| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36241556-36241972 | Common:5; Rare:143; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:36242158-36242209 | Rare:7 | ||||
| chr5:36301875-36302050 | Common:1; Rare:25 | ||||
| chr5:36606456-36606640 | Rare:35 | ||||
| chr5:36876607-36876960 | Common:1; Rare:102; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:36877058-36877155 | Rare:36; Clinvar:1 | ||||
| chr5:37248906-37249084 | Common:3; Rare:32 | ||||
| chr5:37371040-37371327 | Common:1; Rare:75 | ||||
| chr5:37379059-37379392 | Common:3; Rare:88 | ||||
| chr5:38556342-38556931 | Common:3; Rare:190 | ||||
| chr5:38557183-38557304 | Rare:30 | ||||
| chr5:38557353-38557601 | Rare:50 | ||||
| chr5:38845706-38846053 | Common:2; Rare:90 | ||||
| chr5:39074350-39074539 | Common:1; Rare:89 | ||||
| chr5:39202982-39203152 | Rare:37 |