| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:48771134-48771621 | Common:8; Rare:207 | ||||
| chr2:49768396-49768836 | Common:3; Rare:226 | ||||
| chr2:49901077-49902201 | Common:24; Rare:509 | ||||
| chr2:50121634-50122315 | Common:12; Rare:301 | ||||
| chr2:50127001-50127123 | Common:1; Rare:26 | ||||
| chr2:52005973-52006943 | Common:15; Rare:344 | ||||
| chr2:52695205-52695605 | Common:8; Rare:220 | ||||
| chr2:53969296-53970208 | Common:9; Rare:251 | ||||
| chr2:54416175-54416370 | Common:2; Rare:35 | ||||
| chr2:54455245-54455412 | Common:1; Rare:40 | ||||
| chr2:54559730-54560070 | Common:2; Rare:136 | ||||
| chr2:54560435-54560628 | Common:2; Rare:58 | ||||
| chr2:54579479-54580096 | Common:8; Rare:312 | ||||
| chr2:54945861-54946318 | Common:9; Rare:230 | ||||
| chr2:55156590-55157465 | Common:8; Rare:303 |