Variant report

Variant	rs1324584
Chromosome Location	chr6:150310305-150310306
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1853657	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4869784	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4870175	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4870189	0.82[ASN][1000 genomes]
rs4870190	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60874421	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73614697	0.82[ASN][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	nsv886764	chr6:150114745-150393683	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 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	chr6:150308800-150310400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
2	chr6:150309600-150310800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:150309600-150311000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
4	chr6:150309600-150311200	Enhancers	Pancreas	Pancrea
5	chr6:150309600-150311600	ZNF genes & repeats	Lung	lung
6	chr6:150309800-150310400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
7	chr6:150309800-150311000	ZNF genes & repeats	Spleen	Spleen
8	chr6:150309800-150311400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr6:150309800-150313600	Bivalent/Poised TSS	Thymus	Thymus
10	chr6:150310000-150310400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:150310000-150311200	Weak transcription	Right Atrium	heart
12	chr6:150310000-150313400	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
13	chr6:150310200-150310400	Bivalent Enhancer	Brain Hippocampus Middle	brain
14	chr6:150310200-150311000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
15	chr6:150310200-150311200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
16	chr6:150310200-150311400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
17	chr6:150310200-150311400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
18	chr6:150310200-150311800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
19	chr6:150310200-150311800	Bivalent Enhancer	Stomach Mucosa	stomach

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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