| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96267389-96267630 | Common:1; Rare:65 | ||||
| chr2:96761749-96762089 | Rare:79; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr2:96762292-96762343 | Rare:18; Clinvar:1 | ||||
| chr2:96768184-96768421 | Common:2; Rare:43 | ||||
| chr2:96801199-96801521 | Common:2; Rare:54 | ||||
| chr2:96801636-96801798 | Common:4; Rare:44 | ||||
| chr2:96801817-96802039 | Common:1; Rare:45 | ||||
| chr2:99407560-99407580 | Rare:4 | ||||
| chr2:100818634-100818760 | Rare:25 | ||||
| chr2:100819105-100819245 | Common:1; Rare:22 | ||||
| chr2:101008187-101008506 | Common:2; Rare:99 | ||||
| chr2:102694243-102694486 | Common:2; Rare:50 | ||||
| chr2:105375404-105375511 | Common:1; Rare:24 | ||||
| chr2:106698557-106698574 | Rare:3 | ||||
| chr2:108489646-108489960 | Common:2; Rare:66 |