Variant report

Variant	rs60204871
Chromosome Location	chr7:70832915-70832916
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11971278	1.00[AMR][1000 genomes]
rs11971711	1.00[AMR][1000 genomes]
rs11973091	1.00[AMR][1000 genomes]
rs11974045	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11976034	1.00[AMR][1000 genomes]
rs11982964	1.00[AMR][1000 genomes]
rs58768169	1.00[AMR][1000 genomes]
rs59592502	1.00[AMR][1000 genomes]
rs73354290	1.00[AMR][1000 genomes]
rs73356047	1.00[AMR][1000 genomes]
rs73356056	1.00[AMR][1000 genomes]
rs73356066	1.00[AMR][1000 genomes]
rs73358126	1.00[AMR][1000 genomes]
rs73358129	1.00[AMR][1000 genomes]
rs73358132	1.00[AMR][1000 genomes]
rs73358163	1.00[AMR][1000 genomes]
rs73358191	1.00[AMR][1000 genomes]
rs73360114	1.00[AMR][1000 genomes]
rs73360128	1.00[AMR][1000 genomes]
rs73360129	1.00[AMR][1000 genomes]
rs73360132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360136	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360139	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360161	0.88[AFR][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:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70827200-70835000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr7:70829600-70838200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:70829800-70837000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:70831400-70837800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:70831400-70837800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:70831800-70835000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:70832600-70835600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:70832800-70834000	Enhancers	Fetal Brain Male	brain

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links