| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:35094030-35094332 | Not yet | Rare:67 | 166 | ||
| chr1:35186942-35187271 | Not yet | Common:1; Rare:116 | 185 | ||
| chr1:35438463-35438500 | Not yet | Rare:6 | 26 | ||
| chr1:36139721-36140077 | Not yet | Common:3; Rare:72; Clinvar (pathogenic):1 | 165 | ||
| chr1:37575021-37575144 | Not yet | Rare:20 | 102 | ||
| chr1:37809434-37809536 | Not yet | Rare:15 | 93 | ||
| chr1:39115952-39116060 | Not yet | Rare:17 | 107 | ||
| chr1:40267735-40267804 | Not yet | Common:1; Rare:20; Clinvar:1 | 42 | ||
| chr1:40687064-40687157 | Not yet | Common:1; Rare:19 | 81 | ||
| chr1:41168153-41168198 | Not yet | Rare:3 | 39 | ||
| chr1:41432961-41433276 | Not yet | Common:1; Rare:61 | 170 | ||
| chr1:42226331-42226474 | Not yet | Common:2; Rare:28 | 139 | ||
| chr1:42500413-42500678 | Not yet | Common:3; Rare:57 | 171 | ||
| chr1:42693867-42694033 | Not yet | Rare:32 | 90 | ||
| chr1:42752220-42752286 | Not yet | Common:2; Rare:21; Clinvar (benign):1; Clinvar (pathogenic):1 | 72 |