| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49029320-49029800 | Common:6; Rare:544 | ||||
| chr3:49092732-49093137 | Common:2; Rare:205 | ||||
| chr3:49093250-49094835 | Common:18; Rare:1638 | ||||
| chr3:49104307-49104707 | Rare:222; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr3:49104678-49105022 | Common:3; Rare:564; Clinvar:3; Clinvar (benign):23 | ||||
| chr3:49105033-49105433 | Rare:100 | ||||
| chr3:49120570-49121160 | Rare:460; Clinvar:1 | ||||
| chr3:49132584-49133336 | Rare:410; Clinvar:10; Clinvar (benign):1 | ||||
| chr3:49133489-49133889 | Common:1; Rare:88 | ||||
| chr3:49165714-49166570 | Common:8; Rare:544 | ||||
| chr3:49170992-49171392 | Common:1; Rare:139 | ||||
| chr3:49171347-49171681 | Common:16; Rare:347; Clinvar (pathogenic):1 | ||||
| chr3:49339465-49339874 | Common:4; Rare:158 | ||||
| chr3:49339951-49340342 | Common:18; Rare:675 | ||||
| chr3:49340292-49340692 | Common:1; Rare:72 |