| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191678273-191678347 | Rare:15 | ||||
| chr2:191678495-191679120 | Common:1; Rare:198 | ||||
| chr2:191846629-191846849 | Common:2; Rare:60 | ||||
| chr2:191846886-191847173 | Rare:74 | ||||
| chr2:195657060-195657320 | Common:1; Rare:80 | ||||
| chr2:196171351-196171897 | Common:2; Rare:161 | ||||
| chr2:196176296-196176380 | Rare:11 | ||||
| chr2:196242216-196242513 | Common:3; Rare:64 | ||||
| chr2:197197647-197197988 | Common:3; Rare:49 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453244-197453561 | Rare:109 | ||||
| chr2:197499817-197500015 | Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500106-197500430 | Common:1; Rare:135 | ||||
| chr2:197500864-197501148 | Common:1; Rare:71 | ||||
| chr2:197515835-197516094 | Common:2; Rare:94 |