| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140664753-140664907 | Common:2; Rare:39 | ||||
| chr5:140691305-140691662 | Common:1; Rare:131; Clinvar:11; Clinvar (benign):2 | ||||
| chr5:141320742-141320928 | Common:2; Rare:64 | ||||
| chr5:141636800-141637001 | Common:2; Rare:93 | ||||
| chr5:141651387-141651483 | Rare:27 | ||||
| chr5:141923645-141923890 | Common:1; Rare:68 | ||||
| chr5:142108658-142108929 | Common:3; Rare:92 | ||||
| chr5:142324995-142325303 | Rare:95 | ||||
| chr5:143404426-143404604 | Common:2; Rare:42 | ||||
| chr5:144170551-144170784 | Common:1; Rare:82 | ||||
| chr5:145937638-145937758 | Rare:30 | ||||
| chr5:146182500-146182866 | Common:4; Rare:105 | ||||
| chr5:147509930-147510249 | Common:1; Rare:60 | ||||
| chr5:148383872-148384018 | Rare:46 | ||||
| chr5:149063129-149063366 | Rare:42 |