| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134891352-134891626 | Common:3; Rare:75 | ||||
| chr7:134986367-134986668 | Common:6; Rare:96 | ||||
| chr7:134986791-134986856 | Rare:20 | ||||
| chr7:135170393-135170422 | Rare:10 | ||||
| chr7:135170486-135170932 | Common:4; Rare:153 | ||||
| chr7:135211498-135211745 | Common:2; Rare:114 | ||||
| chr7:135510049-135510297 | Common:3; Rare:57 | ||||
| chr7:135662297-135662580 | Common:5; Rare:130 | ||||
| chr7:135977303-135977542 | Common:3; Rare:91 | ||||
| chr7:136868422-136868475 | Rare:13 | ||||
| chr7:136868530-136868841 | Common:1; Rare:66 | ||||
| chr7:136868970-136869096 | Rare:21 | ||||
| chr7:136869130-136869281 | Common:2; Rare:28; Clinvar (benign):3 | ||||
| chr7:137343474-137343690 | Rare:83 | ||||
| chr7:138002045-138002277 | Common:1; Rare:59 |