Variant report

Variant	rs1475300
Chromosome Location	chr10:95928810-95928811
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1108456	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223628	0.97[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1223634	0.97[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1749322	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1776945	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2689694	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2689697	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2689707	0.82[CHB][hapmap]
rs2798001	0.82[CHB][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036676	chr10:95851376-96103876	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95906400-95930800	Weak transcription	Fetal Stomach	stomach
2	chr10:95906800-95930800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr10:95906800-95931200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr10:95923200-95930800	Weak transcription	Fetal Intestine Small	intestine
5	chr10:95923600-95930200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr10:95924800-95947200	Weak transcription	Aorta	Aorta
7	chr10:95925000-95930800	Weak transcription	Colonic Mucosa	Colon
8	chr10:95925800-95938000	Weak transcription	A549	lung
9	chr10:95928200-95930800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr10:95928600-95929600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr10:95928600-95931000	Weak transcription	Duodenum Mucosa	Duodenum
12	chr10:95928600-95931000	Weak transcription	Fetal Intestine Large	intestine
13	chr10:95928800-95930600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr10:95928800-95930800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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