| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084283-37084544 | Common:3; Rare:94 | ||||
| chr2:37231476-37231734 | Common:5; Rare:141; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37671562-37671749 | Common:1; Rare:85 | ||||
| chr2:37925214-37925354 | Rare:55 | ||||
| chr2:38075446-38075716 | Common:1; Rare:68 | ||||
| chr2:38075789-38075921 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:38076004-38076291 | Common:1; Rare:71 | ||||
| chr2:38746924-38747046 | Common:1; Rare:38 | ||||
| chr2:38751235-38751362 | Common:2; Rare:86 | ||||
| chr2:38875892-38876032 | Common:1; Rare:47 | ||||
| chr2:39437276-39437464 | Common:2; Rare:67 | ||||
| chr2:40451932-40452295 | Common:7; Rare:125 | ||||
| chr2:42792197-42792364 | Common:2; Rare:32 | ||||
| chr2:43226559-43226842 | Common:2; Rare:117 | ||||
| chr2:43595978-43596197 | Common:1; Rare:73 |