| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:128091670-128091898 | Rare:52 | ||||
| chr2:128318845-128319030 | Common:1; Rare:71 | ||||
| chr2:130145109-130145177 | Rare:14 | ||||
| chr2:130158201-130158337 | Rare:43 | ||||
| chr2:130181485-130181944 | Common:4; Rare:206 | ||||
| chr2:130182020-130182279 | Common:1; Rare:88 | ||||
| chr2:130182489-130182533 | Common:1; Rare:16 | ||||
| chr2:130342079-130342435 | Common:1; Rare:122; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:130342615-130343014 | Common:8; Rare:141 | ||||
| chr2:130343103-130343202 | Common:1; Rare:37 | ||||
| chr2:130355865-130356092 | Common:3; Rare:60 | ||||
| chr2:130371534-130371757 | Common:1; Rare:32 | ||||
| chr2:130371884-130372033 | Rare:33 | ||||
| chr2:130372082-130372300 | Common:2; Rare:55 | ||||
| chr2:130372328-130372782 | Common:3; Rare:127 |