Variant report

Variant	rs527297
Chromosome Location	chr3:54677383-54677384
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs515920	0.86[ASN][1000 genomes]
rs517729	0.80[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs517738	0.86[ASN][1000 genomes]
rs550210	0.82[ASN][1000 genomes]
rs578032	0.91[ASN][1000 genomes]
rs587384	0.90[ASN][1000 genomes]
rs838022	0.89[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	nsv1014595	chr3:53944473-54846754	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv428084	chr3:54404258-54742756	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv834700	chr3:54637374-54803896	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv525644	chr3:54653316-54709987	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:54663600-54683800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr3:54674200-54677400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:54674400-54677800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr3:54674400-54678000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:54676200-54678000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr3:54676400-54677800	Enhancers	H9 Cell Line	embryonic stem cell
7	chr3:54676400-54679000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:54676600-54677400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr3:54676800-54679200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:54676800-54683200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:54677000-54677800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:54677000-54677800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:54677200-54677400	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
14	chr3:54677200-54677400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr3:54677200-54677800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr3:54677200-54678000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr3:54677200-54678200	Genic enhancers	HUES48 Cell Line	embryonic stem cell
18	chr3:54677200-54685600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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

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