Variant report

Variant	rs17074106
Chromosome Location	chr13:50892520-50892521
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1149867	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1149868	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12585618	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1262860	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17074122	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17074133	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2066688	0.91[ASN][1000 genomes]
rs2580177	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2740532	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs41284822	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	esv2752608	chr13:50550099-51054499	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1249 gene(s)	inside rSNPs	diseases
5	nsv900076	chr13:50710579-50912578	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv561632	chr13:50874346-50912578	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50884600-50892600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr13:50884600-50893000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr13:50884600-50893000	Weak transcription	Thymus	Thymus
4	chr13:50884600-50893200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr13:50885200-50892800	Weak transcription	Fetal Thymus	thymus
6	chr13:50886200-50892800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr13:50886400-50892600	Weak transcription	Primary T cells from cord blood	blood
8	chr13:50887600-50892600	Weak transcription	K562	blood
9	chr13:50892200-50893400	Enhancers	Dnd41	blood
10	chr13:50892400-50895600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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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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