| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85602618-85602904 | Rare:76 | ||||
| chr2:85612001-85612138 | Rare:47 | ||||
| chr2:85615991-85616345 | Common:2; Rare:137 | ||||
| chr2:85888841-85889156 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:86105804-86106300 | Common:4; Rare:171 | ||||
| chr2:86195078-86195169 | Rare:18 | ||||
| chr2:86195392-86195691 | Common:8; Rare:94 | ||||
| chr2:86441842-86442179 | Rare:128 | ||||
| chr2:86563307-86563557 | Common:2; Rare:97 | ||||
| chr2:86623826-86623988 | Common:1; Rare:71 | ||||
| chr2:86720046-86720313 | Rare:106 | ||||
| chr2:86861883-86862042 | Common:3; Rare:31 | ||||
| chr2:88055726-88055923 | Rare:74 | ||||
| chr2:88170146-88170360 | Common:6; Rare:45 | ||||
| chr2:88627782-88627926 | Rare:45 |