| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140564284-140564510 | Common:1; Rare:61 | ||||
| chr5:140564662-140564853 | Rare:57 | ||||
| chr5:140639286-140639530 | Common:3; Rare:63 | ||||
| chr5:140647576-140647751 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140647761-140648082 | Common:17; Rare:112 | ||||
| chr5:140664750-140664926 | Common:2; Rare:50 | ||||
| chr5:140691305-140691668 | Common:1; Rare:133; Clinvar:11; Clinvar (benign):2 | ||||
| chr5:140700270-140700488 | Rare:73 | ||||
| chr5:140868737-140868972 | Common:2; Rare:55 | ||||
| chr5:141094495-141094662 | Rare:40 | ||||
| chr5:141320722-141320928 | Common:3; Rare:71 | ||||
| chr5:141475864-141475977 | Rare:26 | ||||
| chr5:141636801-141637011 | Common:2; Rare:95 | ||||
| chr5:141637330-141637452 | Common:1; Rare:28 | ||||
| chr5:141651370-141651476 | Rare:36 |