| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33599222-33599400 | Rare:68 | ||||
| chr2:36356388-36356498 | Rare:37 | ||||
| chr2:37084276-37084566 | Common:3; Rare:110 | ||||
| chr2:37231478-37231720 | Common:5; Rare:132; Clinvar (benign):3 | ||||
| chr2:37324713-37324909 | Common:1; Rare:78 | ||||
| chr2:37344601-37344843 | Common:1; Rare:98 | ||||
| chr2:37671598-37671884 | Common:11; Rare:118 | ||||
| chr2:38076143-38076291 | Rare:38 | ||||
| chr2:38751230-38751593 | Common:5; Rare:184 | ||||
| chr2:38875886-38876064 | Common:1; Rare:65 | ||||
| chr2:39437078-39437456 | Common:4; Rare:136 | ||||
| chr2:40452009-40452241 | Common:4; Rare:88 | ||||
| chr2:43226188-43226503 | Common:1; Rare:134 | ||||
| chr2:43226587-43226879 | Common:2; Rare:116 | ||||
| chr2:43595931-43596197 | Common:1; Rare:92 |