| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46541520-46542000 | Common:5; Rare:126 | ||||
| chr2:46542494-46542736 | Rare:124 | ||||
| chr2:46616941-46617270 | Common:17; Rare:271 | ||||
| chr2:46698700-46698950 | Common:2; Rare:114 | ||||
| chr2:46698970-46699387 | Common:2; Rare:257 | ||||
| chr2:46915728-46916190 | Common:8; Rare:269; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:46941007-46941584 | Common:7; Rare:300; Clinvar (benign):1 | ||||
| chr2:47175550-47176110 | Common:7; Rare:200 | ||||
| chr2:47176392-47176902 | Common:8; Rare:436; Clinvar (benign):10 | ||||
| chr2:47369486-47370035 | Common:15; Rare:432; Clinvar:20; Clinvar (benign):12 | ||||
| chr2:47402887-47403210 | Common:2; Rare:285; Clinvar:94; Clinvar (benign):60; Clinvar (pathogenic):1 | ||||
| chr2:47782922-47783218 | Common:4; Rare:251; Clinvar:11; Clinvar (benign):23 | ||||
| chr2:47783356-47783586 | Common:2; Rare:80; Clinvar:24; Clinvar (benign):20 | ||||
| chr2:47905000-47906020 | Common:10; Rare:720 | ||||
| chr2:48314130-48314770 | Common:2; Rare:418 |