Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10265903	0.94[ASN][1000 genomes]
rs11972510	0.92[ASN][1000 genomes]
rs11976167	0.96[ASN][1000 genomes]
rs11979289	0.92[ASN][1000 genomes]
rs16869441	0.81[ASN][1000 genomes]
rs2068592	0.90[ASN][1000 genomes]
rs28557230	0.88[ASN][1000 genomes]
rs58011346	0.94[ASN][1000 genomes]
rs59639465	0.88[ASN][1000 genomes]
rs60964959	0.92[ASN][1000 genomes]
rs61455240	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6953864	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6964977	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6969444	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs73360158	0.94[ASN][1000 genomes]
rs73360172	0.92[ASN][1000 genomes]
rs73360174	0.92[ASN][1000 genomes]
rs73360176	0.92[ASN][1000 genomes]
rs73360181	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73360191	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73360192	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73700929	0.92[ASN][1000 genomes]
rs73702892	0.94[ASN][1000 genomes]
rs962293	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519090	chr7:70085934-71071896	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1015261	chr7:70404302-71255933	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70850800-70862200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr7:70853400-70885800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:70854800-70868400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:70856000-70862200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:70856200-70862400	Weak transcription	Fetal Muscle Leg	muscle
6	chr7:70856400-70867800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:70857600-70862400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:70858800-70864200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:70860800-70865800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:70860800-70869600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:70861400-70862200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:70861800-70868000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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