Variant report

Variant	rs9527192
Chromosome Location	chr13:54899067-54899068
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs2784567	1.00[CHB][hapmap]
rs2785948	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2818212	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4883901	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4883902	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4884960	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4884965	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7139767	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7333655	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7334273	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7338467	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9536680	0.92[EUR][1000 genomes]
rs9563213	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9569017	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9569018	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	esv3375545	chr13:54517432-54908108	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1051063	chr13:54777487-54997866	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv541778	chr13:54777487-54997866	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	esv3349795	chr13:54892694-55252030	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54880000-54929800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr13:54892600-54903800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr13:54892800-54923000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr13:54895800-54901600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr13:54896600-54903000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr13:54898000-54901400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:54898200-54902800	Weak transcription	Fetal Heart	heart
8	chr13:54898200-54903400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr13:54898400-54903000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr13:54898600-54899800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr13:54898600-54905000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr13:54898800-54901600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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