Variant report

Variant	rs568640
Chromosome Location	chr11:104782086-104782087
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs502684	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs518128	0.99[AFR][1000 genomes]
rs538596	0.88[AFR][1000 genomes]
rs542762	0.95[AFR][1000 genomes]
rs568071	0.91[AFR][1000 genomes]
rs572557	0.91[AFR][1000 genomes]
rs573451	0.91[AFR][1000 genomes]
rs588533	0.93[AFR][1000 genomes]
rs589417	0.91[AFR][1000 genomes]
rs590178	0.88[AFR][1000 genomes]
rs596397	0.93[AFR][1000 genomes]
rs610997	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs617114	0.98[AFR][1000 genomes]
rs678689	0.85[AFR][1000 genomes]
rs682865	0.91[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1054456	chr11:104358924-104805251	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv832255	chr11:104674918-104846961	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	esv2757474	chr11:104719593-104798545	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv2759862	chr11:104719593-104798545	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv898355	chr11:104730322-104897843	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv1040784	chr11:104763797-104855878	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv468862	chr11:104774014-105243371	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
10	nsv556218	chr11:104774014-105243371	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
11	esv3334824	chr11:104776753-104813836	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv898356	chr11:104779195-104838471	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104769200-104786400	Weak transcription	Lung	lung
2	chr11:104769200-104786600	Weak transcription	Fetal Muscle Leg	muscle
3	chr11:104769200-104787800	Weak transcription	Fetal Lung	lung
4	chr11:104769400-104785400	Weak transcription	Psoas Muscle	Psoas
5	chr11:104769400-104786800	Weak transcription	Duodenum Mucosa	Duodenum
6	chr11:104769600-104785800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr11:104769600-104786800	Weak transcription	Adipose Nuclei	Adipose
8	chr11:104769600-104788000	Weak transcription	Fetal Stomach	stomach
9	chr11:104770400-104786600	Weak transcription	Ovary	ovary
10	chr11:104772600-104783600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:104773800-104785600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr11:104776400-104787200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:104778400-104786800	Weak transcription	Aorta	Aorta
14	chr11:104778400-104788800	Weak transcription	Pancreas	Pancrea
15	chr11:104779000-104783800	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr11:104779000-104784600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr11:104779000-104785400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr11:104779000-104786800	Weak transcription	NHLF	lung
19	chr11:104779200-104788000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr11:104779600-104783600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:104779600-104784600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:104779800-104782200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr11:104779800-104786600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr11:104779800-104786600	Weak transcription	Left Ventricle	heart
25	chr11:104782000-104782400	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr11:104782000-104782600	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr11:104782000-104782800	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr11:104782000-104783400	Enhancers	Dnd41	blood

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