Variant report

Variant	rs2823741
Chromosome Location	chr21:17664730-17664731
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:15)

rs_ID	r²[population]
rs189457	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs239051	0.86[CHB][hapmap];0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs239055	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs239056	0.82[ASN][1000 genomes]
rs239060	0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs239062	0.97[ASN][1000 genomes]
rs239063	0.88[ASN][1000 genomes]
rs239064	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs239065	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs2823735	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap]
rs2823736	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap]
rs2823737	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs2823738	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2823743	1.00[CEU][hapmap]
rs9305762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[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	nsv834051	chr21:17564843-17721764	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1064857	chr21:17628760-18533131	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
3	nsv544382	chr21:17628760-18533131	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
4	nsv521068	chr21:17664676-17667779	Strong transcription Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17634800-17667000	Weak transcription	Hela-S3	cervix
2	chr21:17654800-17666600	Weak transcription	Fetal Heart	heart
3	chr21:17658400-17670200	Weak transcription	Fetal Muscle Leg	muscle
4	chr21:17658600-17674800	Weak transcription	Brain Hippocampus Middle	brain
5	chr21:17658600-17675200	Weak transcription	Ovary	ovary
6	chr21:17658800-17675200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr21:17659600-17674800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr21:17659600-17674800	Weak transcription	Brain Substantia Nigra	brain
9	chr21:17659600-17675000	Weak transcription	Brain Angular Gyrus	brain
10	chr21:17659600-17675200	Weak transcription	Adipose Nuclei	Adipose
11	chr21:17663000-17665800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr21:17664000-17675000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr21:17664200-17666600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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