Variant report

Variant	rs4939129
Chromosome Location	chr11:57050882-57050883
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10732882	0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs10792083	0.81[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs10792085	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10896596	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10896599	0.88[EUR][1000 genomes]
rs10896601	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896602	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10896609	0.81[ASN][1000 genomes]
rs11228971	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11228988	0.91[ASN][1000 genomes]
rs11602501	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11604373	0.88[ASN][1000 genomes]
rs17573746	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1939496	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2155231	0.81[EUR][1000 genomes]
rs2282623	1.00[YRI][hapmap]
rs2511029	0.84[EUR][1000 genomes]
rs2846051	0.85[EUR][1000 genomes]
rs3935069	0.98[ASN][1000 genomes]
rs4939131	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4939134	0.85[ASN][1000 genomes]
rs5012051	0.96[CEU][hapmap];0.93[EUR][1000 genomes]
rs522656	0.83[EUR][1000 genomes]
rs55637147	0.82[ASN][1000 genomes]
rs590240	0.84[EUR][1000 genomes]
rs7130020	0.88[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs746886	1.00[YRI][hapmap]
rs7928905	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7931298	0.93[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7936545	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7943761	0.91[ASN][1000 genomes]
rs7943915	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7948723	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915640	chr11:56814841-57139786	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57045800-57051000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:57045800-57051200	Weak transcription	Esophagus	oesophagus
3	chr11:57045800-57054200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr11:57046000-57051000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr11:57046000-57062000	Weak transcription	Right Atrium	heart
6	chr11:57046200-57051000	Weak transcription	Small Intestine	intestine
7	chr11:57046200-57051000	Weak transcription	Stomach Mucosa	stomach
8	chr11:57046600-57056000	Weak transcription	Adipose Nuclei	Adipose
9	chr11:57046800-57051000	Weak transcription	HSMMtube	muscle
10	chr11:57046800-57051400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:57047000-57051000	Weak transcription	Duodenum Mucosa	Duodenum
12	chr11:57047600-57051200	Weak transcription	Hela-S3	cervix
13	chr11:57048000-57051200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr11:57048000-57051200	Weak transcription	Fetal Intestine Large	intestine
15	chr11:57048200-57051200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr11:57048200-57051200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:57048200-57051200	Weak transcription	HSMM	muscle
18	chr11:57048200-57051400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:57048200-57055200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:57048200-57055600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr11:57048200-57056400	Weak transcription	Gastric	stomach
22	chr11:57048400-57051000	Weak transcription	HMEC	breast
23	chr11:57048400-57051400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr11:57050200-57053800	Enhancers	Placenta	Placenta
25	chr11:57050400-57051400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr11:57050400-57051800	Enhancers	NHDF-Ad	bronchial
27	chr11:57050400-57052200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr11:57050400-57052400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr11:57050400-57052400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr11:57050400-57052600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:57050600-57051000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr11:57050600-57051000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr11:57050600-57051400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr11:57050600-57051400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:57050600-57051600	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr11:57050600-57052000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:57050600-57052000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr11:57050600-57052200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr11:57050800-57051800	Enhancers	Osteobl	bone
40	chr11:57050800-57052400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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