Variant report

Variant	rs73422890
Chromosome Location	chr6:38330227-38330228
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12181218	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58303939	0.85[AMR][1000 genomes]
rs60588879	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9296245	1.00[EUR][1000 genomes]
rs9462430	1.00[EUR][1000 genomes]
rs9470853	1.00[EUR][1000 genomes]
rs9470864	0.85[AMR][1000 genomes]
rs9470869	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9470870	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9470871	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9470872	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	nsv602957	chr6:38305770-38395874	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1032358	chr6:38323745-38415855	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38313800-38331200	Weak transcription	Primary T cells from cord blood	blood
2	chr6:38315800-38339000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:38319200-38334200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:38323200-38331800	Weak transcription	Adipose Nuclei	Adipose
5	chr6:38323600-38330400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:38326200-38331000	Weak transcription	Right Atrium	heart
7	chr6:38326200-38331800	Weak transcription	Lung	lung
8	chr6:38326200-38338600	Weak transcription	Ovary	ovary
9	chr6:38326400-38332000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr6:38326400-38337200	Weak transcription	Psoas Muscle	Psoas
11	chr6:38326600-38331800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:38326600-38332400	Weak transcription	HSMMtube	muscle
13	chr6:38327200-38331200	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr6:38327400-38331600	Weak transcription	Fetal Muscle Leg	muscle
15	chr6:38327400-38338600	Weak transcription	Left Ventricle	heart
16	chr6:38330000-38338000	Weak transcription	Fetal Kidney	kidney
17	chr6:38330200-38330400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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