Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:94129476-94129830 | Common:3; Rare:104 | ||||
chr12:7089370-7089652 | Common:2; Rare:97 | ||||
chr12:76030535-76030621 | Rare:30 | ||||
chr12:108657091-108657305 | Common:1; Rare:31 | ||||
chr12:123260866-123261014 | Rare:16 | ||||
chr14:21364873-21365120 | Common:1; Rare:56 | ||||
chr14:22844470-22844705 | Rare:61 | ||||
chr14:49622706-49622872 | Rare:35 | ||||
chr14:73245966-73246107 | Common:2; Rare:60 | ||||
chr14:75294166-75294446 | Common:1; Rare:75 | ||||
chr14:76761416-76761518 | Common:2; Rare:43 | ||||
chr15:23686188-23686335 | Common:1; Rare:39; Clinvar (benign):1 | ||||
chr15:90231105-90231438 | Common:2; Rare:115 | ||||
chr16:75577144-75577381 | Rare:60 | ||||
chr17:1712012-1712164 | Rare:35 |