Variant report

Variant	rs1717741
Chromosome Location	chr7:38004057-38004058
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12701600	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1376258	0.86[AFR][1000 genomes]
rs1376260	1.00[CEU][hapmap];0.81[JPT][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1376261	1.00[CEU][hapmap];0.81[JPT][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1450849	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1450850	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1616485	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1619560	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1621407	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668347	0.86[AFR][1000 genomes]
rs1668348	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668350	0.84[AFR][1000 genomes]
rs1668353	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1668354	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668356	0.86[AFR][1000 genomes]
rs1668357	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1668358	0.86[AFR][1000 genomes]
rs1668361	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668362	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1668363	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1717732	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1717737	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1717742	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1717743	0.86[AFR][1000 genomes]
rs1717744	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1823522	1.00[CEU][hapmap];0.81[JPT][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1901197	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1993055	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2167267	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2246953	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2598084	0.86[AFR][1000 genomes]
rs2598085	0.83[AFR][1000 genomes]
rs2598086	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2598087	0.86[AFR][1000 genomes]
rs2598088	0.86[AFR][1000 genomes]
rs2598089	0.85[AFR][1000 genomes]
rs2598090	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2598093	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2722274	0.86[ASN][1000 genomes]
rs2722278	1.00[CEU][hapmap];0.81[JPT][hapmap];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2722279	1.00[CEU][hapmap];0.81[JPT][hapmap];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2722283	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2722287	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2722288	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2722296	0.86[AFR][1000 genomes]
rs4723719	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs976798	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8074	chr7:37865340-38210087	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:37992200-38017600	Weak transcription	Ovary	ovary
2	chr7:37992600-38026800	Weak transcription	Pancreas	Pancrea
3	chr7:37993000-38007600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr7:37993800-38007400	Weak transcription	A549	lung
5	chr7:37997600-38010600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:37997800-38005000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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