| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70293676-70293913 | Common:3; Rare:70 | ||||
| chr2:70301952-70302186 | Common:4; Rare:113 | ||||
| chr2:70767291-70767691 | Common:2; Rare:188 | ||||
| chr2:70768162-70768465 | Common:2; Rare:65 | ||||
| chr2:70900361-70900613 | Common:5; Rare:77 | ||||
| chr2:70994806-70995075 | Common:4; Rare:80 | ||||
| chr2:71068182-71068326 | Rare:45 | ||||
| chr2:71068502-71068678 | Rare:93 | ||||
| chr2:71130206-71130367 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130537-71130682 | Common:2; Rare:47 | ||||
| chr2:71130881-71131281 | Common:4; Rare:102 | ||||
| chr2:71226392-71226590 | Rare:57 | ||||
| chr2:71227020-71227450 | Common:2; Rare:105 | ||||
| chr2:71276382-71276613 | Rare:84 | ||||
| chr2:71331586-71331860 | Common:5; Rare:83 |