Variant report

Variant	rs73164312
Chromosome Location	chr22:33455436-33455437
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000230866	Chromatin interaction
ENSG00000240647	Chromatin interaction
ENSG00000251890	Chromatin interaction
ENSG00000237439	Chromatin interaction
ENSG00000184459	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs56105429	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56141125	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73162100	1.00[AMR][1000 genomes]
rs73162102	1.00[AMR][1000 genomes]
rs73164303	1.00[AMR][1000 genomes]
rs73164306	1.00[AMR][1000 genomes]
rs73164308	1.00[AMR][1000 genomes]
rs73164310	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73164320	1.00[AMR][1000 genomes];1.00[EUR][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	nsv531568	chr22:33336868-33480272	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv531587	chr22:33346710-33809338	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv948523	chr22:33414164-34098417	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
4	nsv1067068	chr22:33452180-33851033	Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
5	esv3390652	chr22:33452977-33455825	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33454400-33458400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr22:33454800-33457200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr22:33454800-33457200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr22:33454800-33457600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr22:33454800-33457800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr22:33454800-33458000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr22:33454800-33459800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr22:33454800-33465000	Weak transcription	Fetal Brain Female	brain
9	chr22:33455000-33457200	Weak transcription	iPS-15b 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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