| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24052910-24053190 | Common:1; Rare:78 | ||||
| chr7:24075230-24075940 | Common:40; Rare:308 | ||||
| chr7:26193434-26193686 | Rare:88; Clinvar (benign):2 | ||||
| chr7:26549574-26549707 | Rare:29 | ||||
| chr7:29684750-29685270 | Common:13; Rare:307 | ||||
| chr7:29988761-29989068 | Rare:72 | ||||
| chr7:32728602-32728901 | Common:17; Rare:157 | ||||
| chr7:32942459-32942653 | Common:1; Rare:52 | ||||
| chr7:32943086-32943444 | Common:2; Rare:82 | ||||
| chr7:34036180-34036700 | Common:3; Rare:148 | ||||
| chr7:35249590-35249870 | Common:2; Rare:81 | ||||
| chr7:37666400-37666740 | Common:1; Rare:94 | ||||
| chr7:39733514-39733669 | Rare:32 | ||||
| chr7:40717310-40717590 | Common:4; Rare:83 | ||||
| chr7:40899130-40899500 | Common:5; Rare:188 |