| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139561721-139561794 | Rare:34 | ||||
| chr5:140557405-140557557 | Common:2; Rare:97 | ||||
| chr5:140564546-140564853 | Rare:79 | ||||
| chr5:140647583-140647888 | Common:5; Rare:123; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691313-140691633 | Common:1; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
| chr5:141320742-141320920 | Common:1; Rare:62 | ||||
| chr5:141636810-141637001 | Common:2; Rare:83 | ||||
| chr5:141923721-141923914 | Common:1; Rare:60 | ||||
| chr5:142324979-142325300 | Rare:105 | ||||
| chr5:146182501-146182854 | Common:3; Rare:96 | ||||
| chr5:148383905-148384021 | Rare:37 | ||||
| chr5:149551356-149551722 | Common:1; Rare:98 | ||||
| chr5:149960575-149960915 | Rare:114; Clinvar:7 | ||||
| chr5:150449662-150449843 | Common:4; Rare:61 | ||||
| chr5:150600857-150601091 | Common:1; Rare:58 |