Variant report

Variant	rs7157858
Chromosome Location	chr14:67960437-67960438
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10438155	0.90[AMR][1000 genomes]
rs17184538	1.00[ASN][1000 genomes]
rs45479091	1.00[ASN][1000 genomes]
rs72719106	1.00[ASN][1000 genomes]
rs72719108	1.00[ASN][1000 genomes]
rs72719110	1.00[ASN][1000 genomes]
rs72719115	1.00[ASN][1000 genomes]
rs72719116	1.00[ASN][1000 genomes]
rs72719122	1.00[ASN][1000 genomes]
rs72719129	1.00[ASN][1000 genomes]
rs72719130	1.00[ASN][1000 genomes]
rs72719131	1.00[ASN][1000 genomes]
rs72719134	1.00[ASN][1000 genomes]
rs72719137	1.00[ASN][1000 genomes]
rs72719138	1.00[ASN][1000 genomes]
rs72719140	1.00[ASN][1000 genomes]
rs8006892	1.00[ASN][1000 genomes]
rs8014211	1.00[ASN][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	nsv456331	chr14:67732861-68103780	Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv564961	chr14:67732861-68103780	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv470651	chr14:67732861-68113293	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv902066	chr14:67873128-68103780	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv1035855	chr14:67935684-67964355	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1320	chr14:67938724-67984157	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67935000-67977200	Weak transcription	Brain Angular Gyrus	brain
2	chr14:67956000-67978000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:67956200-67981000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr14:67956800-67961000	ZNF genes & repeats	GM12878-XiMat	blood
5	chr14:67959000-67961600	ZNF genes & repeats	Fetal Intestine Small	intestine
6	chr14:67959200-67960600	ZNF genes & repeats	Dnd41	blood
7	chr14:67959400-67961000	Weak transcription	Pancreas	Pancrea
8	chr14:67959400-67961600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr14:67959400-67979800	Weak transcription	Fetal Brain Male	brain
10	chr14:67959600-67960800	ZNF genes & repeats	Primary B cells from cord blood	blood
11	chr14:67959600-67961600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
12	chr14:67959800-67961400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
13	chr14:67959800-67961600	ZNF genes & repeats	Thymus	Thymus
14	chr14:67960000-67960600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
15	chr14:67960200-67960600	ZNF genes & repeats	Primary T cells from cord blood	blood

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

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