Variant report

Variant	rs60395126
Chromosome Location	chr6:38261754-38261755
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11964509	1.00[EUR][1000 genomes]
rs11967720	1.00[EUR][1000 genomes]
rs56783945	1.00[AMR][1000 genomes]
rs57211386	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58257452	1.00[EUR][1000 genomes]
rs58907208	1.00[AMR][1000 genomes]
rs60148639	1.00[AMR][1000 genomes]
rs60662487	1.00[AMR][1000 genomes]
rs61097716	1.00[AMR][1000 genomes]
rs61104643	1.00[AMR][1000 genomes]
rs6936449	1.00[AMR][1000 genomes]
rs73420800	1.00[AMR][1000 genomes]
rs73420801	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73422812	1.00[AMR][1000 genomes]
rs73422820	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73422823	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73422832	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73422841	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73422843	1.00[EUR][1000 genomes]
rs73422846	1.00[EUR][1000 genomes]
rs73422854	1.00[AMR][1000 genomes]
rs73422856	1.00[AMR][1000 genomes]
rs73422860	1.00[AMR][1000 genomes]
rs73422871	1.00[AMR][1000 genomes]
rs73422874	1.00[AMR][1000 genomes]
rs73422876	1.00[AMR][1000 genomes]
rs73422883	1.00[AMR][1000 genomes]
rs73422884	1.00[AMR][1000 genomes]
rs7748763	1.00[EUR][1000 genomes]
rs7763951	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1021991	chr6:37893949-38738720	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv534620	chr6:38049585-38602064	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv885818	chr6:38147745-38436317	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv885820	chr6:38166511-38468887	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38224400-38267600	Weak transcription	Primary T cells from cord blood	blood
2	chr6:38249200-38275600	Weak transcription	Fetal Brain Male	brain
3	chr6:38256000-38263000	Weak transcription	Lung	lung

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