| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:32014061-32014377 | Not yet | Common:1; Rare:88 | 158 | ||
| chr1:32072764-32072993 | Not yet | Rare:61 | 136 | ||
| chr1:32107968-32108118 | Not yet | Rare:57 | 82 | ||
| chr1:32179627-32179771 | Not yet | Rare:30 | 119 | ||
| chr1:32200495-32200709 | Not yet | Rare:48 | 130 | ||
| chr1:32201585-32201702 | Not yet | Rare:23 | 99 | ||
| chr1:32205505-32205699 | Not yet | Common:1; Rare:78 | 139 | ||
| chr1:32291919-32292167 | Not yet | Common:1; Rare:85 | 132 | ||
| chr1:32351410-32351639 | Not yet | Common:1; Rare:60 | 145 | ||
| chr1:32394385-32394683 | Not yet | Common:1; Rare:90 | 177 | ||
| chr1:32650918-32651318 | Not yet | Common:2; Rare:150 | 188 | ||
| chr1:32702634-32702943 | Not yet | Common:1; Rare:75 | 132 | ||
| chr1:32817257-32817674 | Not yet | Rare:112; Clinvar:5 | 196 | ||
| chr1:33036800-33037155 | Not yet | Rare:127; Clinvar (pathogenic):2 | 178 | ||
| chr1:33080994-33081196 | Not yet | Common:1; Rare:60 | 117 |