| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197602696-197602886 | Common:5; Rare:51 | ||||
| chr3:197627833-197627987 | Common:6; Rare:54 | ||||
| chr4:678757-679119 | Common:2; Rare:125 | ||||
| chr4:760770-760813 | Rare:16 | ||||
| chr4:761108-761314 | Common:2; Rare:71 | ||||
| chr4:896497-896681 | Rare:48 | ||||
| chr4:971646-971841 | Common:1; Rare:46 | ||||
| chr4:1177776-1178057 | Common:3; Rare:60 | ||||
| chr4:1178693-1178736 | Rare:4 | ||||
| chr4:1245981-1246149 | Common:1; Rare:46 | ||||
| chr4:1806073-1806326 | Common:2; Rare:95; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr4:2036998-2037136 | Rare:25 | ||||
| chr4:2761417-2761773 | Common:2; Rare:93 | ||||
| chr4:2762743-2762945 | Common:3; Rare:59 | ||||
| chr4:2939623-2939927 | Common:3; Rare:114 |