| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189763189-189763310 | Common:1; Rare:25 | ||||
| chr2:189783957-189784125 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr2:189784271-189784547 | Common:4; Rare:102; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343868-190343938 | Rare:11 | ||||
| chr2:190880644-190880905 | Common:4; Rare:91 | ||||
| chr2:191014115-191014312 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245061-191245178 | Common:1; Rare:27 | ||||
| chr2:191245219-191245599 | Common:3; Rare:124 | ||||
| chr2:191246163-191246351 | Common:1; Rare:48 | ||||
| chr2:191677846-191678155 | Common:4; Rare:89 | ||||
| chr2:192194876-192195086 | Rare:50 | ||||
| chr2:195656821-195657279 | Common:2; Rare:129 | ||||
| chr2:196068769-196068909 | Common:1; Rare:40 | ||||
| chr2:196926623-196926796 | Common:2; Rare:78 | ||||
| chr2:197310608-197311012 | Common:1; Rare:91 |