| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:195657039-195657327 | Common:1; Rare:85 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453139-197453554 | Rare:139 | ||||
| chr2:197499807-197500427 | Common:1; Rare:238; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515772-197516101 | Common:2; Rare:112 | ||||
| chr2:197675711-197675820 | Rare:13 | ||||
| chr2:199911037-199911409 | Common:1; Rare:115 | ||||
| chr2:200306036-200306291 | Common:1; Rare:57 | ||||
| chr2:200306420-200306566 | Common:2; Rare:34 | ||||
| chr2:200509926-200510075 | Common:1; Rare:59 | ||||
| chr2:200510082-200510128 | Rare:15 | ||||
| chr2:200811324-200811598 | Common:1; Rare:88 | ||||
| chr2:200811766-200812012 | Rare:100 | ||||
| chr2:200864222-200864252 | Rare:8 | ||||
| chr2:200864580-200864811 | Common:1; Rare:86 |