| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16465721-16465865 | Rare:23 | ||||
| chr5:16616973-16617096 | Common:1; Rare:41; Clinvar (benign):5 | ||||
| chr5:31532021-31532361 | Common:3; Rare:96 | ||||
| chr5:32174244-32174562 | Common:4; Rare:101 | ||||
| chr5:32710536-32710695 | Common:1; Rare:33 | ||||
| chr5:32711102-32711536 | Common:1; Rare:76 | ||||
| chr5:32711725-32711804 | Common:1; Rare:19 | ||||
| chr5:32711862-32712016 | Common:1; Rare:47 | ||||
| chr5:33440605-33441076 | Common:6; Rare:125 | ||||
| chr5:34915500-34915800 | Common:1; Rare:82 | ||||
| chr5:35617752-35617970 | Common:1; Rare:51 | ||||
| chr5:36151881-36152204 | Rare:102 | ||||
| chr5:36876623-36876853 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37379054-37379375 | Common:3; Rare:77 | ||||
| chr5:39074367-39074510 | Common:1; Rare:60 |