| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:41870360-41870591 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41903942-41904391 | Common:2; Rare:139 | ||||
| chr5:42756753-42756878 | Common:1; Rare:23 | ||||
| chr5:43064815-43065143 | Common:1; Rare:77 | ||||
| chr5:43067438-43067499 | Rare:10 | ||||
| chr5:43120833-43120975 | Common:4; Rare:67 | ||||
| chr5:43121354-43121648 | Common:1; Rare:110 | ||||
| chr5:43313354-43313624 | Common:3; Rare:73 | ||||
| chr5:43483837-43484001 | Common:1; Rare:54 | ||||
| chr5:43484335-43484457 | Rare:28 | ||||
| chr5:43515030-43515313 | Common:4; Rare:100 | ||||
| chr5:43602501-43602760 | Common:3; Rare:50 | ||||
| chr5:43602886-43603287 | Rare:97 | ||||
| chr5:44388045-44388356 | Common:1; Rare:58 | ||||
| chr5:44389364-44389651 | Common:1; Rare:39 |