Variant report

Variant	rs73914094
Chromosome Location	chr2:10615019-10615020
allele	A/C
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]
rs1641134	1.00[AMR][1000 genomes]
rs1728145	1.00[AMR][1000 genomes]
rs1728146	1.00[AMR][1000 genomes]
rs1728162	1.00[AMR][1000 genomes]
rs58775214	1.00[AMR][1000 genomes]
rs73914105	1.00[AMR][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	nsv530829	chr2:10357105-10655131	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
2	nsv1007185	chr2:10540386-10791743	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv2756905	chr2:10595578-10688969	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2759025	chr2:10595578-10688969	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10590800-10615200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:10601400-10621400	Weak transcription	Right Atrium	heart
3	chr2:10608600-10617200	Weak transcription	Thymus	Thymus
4	chr2:10610600-10617400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr2:10612000-10617600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:10612000-10619600	Enhancers	Fetal Thymus	thymus
7	chr2:10613000-10621200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:10613200-10617200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:10613800-10615800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:10614400-10616200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr2:10615000-10615200	Bivalent Enhancer	Fetal Muscle Leg	muscle

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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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