| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249536-129249680 | Common:1; Rare:45 | ||||
| chr3:129278736-129278899 | Common:4; Rare:49 | ||||
| chr3:129316242-129316340 | Rare:48 | ||||
| chr3:129439847-129440381 | Common:1; Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893574-129893898 | Rare:135 | ||||
| chr3:130746764-130746946 | Common:3; Rare:56 | ||||
| chr3:130893905-130894231 | Common:3; Rare:96 | ||||
| chr3:131026553-131026955 | Common:2; Rare:91 | ||||
| chr3:131381496-131381801 | Common:2; Rare:76 | ||||
| chr3:131502782-131503016 | Common:1; Rare:97 | ||||
| chr3:132417167-132417534 | Common:5; Rare:120 | ||||
| chr3:132659790-132659937 | Common:3; Rare:35 | ||||
| chr3:133038202-133038359 | Common:1; Rare:48 | ||||
| chr3:133661812-133662015 | Rare:49 | ||||
| chr3:134374388-134374667 | Common:1; Rare:79 |