Variant report

Variant	rs11685775
Chromosome Location	chr2:190366824-190366825
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10202029	1.00[JPT][hapmap]
rs11674773	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11677198	1.00[JPT][hapmap]
rs11677494	1.00[JPT][hapmap]
rs11682165	1.00[JPT][hapmap]
rs11694976	1.00[JPT][hapmap]
rs12465339	0.96[CEU][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17198934	1.00[JPT][hapmap]
rs4277558	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4667285	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62187110	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs920266	0.96[EUR][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	nsv533029	chr2:189812229-190554339	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv875615	chr2:190215527-190444392	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv584062	chr2:190272195-190376493	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	esv3439566	chr2:190364328-190376661	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190363800-190367000	Weak transcription	Fetal Lung	lung
2	chr2:190364000-190367000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr2:190365200-190369800	Weak transcription	Small Intestine	intestine
4	chr2:190365400-190371200	Weak transcription	Psoas Muscle	Psoas
5	chr2:190365800-190369800	Weak transcription	HepG2	liver
6	chr2:190366000-190377600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:190366400-190367000	Weak transcription	Ovary	ovary
8	chr2:190366400-190367000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr2:190366400-190367800	Weak transcription	Fetal Intestine Large	intestine
10	chr2:190366400-190369800	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr2:190366400-190369800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr2:190366400-190369800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr2:190366400-190369800	Weak transcription	Fetal Intestine Small	intestine
14	chr2:190366400-190369800	Weak transcription	Stomach Mucosa	stomach
15	chr2:190366400-190369800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr2:190366800-190371200	Weak transcription	HSMMtube	muscle

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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