| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:86617772-86618055 | Common:2; Rare:95 | ||||
| chr5:87267667-87268039 | Common:4; Rare:135 | ||||
| chr5:87268380-87269089 | Common:2; Rare:327; Clinvar:9; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr5:87411953-87412652 | Rare:247 | ||||
| chr5:87412816-87413138 | Common:4; Rare:104 | ||||
| chr5:88268783-88269108 | Rare:96 | ||||
| chr5:88883130-88883447 | Rare:82; Clinvar:6; Clinvar (benign):2 | ||||
| chr5:90409302-90409478 | Common:1; Rare:44 | ||||
| chr5:90409650-90410200 | Common:11; Rare:186 | ||||
| chr5:90473699-90474099 | Common:4; Rare:211 | ||||
| chr5:90474160-90474550 | Common:1; Rare:144 | ||||
| chr5:90474688-90474905 | Common:1; Rare:83 | ||||
| chr5:90529514-90529979 | Common:4; Rare:157 | ||||
| chr5:90558402-90558848 | Common:8; Rare:138; Clinvar (benign):1 | ||||
| chr5:91380029-91380595 | Common:3; Rare:155 |