| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160399518-160399656 | Rare:26 | ||||
| chr3:160565569-160565842 | Common:1; Rare:89 | ||||
| chr3:160676995-160677206 | Common:3; Rare:28 | ||||
| chr3:161104607-161104711 | Common:1; Rare:31 | ||||
| chr3:161105284-161105387 | Common:2; Rare:37 | ||||
| chr3:161221209-161221394 | Common:2; Rare:57 | ||||
| chr3:167734837-167735254 | Common:5; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:169773331-169773424 | Rare:29 | ||||
| chr3:170870175-170870360 | Rare:78 | ||||
| chr3:171771302-171771489 | Common:1; Rare:39 | ||||
| chr3:172750397-172750730 | Common:4; Rare:72 | ||||
| chr3:173397485-173397814 | Common:4; Rare:110 | ||||
| chr3:179604622-179604836 | Common:1; Rare:73 | ||||
| chr3:180601978-180602224 | Common:1; Rare:75 | ||||
| chr3:180989626-180989815 | Rare:82; Clinvar:1; Clinvar (benign):1 |