| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:1233435-1233620 | Common:4; Rare:51 | ||||
| chr2:1246223-1246530 | Common:5; Rare:70 | ||||
| chr2:1388252-1388383 | Rare:27 | ||||
| chr2:1617660-1617983 | Common:16; Rare:111 | ||||
| chr2:1621748-1622250 | Common:29; Rare:200 | ||||
| chr2:1625184-1625709 | Common:10; Rare:249 | ||||
| chr2:1625979-1626176 | Common:1; Rare:44 | ||||
| chr2:1626392-1626508 | Common:1; Rare:27 | ||||
| chr2:1634084-1634526 | Common:5; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:1639347-1640747 | Common:22; Rare:434; Clinvar (benign):1 | ||||
| chr2:1742878-1743156 | Common:2; Rare:45 | ||||
| chr2:1743063-1743395 | Common:1; Rare:96 | ||||
| chr2:1743507-1743811 | Common:8; Rare:120 | ||||
| chr2:1772560-1773240 | Common:7; Rare:106 | ||||
| chr2:2083360-2083740 | Common:1; Rare:65 |