Variant report

Variant	rs1605677
Chromosome Location	chr5:35600210-35600211
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12514911	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12521927	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13359710	0.87[GIH][hapmap]
rs1508662	0.89[EUR][1000 genomes]
rs16902381	0.87[GIH][hapmap]
rs286441	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs406830	1.00[EUR][1000 genomes]
rs430828	1.00[EUR][1000 genomes]
rs60139581	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6878233	0.89[EUR][1000 genomes]
rs73091428	0.89[EUR][1000 genomes]
rs7700662	1.00[GIH][hapmap];0.85[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7725149	0.89[EUR][1000 genomes]
rs7735024	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525477	chr5:35530905-35792990	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv525994	chr5:35577257-35600210	Flanking Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	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	chr5:35600200-35600400	Flanking Active TSS	hESC Derived CD184+ Endoderm 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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