Variant report

Variant	rs477206
Chromosome Location	chr11:107387656-107387657
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1784274	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs477390	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs494029	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs501373	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs533757	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs561680	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs567953	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs580821	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs589316	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs589517	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs589788	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs596149	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs604395	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs613055	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs619172	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs619633	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs621303	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs630480	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs641502	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs648717	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs652320	0.81[EUR][1000 genomes]
rs654093	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs655009	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs664084	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs665905	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs667741	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs668739	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs670393	0.88[ASN][1000 genomes]
rs682334	0.82[EUR][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	nsv898365	chr11:106944975-107430300	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv898366	chr11:106944975-107433835	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv898367	chr11:106944975-107443420	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv898369	chr11:106958304-107443420	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv898370	chr11:107027991-107430300	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv898372	chr11:107049968-107433835	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1038368	chr11:107116577-107664181	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv541163	chr11:107116577-107664181	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv898373	chr11:107124903-107433835	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv556376	chr11:107250851-107486598	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv898376	chr11:107299631-107443420	Weak transcription Active TSS Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv533794	chr11:107349817-108093259	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS 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	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107364000-107394000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:107369200-107406400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:107370000-107433800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr11:107371200-107393000	Weak transcription	Brain Substantia Nigra	brain
5	chr11:107371200-107421200	Weak transcription	Right Ventricle	heart
6	chr11:107372000-107435600	Weak transcription	Colonic Mucosa	Colon
7	chr11:107372800-107389600	Weak transcription	Gastric	stomach
8	chr11:107372800-107409600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:107372800-107434600	Weak transcription	Placenta	Placenta
10	chr11:107373000-107414800	Weak transcription	Brain Anterior Caudate	brain
11	chr11:107373000-107415200	Weak transcription	Osteobl	bone
12	chr11:107373000-107421000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:107373000-107421400	Weak transcription	Brain Germinal Matrix	brain
14	chr11:107373200-107389000	Weak transcription	Fetal Intestine Small	intestine
15	chr11:107373200-107389600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr11:107373200-107390800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:107373200-107393000	Weak transcription	Fetal Stomach	stomach
18	chr11:107373200-107396200	Weak transcription	Small Intestine	intestine
19	chr11:107373200-107405800	Weak transcription	NHEK	skin
20	chr11:107373200-107407400	Weak transcription	Esophagus	oesophagus
21	chr11:107373200-107421000	Weak transcription	Spleen	Spleen
22	chr11:107373200-107423200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr11:107373400-107407400	Weak transcription	GM12878-XiMat	blood
24	chr11:107373800-107409200	Weak transcription	HepG2	liver
25	chr11:107375600-107389000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:107375600-107393000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr11:107375600-107414600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr11:107375800-107388200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:107375800-107388200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:107375800-107388400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:107375800-107389600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr11:107375800-107390000	Weak transcription	HUVEC	blood vessel
33	chr11:107375800-107390800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr11:107375800-107392200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:107375800-107392800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr11:107375800-107393000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr11:107375800-107395800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr11:107375800-107396800	Weak transcription	HSMM	muscle
39	chr11:107375800-107402400	Weak transcription	Fetal Thymus	thymus
40	chr11:107375800-107407000	Weak transcription	Brain Hippocampus Middle	brain
41	chr11:107376000-107389200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr11:107376000-107389200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:107376000-107389800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr11:107376000-107390600	Weak transcription	HMEC	breast
45	chr11:107376000-107392200	Weak transcription	Fetal Intestine Large	intestine
46	chr11:107376000-107402000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr11:107376000-107402400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr11:107376000-107407400	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr11:107376000-107415600	Weak transcription	Brain Angular Gyrus	brain
50	chr11:107376000-107421000	Weak transcription	Thymus	Thymus

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