| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9555457-9555518 | Rare:21 | ||||
| chr2:9555530-9555776 | Common:1; Rare:85; Clinvar:2 | ||||
| chr2:9555798-9556294 | Common:1; Rare:151 | ||||
| chr2:9630411-9630656 | Common:4; Rare:109 | ||||
| chr2:9630743-9630802 | Common:1; Rare:20 | ||||
| chr2:9630816-9631413 | Common:3; Rare:184 | ||||
| chr2:9843191-9843593 | Common:10; Rare:126 | ||||
| chr2:9843615-9843767 | Common:3; Rare:57 | ||||
| chr2:9843866-9843968 | Rare:22 | ||||
| chr2:9951376-9951969 | Common:6; Rare:186 | ||||
| chr2:9952021-9952042 | Rare:5 | ||||
| chr2:10042677-10043025 | Common:5; Rare:107 | ||||
| chr2:10043120-10043655 | Common:27; Rare:203; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:10043725-10044390 | Common:13; Rare:266; Clinvar:1 | ||||
| chr2:10044440-10044521 | Common:1; Rare:24 |