| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437087-39437447 | Common:4; Rare:127 | ||||
| chr2:44361479-44361959 | Common:3; Rare:150 | ||||
| chr2:46617019-46617255 | Common:6; Rare:99 | ||||
| chr2:46915744-46915908 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176456-47176573 | Rare:87; Clinvar (benign):4 | ||||
| chr2:47345052-47345148 | Rare:26 | ||||
| chr2:48440631-48440821 | Common:5; Rare:83 | ||||
| chr2:53786842-53787072 | Rare:76 | ||||
| chr2:53970798-53971152 | Common:10; Rare:127 | ||||
| chr2:54115534-54115681 | Rare:53 | ||||
| chr2:55232256-55232413 | Common:3; Rare:35 | ||||
| chr2:58046419-58046644 | Rare:64 | ||||
| chr2:60881327-60881610 | Common:2; Rare:119 | ||||
| chr2:61017420-61017753 | Common:1; Rare:100; Clinvar:2 | ||||
| chr2:61144949-61145165 | Common:3; Rare:71 |