Variant report

Variant	rs1934614
Chromosome Location	chr1:210968212-210968213
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10465689	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs11119591	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs11119592	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs11119604	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs1122901	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs12117136	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12122556	0.89[EUR][1000 genomes]
rs12122589	0.89[EUR][1000 genomes]
rs12122593	0.89[EUR][1000 genomes]
rs12122869	0.91[EUR][1000 genomes]
rs12134429	0.84[EUR][1000 genomes]
rs12134632	0.82[EUR][1000 genomes]
rs12137464	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs12139273	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs12139474	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs12142954	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12143524	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs12562303	0.83[JPT][hapmap]
rs12562536	0.92[JPT][hapmap]
rs12563193	0.90[JPT][hapmap]
rs12564968	0.83[EUR][1000 genomes]
rs12565452	0.83[JPT][hapmap]
rs12566698	0.82[EUR][1000 genomes]
rs1340124	0.90[EUR][1000 genomes]
rs1340125	0.90[EUR][1000 genomes]
rs1538755	0.92[JPT][hapmap]
rs17016821	0.85[CHB][hapmap];0.92[JPT][hapmap]
rs1934612	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1934613	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs1970589	0.92[CHB][hapmap];0.82[JPT][hapmap];0.80[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2185384	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs4951462	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs4951563	0.85[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs4951566	0.85[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs4951576	0.83[JPT][hapmap]
rs4951591	0.83[JPT][hapmap]
rs4951605	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs56264689	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56383511	0.85[EUR][1000 genomes]
rs61829490	0.85[EUR][1000 genomes]
rs61829492	0.89[EUR][1000 genomes]
rs61829493	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61829496	0.90[EUR][1000 genomes]
rs61829499	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6689950	0.92[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6694502	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[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]
rs73069563	0.83[EUR][1000 genomes]
rs73069573	0.83[EUR][1000 genomes]
rs7519357	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs7532333	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7541814	0.82[EUR][1000 genomes]
rs9430047	0.83[JPT][hapmap]
rs9430049	0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv873153	chr1:210900481-210994339	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv999018	chr1:210907239-210999306	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv832503	chr1:210948760-211103163	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210941800-210978000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:210953400-210974400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr1:210965800-210969800	Weak transcription	HSMMtube	muscle
4	chr1:210965800-210975600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:210966600-210969600	Weak transcription	HSMM	muscle
6	chr1:210966600-210970000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:210966800-210976800	Weak transcription	A549	lung
8	chr1:210967000-210979600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr1:210967200-210970200	Weak transcription	Brain Anterior Caudate	brain
10	chr1:210967400-210973400	Weak transcription	Brain Angular Gyrus	brain
11	chr1:210967400-210985000	Weak transcription	Brain Hippocampus Middle	brain
12	chr1:210968000-210970000	Weak transcription	Brain Inferior Temporal Lobe	brain

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