| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188291615-188292078 | Common:6; Rare:130 | ||||
| chr2:188292716-188292861 | Common:1; Rare:38 | ||||
| chr2:189441072-189441151 | Rare:26 | ||||
| chr2:189783965-189784123 | Common:3; Rare:60; Clinvar (benign):1 | ||||
| chr2:189784276-189784532 | Common:4; Rare:91; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190319736-190319960 | Common:5; Rare:82; Clinvar (benign):5 | ||||
| chr2:190343868-190344031 | Rare:32 | ||||
| chr2:190469606-190469815 | Common:9; Rare:47 | ||||
| chr2:190534696-190534955 | Common:2; Rare:85 | ||||
| chr2:190900395-190900660 | Common:1; Rare:56 | ||||
| chr2:191014143-191014333 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245273-191245554 | Common:2; Rare:87 | ||||
| chr2:191677856-191678163 | Common:4; Rare:88 | ||||
| chr2:196171428-196171912 | Common:1; Rare:143 | ||||
| chr2:197434973-197435176 | Rare:70 |