| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:4686525-4686704 | Common:2; Rare:50 | ||||
| chr20:4823402-4823709 | Common:4; Rare:61 | ||||
| chr20:4823744-4823796 | Rare:15 | ||||
| chr20:5112852-5113179 | Common:1; Rare:118 | ||||
| chr20:5119907-5120174 | Common:1; Rare:90 | ||||
| chr20:5126546-5126780 | Common:3; Rare:65 | ||||
| chr20:5610859-5611154 | Common:2; Rare:99 | ||||
| chr20:5950391-5950720 | Common:8; Rare:101 | ||||
| chr20:10673902-10674040 | Common:3; Rare:52; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:10674042-10674125 | Common:1; Rare:24; Clinvar (benign):2 | ||||
| chr20:11890573-11890943 | Common:3; Rare:125 | ||||
| chr20:13784871-13785112 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13785336-13785394 | Rare:15 | ||||
| chr20:13995241-13995624 | Rare:109 | ||||
| chr20:14337440-14337553 | Rare:31 |