Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:136987134-136987171 | Common:1; Rare:12 | ||||
chr3:139349888-139350240 | Rare:68; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr3:139361079-139361454 | Rare:70 | ||||
chr3:150408878-150409167 | Rare:74 | ||||
chr3:150761921-150762003 | Common:1; Rare:15 | ||||
chr3:152835282-152835521 | Common:1; Rare:70 | ||||
chr3:152870166-152870430 | Rare:47 | ||||
chr3:152873217-152873232 | Rare:3 | ||||
chr3:152875105-152875161 | Common:1; Rare:10 | ||||
chr3:153163448-153163477 | Rare:7 | ||||
chr3:153163512-153163591 | Rare:20 | ||||
chr3:153979469-153979582 | Rare:23 | ||||
chr3:153979953-153980274 | Common:4; Rare:47 | ||||
chr3:156816945-156817107 | Common:1; Rare:66 | ||||
chr3:160039045-160039279 | Common:2; Rare:52 |