| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:135965420-135966142 | Common:6; Rare:603 | ||||
| chr3:136194744-136195246 | Common:1; Rare:236; Clinvar:2 | ||||
| chr3:136195349-136195497 | Rare:45 | ||||
| chr3:136195655-136197040 | Common:20; Rare:2406 | ||||
| chr3:136197030-136197526 | Rare:183 | ||||
| chr3:136197451-136197851 | Common:3; Rare:117 | ||||
| chr3:136250115-136250515 | Common:14; Rare:444; Clinvar:24; Clinvar (benign):20; Clinvar (pathogenic):9 | ||||
| chr3:136250537-136250781 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:136251049-136251449 | Common:3; Rare:228 | ||||
| chr3:136751673-136751894 | Common:5; Rare:178 | ||||
| chr3:136751893-136752293 | Common:2; Rare:156 | ||||
| chr3:136752220-136752920 | Common:7; Rare:937 | ||||
| chr3:136818200-136818484 | Common:2; Rare:61 | ||||
| chr3:136818805-136819205 | Common:15; Rare:430 | ||||
| chr3:136819500-136819840 | Common:4; Rare:130 |