| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138575013-138575287 | Common:2; Rare:78 | ||||
| chr5:138875302-138875427 | Rare:21; Clinvar (benign):1 | ||||
| chr5:139293627-139294022 | Rare:124 | ||||
| chr5:139341824-139341946 | Common:1; Rare:36 | ||||
| chr5:139482651-139482896 | Rare:38 | ||||
| chr5:139561137-139561413 | Common:1; Rare:114 | ||||
| chr5:139561737-139561802 | Rare:27 | ||||
| chr5:140564284-140564846 | Common:1; Rare:144 | ||||
| chr5:140647488-140647896 | Common:5; Rare:168; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:140691282-140691513 | Common:2; Rare:92; Clinvar:9; Clinvar (benign):1 | ||||
| chr5:141320314-141320343 | Rare:8 | ||||
| chr5:141320364-141320461 | Rare:23 | ||||
| chr5:141320725-141320914 | Common:2; Rare:66 | ||||
| chr5:141636809-141636957 | Common:2; Rare:69 | ||||
| chr5:142324958-142325238 | Rare:96 |