| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:166375831-166377241 | Common:33; Rare:904; Clinvar:7; Clinvar (benign):29 | ||||
| chr2:168247330-168248041 | Common:22; Rare:601 | ||||
| chr2:168455584-168455904 | Common:14; Rare:87 | ||||
| chr2:168455901-168456932 | Common:3; Rare:889 | ||||
| chr2:168797449-168797849 | Common:5; Rare:71 | ||||
| chr2:168798301-168798863 | Common:20; Rare:542 | ||||
| chr2:168802021-168803482 | Common:34; Rare:1105 | ||||
| chr2:168890310-168890710 | Common:13; Rare:411 | ||||
| chr2:169072322-169072722 | Common:2; Rare:58 | ||||
| chr2:169072625-169072877 | Common:6; Rare:74 | ||||
| chr2:169479110-169479572 | Common:12; Rare:320; Clinvar (benign):4 | ||||
| chr2:169479611-169480150 | Common:7; Rare:205 | ||||
| chr2:169573165-169573423 | Common:3; Rare:77 | ||||
| chr2:169573570-169574158 | Common:8; Rare:309 | ||||
| chr2:169584126-169584646 | Common:4; Rare:496 |