| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15859742-15860099 | Common:4; Rare:116 | ||||
| chr3:16264872-16265243 | Common:2; Rare:124 | ||||
| chr3:17742569-17742952 | Common:4; Rare:142 | ||||
| chr3:18424202-18424408 | Common:5; Rare:42 | ||||
| chr3:19946974-19947310 | Common:5; Rare:126 | ||||
| chr3:20186176-20186434 | Common:2; Rare:84 | ||||
| chr3:23916872-23917204 | Rare:130 | ||||
| chr3:24494736-24494898 | Rare:44 | ||||
| chr3:24494985-24495072 | Common:2; Rare:25 | ||||
| chr3:25428107-25428296 | Rare:36 | ||||
| chr3:25664759-25665069 | Common:4; Rare:83 | ||||
| chr3:25783386-25783621 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:25789966-25790118 | Common:4; Rare:60 | ||||
| chr3:27484071-27484088 | Rare:5 | ||||
| chr3:28348612-28348747 | Rare:33 |