| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16616973-16617262 | Common:2; Rare:78; Clinvar (benign):5 | ||||
| chr5:16936241-16936447 | Common:3; Rare:53 | ||||
| chr5:31532032-31532378 | Common:3; Rare:99 | ||||
| chr5:31854778-31854856 | Rare:22 | ||||
| chr5:32174252-32174395 | Common:1; Rare:55 | ||||
| chr5:33440617-33441105 | Common:7; Rare:137 | ||||
| chr5:34656164-34656467 | Common:3; Rare:77 | ||||
| chr5:34839270-34839404 | Common:2; Rare:40 | ||||
| chr5:34915462-34915744 | Common:1; Rare:69 | ||||
| chr5:35617728-35617935 | Common:1; Rare:40 | ||||
| chr5:35856803-35856962 | Rare:27 | ||||
| chr5:36151823-36152120 | Rare:73 | ||||
| chr5:36876650-36876942 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36876996-36877155 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37050683-37050831 | Rare:30 |