Variant report

Variant	rs7159823
Chromosome Location	chr14:70266367-70266368
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:70232739..70236319-chr14:70264002..70267714,4	MCF-7	breast:
2	chr14:70261200..70263802-chr14:70264379..70267059,2	MCF-7	breast:
3	chr14:70264666..70266507-chr14:70268472..70271032,2	MCF-7	breast:
4	chr14:70233030..70235263-chr14:70265408..70267829,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRSF5-1	chr14:70265065-70266679	NONHSAT037545

Variant related genes	Relation type
ENSG00000100650	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10130174	0.90[CEU][hapmap];0.94[EUR][1000 genomes]
rs10145643	0.96[EUR][1000 genomes]
rs10498531	0.85[GIH][hapmap]
rs11623504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.85[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11626135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.85[TSI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11626930	0.93[EUR][1000 genomes]
rs11628140	0.89[EUR][1000 genomes]
rs11628646	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[TSI][hapmap];0.94[EUR][1000 genomes]
rs11628755	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11629222	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12431918	0.90[CEU][hapmap];1.00[CHB][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs12434311	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12434937	0.93[EUR][1000 genomes]
rs12436240	1.00[CHB][hapmap]
rs17107282	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[TSI][hapmap];0.94[EUR][1000 genomes]
rs28488181	0.90[EUR][1000 genomes]
rs28595072	0.94[EUR][1000 genomes]
rs2877596	0.93[EUR][1000 genomes]
rs4340264	0.86[EUR][1000 genomes]
rs4341691	0.82[EUR][1000 genomes]
rs45527638	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55663855	0.82[AFR][1000 genomes]
rs56063215	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56154784	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60401303	0.86[AFR][1000 genomes]
rs61982074	0.89[EUR][1000 genomes]
rs61982101	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61982104	0.93[EUR][1000 genomes]
rs61982105	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61982106	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61982107	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72725721	0.90[EUR][1000 genomes]
rs72725750	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73285211	0.85[AFR][1000 genomes]
rs8013586	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8014462	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs8018389	0.94[EUR][1000 genomes]
rs8019166	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8020042	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];0.96[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs943276	1.00[CHB][hapmap];0.85[GIH][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs943277	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];0.85[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][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	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70248200-70271600	Weak transcription	Psoas Muscle	Psoas
2	chr14:70254800-70275600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:70265000-70266600	Enhancers	Liver	Liver
4	chr14:70265400-70268800	Weak transcription	Placenta	Placenta
5	chr14:70265600-70266400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:70265800-70266400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr14:70265800-70266400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr14:70265800-70266600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr14:70266000-70266600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr14:70266000-70273400	Weak transcription	HepG2	liver

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