| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88055722-88055807 | Rare:37 | ||||
| chr2:88055842-88055935 | Rare:29 | ||||
| chr2:88067744-88067920 | Common:1; Rare:54 | ||||
| chr2:88691456-88691743 | Common:2; Rare:107 | ||||
| chr2:95121736-95122074 | Common:1; Rare:117 | ||||
| chr2:95165376-95165453 | Rare:12 | ||||
| chr2:95165640-95165828 | Rare:58 | ||||
| chr2:95207393-95207610 | Rare:86 | ||||
| chr2:95402607-95402762 | Rare:50 | ||||
| chr2:96208248-96208459 | Rare:104 | ||||
| chr2:96208786-96208954 | Common:3; Rare:68 | ||||
| chr2:96265978-96266374 | Common:2; Rare:117 | ||||
| chr2:96305458-96305654 | Common:2; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335719-96335814 | Common:1; Rare:31 | ||||
| chr2:96638282-96638467 | Common:1; Rare:47 |