| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164841798-164841977 | Common:1; Rare:51 | ||||
| chr2:165794164-165794317 | Common:2; Rare:48; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:165953733-165954109 | Common:3; Rare:125; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:169584317-169584630 | Common:1; Rare:120 | ||||
| chr2:169584744-169584816 | Rare:18 | ||||
| chr2:169694348-169694571 | Common:5; Rare:76 | ||||
| chr2:171160302-171160487 | Rare:72 | ||||
| chr2:171433915-171434234 | Common:3; Rare:84 | ||||
| chr2:171999822-171999966 | Common:1; Rare:63 | ||||
| chr2:173354753-173354890 | Rare:43 | ||||
| chr2:173965281-173965478 | Rare:68 | ||||
| chr2:174248460-174248731 | Common:1; Rare:81 | ||||
| chr2:174395555-174395799 | Common:2; Rare:73 | ||||
| chr2:174597800-174597960 | Rare:24 | ||||
| chr2:175181659-175181729 | Common:3; Rare:39 |