| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160565260-160565842 | Common:3; Rare:193 | ||||
| chr3:160755442-160755664 | Common:1; Rare:83 | ||||
| chr3:160756036-160756494 | Rare:111 | ||||
| chr3:160756679-160756709 | Rare:5 | ||||
| chr3:161104966-161105386 | Common:4; Rare:122 | ||||
| chr3:161221159-161221379 | Common:2; Rare:73 | ||||
| chr3:161221451-161221606 | Common:1; Rare:32 | ||||
| chr3:167734781-167735266 | Common:5; Rare:155; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735617-167735752 | Rare:34 | ||||
| chr3:168095801-168095981 | Common:1; Rare:60 | ||||
| chr3:169663566-169663993 | Common:3; Rare:97 | ||||
| chr3:169769586-169769625 | Rare:14 | ||||
| chr3:169769816-169769888 | Common:2; Rare:11 | ||||
| chr3:169772759-169772846 | Rare:20 | ||||
| chr3:169773325-169773424 | Rare:30 |