| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237487136-237487323 | Common:3; Rare:53 | ||||
| chr2:237966736-237967077 | Common:4; Rare:107 | ||||
| chr2:240025297-240025429 | Rare:54; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:240136264-240136404 | Common:1; Rare:63 | ||||
| chr2:240560766-240560800 | Rare:9 | ||||
| chr2:241102265-241102395 | Common:2; Rare:46 | ||||
| chr2:241149445-241149639 | Common:2; Rare:60 | ||||
| chr2:241272807-241272903 | Rare:37 | ||||
| chr2:241315153-241315296 | Common:1; Rare:50 | ||||
| chr2:241315646-241315978 | Common:5; Rare:130 | ||||
| chr2:241508539-241508872 | Common:2; Rare:104 | ||||
| chr2:241637544-241637709 | Common:1; Rare:90 | ||||
| chr20:325218-325583 | Rare:108 | ||||
| chr20:347013-347127 | Rare:36 | ||||
| chr20:543688-543879 | Rare:71 |