| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915462-34915741 | Common:1; Rare:68 | ||||
| chr5:34929687-34929903 | Rare:74 | ||||
| chr5:35617728-35617901 | Common:1; Rare:28 | ||||
| chr5:35856756-35856933 | Rare:26 | ||||
| chr5:36151874-36152120 | Rare:68 | ||||
| chr5:36301875-36302184 | Common:3; Rare:48 | ||||
| chr5:36876650-36876922 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37050570-37050839 | Rare:45 | ||||
| chr5:37379176-37379547 | Rare:115 | ||||
| chr5:38556475-38556803 | Common:3; Rare:114 | ||||
| chr5:38557225-38557364 | Rare:36 | ||||
| chr5:38845718-38846118 | Common:2; Rare:100 | ||||
| chr5:39074363-39074522 | Common:1; Rare:73 | ||||
| chr5:39424929-39425308 | Common:3; Rare:78 | ||||
| chr5:40798152-40798401 | Common:1; Rare:94 |