| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85888940-85889240 | Common:8; Rare:189; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:86105773-86106257 | Common:6; Rare:279 | ||||
| chr2:86194883-86195174 | Common:2; Rare:123 | ||||
| chr2:86195354-86195704 | Common:13; Rare:159 | ||||
| chr2:86199359-86199505 | Common:2; Rare:90 | ||||
| chr2:86440630-86440970 | Common:6; Rare:205 | ||||
| chr2:86563312-86563563 | Common:4; Rare:185 | ||||
| chr2:86623528-86623668 | Rare:44 | ||||
| chr2:86623763-86624034 | Common:3; Rare:223 | ||||
| chr2:88054940-88055650 | Rare:251 | ||||
| chr2:88055712-88055951 | Rare:171 | ||||
| chr2:88627313-88627757 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:88627710-88627900 | Common:1; Rare:55 | ||||
| chr2:88691438-88691853 | Common:5; Rare:320; Clinvar:2 | ||||
| chr2:95121740-95122094 | Common:1; Rare:202 |