Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:37448067-37448174 | Rare:22 | ||||
chr7:37916157-37916208 | Rare:19 | ||||
chr7:38300268-38300415 | Common:1; Rare:41 | ||||
chr7:38311426-38311568 | Common:2; Rare:33 | ||||
chr7:38335551-38335710 | Common:1; Rare:25 | ||||
chr7:38341291-38341421 | Rare:32 | ||||
chr7:38358380-38358490 | Common:1; Rare:53 | ||||
chr7:38359157-38359492 | Common:10; Rare:79 | ||||
chr7:39733546-39733660 | Rare:26 | ||||
chr7:41705407-41705545 | Common:1; Rare:25 | ||||
chr7:42888635-42888815 | Rare:35 | ||||
chr7:44038979-44039221 | Common:5; Rare:40 | ||||
chr7:44039499-44039541 | Common:1; Rare:12 | ||||
chr7:44107915-44108084 | Common:2; Rare:59; Clinvar (pathogenic):1 | ||||
chr7:44467579-44467881 | Common:3; Rare:59 |