| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:226794589-226795164 | Common:2; Rare:133 | ||||
| chr2:226795345-226796295 | Common:4; Rare:346; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:226798949-226799304 | Common:3; Rare:97 | ||||
| chr2:226799721-226800273 | Common:1; Rare:152 | ||||
| chr2:226835866-226836090 | Rare:90 | ||||
| chr2:226836334-226836418 | Common:2; Rare:20 | ||||
| chr2:227325200-227325430 | Common:5; Rare:77 | ||||
| chr2:227352045-227352113 | Common:2; Rare:13 | ||||
| chr2:227472189-227472550 | Common:1; Rare:107 | ||||
| chr2:227537052-227537327 | Rare:38 | ||||
| chr2:227871503-227871682 | Common:5; Rare:63 | ||||
| chr2:229814013-229814290 | Rare:62 | ||||
| chr2:229921927-229922522 | Common:3; Rare:210 | ||||
| chr2:229922875-229922968 | Rare:22 | ||||
| chr2:229923162-229923375 | Common:1; Rare:50 |