Variant report

Variant	rs61918556
Chromosome Location	chr11:93382727-93382728
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	chr11:93373748..93375964-chr11:93381168..93383462,2	K562	blood:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10047479	1.00[ASN][1000 genomes]
rs10047481	1.00[ASN][1000 genomes]
rs10047484	1.00[ASN][1000 genomes]
rs1011993	1.00[ASN][1000 genomes]
rs10128669	1.00[ASN][1000 genomes]
rs10128673	1.00[ASN][1000 genomes]
rs10128725	1.00[ASN][1000 genomes]
rs10128726	1.00[ASN][1000 genomes]
rs10734163	1.00[ASN][1000 genomes]
rs10741472	1.00[ASN][1000 genomes]
rs10741473	1.00[ASN][1000 genomes]
rs10765621	1.00[ASN][1000 genomes]
rs10765622	1.00[ASN][1000 genomes]
rs10765624	1.00[ASN][1000 genomes]
rs10765627	1.00[ASN][1000 genomes]
rs10765629	0.83[ASN][1000 genomes]
rs10765631	1.00[ASN][1000 genomes]
rs10831086	1.00[ASN][1000 genomes]
rs10831088	1.00[ASN][1000 genomes]
rs10831092	1.00[ASN][1000 genomes]
rs11020467	1.00[ASN][1000 genomes]
rs11020468	1.00[ASN][1000 genomes]
rs11020469	1.00[ASN][1000 genomes]
rs11020471	1.00[ASN][1000 genomes]
rs11020474	1.00[ASN][1000 genomes]
rs11822965	1.00[ASN][1000 genomes]
rs11828991	1.00[ASN][1000 genomes]
rs12271543	1.00[ASN][1000 genomes]
rs12272963	1.00[ASN][1000 genomes]
rs12274112	1.00[ASN][1000 genomes]
rs12275974	1.00[ASN][1000 genomes]
rs12277268	1.00[ASN][1000 genomes]
rs12278092	1.00[ASN][1000 genomes]
rs12284176	1.00[ASN][1000 genomes]
rs12295009	1.00[ASN][1000 genomes]
rs13377252	1.00[ASN][1000 genomes]
rs13377541	1.00[ASN][1000 genomes]
rs16919124	1.00[ASN][1000 genomes]
rs1944099	1.00[ASN][1000 genomes]
rs1944102	1.00[ASN][1000 genomes]
rs1944106	1.00[ASN][1000 genomes]
rs4237560	1.00[ASN][1000 genomes]
rs4303195	1.00[ASN][1000 genomes]
rs4753095	1.00[ASN][1000 genomes]
rs4753096	1.00[ASN][1000 genomes]
rs4753489	1.00[ASN][1000 genomes]
rs4753490	1.00[ASN][1000 genomes]
rs4753491	1.00[ASN][1000 genomes]
rs4753495	0.83[ASN][1000 genomes]
rs56705833	1.00[ASN][1000 genomes]
rs58111338	1.00[ASN][1000 genomes]
rs586655	1.00[ASN][1000 genomes]
rs61904920	1.00[ASN][1000 genomes]
rs61904941	1.00[ASN][1000 genomes]
rs61904951	1.00[ASN][1000 genomes]
rs61904958	1.00[ASN][1000 genomes]
rs61906560	1.00[ASN][1000 genomes]
rs61918547	1.00[ASN][1000 genomes]
rs61918549	1.00[ASN][1000 genomes]
rs61918550	1.00[ASN][1000 genomes]
rs61918551	1.00[ASN][1000 genomes]
rs61918553	1.00[ASN][1000 genomes]
rs61918555	1.00[ASN][1000 genomes]
rs61918557	1.00[ASN][1000 genomes]
rs61918558	1.00[ASN][1000 genomes]
rs61921277	1.00[ASN][1000 genomes]
rs628916	1.00[ASN][1000 genomes]
rs629580	1.00[ASN][1000 genomes]
rs642984	1.00[ASN][1000 genomes]
rs655279	1.00[ASN][1000 genomes]
rs674150	1.00[ASN][1000 genomes]
rs688374	0.83[ASN][1000 genomes]
rs7101779	1.00[ASN][1000 genomes]
rs7111581	1.00[ASN][1000 genomes]
rs7113200	1.00[ASN][1000 genomes]
rs7127033	1.00[ASN][1000 genomes]
rs7939834	1.00[ASN][1000 genomes]
rs7939847	1.00[ASN][1000 genomes]
rs7940153	1.00[ASN][1000 genomes]
rs7941230	1.00[ASN][1000 genomes]

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	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv975401	chr11:93364502-93390549	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv898182	chr11:93381845-93637462	Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	108 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93379000-93387800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:93379000-93388800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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