Variant report

Variant	rs4613682
Chromosome Location	chr5:75576455-75576456
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10942765	0.84[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs13174383	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13188781	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[ASN][1000 genomes]
rs1995381	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs2270927	0.84[AMR][1000 genomes]
rs2358710	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2358712	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[ASN][1000 genomes]
rs246813	0.84[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs246814	0.84[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs246815	0.84[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs2937748	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs2937749	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs2937750	0.96[ASN][1000 genomes]
rs2937752	0.96[ASN][1000 genomes]
rs2972836	0.96[ASN][1000 genomes]
rs2972837	0.82[ASN][1000 genomes]
rs2972838	0.96[ASN][1000 genomes]
rs2972839	0.96[ASN][1000 genomes]
rs2972840	0.96[ASN][1000 genomes]
rs31243	0.84[AMR][1000 genomes]
rs31244	0.82[JPT][hapmap];0.96[ASN][1000 genomes]
rs34596551	1.00[ASN][1000 genomes]
rs35662301	0.82[AMR][1000 genomes]
rs35764719	0.91[ASN][1000 genomes]
rs35930860	1.00[ASN][1000 genomes]
rs35966882	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35984318	0.96[ASN][1000 genomes]
rs4352583	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[ASN][1000 genomes]
rs4496693	1.00[CHB][hapmap];0.91[JPT][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4546360	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4566770	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.91[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4566771	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6453213	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6453214	0.84[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs67771044	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6874435	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.91[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6875731	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6876070	1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[ASN][1000 genomes]
rs6891108	1.00[ASN][1000 genomes]
rs7730153	1.00[CHB][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];1.00[ASN][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	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv870415	chr5:75526088-75738412	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75575000-75579600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr5:75576000-75582800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:75576200-75576600	Enhancers	Fetal Muscle Leg	muscle
4	chr5:75576200-75580200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr5:75576200-75583200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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