Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:30556211-30556437 | Rare:65 | ||||
chr6:30556674-30557045 | Common:3; Rare:74 | ||||
chr6:30557090-30557342 | Common:1; Rare:83 | ||||
chr6:30571255-30571490 | Common:1; Rare:79 | ||||
chr6:30686636-30686765 | Common:1; Rare:25 | ||||
chr6:30717243-30717574 | Common:1; Rare:74 | ||||
chr6:30720196-30720543 | Common:1; Rare:82 | ||||
chr6:30742616-30742954 | Common:2; Rare:82 | ||||
chr6:30914193-30914370 | Rare:68; Clinvar (benign):2 | ||||
chr6:31197683-31197760 | Common:3; Rare:19 | ||||
chr6:31272053-31272234 | Common:9; Rare:32 | ||||
chr6:31357089-31357375 | Common:27; Rare:53 | ||||
chr6:31399732-31400073 | Common:7; Rare:60 | ||||
chr6:31541949-31542330 | Common:8; Rare:100 | ||||
chr6:31546569-31546870 | Common:3; Rare:62 |