| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159712336-159712600 | Common:2; Rare:96 | ||||
| chr2:161308329-161308566 | Common:2; Rare:58 | ||||
| chr2:162073983-162074056 | Rare:23 | ||||
| chr2:162074058-162074113 | Rare:19 | ||||
| chr2:162074116-162074349 | Common:1; Rare:62 | ||||
| chr2:163735987-163736110 | Rare:23 | ||||
| chr2:165469540-165469711 | Rare:29 | ||||
| chr2:166375877-166376062 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:169584764-169584809 | Rare:14 | ||||
| chr2:169694360-169694497 | Common:2; Rare:45 | ||||
| chr2:169798767-169798965 | Rare:51 | ||||
| chr2:171433915-171434248 | Common:3; Rare:87 | ||||
| chr2:171522272-171522520 | Common:3; Rare:57 | ||||
| chr2:171687645-171687845 | Rare:58 | ||||
| chr2:171687965-171688016 | Common:1; Rare:9 |