| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:165691774-165691860 | Rare:22 | ||||
| chr2:165886392-165886664 | Common:2; Rare:46 | ||||
| chr2:166091145-166091201 | Rare:6 | ||||
| chr2:166234257-166234420 | Common:3; Rare:21 | ||||
| chr2:166239663-166239842 | Common:1; Rare:35 | ||||
| chr2:166344734-166344953 | Common:1; Rare:37 | ||||
| chr2:166361050-166361066 | Rare:1 | ||||
| chr2:166361382-166361503 | Common:2; Rare:26 | ||||
| chr2:166410957-166411169 | Common:3; Rare:39 | ||||
| chr2:166411290-166411375 | Common:1; Rare:16 | ||||
| chr2:166411643-166411744 | Rare:18 | ||||
| chr2:166411762-166411956 | Common:2; Rare:36 | ||||
| chr2:166958794-166959072 | Common:2; Rare:65 | ||||
| chr2:166959333-166959499 | Rare:22 | ||||
| chr2:166959840-166959887 | Rare:10 |