Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:6673293-6673447 | Common:2; Rare:39 | ||||
chr4:6673809-6673969 | Common:7; Rare:81 | ||||
chr4:15599290-15599592 | Rare:69; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr4:15833917-15834205 | Common:1; Rare:47 | ||||
chr4:20251733-20251909 | Common:1; Rare:70 | ||||
chr4:23945882-23945976 | Rare:22 | ||||
chr4:36913342-36913616 | Rare:57 | ||||
chr4:38754204-38754494 | Common:30; Rare:83 | ||||
chr4:38857725-38857851 | Rare:26 | ||||
chr4:38868326-38868471 | Common:1; Rare:29 | ||||
chr4:38942026-38942234 | Common:2; Rare:36 | ||||
chr4:39544038-39544324 | Common:1; Rare:49 | ||||
chr4:40554130-40554303 | Common:1; Rare:31 | ||||
chr4:40586807-40587007 | Common:1; Rare:42 | ||||
chr4:40594295-40594525 | Common:7; Rare:43 |