| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915709-46915910 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46916007-46916181 | Common:2; Rare:56 | ||||
| chr2:46941694-46941844 | Common:3; Rare:52; Clinvar (benign):1 | ||||
| chr2:47176432-47176864 | Common:4; Rare:192; Clinvar (benign):5 | ||||
| chr2:47402935-47403218 | Common:1; Rare:136; Clinvar:47; Clinvar (benign):33; Clinvar (pathogenic):1 | ||||
| chr2:47782924-47783214 | Common:2; Rare:130; Clinvar:6; Clinvar (benign):10 | ||||
| chr2:47905497-47905847 | Common:3; Rare:172 | ||||
| chr2:48314161-48314781 | Common:1; Rare:214 | ||||
| chr2:48440619-48440833 | Common:6; Rare:96 | ||||
| chr2:53767559-53767984 | Common:5; Rare:158 | ||||
| chr2:53786842-53787229 | Common:1; Rare:146 | ||||
| chr2:53970780-53971163 | Common:12; Rare:141 | ||||
| chr2:54115782-54115993 | Common:5; Rare:81 | ||||
| chr2:54557805-54557960 | Rare:35 | ||||
| chr2:54558621-54558866 | Common:1; Rare:73 |