Variant report

Variant	rs12216096
Chromosome Location	chr6:143925374-143925375
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:143923576..143926302-chr6:143926359..143929305,3	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10214882	0.83[EUR][1000 genomes]
rs10457749	0.89[CEU][hapmap];0.88[MEX][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10484802	0.83[EUR][1000 genomes]
rs12190134	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12191296	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12191485	0.83[EUR][1000 genomes]
rs12196002	0.86[EUR][1000 genomes]
rs12199016	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12203367	0.86[EUR][1000 genomes]
rs12204876	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12205130	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12205256	0.82[EUR][1000 genomes]
rs12206116	0.86[EUR][1000 genomes]
rs12208244	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12210250	0.87[EUR][1000 genomes]
rs12212759	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12213878	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs1338536	0.86[CHB][hapmap];0.87[CHD][hapmap]
rs17072813	0.86[CHB][hapmap];0.94[CHD][hapmap];0.81[ASN][1000 genomes]
rs17072815	0.86[CHB][hapmap]
rs17072817	0.86[CHB][hapmap]
rs17368239	0.89[CEU][hapmap];0.88[MEX][hapmap];0.93[TSI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17368267	0.89[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2027280	0.83[EUR][1000 genomes]
rs4142502	0.85[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55854171	0.88[EUR][1000 genomes]
rs58388072	0.83[EUR][1000 genomes]
rs6899521	0.86[CHB][hapmap]
rs6919613	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72995603	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73003366	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73005383	0.89[EUR][1000 genomes]
rs7744771	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9321924	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9321928	0.81[EUR][1000 genomes]
rs9321929	0.80[EUR][1000 genomes]
rs9321930	0.83[EUR][1000 genomes]
rs9403513	0.82[EUR][1000 genomes]
rs9484777	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9496663	0.84[CEU][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9496677	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9496694	0.80[EUR][1000 genomes]
rs9496701	0.85[CHB][hapmap]
rs9496702	0.85[CHB][hapmap]
rs9496703	0.86[CHB][hapmap];0.94[CHD][hapmap]
rs9496704	0.86[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758084	chr6:143916621-144079976	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759476	chr6:143916621-144079976	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1032369	chr6:143925374-144007513	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143911200-143929200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr6:143913200-143928400	Weak transcription	Aorta	Aorta
3	chr6:143917000-143973600	Weak transcription	Fetal Intestine Small	intestine
4	chr6:143917200-143929000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr6:143917200-143941400	Weak transcription	Fetal Intestine Large	intestine
6	chr6:143918200-143929200	Weak transcription	Lung	lung
7	chr6:143919800-143930400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr6:143919800-143930600	Weak transcription	Stomach Mucosa	stomach
9	chr6:143920000-143935200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr6:143920200-143935000	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr6:143920600-143934800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr6:143923000-143926400	Weak transcription	Placenta	Placenta
13	chr6:143923800-143929200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:143923800-143929200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:143924000-143925600	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:143924400-143925400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:143924800-143925600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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