Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:100602167-100602630 | Common:3; Rare:124 | ||||
chr15:101295174-101295354 | Rare:55 | ||||
chr15:101652329-101652465 | Common:2; Rare:68 | ||||
chr16:53590-53889 | Common:7; Rare:101 | ||||
chr16:78165-78322 | Common:3; Rare:56 | ||||
chr16:275907-275962 | Rare:14 | ||||
chr16:282921-283378 | Common:13; Rare:155 | ||||
chr16:284351-284401 | Rare:31 | ||||
chr16:396969-397311 | Common:8; Rare:82 | ||||
chr16:401654-401952 | Common:2; Rare:133 | ||||
chr16:649291-649365 | Rare:25 | ||||
chr16:681153-681505 | Rare:111; Clinvar (pathogenic):4 | ||||
chr16:721076-721162 | Common:2; Rare:19 | ||||
chr16:740973-741144 | Rare:56 | ||||
chr16:970851-971139 | Common:7; Rare:136 |