Variant report

Variant	rs4124453
Chromosome Location	chr1:57633048-57633049
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:14)

rs_ID	r²[population]
rs10465836	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11206992	0.81[CEU][hapmap]
rs12072527	0.81[AMR][1000 genomes]
rs17115233	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17115240	0.90[CEU][hapmap];0.91[EUR][1000 genomes]
rs636943	0.83[CEU][hapmap];0.90[EUR][1000 genomes]
rs66474646	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66665045	0.91[EUR][1000 genomes]
rs72672662	0.91[EUR][1000 genomes]
rs72672663	0.89[EUR][1000 genomes]
rs72672669	0.91[EUR][1000 genomes]
rs72672676	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72672678	0.91[EUR][1000 genomes]
rs7533282	1.00[CEU][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr1:57623200-57635400	Weak transcription	Fetal Intestine Small	intestine
2	chr1:57624000-57644800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:57629200-57633200	Weak transcription	Pancreas	Pancrea
4	chr1:57631800-57636400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:57631800-57636800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:57632000-57636400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr1:57632000-57636600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr1:57632000-57636600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:57632000-57637000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:57632000-57637400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:57632000-57637800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:57632200-57636000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr1:57632200-57636200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:57632200-57636400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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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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