Variant report

Variant	rs2072218
Chromosome Location	chr7:21742151-21742152
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11535172	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17145080	1.00[AMR][1000 genomes]
rs17145107	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs17145111	0.84[CHB][hapmap];1.00[EUR][1000 genomes]
rs17145143	1.00[EUR][1000 genomes]
rs17150374	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2074758	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4404825	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs61238310	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6948826	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6950508	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6951003	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs6955998	1.00[AMR][1000 genomes]
rs6961486	0.87[YRI][hapmap]
rs6966598	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6975974	1.00[AMR][1000 genomes]
rs73682683	1.00[EUR][1000 genomes]
rs7800141	0.89[CHB][hapmap];0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv5655	chr7:21728469-21773203	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1018133	chr7:21740118-22055283	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1016063	chr7:21740433-21808410	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21742000-21742400	Enhancers	Fetal Heart	heart

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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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