| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177392925-177393069 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:178451098-178451424 | Common:5; Rare:98; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:186485998-186486367 | Common:3; Rare:109 | ||||
| chr2:187554297-187554548 | Rare:51 | ||||
| chr2:188292694-188292854 | Common:1; Rare:38 | ||||
| chr2:188293001-188293031 | Rare:5 | ||||
| chr2:189441151-189441501 | Common:2; Rare:103 | ||||
| chr2:189783960-189784133 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784275-189784547 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343910-190344053 | Rare:29 | ||||
| chr2:190534707-190534827 | Rare:37 | ||||
| chr2:197499829-197500429 | Common:1; Rare:237; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:200510049-200510206 | Rare:47 | ||||
| chr2:200811318-200811581 | Common:1; Rare:79 | ||||
| chr2:200889263-200889444 | Common:2; Rare:69 |