| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138575231-138575476 | Common:1; Rare:121 | ||||
| chr5:138575645-138576018 | Rare:99 | ||||
| chr5:138754301-138754391 | Rare:16 | ||||
| chr5:138930644-138930873 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:139293607-139294022 | Rare:130 | ||||
| chr5:139294425-139294530 | Rare:51 | ||||
| chr5:139561066-139561399 | Common:1; Rare:132 | ||||
| chr5:139561466-139561630 | Rare:64 | ||||
| chr5:139561692-139561811 | Rare:42 | ||||
| chr5:139648194-139648426 | Common:1; Rare:70 | ||||
| chr5:139648780-139648983 | Rare:56 | ||||
| chr5:139682579-139682887 | Common:2; Rare:78 | ||||
| chr5:140175057-140175222 | Rare:47 | ||||
| chr5:140303048-140303187 | Common:1; Rare:45 | ||||
| chr5:140402043-140402273 | Common:1; Rare:75 |