Variant report

Variant	rs2860600
Chromosome Location	chr12:68396354-68396355
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1035151	1.00[MEX][hapmap]
rs2906861	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57329873	1.00[EUR][1000 genomes]
rs58233262	1.00[EUR][1000 genomes]
rs58752621	1.00[EUR][1000 genomes]
rs7297341	1.00[EUR][1000 genomes]
rs7309983	1.00[MEX][hapmap];0.84[MKK][hapmap]
rs73320687	1.00[EUR][1000 genomes]
rs74099722	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3411149	chr12:68066948-68435533	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv1039638	chr12:68293351-68399871	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv975509	chr12:68382193-68405026	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:68386400-68404200	Weak transcription	Primary B cells from cord blood	blood
2	chr12:68386800-68404600	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr12:68391400-68405400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:68392400-68404600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr12:68392400-68404800	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr12:68392600-68413800	Weak transcription	Primary T cells from cord blood	blood
7	chr12:68392800-68405200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr12:68393000-68405000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr12:68395800-68398200	Weak transcription	Primary B cells from peripheral blood	blood
10	chr12:68395800-68404400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr12:68396200-68397200	Weak transcription	Liver	Liver

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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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