| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:13268368-13268465 | Rare:9 | ||||
| chr20:15571010-15571289 | Common:1; Rare:54 | ||||
| chr20:15580491-15580600 | Rare:17 | ||||
| chr20:15679466-15679624 | Common:1; Rare:35 | ||||
| chr20:17568152-17568189 | Common:1; Rare:5 | ||||
| chr20:17570858-17570920 | Rare:8 | ||||
| chr20:17615927-17616307 | Common:4; Rare:107 | ||||
| chr20:17627341-17627667 | Common:2; Rare:146 | ||||
| chr20:19756450-19756707 | Common:3; Rare:55 | ||||
| chr20:19757461-19757704 | Common:3; Rare:69 | ||||
| chr20:19757920-19758289 | Common:5; Rare:127 | ||||
| chr20:19823921-19823944 | Rare:7 | ||||
| chr20:19940682-19940920 | Rare:47 | ||||
| chr20:23025627-23025760 | Common:3; Rare:27 | ||||
| chr20:23047467-23047661 | Common:1; Rare:45; Clinvar (benign):2 |