| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11465844-11466213 | Common:5; Rare:117 | ||||
| chr2:11746401-11746671 | Common:2; Rare:77; Clinvar:4 | ||||
| chr2:12716748-12717069 | Common:1; Rare:91 | ||||
| chr2:16665794-16665962 | Common:4; Rare:36 | ||||
| chr2:17753338-17753408 | Common:4; Rare:20 | ||||
| chr2:17753655-17754160 | Common:4; Rare:161; Clinvar (benign):1 | ||||
| chr2:18560308-18560571 | Rare:104 | ||||
| chr2:18560643-18560808 | Rare:48 | ||||
| chr2:19358508-19358903 | Common:1; Rare:86 | ||||
| chr2:19901602-19902013 | Common:2; Rare:165 | ||||
| chr2:19990046-19990229 | Rare:51 | ||||
| chr2:20051466-20051816 | Common:1; Rare:107 | ||||
| chr2:20350609-20351092 | Common:2; Rare:176 | ||||
| chr2:20446841-20447113 | Common:4; Rare:120 | ||||
| chr2:20447239-20447552 | Common:2; Rare:105 |