Variant report

Variant	rs11038615
Chromosome Location	chr11:45703540-45703541
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	chr11:45701838..45704783-chr11:45706711..45709522,2	K562	blood:

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10742762	0.87[CEU][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10742763	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10769161	0.87[CEU][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10769162	0.87[CEU][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10838493	1.00[ASN][1000 genomes]
rs10838494	1.00[ASN][1000 genomes]
rs10838495	1.00[ASN][1000 genomes]
rs10838496	1.00[ASN][1000 genomes]
rs10838497	1.00[ASN][1000 genomes]
rs11038524	1.00[ASN][1000 genomes]
rs11038525	1.00[ASN][1000 genomes]
rs11038528	1.00[ASN][1000 genomes]
rs11038530	1.00[ASN][1000 genomes]
rs11038531	1.00[ASN][1000 genomes]
rs11038533	1.00[ASN][1000 genomes]
rs11038538	1.00[ASN][1000 genomes]
rs11038539	1.00[ASN][1000 genomes]
rs11038543	1.00[ASN][1000 genomes]
rs11038544	1.00[ASN][1000 genomes]
rs11038549	1.00[ASN][1000 genomes]
rs11038550	1.00[ASN][1000 genomes]
rs11038552	0.82[CEU][hapmap];1.00[ASN][1000 genomes]
rs11038559	1.00[ASN][1000 genomes]
rs11038560	1.00[ASN][1000 genomes]
rs11038563	1.00[ASN][1000 genomes]
rs11038566	1.00[ASN][1000 genomes]
rs11038567	1.00[ASN][1000 genomes]
rs11038568	1.00[ASN][1000 genomes]
rs11038569	1.00[ASN][1000 genomes]
rs11038570	1.00[ASN][1000 genomes]
rs11038571	1.00[ASN][1000 genomes]
rs11038572	1.00[ASN][1000 genomes]
rs11038573	1.00[ASN][1000 genomes]
rs11038575	1.00[ASN][1000 genomes]
rs11038576	1.00[ASN][1000 genomes]
rs11038581	1.00[ASN][1000 genomes]
rs11038582	1.00[ASN][1000 genomes]
rs11038594	1.00[ASN][1000 genomes]
rs11038596	1.00[ASN][1000 genomes]
rs11038598	1.00[ASN][1000 genomes]
rs11038599	1.00[ASN][1000 genomes]
rs11038600	1.00[ASN][1000 genomes]
rs11038601	1.00[ASN][1000 genomes]
rs11038603	1.00[ASN][1000 genomes]
rs11038606	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12362568	1.00[ASN][1000 genomes]
rs12362984	1.00[ASN][1000 genomes]
rs12363116	1.00[ASN][1000 genomes]
rs12363231	1.00[ASN][1000 genomes]
rs12364128	1.00[ASN][1000 genomes]
rs12364847	1.00[ASN][1000 genomes]
rs12365421	1.00[ASN][1000 genomes]
rs12365436	1.00[ASN][1000 genomes]
rs12365703	1.00[ASN][1000 genomes]
rs12366014	1.00[ASN][1000 genomes]
rs1387058	1.00[ASN][1000 genomes]
rs1488677	1.00[ASN][1000 genomes]
rs1562461	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17724240	1.00[ASN][1000 genomes]
rs17724446	1.00[ASN][1000 genomes]
rs17786178	1.00[ASN][1000 genomes]
rs17786436	1.00[ASN][1000 genomes]
rs2028985	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs275597	1.00[ASN][1000 genomes]
rs45627537	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756007	1.00[ASN][1000 genomes]
rs4756013	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756014	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6485637	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7104214	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7105647	0.87[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7116428	1.00[ASN][1000 genomes]
rs7121818	0.87[CEU][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7121848	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72895235	1.00[ASN][1000 genomes]
rs72895236	1.00[ASN][1000 genomes]
rs72895273	1.00[ASN][1000 genomes]
rs72896754	1.00[ASN][1000 genomes]
rs72896772	1.00[ASN][1000 genomes]
rs72896789	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72898653	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72898676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899255	1.00[ASN][1000 genomes]
rs72899271	1.00[ASN][1000 genomes]
rs72899280	1.00[ASN][1000 genomes]
rs72904957	1.00[ASN][1000 genomes]
rs72904980	1.00[ASN][1000 genomes]
rs72904984	1.00[ASN][1000 genomes]
rs72904993	1.00[ASN][1000 genomes]
rs72904994	1.00[ASN][1000 genomes]
rs72904997	1.00[ASN][1000 genomes]
rs72910675	1.00[ASN][1000 genomes]
rs72910679	1.00[ASN][1000 genomes]
rs7947626	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs895718	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs901907	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	nsv467870	chr11:45684557-45757401	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv554199	chr11:45684557-45757401	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 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	chr11:45700000-45704800	Weak transcription	Fetal Heart	heart
2	chr11:45700600-45706000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:45700800-45717800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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