Variant report

Variant	rs740935
Chromosome Location	chr4:82327761-82327762
allele	C/T
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:8)

rs_ID	r²[population]
rs10488932	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11724446	1.00[ASN][1000 genomes]
rs1377055	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1712373	1.00[ASN][1000 genomes]
rs62302274	1.00[ASN][1000 genomes]
rs740936	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs740937	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7687899	1.00[ASN][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	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829985	chr4:82199328-82353656	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv980406	chr4:82310479-82337709	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv517921	chr4:82315470-82346835	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82321000-82335800	Weak transcription	Right Atrium	heart
2	chr4:82326800-82327800	Enhancers	Brain Hippocampus Middle	brain
3	chr4:82327400-82331200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:82327400-82331400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:82327400-82332000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr4:82327600-82329000	Weak transcription	NHEK	skin
7	chr4:82327600-82329200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:82327600-82333200	Weak transcription	Fetal Intestine Small	intestine

Quick Search:

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

what's new

Quick links