Variant report

Variant	rs1678745
Chromosome Location	chr6:38820101-38820102
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:13)

rs_ID	r²[population]
rs1678744	1.00[MEX][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1678746	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1678747	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1738185	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1738186	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1738187	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41376545	1.00[MEX][hapmap]
rs55675276	1.00[EUR][1000 genomes]
rs7772516	1.00[EUR][1000 genomes]
rs7774152	1.00[EUR][1000 genomes]
rs862421	0.91[LWK][hapmap];1.00[MEX][hapmap]
rs862423	0.91[LWK][hapmap];1.00[MEX][hapmap]
rs862432	0.91[LWK][hapmap]

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	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv830643	chr6:38726675-38905589	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38766800-38824400	Weak transcription	K562	blood
2	chr6:38804600-38821000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:38812600-38821000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:38819600-38820600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr6:38819800-38821200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:38820000-38820800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:38820000-38821000	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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