Variant report

Variant	rs1534049
Chromosome Location	chr6:71313194-71313195
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:71139434..71142286-chr6:71311712..71314259,2	K562	blood:

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10214805	0.90[CEU][hapmap]
rs10455706	0.81[CEU][hapmap]
rs1048886	0.81[CEU][hapmap]
rs10945230	0.90[CEU][hapmap]
rs10945231	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11965656	0.81[CEU][hapmap]
rs12197942	0.90[CEU][hapmap]
rs12197963	0.89[CEU][hapmap]
rs12200777	0.90[CEU][hapmap]
rs12203298	0.90[CEU][hapmap]
rs12209965	0.90[CEU][hapmap]
rs12216376	0.90[CEU][hapmap]
rs12524814	0.90[CEU][hapmap]
rs12526164	0.90[CEU][hapmap]
rs12526787	0.90[CEU][hapmap]
rs12526827	0.81[CEU][hapmap]
rs12527634	0.81[CEU][hapmap]
rs12529284	0.90[CEU][hapmap]
rs12529309	0.90[CEU][hapmap]
rs12530057	0.90[CEU][hapmap]
rs16869370	0.81[CEU][hapmap]
rs16869371	0.90[CEU][hapmap]
rs16869373	0.90[CEU][hapmap]
rs1739338	0.81[CEU][hapmap]
rs17634272	0.90[CEU][hapmap]
rs17634491	0.89[CEU][hapmap]
rs17635446	0.90[CEU][hapmap]
rs17635510	0.90[CEU][hapmap]
rs17706748	0.90[CEU][hapmap]
rs17706833	0.90[CEU][hapmap]
rs17713105	0.90[CEU][hapmap]
rs17713212	0.90[CEU][hapmap]
rs17713547	0.90[CEU][hapmap]
rs1917346	1.00[ASN][1000 genomes]
rs1983455	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2207423	0.90[CEU][hapmap]
rs2207425	0.90[CEU][hapmap]
rs2273210	0.81[CEU][hapmap]
rs2293297	1.00[CEU][hapmap]
rs2295200	0.81[CEU][hapmap]
rs2346889	0.81[CEU][hapmap]
rs2346890	0.81[CEU][hapmap]
rs2639297	0.81[CEU][hapmap]
rs2691486	0.88[CEU][hapmap]
rs2691496	0.81[CEU][hapmap]
rs2747702	0.81[CEU][hapmap]
rs2842063	0.81[CEU][hapmap]
rs2842073	1.00[ASN][1000 genomes]
rs2842076	0.87[EUR][1000 genomes]
rs3193656	0.90[CEU][hapmap]
rs3846750	0.81[CEU][hapmap]
rs3889007	0.81[CEU][hapmap]
rs4283855	0.81[CEU][hapmap]
rs4496758	0.90[CEU][hapmap]
rs6455370	0.90[CEU][hapmap]
rs6906592	0.81[CEU][hapmap]
rs6911812	0.81[CEU][hapmap]
rs6911983	0.90[CEU][hapmap]
rs6916974	0.90[CEU][hapmap]
rs6933150	0.81[CEU][hapmap]
rs6942012	0.90[CEU][hapmap]
rs7740873	0.90[CEU][hapmap]
rs7741265	0.89[CEU][hapmap]
rs7752409	0.81[CEU][hapmap]
rs7753355	0.81[CEU][hapmap]
rs7756774	0.90[CEU][hapmap]
rs7757026	0.90[CEU][hapmap]
rs7759464	0.81[CEU][hapmap]
rs7766075	0.81[CEU][hapmap]
rs7769582	0.81[CEU][hapmap]
rs7775962	0.81[CEU][hapmap]
rs9283835	0.90[CEU][hapmap]
rs9294868	0.81[CEU][hapmap]
rs9294872	0.81[CEU][hapmap]
rs9294874	0.81[CEU][hapmap]
rs9294876	0.90[CEU][hapmap]
rs9446245	0.81[CEU][hapmap]
rs9446248	0.81[CEU][hapmap]
rs9446267	0.90[CEU][hapmap]
rs9455092	0.81[CEU][hapmap]
rs9455097	0.81[CEU][hapmap]
rs9455104	0.81[CEU][hapmap]
rs9455105	0.81[CEU][hapmap]
rs9455113	0.81[CEU][hapmap]
rs9455121	0.81[CEU][hapmap]
rs9455132	0.81[CEU][hapmap]
rs9455150	0.90[CEU][hapmap]
rs9455151	0.90[CEU][hapmap]
rs9455158	0.90[CEU][hapmap]
rs9455160	0.90[CEU][hapmap]
rs9455162	0.90[CEU][hapmap]
rs9455163	0.90[CEU][hapmap]

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	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1027049	chr6:70961610-71561488	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv524328	chr6:70961833-71558805	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv917312	chr6:70961903-71601688	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv886145	chr6:71119524-71317480	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv886146	chr6:71219464-71317480	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv886147	chr6:71273253-71471863	Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71295400-71314000	Weak transcription	Aorta	Aorta
2	chr6:71311600-71313800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:71312000-71319000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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