| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24793133-24793174 | Rare:20 | ||||
| chr2:24971915-24972191 | Common:1; Rare:89 | ||||
| chr2:25252075-25252454 | Rare:91 | ||||
| chr2:25342460-25342484 | Rare:1 | ||||
| chr2:25673542-25673779 | Common:1; Rare:86 | ||||
| chr2:26033792-26034160 | Common:3; Rare:131 | ||||
| chr2:26034267-26034702 | Common:4; Rare:108 | ||||
| chr2:26244577-26244963 | Common:2; Rare:143; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345758-26346172 | Common:2; Rare:125 | ||||
| chr2:27032857-27033011 | Rare:61 | ||||
| chr2:27086551-27086790 | Rare:68 | ||||
| chr2:27211916-27212027 | Common:3; Rare:41 | ||||
| chr2:27212266-27212390 | Common:2; Rare:64 | ||||
| chr2:27217087-27217539 | Common:1; Rare:148 | ||||
| chr2:27323051-27323141 | Rare:23; Clinvar (benign):1 |