| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:135170466-135170977 | Common:7; Rare:169 | ||||
| chr7:135662370-135662550 | Common:3; Rare:83 | ||||
| chr7:135977303-135977530 | Common:2; Rare:88 | ||||
| chr7:139109334-139109449 | Common:1; Rare:36 | ||||
| chr7:139133691-139133809 | Rare:29 | ||||
| chr7:139341245-139341379 | Rare:30 | ||||
| chr7:139359452-139359512 | Rare:20 | ||||
| chr7:139359690-139359982 | Common:3; Rare:116 | ||||
| chr7:139777708-139778075 | Common:2; Rare:98 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738628 | Common:5; Rare:165 | ||||
| chr7:143380863-143381315 | Common:2; Rare:130 | ||||
| chr7:143902099-143902304 | Common:6; Rare:65 | ||||
| chr7:144835966-144836054 | Common:1; Rare:23; Clinvar (benign):2 | ||||
| chr7:148884206-148884440 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):1 |