| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37196369-37196534 | Rare:63 | ||||
| chr2:37231499-37231703 | Common:5; Rare:110; Clinvar (benign):3 | ||||
| chr2:37324724-37324911 | Common:1; Rare:75 | ||||
| chr2:37344619-37344745 | Common:1; Rare:52 | ||||
| chr2:37671599-37671823 | Common:10; Rare:99 | ||||
| chr2:37672164-37672244 | Common:2; Rare:31 | ||||
| chr2:37925250-37925296 | Rare:16 | ||||
| chr2:38075899-38075969 | Common:1; Rare:17 | ||||
| chr2:38076038-38076265 | Common:1; Rare:54 | ||||
| chr2:38602867-38603070 | Common:3; Rare:91 | ||||
| chr2:38751336-38751441 | Rare:55 | ||||
| chr2:38875886-38876064 | Common:1; Rare:65 | ||||
| chr2:39121021-39121127 | Rare:33 | ||||
| chr2:39437094-39437453 | Common:4; Rare:127 | ||||
| chr2:42169177-42169436 | Common:1; Rare:131 |