| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:13785048-13785702 | Common:12; Rare:480; Clinvar:7; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr20:16573240-16573640 | Common:10; Rare:625 | ||||
| chr20:16729750-16730200 | Common:4; Rare:358 | ||||
| chr20:17558700-17559121 | Common:5; Rare:134 | ||||
| chr20:17568956-17570191 | Common:36; Rare:1014 | ||||
| chr20:17681357-17682084 | Common:5; Rare:211 | ||||
| chr20:17682151-17682652 | Common:25; Rare:661 | ||||
| chr20:17682661-17683061 | Rare:85 | ||||
| chr20:17967491-17968171 | Common:15; Rare:229 | ||||
| chr20:17968181-17968710 | Common:28; Rare:537 | ||||
| chr20:17968640-17969171 | Common:29; Rare:1014 | ||||
| chr20:17969339-17969744 | Common:4; Rare:192 | ||||
| chr20:17969757-17971054 | Common:7; Rare:709; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr20:18137625-18138025 | Common:7; Rare:369 | ||||
| chr20:18138071-18138572 | Common:8; Rare:316 |