| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240025282-240025480 | Common:1; Rare:78; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560910 | Common:2; Rare:71 | ||||
| chr2:241102259-241102360 | Common:2; Rare:42 | ||||
| chr2:241149434-241149606 | Common:2; Rare:57 | ||||
| chr2:241272794-241272947 | Rare:64 | ||||
| chr2:241315141-241315409 | Common:5; Rare:88 | ||||
| chr2:241315649-241315981 | Common:5; Rare:129 | ||||
| chr2:241637555-241637704 | Common:1; Rare:80 | ||||
| chr20:346882-347121 | Common:1; Rare:66 | ||||
| chr20:348164-348261 | Common:1; Rare:24 | ||||
| chr20:1118434-1118660 | Common:4; Rare:75 | ||||
| chr20:1392930-1393177 | Common:1; Rare:91 | ||||
| chr20:2508872-2509210 | Common:1; Rare:66 | ||||
| chr20:2652408-2652661 | Common:9; Rare:94 | ||||
| chr20:2664186-2664235 | Rare:27 |