| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43053694-43054047 | Common:3; Rare:188; Clinvar:10; Clinvar (benign):1 | ||||
| chr6:43059803-43059913 | Rare:35 | ||||
| chr6:43059822-43059955 | Common:1; Rare:40 | ||||
| chr6:43171054-43171548 | Rare:276 | ||||
| chr6:43182045-43182238 | Rare:93 | ||||
| chr6:43369455-43369930 | Common:6; Rare:255 | ||||
| chr6:43427443-43427599 | Rare:82 | ||||
| chr6:43427761-43427984 | Rare:104 | ||||
| chr6:43455530-43455950 | Common:10; Rare:151 | ||||
| chr6:43477507-43477742 | Common:1; Rare:92 | ||||
| chr6:43516744-43517169 | Common:11; Rare:286; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:43575876-43576231 | Common:3; Rare:252; Clinvar:15 | ||||
| chr6:43627287-43627560 | Common:1; Rare:65 | ||||
| chr6:43628752-43628952 | Rare:74 | ||||
| chr6:43629064-43629500 | Common:3; Rare:124 |