| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218671970-218672086 | Rare:41 | ||||
| chr2:218880060-218880346 | Common:2; Rare:43 | ||||
| chr2:218880674-218880870 | Common:1; Rare:57; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:219176223-219176405 | Common:2; Rare:67 | ||||
| chr2:219176911-219177112 | Common:4; Rare:62 | ||||
| chr2:219206642-219206936 | Rare:106 | ||||
| chr2:219229568-219229920 | Common:2; Rare:107 | ||||
| chr2:219245420-219245554 | Common:1; Rare:42 | ||||
| chr2:219253889-219254084 | Common:2; Rare:60 | ||||
| chr2:219254715-219254992 | Rare:32 | ||||
| chr2:219278223-219278361 | Rare:24 | ||||
| chr2:219279136-219279514 | Common:2; Rare:116 | ||||
| chr2:219498711-219498941 | Common:2; Rare:51 | ||||
| chr2:223957257-223957470 | Common:4; Rare:79 | ||||
| chr2:226835871-226836088 | Rare:88 |