| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161136800-161136979 | Rare:24 | ||||
| chr2:161160209-161160480 | Common:2; Rare:77 | ||||
| chr2:161308355-161308561 | Common:2; Rare:49 | ||||
| chr2:162343858-162344210 | Common:1; Rare:112 | ||||
| chr2:164840725-164840756 | Common:1; Rare:6 | ||||
| chr2:164841778-164841963 | Common:1; Rare:51 | ||||
| chr2:165794181-165794336 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:165794670-165794834 | Common:1; Rare:32 | ||||
| chr2:169584744-169584816 | Rare:18 | ||||
| chr2:169694349-169694529 | Common:4; Rare:63 | ||||
| chr2:170928929-170929338 | Common:4; Rare:125 | ||||
| chr2:171433905-171434248 | Common:3; Rare:88 | ||||
| chr2:171522291-171522498 | Common:3; Rare:43 | ||||
| chr2:171687979-171688075 | Rare:23 | ||||
| chr2:171922306-171922503 | Rare:78 |