Variant report

Variant	rs357375
Chromosome Location	chr7:137984146-137984147
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	UBTF	chr7:137984035-137984156	K562	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000213238	TF binding region

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1035329	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11536612	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs357370	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs357374	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs357380	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs357405	0.93[AFR][1000 genomes]
rs357410	0.93[AFR][1000 genomes]
rs357415	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs357416	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs357417	0.93[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs357419	0.80[EUR][1000 genomes]
rs357420	0.83[EUR][1000 genomes]
rs357434	0.93[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs357436	0.93[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs357439	0.86[EUR][1000 genomes]
rs368043	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs368370	0.80[ASN][1000 genomes]
rs373089	0.80[ASN][1000 genomes]
rs378745	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs386059	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs396783	0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs401454	0.83[ASN][1000 genomes]
rs402615	0.84[ASN][1000 genomes]
rs403675	0.82[ASN][1000 genomes]
rs407702	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs409365	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs410156	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs410187	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs424197	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs424335	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs424847	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs443184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831152	chr7:137884311-138033117	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1029101	chr7:137952620-138005671	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv517949	chr7:137962186-137992969	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr7:137981800-137988200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:137983200-137988000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:137984000-137984400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:137984000-137984600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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