| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2242161-2242292 | Common:4; Rare:143 | ||||
| chr7:2249690-2249960 | Common:1; Rare:100 | ||||
| chr7:2353971-2354142 | Common:7; Rare:127 | ||||
| chr7:2354269-2354961 | Common:11; Rare:434 | ||||
| chr7:2403278-2403631 | Common:1; Rare:138 | ||||
| chr7:2519554-2519805 | Common:4; Rare:232 | ||||
| chr7:2522852-2523830 | Common:7; Rare:388 | ||||
| chr7:2555465-2555950 | Common:10; Rare:207 | ||||
| chr7:2558908-2559176 | Common:4; Rare:190 | ||||
| chr7:2631609-2632045 | Common:6; Rare:237 | ||||
| chr7:2844143-2844751 | Common:8; Rare:275 | ||||
| chr7:4682042-4682305 | Common:2; Rare:196 | ||||
| chr7:4775337-4775764 | Common:13; Rare:285; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:5045777-5045938 | Common:6; Rare:149 | ||||
| chr7:5046282-5046481 | Rare:81 |