| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46163363-46163474 | Rare:16 | ||||
| chr3:46163550-46164190 | Common:2; Rare:271 | ||||
| chr3:46406775-46407463 | Common:2; Rare:167 | ||||
| chr3:46566420-46566780 | Common:1; Rare:60 | ||||
| chr3:46693189-46693589 | Common:2; Rare:84 | ||||
| chr3:46693490-46693818 | Common:4; Rare:105 | ||||
| chr3:46892329-46892750 | Common:2; Rare:167 | ||||
| chr3:46976621-46977139 | Common:11; Rare:309 | ||||
| chr3:46979425-46979923 | Common:9; Rare:328; Clinvar:6 | ||||
| chr3:46981881-46982158 | Common:1; Rare:90 | ||||
| chr3:47163871-47164522 | Common:4; Rare:357; Clinvar (pathogenic):1 | ||||
| chr3:47281717-47281821 | Rare:15 | ||||
| chr3:47282360-47282739 | Common:3; Rare:145 | ||||
| chr3:47283030-47283897 | Rare:390 | ||||
| chr3:47380529-47381113 | Common:2; Rare:409 |