| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:676285-676367 | Common:1; Rare:12 | ||||
| chr2:677339-677505 | Common:1; Rare:70 | ||||
| chr2:1744500-1744568 | Common:1; Rare:30 | ||||
| chr2:3377781-3377913 | Rare:40 | ||||
| chr2:3379594-3379785 | Common:2; Rare:78 | ||||
| chr2:3472508-3472561 | Common:1; Rare:8 | ||||
| chr2:3478835-3479293 | Common:3; Rare:137; Clinvar (pathogenic):1 | ||||
| chr2:3519381-3519668 | Common:2; Rare:83 | ||||
| chr2:3558216-3558758 | Common:6; Rare:192 | ||||
| chr2:3558885-3558955 | Rare:17 | ||||
| chr2:3575098-3575384 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:8679095-8679251 | Rare:62 | ||||
| chr2:8837483-8837766 | Common:1; Rare:101 | ||||
| chr2:9422941-9423734 | Common:2; Rare:193 | ||||
| chr2:9474493-9474632 | Common:6; Rare:65 |