| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42568414-42568767 | Common:6; Rare:90 | ||||
| chr2:43226597-43226847 | Common:1; Rare:96 | ||||
| chr2:44361772-44362002 | Common:1; Rare:67 | ||||
| chr2:46616974-46617270 | Common:7; Rare:131 | ||||
| chr2:46915744-46915882 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47905493-47905848 | Common:3; Rare:175 | ||||
| chr2:53786856-53787086 | Rare:78 | ||||
| chr2:53970983-53971113 | Common:3; Rare:52 | ||||
| chr2:55050348-55050782 | Common:5; Rare:128 | ||||
| chr2:55232256-55232759 | Common:4; Rare:146 | ||||
| chr2:55232764-55232810 | Common:1; Rare:19 | ||||
| chr2:55519455-55519779 | Common:1; Rare:93 | ||||
| chr2:61017185-61017753 | Common:4; Rare:165; Clinvar:2 | ||||
| chr2:61144971-61145128 | Common:2; Rare:49 | ||||
| chr2:61538008-61538138 | Common:2; Rare:23 |