| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196965-197334 | Common:3; Rare:130 | ||||
| chr3:3126806-3126984 | Common:4; Rare:75; Clinvar (benign):1 | ||||
| chr3:4303256-4303412 | Common:1; Rare:62 | ||||
| chr3:4493165-4493504 | Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:5187304-5187639 | Common:5; Rare:128 | ||||
| chr3:8501621-8501937 | Common:2; Rare:119 | ||||
| chr3:9362934-9363127 | Common:2; Rare:67 | ||||
| chr3:9397437-9397891 | Common:1; Rare:143 | ||||
| chr3:9749814-9750007 | Rare:64 | ||||
| chr3:9792414-9792570 | Rare:40 | ||||
| chr3:9792726-9793123 | Common:3; Rare:140 | ||||
| chr3:9890503-9890667 | Common:2; Rare:57 | ||||
| chr3:9933502-9933882 | Common:2; Rare:154; Clinvar:3 | ||||
| chr3:9934028-9934087 | Rare:16 | ||||
| chr3:10026299-10026434 | Rare:48 |