| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:218114-218369 | Common:3; Rare:107; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:443084-443275 | Common:10; Rare:87 | ||||
| chr5:612211-612357 | Rare:58 | ||||
| chr5:693286-693586 | Common:6; Rare:88 | ||||
| chr5:892540-892921 | Common:5; Rare:117 | ||||
| chr5:1799785-1799993 | Common:7; Rare:98 | ||||
| chr5:1801286-1801460 | Common:4; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422311-5422714 | Common:3; Rare:139 | ||||
| chr5:6632996-6633390 | Common:8; Rare:128; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:7868991-7869209 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:9546042-9546383 | Common:7; Rare:77 | ||||
| chr5:10249853-10250157 | Common:16; Rare:147 | ||||
| chr5:10353597-10353910 | Common:3; Rare:114 | ||||
| chr5:10441692-10441923 | Rare:64 | ||||
| chr5:14144225-14144317 | Common:1; Rare:23 |