| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359690-139359982 | Common:3; Rare:116 | ||||
| chr7:139777713-139778076 | Common:2; Rare:98 | ||||
| chr7:140479179-140479324 | Common:1; Rare:63 | ||||
| chr7:140924705-140925092 | Common:3; Rare:143; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:141014920-141015123 | Rare:45 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141737980-141738619 | Common:5; Rare:177 | ||||
| chr7:142854990-142855220 | Common:4; Rare:62 | ||||
| chr7:143263392-143263543 | Rare:50 | ||||
| chr7:143288122-143288451 | Common:1; Rare:112 | ||||
| chr7:143361266-143361501 | Rare:45 | ||||
| chr7:143362040-143362298 | Rare:43 | ||||
| chr7:143362582-143362895 | Common:1; Rare:76 | ||||
| chr7:143380964-143381315 | Common:1; Rare:110 | ||||
| chr7:143882793-143882983 | Rare:48 |