Variant report

Variant	rs11900092
Chromosome Location	chr2:141155667-141155668
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10803583	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13018061	0.90[ASN][1000 genomes]
rs1518439	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17477262	0.81[EUR][1000 genomes]
rs1829364	0.95[ASN][1000 genomes]
rs1968910	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35546150	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4954836	0.90[ASN][1000 genomes]
rs59982045	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs649083	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs670617	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72894082	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72894090	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72896235	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72896239	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72896256	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72898260	0.95[ASN][1000 genomes]
rs72898263	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754266	chr2:141023643-141270786	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875185	chr2:141055080-141179257	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv1002168	chr2:141056296-141157971	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv875186	chr2:141123496-141217244	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv459507	chr2:141130097-141170340	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv583190	chr2:141130097-141170340	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv470488	chr2:141133405-141170339	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141152200-141157600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:141153200-141159000	Weak transcription	Fetal Intestine Large	intestine

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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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