| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140691353-140691627 | Common:1; Rare:84; Clinvar:6; Clinvar (benign):1 | ||||
| chr5:141320762-141320910 | Common:1; Rare:45 | ||||
| chr5:141636821-141636997 | Common:1; Rare:72 | ||||
| chr5:142325008-142325183 | Rare:59 | ||||
| chr5:149345332-149345529 | Common:1; Rare:63 | ||||
| chr5:149551364-149551631 | Rare:62 | ||||
| chr5:150449627-150449795 | Common:4; Rare:55 | ||||
| chr5:150701036-150701147 | Common:2; Rare:39 | ||||
| chr5:151080935-151081204 | Common:1; Rare:91 | ||||
| chr5:154038884-154038999 | Common:1; Rare:36 | ||||
| chr5:159263225-159263321 | Common:1; Rare:30 | ||||
| chr5:163460053-163460159 | Common:2; Rare:45 | ||||
| chr5:163460365-163460643 | Common:4; Rare:57 | ||||
| chr5:169583580-169583801 | Common:6; Rare:77 | ||||
| chr5:172834162-172834384 | Common:1; Rare:51 |