Variant report

Variant	rs11043277
Chromosome Location	chr12:122411101-122411102
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10431199	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10840642	0.81[EUR][1000 genomes]
rs11043255	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11043263	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11043285	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11043286	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11043290	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11043292	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11043295	0.97[ASN][1000 genomes]
rs11829607	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12230823	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34768683	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4069668	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56040016	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56122558	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56142842	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58326739	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59922210	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7138296	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73415674	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73415687	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73415696	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7961660	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7971538	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7978386	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529868	chr12:121956483-122944265	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	173 gene(s)	inside rSNPs	diseases
2	nsv916686	chr12:122240149-122714056	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	nsv899568	chr12:122254713-122456524	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	esv34001	chr12:122298737-122521637	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122375800-122415800	Weak transcription	Liver	Liver
2	chr12:122376000-122413000	Weak transcription	Aorta	Aorta
3	chr12:122394000-122429800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr12:122394200-122411200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr12:122396600-122439200	Weak transcription	Brain Anterior Caudate	brain
6	chr12:122402000-122412400	Weak transcription	Ovary	ovary
7	chr12:122402000-122412800	Weak transcription	Spleen	Spleen
8	chr12:122403400-122417200	Weak transcription	NHDF-Ad	bronchial
9	chr12:122403800-122412400	Weak transcription	HSMM	muscle
10	chr12:122403800-122412600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:122404000-122412400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:122405200-122412400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:122406200-122416800	Weak transcription	K562	blood
14	chr12:122406400-122411200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr12:122406600-122418200	Weak transcription	Osteobl	bone
16	chr12:122407000-122412800	Weak transcription	Right Atrium	heart
17	chr12:122407600-122412200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr12:122408000-122411200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr12:122408600-122414400	Weak transcription	NHLF	lung
20	chr12:122408800-122411200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:122409200-122412200	Weak transcription	Right Ventricle	heart
22	chr12:122409200-122412400	Weak transcription	Pancreas	Pancrea
23	chr12:122409400-122412000	Weak transcription	Fetal Heart	heart
24	chr12:122409400-122412000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr12:122409400-122412200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr12:122409400-122412200	Weak transcription	HSMMtube	muscle
27	chr12:122409400-122412400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:122409400-122412400	Weak transcription	Left Ventricle	heart
29	chr12:122409800-122427200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr12:122409800-122428400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:122409800-122428400	Weak transcription	NHEK	skin
32	chr12:122410000-122413600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr12:122410000-122428600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr12:122410800-122411400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:122410800-122411600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr12:122411000-122411200	ZNF genes & repeats	Fetal Thymus	thymus
37	chr12:122411000-122411400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr12:122411000-122411400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr12:122411000-122411400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr12:122411000-122411600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:122411000-122411600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:122411000-122411600	ZNF genes & repeats	Thymus	Thymus

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