Variant report

Variant	rs28702991
Chromosome Location	chr5:147263377-147263378
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10071367	0.94[AFR][1000 genomes]
rs10075468	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11505126	0.81[AFR][1000 genomes]
rs73261368	0.82[AFR][1000 genomes]
rs73261375	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73261387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73261392	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021356	chr5:147103627-147310531	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1033907	chr5:147109014-147309076	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv537916	chr5:147109014-147309076	Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv3334831	chr5:147165950-147339765	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv933308	chr5:147173804-147269006	Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1028477	chr5:147255013-147416217	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147259800-147267200	Enhancers	Fetal Heart	heart
2	chr5:147261400-147267400	Weak transcription	Aorta	Aorta
3	chr5:147262600-147266800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:147262600-147272600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:147262800-147266400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr5:147262800-147266400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr5:147262800-147266400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr5:147262800-147272200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr5:147262800-147275600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:147263000-147266400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:147263000-147267000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:147263000-147267400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:147263200-147266400	Weak transcription	HUES6 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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