Variant report

Variant	rs12617281
Chromosome Location	chr2:142791913-142791914
allele	C/T
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:14)

rs_ID	r²[population]
rs10496911	1.00[GIH][hapmap]
rs12617185	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12617190	0.90[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12617257	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12617322	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs12617486	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12620001	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12623786	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs16847914	1.00[MEX][hapmap];0.83[TSI][hapmap]
rs16847915	1.00[MEX][hapmap];0.83[TSI][hapmap]
rs16847916	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16847936	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59095262	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6739226	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[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	nsv530398	chr2:142474842-142843839	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv997274	chr2:142760393-143599193	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv526107	chr2:142768518-142884248	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142791200-142792200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:142791400-142794400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:142791600-142794400	Weak transcription	NH-A	brain
4	chr2:142791800-142794600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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