Variant report

Variant	rs17016490
Chromosome Location	chr1:210739089-210739090
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs17016399	1.00[EUR][1000 genomes]
rs17016416	1.00[EUR][1000 genomes]
rs17016429	1.00[EUR][1000 genomes]
rs17016432	1.00[EUR][1000 genomes]
rs17016440	1.00[EUR][1000 genomes]
rs17016444	1.00[EUR][1000 genomes]
rs17016448	1.00[EUR][1000 genomes]
rs17016452	1.00[EUR][1000 genomes]
rs17016455	1.00[EUR][1000 genomes]
rs17016457	1.00[EUR][1000 genomes]
rs17016460	1.00[EUR][1000 genomes]
rs17016461	1.00[EUR][1000 genomes]
rs17016468	1.00[EUR][1000 genomes]
rs17016475	1.00[EUR][1000 genomes]
rs17016478	1.00[EUR][1000 genomes]
rs17016485	1.00[EUR][1000 genomes]
rs17016492	1.00[EUR][1000 genomes]
rs17016497	1.00[EUR][1000 genomes]
rs56769280	1.00[EUR][1000 genomes]
rs57610416	1.00[EUR][1000 genomes]
rs58026648	1.00[EUR][1000 genomes]
rs58332712	1.00[EUR][1000 genomes]
rs58812985	1.00[EUR][1000 genomes]
rs59420061	1.00[EUR][1000 genomes]
rs60950440	1.00[EUR][1000 genomes]
rs61284248	1.00[EUR][1000 genomes]
rs7550703	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv1014480	chr1:210717288-210743026	Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210730000-210742400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:210738600-210739400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:210738800-210739200	Weak transcription	HSMMtube	muscle
4	chr1:210739000-210739400	Enhancers	NHDF-Ad	bronchial

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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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