Variant report

Variant	rs62220272
Chromosome Location	chr21:16643496-16643497
allele	C/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:18)

rs_ID	r²[population]
rs16980826	1.00[EUR][1000 genomes]
rs16980835	1.00[EUR][1000 genomes]
rs16980843	1.00[EUR][1000 genomes]
rs16980928	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17275037	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220271	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220273	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220274	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220275	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220276	1.00[EUR][1000 genomes]
rs62220277	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220278	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62220304	1.00[AFR][1000 genomes]
rs62220306	1.00[AFR][1000 genomes]
rs62220308	1.00[AFR][1000 genomes]
rs7276931	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7277875	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7278014	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063385	chr21:16521617-16926212	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 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	chr21:16636200-16653200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr21:16642400-16644400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr21:16643000-16644000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr21:16643200-16647000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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