Variant report

Variant	rs6721015
Chromosome Location	chr2:187813262-187813263
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10205822	0.86[CEU][hapmap]
rs11675678	0.86[ASN][1000 genomes]
rs12464291	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12465733	0.86[CEU][hapmap];0.87[GIH][hapmap];0.87[JPT][hapmap]
rs12471570	0.86[CEU][hapmap];0.86[JPT][hapmap]
rs12476385	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12614343	0.86[CEU][hapmap];0.87[GIH][hapmap];0.87[JPT][hapmap]
rs13008273	0.89[ASN][1000 genomes]
rs2370734	0.86[CEU][hapmap];0.87[GIH][hapmap]
rs2370735	0.86[CEU][hapmap];0.86[JPT][hapmap]
rs28558491	0.83[ASN][1000 genomes]
rs34938912	0.86[CEU][hapmap];0.87[GIH][hapmap];0.82[JPT][hapmap]
rs4667138	0.86[CEU][hapmap]
rs6434200	0.82[ASN][1000 genomes]
rs71432473	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7571809	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949700	chr2:187713412-188361211	Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv528437	chr2:187778830-187907901	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv999207	chr2:187787121-187924667	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv536084	chr2:187787121-187924667	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv528930	chr2:187808330-187832004	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6721015	TMEM194B	cis	parietal	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187809400-187826800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:187813000-187814000	Enhancers	Pancreas	Pancrea

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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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