Variant report

Variant	rs11134488
Chromosome Location	chr5:167542656-167542657
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1077046	0.86[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs11741507	0.86[CHB][hapmap];0.87[ASN][1000 genomes]
rs11741618	0.90[CHB][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs11748226	0.85[CHB][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs12153437	0.83[ASN][1000 genomes]
rs12186523	0.90[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs12186726	0.86[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs12186727	0.81[ASN][1000 genomes]
rs12187313	0.90[CHD][hapmap];0.82[ASN][1000 genomes]
rs12187477	0.85[ASN][1000 genomes]
rs12188893	0.86[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs1529681	0.90[CHD][hapmap];0.80[ASN][1000 genomes]
rs1529683	0.80[ASN][1000 genomes]
rs1529684	0.90[CHD][hapmap]
rs1897558	0.92[CHD][hapmap]
rs2337119	0.92[CHD][hapmap]
rs2337120	0.86[CHB][hapmap]
rs2569036	0.82[CHD][hapmap]
rs2569040	0.92[CHD][hapmap]
rs2569049	0.92[CHD][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs2617971	0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs3101758	0.92[CHD][hapmap];0.81[ASN][1000 genomes]
rs34000130	0.84[ASN][1000 genomes]
rs4246812	0.86[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs4404700	0.81[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs4976536	0.86[JPT][hapmap]
rs4976573	0.95[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4976574	0.95[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6555783	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6876251	0.81[CHB][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs6885364	0.88[CHD][hapmap];0.82[JPT][hapmap]
rs7708643	0.87[CHD][hapmap]
rs7712718	0.90[CHD][hapmap]
rs891931	0.81[CHB][hapmap]
rs919738	0.90[CHD][hapmap]
rs984228	0.82[ASN][1000 genomes]

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167526800-167552800	Weak transcription	Fetal Heart	heart
2	chr5:167532000-167544800	Weak transcription	Gastric	stomach
3	chr5:167532600-167552800	Weak transcription	Right Ventricle	heart
4	chr5:167533800-167559200	Weak transcription	NH-A	brain
5	chr5:167534000-167545200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr5:167534200-167549600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:167537000-167544800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:167537000-167550800	Weak transcription	HSMM	muscle
9	chr5:167537800-167545200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr5:167538400-167544800	Weak transcription	Left Ventricle	heart
11	chr5:167538800-167542800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:167538800-167544600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:167538800-167544800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:167539400-167542800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:167540000-167544800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:167541400-167550600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:167542400-167543000	Enhancers	Lung	lung
18	chr5:167542600-167544000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:167542600-167547000	Strong transcription	NHEK	skin

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