| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:168456121-168456261 | Rare:33 | ||||
| chr2:169584703-169584852 | Rare:43 | ||||
| chr2:169694275-169694588 | Common:6; Rare:115 | ||||
| chr2:169798786-169798973 | Rare:47 | ||||
| chr2:169808826-169808882 | Rare:17 | ||||
| chr2:170928818-170929386 | Common:7; Rare:165 | ||||
| chr2:171160509-171160665 | Common:1; Rare:46 | ||||
| chr2:171433889-171434328 | Common:3; Rare:119 | ||||
| chr2:171434614-171434709 | Rare:24 | ||||
| chr2:171434711-171435146 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:171522311-171522532 | Common:2; Rare:50 | ||||
| chr2:171687322-171687828 | Common:2; Rare:114 | ||||
| chr2:171688110-171688140 | Rare:10 | ||||
| chr2:171922285-171922560 | Rare:99 | ||||
| chr2:171999837-171999983 | Common:1; Rare:59 |