| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151874-36152185 | Rare:98 | ||||
| chr5:36876616-36876907 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371040-37371433 | Common:2; Rare:99 | ||||
| chr5:37379156-37379370 | Common:1; Rare:55 | ||||
| chr5:39074327-39074539 | Common:1; Rare:105 | ||||
| chr5:39424935-39425308 | Common:3; Rare:77 | ||||
| chr5:40679303-40679467 | Common:2; Rare:32 | ||||
| chr5:40679623-40679956 | Common:2; Rare:87 | ||||
| chr5:40798152-40798448 | Common:1; Rare:116 | ||||
| chr5:43064815-43065137 | Rare:76 | ||||
| chr5:43067422-43067568 | Rare:25 | ||||
| chr5:43121404-43121667 | Common:1; Rare:102 | ||||
| chr5:43483831-43483970 | Common:1; Rare:48 | ||||
| chr5:43602572-43602731 | Common:2; Rare:27 | ||||
| chr5:43602886-43603277 | Rare:97 |