Variant report

Variant	rs72787311
Chromosome Location	chr10:53967361-53967362
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:6)

rs_ID	r²[population]
rs10823983	1.00[AFR][1000 genomes]
rs11001232	1.00[AFR][1000 genomes]
rs11001441	1.00[AFR][1000 genomes]
rs11001714	1.00[AFR][1000 genomes]
rs12219130	1.00[AFR][1000 genomes]
rs72787319	1.00[AFR][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	nsv1045692	chr10:53301450-54086823	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	esv2750961	chr10:53726294-54010594	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv895399	chr10:53900872-54219820	Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:53881000-53971800	Weak transcription	Aorta	Aorta
2	chr10:53951200-53971800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr10:53963000-53973200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:53965400-53969400	Weak transcription	HSMMtube	muscle
5	chr10:53965400-53969600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr10:53965600-53969600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr10:53965600-53971800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr10:53965600-53977400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr10:53966000-53971000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr10:53966200-53967800	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr10:53966400-53967600	Enhancers	Psoas Muscle	Psoas
12	chr10:53966600-53968400	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr10:53967000-53967600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:53967000-53972000	Weak transcription	Pancreas	Pancrea
15	chr10:53967200-53967600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:53967200-53967800	Enhancers	H9 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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