Variant report

Variant	rs6042711
Chromosome Location	chr20:1492590-1492591
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1121670	0.93[ASN][1000 genomes]
rs1121671	0.93[ASN][1000 genomes]
rs1121672	0.93[ASN][1000 genomes]
rs2251801	0.91[ASN][1000 genomes]
rs2251811	0.81[ASN][1000 genomes]
rs2422576	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2422577	0.94[ASN][1000 genomes]
rs2422578	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2422579	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2422580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2422582	0.93[ASN][1000 genomes]
rs2422584	0.93[ASN][1000 genomes]
rs2422585	0.93[ASN][1000 genomes]
rs2422586	0.93[ASN][1000 genomes]
rs2422587	0.93[ASN][1000 genomes]
rs2422588	0.93[ASN][1000 genomes]
rs2422592	0.87[ASN][1000 genomes]
rs2422593	0.93[ASN][1000 genomes]
rs2422594	0.93[ASN][1000 genomes]
rs2422595	0.93[ASN][1000 genomes]
rs2422597	0.92[ASN][1000 genomes]
rs2422599	0.92[ASN][1000 genomes]
rs2422600	0.92[ASN][1000 genomes]
rs2422601	0.92[ASN][1000 genomes]
rs2422602	0.92[ASN][1000 genomes]
rs2422603	0.92[ASN][1000 genomes]
rs2422604	0.92[ASN][1000 genomes]
rs2422605	0.92[ASN][1000 genomes]
rs2422606	0.91[ASN][1000 genomes]
rs2422607	0.91[ASN][1000 genomes]
rs2422608	0.91[ASN][1000 genomes]
rs2422610	0.91[ASN][1000 genomes]
rs2422611	0.91[ASN][1000 genomes]
rs4476414	0.93[ASN][1000 genomes]
rs4813157	0.93[ASN][1000 genomes]
rs4813158	0.93[ASN][1000 genomes]
rs6042710	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6135158	0.92[ASN][1000 genomes]
rs761450	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs761451	0.93[ASN][1000 genomes]
rs975409	0.93[ASN][1000 genomes]
rs975410	0.91[ASN][1000 genomes]
rs976192	0.90[AMR][1000 genomes];0.92[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	nsv522008	chr20:1340390-1638578	Flanking Active TSS Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv585206	chr20:1386473-1714362	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv833893	chr20:1414615-1527779	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	esv2758509	chr20:1476781-1679256	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	esv2758777	chr20:1476781-1679256	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv428374	chr20:1476781-1679256	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv912596	chr20:1486637-1877150	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1482000-1497600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr20:1490600-1493400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr20:1492400-1492600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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