| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105399016-105399186 | Rare:53 | ||||
| chr2:106194250-106194568 | Common:6; Rare:133 | ||||
| chr2:108377829-108377972 | Common:1; Rare:35 | ||||
| chr2:108449098-108449277 | Rare:73 | ||||
| chr2:108534186-108534498 | Common:7; Rare:125 | ||||
| chr2:108719311-108719558 | Common:2; Rare:107 | ||||
| chr2:110204953-110205064 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110677987-110678212 | Rare:75 | ||||
| chr2:111884117-111884257 | Rare:41 | ||||
| chr2:111898330-111898611 | Common:2; Rare:65 | ||||
| chr2:112254998-112255128 | Common:1; Rare:57 | ||||
| chr2:112275399-112275631 | Common:1; Rare:76 | ||||
| chr2:112542148-112542485 | Common:1; Rare:104 | ||||
| chr2:112584362-112584633 | Common:1; Rare:72 | ||||
| chr2:112764578-112764773 | Common:1; Rare:64; Clinvar (pathogenic):1 |