| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10643613-10643647 | Rare:8 | ||||
| chr20:10645393-10645729 | Common:2; Rare:60; Clinvar (benign):2 | ||||
| chr20:10863971-10864330 | Common:1; Rare:61 | ||||
| chr20:10864338-10864616 | Common:4; Rare:64 | ||||
| chr20:17614738-17615058 | Common:2; Rare:111 | ||||
| chr20:17621456-17621776 | Common:4; Rare:101 | ||||
| chr20:17633451-17633768 | Rare:86 | ||||
| chr20:18022858-18022999 | Rare:19 | ||||
| chr20:18056798-18057043 | Rare:79 | ||||
| chr20:18793974-18794123 | Rare:49 | ||||
| chr20:19214261-19214327 | Common:1; Rare:17 | ||||
| chr20:19756347-19756707 | Common:5; Rare:75 | ||||
| chr20:19757007-19757135 | Common:1; Rare:21 | ||||
| chr20:19757499-19757826 | Common:3; Rare:86 | ||||
| chr20:19757884-19757916 | Rare:5 |