| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96265911-96266381 | Common:2; Rare:140; Clinvar:3 | ||||
| chr2:96305435-96306022 | Common:5; Rare:170; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96324848-96324959 | Rare:19 | ||||
| chr2:96325168-96325412 | Rare:63 | ||||
| chr2:96326053-96326282 | Common:1; Rare:54 | ||||
| chr2:96335570-96336155 | Common:4; Rare:170 | ||||
| chr2:96505295-96505475 | Rare:34 | ||||
| chr2:96505576-96505749 | Rare:26 | ||||
| chr2:96536561-96536813 | Common:1; Rare:73 | ||||
| chr2:96536915-96537438 | Common:3; Rare:114 | ||||
| chr2:96637894-96638578 | Common:1; Rare:179 | ||||
| chr2:96739981-96740302 | Common:5; Rare:95 | ||||
| chr2:96760572-96760924 | Common:2; Rare:96 | ||||
| chr2:96760983-96761112 | Rare:35; Clinvar:3 | ||||
| chr2:96815902-96816335 | Common:5; Rare:149 |