| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:192194886-192195115 | Rare:62 | ||||
| chr2:196068782-196068910 | Common:1; Rare:37 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453089-197453571 | Rare:161 | ||||
| chr2:197499773-197500434 | Common:2; Rare:251; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:197515925-197516107 | Rare:75 | ||||
| chr2:197675680-197675820 | Rare:21 | ||||
| chr2:197705149-197705396 | Common:3; Rare:104 | ||||
| chr2:199911104-199911335 | Rare:65 | ||||
| chr2:200306420-200306572 | Common:2; Rare:39 | ||||
| chr2:200510040-200510210 | Rare:56 | ||||
| chr2:200811431-200811572 | Common:1; Rare:50 | ||||
| chr2:200864229-200864256 | Rare:8 | ||||
| chr2:200864569-200864811 | Common:1; Rare:88 | ||||
| chr2:200888970-200889455 | Common:3; Rare:153 |