Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15861211..15863837-chr6:16050426..16052847,2	K562	blood:
2	chr6:15857919..15863956-chr6:16127859..16131568,7	K562	blood:

Variant related genes	Relation type
ENSG00000007944	Chromatin interaction

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10484352	0.87[CEU][hapmap];0.84[EUR][1000 genomes]
rs16877105	0.81[EUR][1000 genomes]
rs17418707	0.83[EUR][1000 genomes]
rs17419263	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17478963	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34459959	0.84[EUR][1000 genomes]
rs35387263	0.88[EUR][1000 genomes]
rs41499644	0.84[EUR][1000 genomes]
rs4712259	0.82[EUR][1000 genomes]
rs4716000	0.83[EUR][1000 genomes]
rs4716002	0.81[EUR][1000 genomes]
rs4716003	0.82[EUR][1000 genomes]
rs4989041	0.83[EUR][1000 genomes]
rs55715119	0.84[EUR][1000 genomes]
rs55756972	0.84[EUR][1000 genomes]
rs56207716	0.84[EUR][1000 genomes]
rs56314144	0.83[EUR][1000 genomes]
rs67428710	0.82[EUR][1000 genomes]
rs73366628	0.83[EUR][1000 genomes]
rs7745776	0.83[EUR][1000 genomes]
rs7748171	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7749868	0.87[CEU][hapmap];0.83[EUR][1000 genomes]
rs7750026	0.83[EUR][1000 genomes]
rs881017	0.87[CEU][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3442648	chr6:15863446-15863907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15863400-15872600	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:15863800-15864200	Weak transcription	HSMMtube	muscle

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