| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564556-140564845 | Rare:76 | ||||
| chr5:140647530-140647919 | Common:5; Rare:165; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:140664738-140664908 | Common:3; Rare:41 | ||||
| chr5:140691313-140691661 | Common:1; Rare:124; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320730-141320935 | Common:3; Rare:72 | ||||
| chr5:141343744-141343893 | Rare:33 | ||||
| chr5:141475932-141476022 | Rare:22 | ||||
| chr5:141636810-141636957 | Common:2; Rare:69 | ||||
| chr5:141682191-141682328 | Common:1; Rare:45 | ||||
| chr5:141923658-141923964 | Common:1; Rare:94 | ||||
| chr5:142012986-142013114 | Rare:39 | ||||
| chr5:142108685-142108970 | Common:2; Rare:96 | ||||
| chr5:142324973-142325310 | Rare:108 | ||||
| chr5:142686035-142686202 | Rare:34 | ||||
| chr5:142697880-142698186 | Common:4; Rare:49 |