| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:48440619-48440858 | Common:8; Rare:113 | ||||
| chr2:53767618-53767839 | Common:3; Rare:74 | ||||
| chr2:53786842-53787213 | Common:1; Rare:143 | ||||
| chr2:53970797-53971168 | Common:11; Rare:135 | ||||
| chr2:55050441-55050754 | Common:4; Rare:95 | ||||
| chr2:55232243-55232732 | Common:3; Rare:137 | ||||
| chr2:58046620-58046845 | Rare:68 | ||||
| chr2:60881307-60881664 | Common:2; Rare:135 | ||||
| chr2:61017177-61017756 | Common:4; Rare:168; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144921-61145164 | Common:3; Rare:82 | ||||
| chr2:61177197-61177465 | Common:5; Rare:114 | ||||
| chr2:61470675-61470991 | Rare:104 | ||||
| chr2:61471247-61471386 | Common:2; Rare:50 | ||||
| chr2:61888491-61888723 | Common:1; Rare:98 | ||||
| chr2:63588627-63589025 | Common:1; Rare:123; Clinvar (benign):1 |