Variant report

Variant	rs6689909
Chromosome Location	chr1:75670877-75670878
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11162738	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11162810	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11162944	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11163114	0.81[CEU][hapmap]
rs11163154	0.81[CEU][hapmap]
rs1144297	0.89[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes]
rs1144298	0.86[EUR][1000 genomes]
rs12039281	0.84[ASN][1000 genomes]
rs12042874	0.85[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12044451	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1249655	0.95[CEU][hapmap]
rs1249656	0.81[CEU][hapmap]
rs12726507	0.80[CEU][hapmap]
rs12741793	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12756704	0.81[CEU][hapmap]
rs1394736	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1700893	0.88[CEU][hapmap]
rs1948874	1.00[CEU][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2202473	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs599291	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs600734	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs609574	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs611899	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs615372	0.91[ASN][1000 genomes]
rs627494	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs642145	0.91[ASN][1000 genomes]
rs645287	0.91[ASN][1000 genomes]
rs686453	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs687715	0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs7516812	0.86[EUR][1000 genomes]
rs7534079	0.92[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap]
rs975152	0.85[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[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	nsv871743	chr1:75235082-75714554	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3368999	chr1:75524762-75933220	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr1:75666000-75675000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:75669600-75673000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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