| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70686928-70687148 | Common:2; Rare:56 | ||||
| chr2:70748450-70748780 | Common:1; Rare:55 | ||||
| chr2:70789510-70789940 | Common:4; Rare:79 | ||||
| chr2:70861836-70862070 | Common:2; Rare:41 | ||||
| chr2:70947615-70948015 | Common:4; Rare:86 | ||||
| chr2:70948498-70948704 | Common:2; Rare:43 | ||||
| chr2:70964940-70965310 | Common:3; Rare:103; Clinvar:5; Clinvar (benign):4 | ||||
| chr2:70976942-70977052 | Common:1; Rare:20 | ||||
| chr2:70977074-70977535 | Common:8; Rare:91 | ||||
| chr2:71545338-71545463 | Common:3; Rare:22 | ||||
| chr2:71742952-71743096 | Rare:30 | ||||
| chr2:71747764-71748069 | Rare:50 | ||||
| chr2:71785092-71785237 | Rare:26 | ||||
| chr2:71843482-71843586 | Common:1; Rare:9 | ||||
| chr2:71871679-71871853 | Common:1; Rare:36 |