| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44475772-44475957 | Common:1; Rare:80 | ||||
| chr20:44521986-44522213 | Common:2; Rare:73 | ||||
| chr20:44651688-44651839 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr20:44960362-44960422 | Common:1; Rare:30 | ||||
| chr20:44966351-44966571 | Common:2; Rare:86 | ||||
| chr20:45405833-45406066 | Common:2; Rare:59 | ||||
| chr20:45406537-45406729 | Rare:52 | ||||
| chr20:45791913-45791989 | Rare:26 | ||||
| chr20:45857353-45857620 | Common:3; Rare:65 | ||||
| chr20:45881111-45881234 | Common:1; Rare:26 | ||||
| chr20:45891256-45891379 | Common:1; Rare:44; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45912106-45912305 | Common:3; Rare:47 | ||||
| chr20:45934411-45934710 | Common:2; Rare:127 | ||||
| chr20:46364386-46364570 | Common:1; Rare:69 | ||||
| chr20:46406565-46406766 | Common:2; Rare:51 |