Variant report

Variant	rs7137682
Chromosome Location	chr12:9020070-9020071
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs16917867	0.94[EUR][1000 genomes]
rs16917872	0.96[EUR][1000 genomes]
rs17729753	0.95[AFR][1000 genomes]
rs1894817	0.96[EUR][1000 genomes]
rs1894818	0.96[EUR][1000 genomes]
rs55776445	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56206826	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs59933620	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61749073	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7136954	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7311897	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73234371	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73234380	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73236241	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][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	nsv1049949	chr12:9008609-9049198	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8982200-9022000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:8987600-9040000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr12:8996000-9040000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:9007000-9029600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr12:9007200-9027600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:9011800-9021600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:9011800-9029800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:9012600-9020400	Weak transcription	Esophagus	oesophagus
9	chr12:9013600-9029400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:9013800-9033800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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

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