| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149749589-149749805 | Rare:109 | ||||
| chr6:151391500-151391837 | Common:3; Rare:98 | ||||
| chr6:151452022-151452548 | Common:5; Rare:188; Clinvar (benign):3 | ||||
| chr6:152302041-152302237 | Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152983005-152983281 | Common:2; Rare:83 | ||||
| chr6:152983499-152983778 | Common:4; Rare:108 | ||||
| chr6:153002681-153002838 | Common:2; Rare:49 | ||||
| chr6:155183044-155183325 | Rare:66 | ||||
| chr6:155314456-155314844 | Common:10; Rare:130 | ||||
| chr6:157323505-157323630 | Common:2; Rare:37 | ||||
| chr6:158168219-158168388 | Common:2; Rare:61 | ||||
| chr6:158644715-158644816 | Common:2; Rare:46 | ||||
| chr6:158819316-158819437 | Common:2; Rare:48 | ||||
| chr6:158999762-158999886 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159044965-159045274 | Rare:54 |