| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139109328-139109460 | Common:1; Rare:40 | ||||
| chr7:139133654-139133833 | Rare:46 | ||||
| chr7:139231006-139231277 | Common:2; Rare:97 | ||||
| chr7:139341234-139341380 | Rare:34 | ||||
| chr7:139359672-139360008 | Common:3; Rare:130 | ||||
| chr7:140479359-140479411 | Rare:12 | ||||
| chr7:140696646-140696995 | Common:2; Rare:115 | ||||
| chr7:140697115-140697248 | Rare:41 | ||||
| chr7:141014617-141014744 | Rare:22 | ||||
| chr7:141014924-141015106 | Rare:41 | ||||
| chr7:141551265-141551423 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738177-141738619 | Common:1; Rare:137 | ||||
| chr7:142854998-142855138 | Common:2; Rare:43 | ||||
| chr7:143362064-143362287 | Rare:34 | ||||
| chr7:143362622-143362884 | Common:1; Rare:65 |