| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9555187-9555633 | Rare:287; Clinvar:4 | ||||
| chr2:9555620-9556132 | Common:16; Rare:806 | ||||
| chr2:9556195-9556595 | Common:10; Rare:108 | ||||
| chr2:9629389-9630322 | Common:9; Rare:488 | ||||
| chr2:9630310-9630890 | Common:24; Rare:810 | ||||
| chr2:9630909-9631363 | Common:10; Rare:482 | ||||
| chr2:9842972-9843950 | Common:64; Rare:1022 | ||||
| chr2:9844016-9844506 | Common:14; Rare:214 | ||||
| chr2:9951338-9951807 | Common:11; Rare:537 | ||||
| chr2:10042677-10042962 | Common:3; Rare:157 | ||||
| chr2:10043100-10043710 | Common:66; Rare:943; Clinvar:11; Clinvar (benign):3 | ||||
| chr2:10043780-10044340 | Common:44; Rare:767 | ||||
| chr2:10044241-10044727 | Common:13; Rare:261 | ||||
| chr2:10121188-10122250 | Common:7; Rare:416 | ||||
| chr2:10122153-10123899 | Common:46; Rare:1920 |