Variant report

Variant	rs12071084
Chromosome Location	chr1:196203694-196203695
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10922061	1.00[CEU][hapmap]
rs10922064	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.85[YRI][hapmap]
rs10922065	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.85[YRI][hapmap]
rs12060609	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12070331	1.00[CEU][hapmap];0.85[YRI][hapmap]
rs12082579	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.85[ASN][1000 genomes]
rs12092252	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1325299	0.95[ASN][1000 genomes]
rs1925337	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[ASN][1000 genomes]
rs1998652	1.00[CHB][hapmap];0.90[CHD][hapmap];0.95[ASN][1000 genomes]
rs2477556	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs558895	1.00[CHB][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59729886	0.85[ASN][1000 genomes]
rs606473	0.95[ASN][1000 genomes]
rs6658286	1.00[CEU][hapmap]
rs994454	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872948	chr1:195872295-196236425	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv534209	chr1:196011881-196208885	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv872952	chr1:196174790-196304223	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv548741	chr1:196186750-196293493	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:196194800-196205200	Strong transcription	Liver	Liver
2	chr1:196195600-196210600	Weak transcription	Fetal Brain Male	brain
3	chr1:196197400-196213000	Weak transcription	Ovary	ovary
4	chr1:196197800-196218400	Weak transcription	Fetal Muscle Trunk	muscle

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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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