| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152175882-152176118 | Common:1; Rare:58 | ||||
| chr2:152717829-152717942 | Rare:47 | ||||
| chr2:152717999-152718305 | Common:1; Rare:100 | ||||
| chr2:159712358-159712591 | Common:2; Rare:91 | ||||
| chr2:161308334-161308560 | Common:2; Rare:55 | ||||
| chr2:165794128-165794298 | Common:2; Rare:46; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794693-165794764 | Common:1; Rare:9 | ||||
| chr2:169584744-169584800 | Rare:9 | ||||
| chr2:169694360-169694497 | Common:2; Rare:45 | ||||
| chr2:169798779-169798965 | Rare:47 | ||||
| chr2:170928899-170929301 | Common:5; Rare:109 | ||||
| chr2:171433941-171434248 | Common:3; Rare:79 | ||||
| chr2:171894217-171894364 | Rare:62; Clinvar:1 | ||||
| chr2:173354612-173354901 | Common:1; Rare:87 | ||||
| chr2:174248454-174248751 | Common:1; Rare:91 |