| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33717933-33718449 | Rare:777 | ||||
| chr3:33718351-33719006 | Common:1; Rare:171 | ||||
| chr3:33798310-33798720 | Common:14; Rare:602 | ||||
| chr3:33798856-33799440 | Common:1; Rare:561 | ||||
| chr3:36908067-36908192 | Common:1; Rare:19 | ||||
| chr3:36908300-36908910 | Common:4; Rare:152 | ||||
| chr3:36992063-36992506 | Rare:154 | ||||
| chr3:36992752-36993612 | Common:13; Rare:1301; Clinvar:211; Clinvar (benign):95; Clinvar (pathogenic):23 | ||||
| chr3:36993630-36994000 | Common:1; Rare:418; Clinvar:18; Clinvar (benign):11 | ||||
| chr3:37175361-37176123 | Common:9; Rare:417 | ||||
| chr3:37176090-37176750 | Common:4; Rare:627 | ||||
| chr3:37242523-37242964 | Common:6; Rare:228 | ||||
| chr3:37243042-37243384 | Common:15; Rare:402 | ||||
| chr3:37243511-37244040 | Common:10; Rare:519 | ||||
| chr3:37861432-37862271 | Common:9; Rare:711 |