| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:13995280-13995557 | Rare:70 | ||||
| chr20:14337515-14337655 | Rare:33 | ||||
| chr20:16573343-16573547 | Common:1; Rare:57 | ||||
| chr20:16729827-16730065 | Common:1; Rare:72 | ||||
| chr20:17226600-17227070 | Common:1; Rare:129 | ||||
| chr20:17531051-17531451 | Common:8; Rare:163; Clinvar (benign):1 | ||||
| chr20:17531462-17531702 | Rare:43 | ||||
| chr20:17569090-17569420 | Common:2; Rare:72 | ||||
| chr20:17569942-17570143 | Common:3; Rare:84 | ||||
| chr20:17682230-17682624 | Common:5; Rare:126 | ||||
| chr20:17967990-17968511 | Common:8; Rare:288 | ||||
| chr20:17968636-17969150 | Common:5; Rare:179 | ||||
| chr20:17969904-17970119 | Rare:68; Clinvar (benign):2 | ||||
| chr20:18137733-18137927 | Common:1; Rare:64 | ||||
| chr20:18288113-18288283 | Rare:50 |