| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2843603-2844038 | Common:10; Rare:410 | ||||
| chr4:2907989-2908180 | Common:1; Rare:36 | ||||
| chr4:2934395-2934599 | Common:3; Rare:32 | ||||
| chr4:2934739-2935027 | Common:14; Rare:291 | ||||
| chr4:2935110-2935357 | Common:1; Rare:57 | ||||
| chr4:2962690-2962979 | Rare:105 | ||||
| chr4:2963264-2963674 | Common:9; Rare:417 | ||||
| chr4:2963907-2964112 | Common:4; Rare:137 | ||||
| chr4:3073900-3074450 | Common:10; Rare:145 | ||||
| chr4:3074492-3075526 | Common:56; Rare:633; Clinvar:4; Clinvar (benign):4 | ||||
| chr4:3292657-3293161 | Common:9; Rare:476 | ||||
| chr4:3342470-3342740 | Common:2; Rare:105 | ||||
| chr4:3463102-3463545 | Common:9; Rare:388; Clinvar:2; Clinvar (benign):10 | ||||
| chr4:3484325-3484981 | Common:13; Rare:245 | ||||
| chr4:3484969-3485752 | Common:21; Rare:447; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):6 |