Variant report

Variant	rs11241476
Chromosome Location	chr5:118160928-118160929
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:117502319..117505069-chr5:118158604..118161182,2	K562	blood:
2	chr5:118159743..118162265-chr5:118287763..118289308,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10447237	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10447238	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10447266	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11959589	1.00[JPT][hapmap]
rs12109252	1.00[JPT][hapmap]
rs12187606	1.00[CHB][hapmap]
rs12659444	0.90[CEU][hapmap]
rs13166967	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1448479	1.00[JPT][hapmap]
rs17132673	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17144552	1.00[JPT][hapmap]
rs17144708	0.81[EUR][1000 genomes]
rs17144714	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17144715	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs17144716	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs17144806	1.00[CHB][hapmap]
rs17144872	1.00[JPT][hapmap]
rs17144877	1.00[JPT][hapmap]
rs17381247	1.00[JPT][hapmap]
rs17440213	1.00[JPT][hapmap]
rs1864109	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2029036	1.00[JPT][hapmap]
rs2081957	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2084460	1.00[JPT][hapmap]
rs2099092	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115301	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115302	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2162888	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3813297	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3813298	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs383585	1.00[ASN][1000 genomes]
rs386288	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs406335	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4392657	1.00[JPT][hapmap]
rs4895183	1.00[CHB][hapmap]
rs4895184	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs4895353	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4895354	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55821851	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55876313	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56004980	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs581887	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs635083	0.83[EUR][1000 genomes]
rs6862297	1.00[JPT][hapmap]
rs6871241	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs6874109	1.00[CHB][hapmap]
rs6881583	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73234502	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236920	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7706037	1.00[JPT][hapmap]
rs7709381	0.92[EUR][1000 genomes]
rs7710339	1.00[JPT][hapmap]
rs7724403	1.00[JPT][hapmap]
rs7724753	1.00[JPT][hapmap]
rs822743	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs849728	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][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	nsv882767	chr5:117931730-118385691	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv599562	chr5:118122504-118230640	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118143400-118178200	Weak transcription	Left Ventricle	heart
2	chr5:118158200-118176400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr5:118158400-118169200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:118159800-118161800	Enhancers	Fetal Heart	heart
5	chr5:118160200-118171600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:118160200-118178200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:118160200-118180200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:118160600-118161600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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