| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139109327-139109473 | Common:1; Rare:44 | ||||
| chr7:139109712-139109811 | Common:1; Rare:26 | ||||
| chr7:139133675-139133816 | Rare:34 | ||||
| chr7:139341216-139341380 | Rare:40 | ||||
| chr7:139359716-139359988 | Common:3; Rare:97 | ||||
| chr7:139777608-139777675 | Common:1; Rare:16 | ||||
| chr7:139778038-139778308 | Common:2; Rare:60 | ||||
| chr7:140398441-140398589 | Common:1; Rare:51 | ||||
| chr7:140696627-140696745 | Common:1; Rare:43 | ||||
| chr7:141014628-141014744 | Rare:18 | ||||
| chr7:141014920-141015019 | Rare:23 | ||||
| chr7:141551256-141551434 | Common:2; Rare:51; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141737907-141738474 | Common:5; Rare:161 | ||||
| chr7:142854990-142855153 | Common:2; Rare:46 | ||||
| chr7:143263392-143263560 | Rare:53 |