| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:165469540-165469711 | Rare:29 | ||||
| chr2:169362472-169362732 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169584744-169584811 | Rare:15 | ||||
| chr2:169694370-169694490 | Common:2; Rare:38 | ||||
| chr2:169733746-169733963 | Common:2; Rare:66 | ||||
| chr2:170928875-170929313 | Common:5; Rare:125 | ||||
| chr2:171433934-171434225 | Common:3; Rare:78 | ||||
| chr2:171922222-171922515 | Rare:108 | ||||
| chr2:171999831-171999996 | Common:1; Rare:68 | ||||
| chr2:173354584-173354893 | Common:1; Rare:90 | ||||
| chr2:173965360-173965547 | Common:2; Rare:77 | ||||
| chr2:174248456-174248786 | Common:2; Rare:107 | ||||
| chr2:174395629-174395794 | Common:1; Rare:55 | ||||
| chr2:174409913-174410049 | Common:5; Rare:22 | ||||
| chr2:175005189-175005505 | Common:2; Rare:112; Clinvar:1 |