| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:189940547-189940964 | Common:11; Rare:132 | ||||
| chr5:218114-218361 | Common:3; Rare:100; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:443080-443272 | Common:10; Rare:87 | ||||
| chr5:612211-612351 | Rare:55 | ||||
| chr5:892738-892992 | Common:2; Rare:102 | ||||
| chr5:1799784-1799988 | Common:7; Rare:96 | ||||
| chr5:1801287-1801447 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:7868987-7869198 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr5:10249869-10250417 | Common:19; Rare:255; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353590-10353901 | Common:3; Rare:116 | ||||
| chr5:16465709-16465913 | Rare:42 | ||||
| chr5:31532070-31532367 | Common:2; Rare:88 | ||||
| chr5:33440615-33441058 | Common:6; Rare:115 | ||||
| chr5:33891982-33892303 | Rare:76 | ||||
| chr5:34915472-34915755 | Common:1; Rare:75 |