| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46617019-46617252 | Common:6; Rare:92 | ||||
| chr2:46915738-46915869 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:48440631-48440827 | Common:5; Rare:89 | ||||
| chr2:53767559-53767839 | Common:4; Rare:96 | ||||
| chr2:53786842-53787078 | Rare:81 | ||||
| chr2:53970788-53971110 | Common:9; Rare:106 | ||||
| chr2:55269201-55269310 | Common:2; Rare:30 | ||||
| chr2:55519452-55519746 | Common:1; Rare:79 | ||||
| chr2:58241300-58241431 | Rare:73; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:61017429-61017731 | Common:1; Rare:83; Clinvar:1 | ||||
| chr2:61144950-61145164 | Common:3; Rare:70 | ||||
| chr2:61888508-61888693 | Common:1; Rare:79 | ||||
| chr2:63588939-63589019 | Rare:30 | ||||
| chr2:63840807-63841143 | Common:1; Rare:96 | ||||
| chr2:63841705-63841941 | Common:1; Rare:85 |