Variant report

Variant	rs62110193
Chromosome Location	chr19:38306014-38306015
allele	A/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:25)

rs_ID	r²[population]
rs16975881	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16975884	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16975930	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3810359	0.81[EUR][1000 genomes]
rs62108264	0.81[EUR][1000 genomes]
rs62108302	0.81[EUR][1000 genomes]
rs62108350	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62110188	0.80[AMR][1000 genomes]
rs62110190	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62110192	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62110194	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62110195	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62110217	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62110222	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62110229	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs62110230	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs62110232	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs62112272	0.85[AMR][1000 genomes]
rs62112273	0.85[AMR][1000 genomes]
rs7245965	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7246147	0.80[AMR][1000 genomes]
rs7247345	0.80[AMR][1000 genomes]
rs7251502	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8100469	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8105754	0.86[AMR][1000 genomes];0.92[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	nsv949296	chr19:38034722-38763140	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv833820	chr19:38190721-38414049	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1057428	chr19:38282158-38320814	Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1062040	chr19:38294465-38370456	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38304200-38307400	Weak transcription	Ovary	ovary
2	chr19:38304200-38307600	Weak transcription	Aorta	Aorta

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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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