| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129183810-129184075 | Common:2; Rare:90 | ||||
| chr3:129439876-129440324 | Common:1; Rare:134; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129560548-129560669 | Rare:33 | ||||
| chr3:130893885-130894253 | Common:3; Rare:112 | ||||
| chr3:131381487-131381811 | Common:2; Rare:82 | ||||
| chr3:131502868-131503023 | Common:1; Rare:61 | ||||
| chr3:132659627-132660005 | Common:3; Rare:99; Clinvar:1 | ||||
| chr3:133661849-133661998 | Rare:35 | ||||
| chr3:134250853-134251080 | Rare:74 | ||||
| chr3:134485714-134485760 | Rare:19 | ||||
| chr3:134485969-134486046 | Common:2; Rare:32 | ||||
| chr3:136862017-136862275 | Common:1; Rare:75 | ||||
| chr3:138946789-138947291 | Common:3; Rare:111; Clinvar (benign):1 | ||||
| chr3:139389578-139389837 | Common:1; Rare:84 | ||||
| chr3:140941715-140941862 | Common:1; Rare:46 |