| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139273952-139274160 | Rare:96 | ||||
| chr5:139341779-139341930 | Common:1; Rare:41 | ||||
| chr5:139404043-139404182 | Rare:47 | ||||
| chr5:139439453-139439646 | Common:2; Rare:52 | ||||
| chr5:139561094-139561408 | Common:1; Rare:125 | ||||
| chr5:139561721-139561796 | Rare:34 | ||||
| chr5:139650840-139651101 | Common:1; Rare:60 | ||||
| chr5:140174919-140175237 | Rare:100 | ||||
| chr5:140303065-140303203 | Common:1; Rare:46 | ||||
| chr5:140557413-140557557 | Common:2; Rare:92 | ||||
| chr5:140564572-140564837 | Rare:73 | ||||
| chr5:140639329-140639478 | Common:2; Rare:39 | ||||
| chr5:140647576-140648085 | Common:19; Rare:196; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664741-140664874 | Common:1; Rare:28 | ||||
| chr5:140691305-140691646 | Common:1; Rare:122; Clinvar:10; Clinvar (benign):1 |