Variant report

Variant	rs1355960
Chromosome Location	chr13:61660480-61660481
allele	A/C
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:19)

rs_ID	r²[population]
rs1355959	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1399310	0.97[AFR][1000 genomes]
rs1514543	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1913556	0.97[AFR][1000 genomes]
rs2203395	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2221987	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3106602	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3121779	0.84[AMR][1000 genomes]
rs3121789	0.97[AFR][1000 genomes]
rs3121791	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3121793	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs3127304	0.81[AFR][1000 genomes]
rs6562151	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7981971	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9317157	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9528288	1.00[EUR][1000 genomes]
rs9539011	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9539021	1.00[EUR][1000 genomes]
rs9539035	0.83[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	nsv832626	chr13:61545191-61698233	Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	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

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61654600-61663800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr13:61655200-61662000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:61657000-61661000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:61658200-61660800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr13:61658200-61661000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr13:61658600-61660800	Enhancers	NHEK	skin
7	chr13:61659600-61660600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:61659800-61660600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:61659800-61660600	Enhancers	Placenta Amnion	Placenta Amnion
10	chr13:61659800-61668600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr13:61660200-61668600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr13:61660400-61660600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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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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