| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201071586-201072058 | Rare:104 | ||||
| chr2:201115941-201116467 | Common:2; Rare:96 | ||||
| chr2:201117295-201117598 | Rare:41 | ||||
| chr2:201118452-201118539 | Rare:11 | ||||
| chr2:201118620-201118879 | Rare:37 | ||||
| chr2:201451435-201451907 | Common:3; Rare:113 | ||||
| chr2:201642637-201642727 | Rare:45 | ||||
| chr2:201643408-201643553 | Common:1; Rare:46; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:201780876-201781004 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238492-202238621 | Rare:41 | ||||
| chr2:202634804-202635012 | Common:4; Rare:78 | ||||
| chr2:202911892-202912300 | Common:2; Rare:112 | ||||
| chr2:202912383-202912548 | Common:2; Rare:41 | ||||
| chr2:203014676-203014933 | Common:1; Rare:77 | ||||
| chr2:203238743-203239050 | Common:2; Rare:105 |