| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3558256-3558630 | Common:6; Rare:139 | ||||
| chr2:3575129-3575358 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423169-9423257 | Common:1; Rare:22 | ||||
| chr2:9423411-9423686 | Rare:83 | ||||
| chr2:9555712-9555992 | Common:2; Rare:95 | ||||
| chr2:10302713-10302939 | Common:4; Rare:77 | ||||
| chr2:10448303-10448716 | Common:1; Rare:129 | ||||
| chr2:11746420-11746674 | Common:2; Rare:74; Clinvar:4 | ||||
| chr2:17753757-17754168 | Common:4; Rare:130; Clinvar (benign):1 | ||||
| chr2:19358602-19358759 | Rare:38 | ||||
| chr2:23940406-23940506 | Common:3; Rare:36 | ||||
| chr2:24076299-24076498 | Rare:57 | ||||
| chr2:24793133-24793425 | Rare:131; Clinvar:1 | ||||
| chr2:24971902-24972138 | Common:1; Rare:77 | ||||
| chr2:26244579-26244943 | Common:2; Rare:133; Clinvar:6; Clinvar (benign):8 |