| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190343958-190344038 | Rare:15 | ||||
| chr2:191245123-191245515 | Common:3; Rare:123 | ||||
| chr2:197499802-197500416 | Common:1; Rare:235; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:200510060-200510141 | Rare:21 | ||||
| chr2:200585962-200586081 | Rare:33 | ||||
| chr2:200889239-200889444 | Common:2; Rare:77 | ||||
| chr2:201071634-201071802 | Rare:39 | ||||
| chr2:201451518-201451753 | Rare:52 | ||||
| chr2:203238930-203239021 | Rare:32 | ||||
| chr2:203328206-203328411 | Common:2; Rare:80 | ||||
| chr2:206085772-206085981 | Common:1; Rare:60 | ||||
| chr2:206159345-206159729 | Common:3; Rare:112; Clinvar (benign):1 | ||||
| chr2:206765284-206765663 | Common:3; Rare:104; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165925-207166141 | Rare:43 | ||||
| chr2:208255032-208255233 | Common:2; Rare:52 |