Variant report

Variant	rs1223528
Chromosome Location	chr6:13144257-13144258
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1223509	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1223514	1.00[ASN][1000 genomes]
rs1223515	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223516	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223517	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223518	1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223522	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223523	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223524	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223525	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1223526	1.00[YRI][hapmap]
rs1223530	0.97[ASN][1000 genomes]
rs1223533	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1223536	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1223537	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1753554	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1753555	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1753562	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1937769	0.85[CHB][hapmap];0.80[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv600992	chr6:12961922-13218549	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13132800-13153000	Weak transcription	Aorta	Aorta
2	chr6:13138800-13144400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr6:13140400-13146000	Weak transcription	Brain Substantia Nigra	brain
4	chr6:13140400-13147800	Weak transcription	Fetal Kidney	kidney
5	chr6:13142200-13145600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr6:13142400-13145400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:13142400-13145400	Weak transcription	Brain Anterior Caudate	brain
8	chr6:13142400-13145600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr6:13142400-13159400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:13142600-13145200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:13143200-13144600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr6:13143800-13144400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:13143800-13144600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr6:13144000-13149000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr6:13144200-13144800	Weak transcription	Pancreas	Pancrea

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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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