Variant report

Variant	rs16880714
Chromosome Location	chr5:8504245-8504246
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10068072	0.83[ASN][1000 genomes]
rs1394642	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16880716	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16880725	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16880754	0.95[ASN][1000 genomes]
rs2166872	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs365719	0.95[ASN][1000 genomes]
rs368753	0.97[ASN][1000 genomes]
rs371677	0.97[ASN][1000 genomes]
rs372326	0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs372588	0.86[CHB][hapmap];0.86[JPT][hapmap];0.97[ASN][1000 genomes]
rs372695	0.97[ASN][1000 genomes]
rs374142	0.93[CHB][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs374856	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs376041	0.97[ASN][1000 genomes]
rs376478	0.95[ASN][1000 genomes]
rs377644	1.00[CHB][hapmap];0.91[CHD][hapmap];0.85[GIH][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs377721	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs383026	0.97[ASN][1000 genomes]
rs384423	0.93[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];0.81[JPT][hapmap];0.97[ASN][1000 genomes]
rs384797	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs386120	0.97[ASN][1000 genomes]
rs386332	0.85[CEU][hapmap];0.93[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.95[ASN][1000 genomes]
rs391942	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs392469	0.97[ASN][1000 genomes]
rs393704	0.97[ASN][1000 genomes]
rs394114	0.97[ASN][1000 genomes]
rs394670	0.97[ASN][1000 genomes]
rs395753	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs396042	0.97[ASN][1000 genomes]
rs396055	0.95[ASN][1000 genomes]
rs397939	0.87[CHB][hapmap];0.86[JPT][hapmap];0.97[ASN][1000 genomes]
rs398188	0.97[ASN][1000 genomes]
rs398928	0.97[ASN][1000 genomes]
rs402359	0.97[ASN][1000 genomes]
rs404767	0.97[ASN][1000 genomes]
rs414613	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs418698	0.97[ASN][1000 genomes]
rs432221	0.90[ASN][1000 genomes]
rs432665	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs438193	0.92[CHB][hapmap];0.88[JPT][hapmap];0.97[ASN][1000 genomes]
rs443746	0.97[ASN][1000 genomes]
rs444945	0.94[ASN][1000 genomes]
rs446916	0.97[ASN][1000 genomes]
rs447586	0.97[ASN][1000 genomes]
rs449352	0.95[ASN][1000 genomes]
rs57085808	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59216168	0.95[ASN][1000 genomes]
rs60932532	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6870322	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7718126	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033505	chr5:8258074-8657627	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv537634	chr5:8258074-8657627	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1026496	chr5:8275119-8681693	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
4	nsv537635	chr5:8275119-8681693	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
5	nsv427709	chr5:8353876-8519855	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv880933	chr5:8467174-8688962	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv461929	chr5:8467900-8664747	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv597028	chr5:8467900-8664747	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv470987	chr5:8467900-8680327	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:8503400-8517400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:8504000-8505400	Enhancers	Dnd41	blood
3	chr5:8504200-8504800	Enhancers	Fetal Intestine Small	intestine
4	chr5:8504200-8506600	Enhancers	Primary hematopoietic stem cells	blood

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