Variant report

Variant	rs56735831
Chromosome Location	chr3:112147945-112147946
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1072896	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1473485	0.86[ASN][1000 genomes]
rs1488265	0.90[ASN][1000 genomes]
rs1488266	0.90[ASN][1000 genomes]
rs16859561	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16859562	0.83[AFR][1000 genomes]
rs16859563	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16859568	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16859570	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16859573	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16859587	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2683893	0.86[ASN][1000 genomes]
rs2705538	0.93[ASN][1000 genomes]
rs56713746	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs56830153	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs57048961	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57240433	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58144611	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58164505	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58315065	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58441702	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58953251	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs59191788	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59429955	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59650289	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59925989	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60001227	0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs60044977	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs60202763	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60340975	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60413363	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs60733172	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60819545	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60882964	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs61147417	1.00[ASN][1000 genomes]
rs61446034	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72936206	0.83[AFR][1000 genomes]
rs72936230	0.83[AFR][1000 genomes]
rs72936241	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72936252	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72936259	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72936271	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs72954456	0.83[AFR][1000 genomes]
rs924310	0.90[ASN][1000 genomes]
rs953716	0.93[ASN][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	nsv591294	chr3:112091220-112208750	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1010208	chr3:112098542-112227212	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1003936	chr3:112125931-112274613	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv998309	chr3:112130290-112278804	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	esv3331778	chr3:112134311-112164058	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv591300	chr3:112144026-112270857	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv1006065	chr3:112147080-112276983	Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112137000-112150400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:112144400-112150400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr3:112145400-112151000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:112145600-112150400	Weak transcription	GM12878-XiMat	blood
5	chr3:112145600-112150600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr3:112145600-112150800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr3:112146200-112149800	Weak transcription	Primary B cells from cord blood	blood
8	chr3:112147400-112148200	Enhancers	Fetal Intestine Large	intestine
9	chr3:112147600-112150600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:112147800-112148400	Enhancers	Cortex derived primary cultured neurospheres	brain

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