| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45686800-45687621 | Common:16; Rare:786 | ||||
| chr1:45687900-45688302 | Common:6; Rare:390 | ||||
| chr1:45688281-45688726 | Common:14; Rare:297 | ||||
| chr1:45750000-45752062 | Common:16; Rare:1212 | ||||
| chr1:45803255-45803689 | Common:11; Rare:624 | ||||
| chr1:46132251-46133237 | Common:22; Rare:997 | ||||
| chr1:46133219-46133619 | Common:3; Rare:162 | ||||
| chr1:46174410-46175070 | Common:4; Rare:178 | ||||
| chr1:46197960-46198751 | Common:38; Rare:1036; Clinvar:8; Clinvar (benign):15 | ||||
| chr1:46203030-46203470 | Rare:196 | ||||
| chr1:46246525-46247202 | Common:1; Rare:119 | ||||
| chr1:46247215-46247896 | Common:33; Rare:639 | ||||
| chr1:46248074-46248576 | Common:5; Rare:428 | ||||
| chr1:46285784-46286415 | Common:1; Rare:422 | ||||
| chr1:46300091-46301150 | Common:6; Rare:311 |