| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191014122-191014353 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677856-191678155 | Common:4; Rare:86 | ||||
| chr2:192194864-192195119 | Common:1; Rare:69 | ||||
| chr2:195656837-195657148 | Common:1; Rare:90 | ||||
| chr2:196593525-196593620 | Rare:26 | ||||
| chr2:196639473-196639692 | Rare:56 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453233-197453554 | Rare:107 | ||||
| chr2:197499791-197500461 | Common:2; Rare:255; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515898-197516107 | Common:1; Rare:81 | ||||
| chr2:197675680-197675817 | Rare:20 | ||||
| chr2:197675996-197676136 | Rare:35 | ||||
| chr2:199911136-199911366 | Rare:66 | ||||
| chr2:200306006-200306075 | Rare:10 | ||||
| chr2:200306210-200306562 | Common:5; Rare:82 |