Variant report

Variant	rs6664453
Chromosome Location	chr1:158954127-158954128
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:8)

rs_ID	r²[population]
rs3026924	1.00[AMR][1000 genomes]
rs57160839	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59448416	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59635124	1.00[AMR][1000 genomes]
rs59654278	1.00[AMR][1000 genomes]
rs7519244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7539283	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7556046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002401	chr1:158712627-158972031	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv3376764	chr1:158761947-158998617	Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3369957	chr1:158915589-159003393	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158946200-158954200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr1:158949200-158956400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr1:158949800-158959400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr1:158950800-158965600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:158951200-158965600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr1:158952200-158955400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
7	chr1:158953400-158955800	Strong transcription	Primary T helper cells PMA-I stimulated	--
8	chr1:158953400-158960200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr1:158953600-158965400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr1:158953600-158965600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr1:158953800-158954200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr1:158953800-158960400	Weak transcription	Primary B cells from cord blood	blood
13	chr1:158954000-158960600	Weak transcription	Primary T cells fromperipheralblood	blood

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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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