Variant report

Variant	rs6936142
Chromosome Location	chr6:145719474-145719475
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1396644	0.89[AMR][1000 genomes]
rs17075151	0.89[AMR][1000 genomes]
rs34729185	0.83[ASN][1000 genomes]
rs35303723	1.00[ASN][1000 genomes]
rs3901447	1.00[ASN][1000 genomes]
rs56055951	1.00[ASN][1000 genomes]
rs56291136	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56323244	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57980525	1.00[ASN][1000 genomes]
rs6922956	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6935624	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73785028	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9484976	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9484977	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9484978	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9484979	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9484980	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9484981	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9484984	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9484985	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9484989	0.89[AMR][1000 genomes]
rs9497276	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9497277	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9497278	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9497281	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9497282	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9497298	0.89[AMR][1000 genomes]
rs9497300	0.89[AMR][1000 genomes]
rs9497302	0.89[AMR][1000 genomes]
rs9497310	0.89[AMR][1000 genomes]
rs9497312	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017166	chr6:145677071-145808448	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv604838	chr6:145709371-145841146	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145718200-145720600	Enhancers	Stomach Mucosa	stomach
2	chr6:145718600-145719800	Enhancers	Hela-S3	cervix

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