Variant report

Variant	rs324804
Chromosome Location	chr12:83931993-83931994
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10862676	0.85[EUR][1000 genomes]
rs10862688	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11115900	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2201718	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2403097	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3103477	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3103498	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3110203	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs324805	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs324807	0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs370604	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs401687	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs419637	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs439870	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs568559	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]

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	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1042674	chr12:83620899-83942628	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83929600-83932200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:83930800-83933000	Enhancers	Colon Smooth Muscle	Colon
3	chr12:83931000-83932400	Enhancers	Rectal Smooth Muscle	rectum
4	chr12:83931400-83932400	Enhancers	Stomach Smooth Muscle	stomach
5	chr12:83931600-83932000	Enhancers	Fetal Muscle Leg	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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