| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:195657060-195657320 | Common:1; Rare:80 | ||||
| chr2:196068770-196068928 | Common:1; Rare:48 | ||||
| chr2:196639553-196639692 | Rare:35 | ||||
| chr2:196926656-196926797 | Common:2; Rare:64 | ||||
| chr2:197434970-197435194 | Rare:75 | ||||
| chr2:197497285-197497588 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197499791-197500439 | Common:2; Rare:246; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515976-197516089 | Rare:47 | ||||
| chr2:197675571-197675804 | Common:10; Rare:49 | ||||
| chr2:200510040-200510135 | Rare:32 | ||||
| chr2:200864190-200864286 | Rare:41 | ||||
| chr2:200864562-200864788 | Common:1; Rare:83 | ||||
| chr2:200889005-200889455 | Common:3; Rare:145 | ||||
| chr2:200963587-200963905 | Common:1; Rare:84 | ||||
| chr2:201071601-201072067 | Rare:100 |