Variant report

Variant	rs3102192
Chromosome Location	chr13:61787193-61787194
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:16)

rs_ID	r²[population]
rs12428507	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs3102178	0.86[TSI][hapmap]
rs3102187	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs3102189	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs3102190	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs3102191	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs3127278	0.80[JPT][hapmap]
rs3127279	0.82[JPT][hapmap];0.80[MEX][hapmap];0.87[TSI][hapmap]
rs3127296	0.82[AMR][1000 genomes]
rs3127300	0.83[AMR][1000 genomes]
rs3127302	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs3127306	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs7317870	0.81[AMR][1000 genomes]
rs9598244	0.87[AMR][1000 genomes]
rs9598245	0.87[AMR][1000 genomes]
rs963838	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]

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	nsv832627	chr13:61642811-61829217	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
2	nsv900243	chr13:61711163-61799269	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
3	nsv900244	chr13:61769349-61856666	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 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	chr13:61786400-61788400	Weak transcription	Fetal Lung	lung

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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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