| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70293613-70293848 | Common:4; Rare:141 | ||||
| chr2:70301964-70302109 | Common:1; Rare:87 | ||||
| chr2:70554150-70554460 | Rare:115 | ||||
| chr2:70900356-70900685 | Common:11; Rare:176 | ||||
| chr2:70994707-70995075 | Common:8; Rare:192 | ||||
| chr2:71068060-71068290 | Rare:58 | ||||
| chr2:71068516-71068703 | Rare:166 | ||||
| chr2:71129940-71130130 | Common:2; Rare:54 | ||||
| chr2:71130168-71130677 | Common:12; Rare:290; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:71332060-71332940 | Common:6; Rare:361 | ||||
| chr2:72887314-72887452 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:72917260-72917630 | Common:8; Rare:184 | ||||
| chr2:73020924-73021148 | Common:2; Rare:36 | ||||
| chr2:73071213-73071518 | Common:3; Rare:197 | ||||
| chr2:73071668-73071863 | Common:4; Rare:135 |