| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47782918-47783236 | Common:2; Rare:146; Clinvar:8; Clinvar (benign):20 | ||||
| chr2:48440631-48440824 | Common:5; Rare:87 | ||||
| chr2:51032099-51032203 | Rare:30; Clinvar:2 | ||||
| chr2:53767469-53767891 | Common:5; Rare:138 | ||||
| chr2:53786836-53787285 | Common:1; Rare:176 | ||||
| chr2:53970762-53971116 | Common:9; Rare:119 | ||||
| chr2:54558196-54558428 | Common:2; Rare:75 | ||||
| chr2:55050302-55050583 | Common:4; Rare:103 | ||||
| chr2:55232235-55232872 | Common:6; Rare:200 | ||||
| chr2:55419823-55420125 | Common:4; Rare:118 | ||||
| chr2:55519409-55519804 | Common:1; Rare:123 | ||||
| chr2:58046625-58046877 | Common:2; Rare:78 | ||||
| chr2:58241306-58241416 | Rare:65; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:60550899-60550978 | Rare:23 | ||||
| chr2:61017388-61017753 | Common:1; Rare:113; Clinvar:2 |