Variant report

Variant	rs73909215
Chromosome Location	chr21:46069089-46069090
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs56066521	0.81[AFR][1000 genomes]
rs57334195	1.00[AMR][1000 genomes]
rs59256622	1.00[AMR][1000 genomes]
rs73907078	1.00[AMR][1000 genomes]
rs73907084	1.00[AMR][1000 genomes]
rs73907085	1.00[AMR][1000 genomes]
rs73907089	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73909205	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73909206	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73909214	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73909222	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065798	chr21:45941000-46097463	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv869108	chr21:45941000-46097463	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv544476	chr21:45941000-46097463	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv913950	chr21:45985068-46097463	Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46065800-46071000	Weak transcription	Right Atrium	heart
2	chr21:46066600-46069400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr21:46066800-46069800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr21:46067200-46073000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr21:46067800-46069600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr21:46068600-46069600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr21:46068800-46069200	Bivalent Enhancer	Placenta	Placenta
8	chr21:46069000-46073600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr21:46069000-46073800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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