Variant report

Variant	rs11229810
Chromosome Location	chr11:58879846-58879847
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
2	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1048374	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11229787	0.83[AFR][1000 genomes]
rs11229788	0.89[AMR][1000 genomes]
rs11229792	0.89[AMR][1000 genomes]
rs11229802	0.98[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs11229821	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11229825	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11229829	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11229831	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11229832	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11229835	0.86[CHB][hapmap];1.00[EUR][1000 genomes]
rs11229836	0.86[CHB][hapmap];1.00[EUR][1000 genomes]
rs11229838	1.00[EUR][1000 genomes]
rs11229841	0.84[CHB][hapmap];1.00[EUR][1000 genomes]
rs11229842	1.00[EUR][1000 genomes]
rs11229843	1.00[EUR][1000 genomes]
rs11229844	1.00[EUR][1000 genomes]
rs11229845	0.86[CHB][hapmap];1.00[EUR][1000 genomes]
rs11229847	0.86[CHB][hapmap];1.00[EUR][1000 genomes]
rs11229853	1.00[CHB][hapmap]
rs12221768	0.84[CHB][hapmap];1.00[EUR][1000 genomes]
rs12222675	0.84[CHB][hapmap];0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12223085	0.86[CHB][hapmap]
rs12223473	0.84[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12225532	0.86[CHB][hapmap];1.00[EUR][1000 genomes]
rs12225972	0.86[CHB][hapmap]
rs12226515	0.93[AFR][1000 genomes]
rs17153381	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2020039	0.83[AFR][1000 genomes]
rs2154626	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2154627	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2154964	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2154965	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35732637	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55742277	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56349021	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57969871	1.00[EUR][1000 genomes]
rs60519524	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60795438	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60883299	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv948365	chr11:58515163-59156405	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	esv3393019	chr11:58679419-58880845	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv2758272	chr11:58700092-59008673	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv2759830	chr11:58700092-59008673	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv469559	chr11:58730785-58887639	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv482906	chr11:58730785-58887639	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv471671	chr11:58730786-58887639	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	esv2757447	chr11:58746238-58906018	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
10	nsv975329	chr11:58767290-58907813	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
11	nsv430388	chr11:58769524-58925824	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
12	nsv468578	chr11:58790628-58901763	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv555147	chr11:58790628-58901763	Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1043956	chr11:58818144-58882570	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58875200-58909600	Weak transcription	Stomach Mucosa	stomach
2	chr11:58875400-58883400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:58875400-58884000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr11:58875400-58884000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:58875400-58884000	Weak transcription	Esophagus	oesophagus
6	chr11:58875400-58885000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:58875400-58909600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr11:58875600-58881400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr11:58875800-58883200	Weak transcription	NH-A	brain
10	chr11:58876000-58880600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:58876000-58880800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:58876000-58880800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr11:58876000-58880800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr11:58876000-58880800	Weak transcription	Fetal Muscle Leg	muscle
15	chr11:58876000-58880800	Weak transcription	Fetal Stomach	stomach
16	chr11:58876000-58880800	Weak transcription	Thymus	Thymus
17	chr11:58876000-58881000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr11:58876000-58881000	Weak transcription	Fetal Intestine Small	intestine
19	chr11:58876000-58881600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:58876000-58881800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr11:58876000-58881800	Weak transcription	Small Intestine	intestine
22	chr11:58876000-58882800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr11:58876000-58883200	Weak transcription	Fetal Muscle Trunk	muscle
24	chr11:58876000-58883800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:58876000-58884000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:58876000-58884200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:58876000-58884400	Weak transcription	Fetal Brain Female	brain
28	chr11:58876000-58884600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr11:58876000-58885000	Weak transcription	Fetal Intestine Large	intestine
30	chr11:58876000-58886400	Weak transcription	HSMM	muscle
31	chr11:58876000-58888000	Weak transcription	Fetal Kidney	kidney
32	chr11:58876200-58880800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr11:58876200-58880800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr11:58876200-58880800	Weak transcription	NHEK	skin
35	chr11:58876200-58881600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:58876200-58883200	Weak transcription	Fetal Lung	lung
37	chr11:58876200-58883400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr11:58876200-58884000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr11:58876200-58884200	Weak transcription	A549	lung
40	chr11:58876200-58884600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:58876200-58885000	Weak transcription	HepG2	liver
42	chr11:58876200-58885600	Weak transcription	HUVEC	blood vessel
43	chr11:58876200-58891800	Weak transcription	Fetal Heart	heart
44	chr11:58876200-58892000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr11:58876600-58880800	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr11:58876600-58883200	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr11:58876600-58884000	Strong transcription	Fetal Thymus	thymus
48	chr11:58876600-58884400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr11:58876600-58884600	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr11:58876600-58884600	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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