| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:81761471-81761615 | Common:5; Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:101576978-101577093 | Common:1; Rare:32 | ||||
| chr3:101676275-101676522 | Common:1; Rare:86 | ||||
| chr3:101680973-101681158 | Common:2; Rare:40 | ||||
| chr3:105868315-105868470 | Rare:39 | ||||
| chr3:107240557-107240836 | Rare:101 | ||||
| chr3:110969802-110970167 | Rare:64 | ||||
| chr3:110971284-110971493 | Common:1; Rare:41 | ||||
| chr3:112333790-112334093 | Common:2; Rare:53 | ||||
| chr3:114214037-114214370 | Common:2; Rare:59 | ||||
| chr3:115475649-115476025 | Common:2; Rare:72 | ||||
| chr3:115508608-115508755 | Common:1; Rare:27 | ||||
| chr3:115512621-115512797 | Common:1; Rare:51 | ||||
| chr3:115624363-115624430 | Common:1; Rare:6 | ||||
| chr3:115625107-115625294 | Common:3; Rare:24 |