Variant report

Variant	rs35146319
Chromosome Location	chr7:124575949-124575950
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:124570250..124573246-chr7:124575640..124577419,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10281773	0.80[EUR][1000 genomes]
rs11766412	0.86[EUR][1000 genomes]
rs11767519	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11768553	0.86[EUR][1000 genomes]
rs11770818	0.86[EUR][1000 genomes]
rs11972411	0.91[EUR][1000 genomes]
rs11978268	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12533661	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12534983	0.86[EUR][1000 genomes]
rs12537983	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12538061	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12539481	0.88[EUR][1000 genomes]
rs12706625	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12706627	0.91[EUR][1000 genomes]
rs13222197	0.88[EUR][1000 genomes]
rs13228358	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13240050	0.80[EUR][1000 genomes]
rs1481334	0.80[EUR][1000 genomes]
rs17147723	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2101100	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2127968	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2127969	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2127970	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2291207	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2402761	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28820412	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs33964002	0.89[EUR][1000 genomes]
rs35423300	0.85[EUR][1000 genomes]
rs4501522	0.86[EUR][1000 genomes]
rs60678110	0.89[EUR][1000 genomes]
rs62480260	0.86[EUR][1000 genomes]
rs62480274	0.88[EUR][1000 genomes]
rs6466959	0.89[EUR][1000 genomes]
rs6945563	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6946962	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs719974	0.80[EUR][1000 genomes]
rs727521	0.80[EUR][1000 genomes]
rs73432439	0.90[ASN][1000 genomes]
rs7784285	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7786989	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7787570	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7801755	0.89[EUR][1000 genomes]
rs7804052	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7806890	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429809	chr7:123937674-124835925	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
2	esv3446198	chr7:124358002-124586856	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv889135	chr7:124462081-124584834	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv889137	chr7:124513770-124584834	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv889138	chr7:124518766-124584834	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv608342	chr7:124549573-124600505	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv1016655	chr7:124575684-124684279	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr7:124570200-124585400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:124575400-124580200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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