| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63367138-63367401 | Common:1; Rare:91 | ||||
| chr18:63422360-63422716 | Common:2; Rare:105 | ||||
| chr18:67516713-67517031 | Common:5; Rare:83 | ||||
| chr18:68714982-68715317 | Common:7; Rare:139 | ||||
| chr18:70205659-70205784 | Common:3; Rare:51; Clinvar (benign):2 | ||||
| chr18:70288788-70289078 | Common:3; Rare:91 | ||||
| chr18:74148295-74148555 | Common:2; Rare:99 | ||||
| chr18:74291906-74292245 | Common:3; Rare:95 | ||||
| chr18:74496029-74496402 | Common:4; Rare:118 | ||||
| chr18:74597548-74597929 | Common:2; Rare:104 | ||||
| chr18:76822236-76822591 | Common:11; Rare:99 | ||||
| chr18:79988274-79988671 | Common:4; Rare:130; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344788-344925 | Common:3; Rare:43 | ||||
| chr19:409083-409287 | Common:2; Rare:72 | ||||
| chr19:633520-633710 | Common:8; Rare:86 |