| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:924730-925160 | Not yet | Common:8; Rare:286 | 154 | ||
| chr1:925559-925951 | Not yet | Common:4; Rare:183 | 137 | ||
| chr1:940130-940430 | Not yet | Common:7; Rare:120 | 157 | ||
| chr1:941687-942116 | Not yet | Common:5; Rare:457 | 155 | ||
| chr1:959047-959585 | Not yet | Common:11; Rare:729 | 187 | ||
| chr1:960345-961477 | Not yet | Common:21; Rare:1099 | 185 | ||
| chr1:966241-966641 | Not yet | Common:13; Rare:337 | 141 | ||
| chr1:966841-967241 | Not yet | Common:2; Rare:480 | 161 | ||
| chr1:980630-981010 | Not yet | Common:4; Rare:117 | 154 | ||
| chr1:999513-999913 | Not yet | Common:4; Rare:205 | 161 | ||
| chr1:999952-1000557 | Not yet | Common:49; Rare:966 | 180 | ||
| chr1:1000570-1001140 | Not yet | Common:20; Rare:559 | 228 | ||
| chr1:1001193-1001593 | Not yet | Common:3; Rare:80 | 192 | ||
| chr1:1013070-1013690 | Not yet | Common:25; Rare:402 | 239 | ||
| chr1:1019248-1020436 | Not yet | Common:21; Rare:947; Clinvar:7; Clinvar (benign):2 | 209 |