Variant report

Variant	rs74117007
Chromosome Location	chr10:4067992-4067993
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10218901	1.00[ASN][1000 genomes]
rs11252250	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260537	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12261882	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17132022	1.00[ASN][1000 genomes]
rs17132024	1.00[ASN][1000 genomes]
rs17132053	1.00[ASN][1000 genomes]
rs4242768	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56043214	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59137764	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61829210	1.00[ASN][1000 genomes]
rs61829222	1.00[ASN][1000 genomes]
rs61829235	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7072426	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7074419	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][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	nsv1051297	chr10:3908706-4277678	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv831772	chr10:4039292-4212218	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1046213	chr10:4059937-4144692	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv540460	chr10:4059937-4144692	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr10:4056600-4068800	Weak transcription	NHDF-Ad	bronchial
2	chr10:4065000-4068200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:4066400-4068000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr10:4066400-4068200	Enhancers	Placenta	Placenta
5	chr10:4066400-4081200	Weak transcription	Gastric	stomach
6	chr10:4067400-4077000	Weak transcription	Right Atrium	heart
7	chr10:4067600-4068000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:4067600-4070200	Weak transcription	Lung	lung
9	chr10:4067800-4070000	Weak transcription	Placenta Amnion	Placenta Amnion

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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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