| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44651687-44651789 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr20:44885393-44885838 | Common:8; Rare:138 | ||||
| chr20:44960334-44960555 | Common:1; Rare:89 | ||||
| chr20:44966361-44966566 | Common:1; Rare:83 | ||||
| chr20:45348388-45348593 | Common:1; Rare:60 | ||||
| chr20:45362933-45363232 | Rare:89 | ||||
| chr20:45363357-45363537 | Common:1; Rare:47 | ||||
| chr20:45406537-45406723 | Rare:49 | ||||
| chr20:45416026-45416183 | Rare:57; Clinvar:1 | ||||
| chr20:45791888-45792030 | Common:2; Rare:57 | ||||
| chr20:45812286-45812774 | Common:5; Rare:143 | ||||
| chr20:45812968-45813180 | Common:2; Rare:35 | ||||
| chr20:45833718-45833851 | Common:3; Rare:31 | ||||
| chr20:45834076-45834207 | Rare:48 | ||||
| chr20:45857292-45857639 | Common:4; Rare:101 |