| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46617019-46617255 | Common:6; Rare:99 | ||||
| chr2:46915736-46916122 | Common:4; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941715-46941844 | Common:2; Rare:42; Clinvar (benign):1 | ||||
| chr2:53786862-53787184 | Common:1; Rare:120 | ||||
| chr2:53970788-53971119 | Common:9; Rare:108 | ||||
| chr2:54558656-54558776 | Common:1; Rare:33 | ||||
| chr2:55050441-55050784 | Common:4; Rare:103 | ||||
| chr2:55232249-55232413 | Common:3; Rare:38 | ||||
| chr2:55269201-55269332 | Common:2; Rare:38 | ||||
| chr2:55519421-55519746 | Common:1; Rare:90 | ||||
| chr2:61017428-61017770 | Common:1; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144926-61145165 | Common:3; Rare:79 | ||||
| chr2:61470664-61470990 | Rare:109 | ||||
| chr2:61888564-61888727 | Common:1; Rare:66 | ||||
| chr2:63588632-63589025 | Common:1; Rare:122; Clinvar (benign):1 |