| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139561733-139561800 | Rare:28 | ||||
| chr5:139648168-139648379 | Rare:60 | ||||
| chr5:139659203-139659359 | Rare:39 | ||||
| chr5:140174797-140175202 | Rare:123 | ||||
| chr5:140303057-140303182 | Common:1; Rare:39 | ||||
| chr5:140557378-140557557 | Common:3; Rare:118 | ||||
| chr5:140564309-140564449 | Common:1; Rare:43 | ||||
| chr5:140564556-140564841 | Rare:75 | ||||
| chr5:140647589-140648096 | Common:19; Rare:189; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664583-140664926 | Common:4; Rare:82 | ||||
| chr5:140691309-140691641 | Common:1; Rare:115; Clinvar:8; Clinvar (benign):1 | ||||
| chr5:141135135-141135299 | Rare:33 | ||||
| chr5:141320692-141320928 | Common:3; Rare:82 | ||||
| chr5:141636810-141637001 | Common:2; Rare:83 | ||||
| chr5:141682191-141682348 | Common:1; Rare:47 |