Variant report

Variant	rs12523732
Chromosome Location	chr6:161302716-161302717
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12525459	1.00[ASN][1000 genomes]
rs12528526	1.00[ASN][1000 genomes]
rs12530268	1.00[ASN][1000 genomes]
rs12530382	1.00[ASN][1000 genomes]
rs4127338	1.00[ASN][1000 genomes]
rs57314213	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60015872	1.00[EUR][1000 genomes];1.00[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	esv3352911	chr6:161140543-161324358	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv830853	chr6:161180005-161376481	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2422347	chr6:161211171-161442377	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1837673	chr6:161216608-161318009	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161294200-161304200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:161296000-161313000	Weak transcription	Right Atrium	heart
3	chr6:161298000-161303800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:161298200-161305200	Weak transcription	Pancreas	Pancrea
5	chr6:161298800-161305000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:161299200-161304200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:161301400-161303800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr6:161302000-161303800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:161302000-161304200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr6:161302000-161304200	Enhancers	Fetal Lung	lung
11	chr6:161302000-161304400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:161302000-161304400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr6:161302200-161303600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:161302200-161303600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:161302200-161304400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr6:161302400-161304200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr6:161302400-161304400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:161302400-161306200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:161302600-161302800	Enhancers	Ovary	ovary

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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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