| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35699305-35699475 | Rare:59; Clinvar (benign):3 | ||||
| chr20:35742136-35742651 | Common:5; Rare:162 | ||||
| chr20:35771781-35772060 | Common:2; Rare:85 | ||||
| chr20:36236440-36236491 | Rare:9 | ||||
| chr20:36541386-36541555 | Common:2; Rare:50 | ||||
| chr20:36605495-36605809 | Common:2; Rare:114 | ||||
| chr20:36746044-36746304 | Common:2; Rare:94 | ||||
| chr20:36773733-36773944 | Common:3; Rare:76 | ||||
| chr20:36951640-36951742 | Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:37178865-37179243 | Rare:110 | ||||
| chr20:37289507-37289669 | Common:1; Rare:46 | ||||
| chr20:37520978-37521262 | Common:1; Rare:67 | ||||
| chr20:37527820-37528186 | Common:5; Rare:129 | ||||
| chr20:38033416-38033764 | Common:2; Rare:100 | ||||
| chr20:38165188-38165390 | Common:1; Rare:71 |