| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38377199-38377495 | Common:5; Rare:241 | ||||
| chr2:38602792-38603187 | Common:8; Rare:292 | ||||
| chr2:38665978-38666151 | Common:4; Rare:92 | ||||
| chr2:38751224-38751486 | Common:3; Rare:217 | ||||
| chr2:38777980-38778250 | Common:2; Rare:102 | ||||
| chr2:38875843-38876072 | Common:3; Rare:148 | ||||
| chr2:39120020-39120790 | Common:4; Rare:417; Clinvar:4; Clinvar (benign):16 | ||||
| chr2:39120954-39121127 | Common:2; Rare:117 | ||||
| chr2:39124190-39124590 | Common:2; Rare:166 | ||||
| chr2:39437051-39437469 | Common:7; Rare:237 | ||||
| chr2:39779138-39779323 | Common:3; Rare:72 | ||||
| chr2:41954630-41955320 | Common:3; Rare:128 | ||||
| chr2:42047737-42048027 | Common:7; Rare:173 | ||||
| chr2:42169168-42169474 | Common:2; Rare:283 | ||||
| chr2:43225660-43226190 | Common:5; Rare:278 |