Variant report

Variant	rs17775827
Chromosome Location	chr5:100026421-100026422
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs17159001	0.85[EUR][1000 genomes]
rs17718624	0.82[CEU][hapmap]
rs17718723	0.82[CEU][hapmap];0.91[AMR][1000 genomes]
rs17719528	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17720901	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17721341	0.83[AMR][1000 genomes]
rs17721790	0.83[AMR][1000 genomes]
rs17722713	0.83[AMR][1000 genomes]
rs17723146	0.83[AMR][1000 genomes]
rs17725086	0.83[AMR][1000 genomes]
rs17775060	0.82[CEU][hapmap]
rs17775983	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17776515	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17776916	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17777079	0.85[EUR][1000 genomes]
rs17777349	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17778120	0.83[AMR][1000 genomes]
rs17778217	0.83[AMR][1000 genomes]
rs17778313	0.83[AMR][1000 genomes]
rs17778440	0.83[AMR][1000 genomes]
rs17778487	0.83[AMR][1000 genomes]
rs17778598	0.83[AMR][1000 genomes]
rs17778786	0.83[AMR][1000 genomes]
rs17779305	0.83[AMR][1000 genomes]
rs17779694	0.83[AMR][1000 genomes]
rs17779731	0.83[AMR][1000 genomes]
rs17780072	0.83[AMR][1000 genomes]
rs17780121	0.83[AMR][1000 genomes]
rs17780854	0.83[AMR][1000 genomes]
rs17780992	0.83[AMR][1000 genomes]
rs17781289	0.83[AMR][1000 genomes]
rs57652761	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6866516	0.83[AMR][1000 genomes]
rs73777435	0.83[AMR][1000 genomes]
rs73777437	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599165	chr5:99469004-100063039	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv948969	chr5:99534096-100133827	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1021183	chr5:99625857-100221426	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv882462	chr5:99745767-100060150	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1017420	chr5:99745775-100133140	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv537825	chr5:99745775-100133140	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv1023765	chr5:99915011-100733755	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
8	nsv882466	chr5:99936090-100029620	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv882467	chr5:99952282-100100157	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv882468	chr5:99959205-100029620	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv882469	chr5:100018392-100082355	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv882470	chr5:100018392-100100157	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:100025600-100028200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr5:100025600-100028200	Enhancers	Osteobl	bone
3	chr5:100026400-100026800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:100026400-100028200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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