| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:107522730-107523052 | Common:4; Rare:269 | ||||
| chr3:107523196-107523895 | Common:7; Rare:263 | ||||
| chr3:107523805-107524980 | Common:10; Rare:450 | ||||
| chr3:107525141-107525541 | Common:2; Rare:126 | ||||
| chr3:108090250-108091198 | Common:4; Rare:583 | ||||
| chr3:108222330-108222753 | Common:18; Rare:568 | ||||
| chr3:108589250-108589790 | Common:22; Rare:831 | ||||
| chr3:109117979-109118379 | Common:5; Rare:196 | ||||
| chr3:111071229-111072217 | Common:9; Rare:582 | ||||
| chr3:111542083-111543085 | Common:13; Rare:295; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:111674387-111674787 | Rare:303 | ||||
| chr3:111978747-111979150 | Common:21; Rare:495 | ||||
| chr3:111979207-111979353 | Rare:43 | ||||
| chr3:111979388-111979788 | Common:1; Rare:71 | ||||
| chr3:112086225-112086871 | Common:13; Rare:578 |