| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188292689-188292854 | Common:1; Rare:39 | ||||
| chr2:188293000-188293064 | Rare:7 | ||||
| chr2:189441050-189441501 | Common:3; Rare:139 | ||||
| chr2:189783957-189784123 | Common:3; Rare:61; Clinvar (benign):1 | ||||
| chr2:189784271-189784543 | Common:4; Rare:101; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343880-190343924 | Rare:5 | ||||
| chr2:190343961-190344050 | Rare:17 | ||||
| chr2:190469907-190469971 | Rare:9 | ||||
| chr2:190534688-190534847 | Common:1; Rare:54 | ||||
| chr2:190648709-190648906 | Common:1; Rare:74 | ||||
| chr2:190880644-190880834 | Common:3; Rare:61 | ||||
| chr2:191014133-191014333 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245257-191245525 | Common:2; Rare:82 | ||||
| chr2:191246162-191246305 | Common:1; Rare:41 | ||||
| chr2:191677856-191678173 | Common:4; Rare:91 |