| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140504924-140505206 | Rare:63 | ||||
| chr5:140564369-140564856 | Common:1; Rare:122 | ||||
| chr5:140641353-140641635 | Rare:35 | ||||
| chr5:140647485-140647924 | Common:5; Rare:183; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:140664575-140664936 | Common:4; Rare:87 | ||||
| chr5:140691258-140691738 | Common:2; Rare:178; Clinvar:12; Clinvar (benign):3 | ||||
| chr5:140966382-140966535 | Rare:48 | ||||
| chr5:141320311-141320360 | Rare:14 | ||||
| chr5:141320364-141320416 | Rare:14 | ||||
| chr5:141320489-141320689 | Rare:41 | ||||
| chr5:141320700-141320920 | Common:2; Rare:77 | ||||
| chr5:141636792-141636961 | Common:2; Rare:86 | ||||
| chr5:141637333-141637449 | Common:1; Rare:28 | ||||
| chr5:141682180-141682346 | Common:1; Rare:49 | ||||
| chr5:141923783-141923972 | Rare:58 |