| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47369457-47369539 | Common:1; Rare:47; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:47402865-47403192 | Common:1; Rare:154; Clinvar:49; Clinvar (benign):27 | ||||
| chr2:47782953-47783161 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:47783810-47783980 | Common:6; Rare:34 | ||||
| chr2:48314413-48314764 | Rare:124 | ||||
| chr2:48440631-48440818 | Common:5; Rare:80 | ||||
| chr2:53767559-53767898 | Common:5; Rare:124 | ||||
| chr2:53786856-53787213 | Common:1; Rare:136 | ||||
| chr2:53970774-53971126 | Common:10; Rare:120 | ||||
| chr2:55050309-55050402 | Common:1; Rare:34 | ||||
| chr2:55050441-55050763 | Common:4; Rare:96 | ||||
| chr2:55232235-55232892 | Common:7; Rare:212 | ||||
| chr2:55269176-55269355 | Common:2; Rare:53 | ||||
| chr2:55519414-55519746 | Common:1; Rare:92 | ||||
| chr2:55693793-55693930 | Rare:57; Clinvar (benign):2 |