| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49689461-49689613 | Rare:47 | ||||
| chr3:49723937-49724227 | Common:8; Rare:101 | ||||
| chr3:49813903-49813979 | Common:1; Rare:11 | ||||
| chr3:49929746-49930026 | Rare:94 | ||||
| chr3:50267405-50267659 | Common:2; Rare:83 | ||||
| chr3:50299355-50299671 | Common:1; Rare:81 | ||||
| chr3:50303562-50303853 | Common:3; Rare:55; Clinvar:1 | ||||
| chr3:50328161-50328353 | Rare:58 | ||||
| chr3:50350705-50350897 | Common:1; Rare:29 | ||||
| chr3:50359344-50359712 | Common:3; Rare:106 | ||||
| chr3:50365137-50365381 | Common:1; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:50567593-50567895 | Common:1; Rare:91 | ||||
| chr3:50569406-50569527 | Rare:27 | ||||
| chr3:50611702-50611889 | Rare:43 | ||||
| chr3:51385025-51385356 | Common:2; Rare:102 |