| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37762503-37762737 | Common:3; Rare:95; Clinvar (benign):1 | ||||
| chr8:37849818-37850024 | Common:2; Rare:74 | ||||
| chr8:38030283-38030643 | Common:3; Rare:104 | ||||
| chr8:38105340-38105575 | Common:3; Rare:76 | ||||
| chr8:38105779-38105966 | Rare:54 | ||||
| chr8:38176412-38176564 | Common:1; Rare:59 | ||||
| chr8:38176648-38176906 | Common:5; Rare:73 | ||||
| chr8:38231685-38231858 | Rare:38 | ||||
| chr8:38269110-38269235 | Rare:54 | ||||
| chr8:38727984-38728391 | Common:5; Rare:73 | ||||
| chr8:38728394-38728681 | Common:1; Rare:57 | ||||
| chr8:38787012-38787249 | Rare:89 | ||||
| chr8:38901061-38901339 | Common:2; Rare:61 | ||||
| chr8:38901682-38901856 | Common:3; Rare:29 | ||||
| chr8:38996435-38997114 | Common:7; Rare:258 |