| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:138459933-138460319 | Rare:113 | ||||
| chr7:138460858-138461059 | Common:1; Rare:60 | ||||
| chr7:139109334-139109458 | Common:1; Rare:37 | ||||
| chr7:139133438-139133809 | Common:1; Rare:83 | ||||
| chr7:139231087-139231262 | Common:2; Rare:67 | ||||
| chr7:139340386-139340503 | Rare:32 | ||||
| chr7:139341188-139341380 | Rare:47 | ||||
| chr7:139359456-139359534 | Rare:24 | ||||
| chr7:139359690-139360008 | Common:3; Rare:123 | ||||
| chr7:140398434-140398591 | Common:1; Rare:52 | ||||
| chr7:140479169-140479429 | Common:2; Rare:91 | ||||
| chr7:140479471-140479639 | Rare:56 | ||||
| chr7:140696602-140696797 | Common:1; Rare:72 | ||||
| chr7:140924702-140925103 | Common:3; Rare:151; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:141014617-141014744 | Rare:22 |