Rare:68 | ||||
chr3:45076301-45076598 | Common:2; Rare:49 | ||||
chr3:46097776-46098039 | Common:2; Rare:45 | ||||
chr3:46111176-46111465 | Common:2; Rare:63 | ||||
chr3:46883901-46884068 | Common:2; Rare:25 |