| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183078666-183078799 | Rare:50 | ||||
| chr2:186485884-186486408 | Common:6; Rare:256 | ||||
| chr2:186589894-186590356 | Rare:277 | ||||
| chr2:187554360-187554505 | Rare:33 | ||||
| chr2:189441030-189441527 | Common:6; Rare:309 | ||||
| chr2:189580752-189580941 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:189674422-189674765 | Common:5; Rare:156 | ||||
| chr2:189762415-189763385 | Common:5; Rare:368 | ||||
| chr2:189783942-189784140 | Common:9; Rare:139; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:189784264-189784590 | Common:8; Rare:217; Clinvar:16; Clinvar (benign):5 | ||||
| chr2:190319714-190320011 | Common:10; Rare:200; Clinvar (benign):10 | ||||
| chr2:190343427-190343674 | Common:2; Rare:54 | ||||
| chr2:190343743-190344077 | Common:1; Rare:142 | ||||
| chr2:190534330-190534608 | Common:14; Rare:136 | ||||
| chr2:190534633-190534846 | Common:4; Rare:106 |