Variant report

Variant	rs326175
Chromosome Location	chr5:7829813-7829814
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:7822314..7823878-chr5:7829046..7830943,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10474820	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10474821	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10475395	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs162054	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16879202	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16879204	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs179044	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs191261	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2287778	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs326171	0.92[CEU][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs326173	0.92[CEU][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs326174	0.92[CEU][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs326184	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4702502	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs66820699	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6870733	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6879836	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6887726	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7703102	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9313204	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs989632	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs989633	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs989634	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs989635	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916892	chr5:7634377-8158890	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv949492	chr5:7682909-7953909	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv533983	chr5:7701457-8275379	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv461927	chr5:7757812-7854289	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv597004	chr5:7757812-7854289	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7820000-7830200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:7825600-7830200	Weak transcription	Aorta	Aorta
3	chr5:7827600-7830200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:7827600-7830600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr5:7827600-7831000	Weak transcription	Fetal Stomach	stomach
6	chr5:7827600-7833600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:7827600-7834000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr5:7827800-7830000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr5:7828200-7833600	Weak transcription	Fetal Brain Male	brain
10	chr5:7828400-7839000	Weak transcription	Fetal Brain Female	brain
11	chr5:7829200-7831600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:7829200-7834600	Weak transcription	Brain Germinal Matrix	brain
13	chr5:7829200-7837200	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr5:7829200-7842400	Weak transcription	Brain Anterior Caudate	brain

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