| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129278736-129278888 | Common:4; Rare:48 | ||||
| chr3:129316233-129316350 | Rare:56 | ||||
| chr3:129439753-129440382 | Common:1; Rare:186; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129558498-129558764 | Common:1; Rare:58 | ||||
| chr3:129565947-129566196 | Common:2; Rare:50 | ||||
| chr3:129570840-129571164 | Common:3; Rare:95 | ||||
| chr3:129893373-129893498 | Rare:35 | ||||
| chr3:129893514-129893887 | Rare:140 | ||||
| chr3:130081665-130081822 | Common:1; Rare:8 | ||||
| chr3:130746753-130746913 | Common:3; Rare:52 | ||||
| chr3:130893905-130894231 | Common:3; Rare:96 | ||||
| chr3:131026716-131026942 | Common:2; Rare:56 | ||||
| chr3:131381451-131381832 | Common:3; Rare:103 | ||||
| chr3:131502754-131502997 | Common:1; Rare:104 | ||||
| chr3:132417177-132417534 | Common:5; Rare:117 |