| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237085809-237085951 | Common:1; Rare:57 | ||||
| chr2:237487136-237487323 | Common:3; Rare:53 | ||||
| chr2:237590671-237591220 | Common:10; Rare:113 | ||||
| chr2:237627469-237627675 | Common:2; Rare:75 | ||||
| chr2:237691787-237692110 | Common:3; Rare:51 | ||||
| chr2:237968650-237968812 | Common:2; Rare:30 | ||||
| chr2:238060734-238061143 | Common:6; Rare:127 | ||||
| chr2:238203583-238203821 | Common:3; Rare:101 | ||||
| chr2:238320275-238320653 | Common:2; Rare:127 | ||||
| chr2:238426895-238427067 | Common:1; Rare:63 | ||||
| chr2:239401635-239401791 | Rare:84 | ||||
| chr2:240025225-240025455 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240136212-240136404 | Common:1; Rare:85 | ||||
| chr2:240140340-240140699 | Common:3; Rare:61 | ||||
| chr2:240560754-240560906 | Common:2; Rare:69 |