Variant report

Variant	rs61018857
Chromosome Location	chr11:73274832-73274833
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10898921	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235736	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11235772	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235783	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235784	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235786	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235787	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235789	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235790	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235791	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235792	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235796	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235802	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235803	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11235807	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235810	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11235811	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11235816	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12417351	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12417890	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12417977	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12418558	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12420228	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12421012	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17132126	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17244589	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1808095	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1939383	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3087498	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34493385	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55885773	0.88[EUR][1000 genomes]
rs56277844	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56375530	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56394842	0.95[EUR][1000 genomes]
rs57225667	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60203229	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];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	esv3395161	chr11:73084616-73461577	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv530624	chr11:73114283-73646329	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv983188	chr11:73273934-73307064	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73243400-73279600	Weak transcription	Fetal Stomach	stomach
2	chr11:73249600-73276000	Weak transcription	Fetal Muscle Leg	muscle
3	chr11:73250000-73307800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr11:73250200-73278800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr11:73250800-73282800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr11:73251000-73288800	Weak transcription	Thymus	Thymus
7	chr11:73253800-73307000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr11:73258800-73278000	Weak transcription	Primary B cells from cord blood	blood
9	chr11:73262200-73281000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:73262600-73276800	Weak transcription	Brain Germinal Matrix	brain
11	chr11:73263200-73276000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr11:73263200-73306000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:73263800-73288800	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:73264200-73276800	Weak transcription	Hela-S3	cervix
15	chr11:73264600-73287000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr11:73264800-73276000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr11:73265400-73287200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:73266400-73280000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:73266600-73275000	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr11:73266600-73307800	Weak transcription	Fetal Intestine Small	intestine
21	chr11:73266800-73275000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr11:73267000-73275000	Weak transcription	Brain Anterior Caudate	brain
23	chr11:73267200-73277000	Weak transcription	Primary T cells from cord blood	blood
24	chr11:73267400-73275000	Weak transcription	Psoas Muscle	Psoas
25	chr11:73267400-73281400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:73267400-73284800	Weak transcription	Right Atrium	heart
27	chr11:73268400-73281000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr11:73269800-73279600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:73270600-73288000	Weak transcription	NHLF	lung
30	chr11:73271400-73277400	Weak transcription	Left Ventricle	heart
31	chr11:73271400-73277600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:73272000-73277800	Weak transcription	Esophagus	oesophagus
33	chr11:73272200-73307600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr11:73274400-73275400	Enhancers	GM12878-XiMat	blood
35	chr11:73274600-73287000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr11:73274600-73287000	Weak transcription	Brain Substantia Nigra	brain
37	chr11:73274800-73275000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr11:73274800-73275200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr11:73274800-73290800	Weak transcription	Primary T cells fromperipheralblood	blood

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