| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:15847426-15847929 | Rare:316 | ||||
| chr1:15976062-15976216 | Common:4; Rare:62 | ||||
| chr1:16146266-16146687 | Common:7; Rare:168 | ||||
| chr1:16155998-16156178 | Rare:80; Clinvar:4 | ||||
| chr1:16206460-16206830 | Common:14; Rare:184 | ||||
| chr1:16237137-16237333 | Common:1; Rare:113 | ||||
| chr1:16352416-16352630 | Common:6; Rare:202 | ||||
| chr1:16366907-16367260 | Common:2; Rare:194 | ||||
| chr1:16440522-16440771 | Common:3; Rare:123 | ||||
| chr1:16613371-16613703 | Common:6; Rare:1 | ||||
| chr1:17011868-17012025 | Common:1; Rare:45; Clinvar:2 | ||||
| chr1:17053982-17054383 | Common:6; Rare:233; Clinvar:20; Clinvar (benign):18 | ||||
| chr1:17348300-17348750 | Common:16; Rare:110 | ||||
| chr1:17439627-17439975 | Rare:186 | ||||
| chr1:17539506-17539845 | Rare:86 |