Variant report

Variant	rs13158674
Chromosome Location	chr5:52649748-52649749
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13153694	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13156370	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13159322	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13171311	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13179965	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13180278	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16881303	1.00[EUR][1000 genomes]
rs34645246	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34779217	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34951553	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34953700	1.00[EUR][1000 genomes]
rs35159810	1.00[AMR][1000 genomes]
rs35285333	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35384598	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35412043	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35689181	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6450129	0.83[AFR][1000 genomes]
rs71619950	1.00[EUR][1000 genomes]
rs71633452	1.00[AMR][1000 genomes]
rs71633454	1.00[EUR][1000 genomes]
rs7710977	1.00[AFR][1000 genomes]
rs7732512	1.00[AFR][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	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv830297	chr5:52492494-52707758	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv508356	chr5:52646168-52703120	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52642800-52656000	Weak transcription	Aorta	Aorta
2	chr5:52646400-52650400	Weak transcription	Osteobl	bone
3	chr5:52646400-52651200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:52647400-52650600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:52647400-52651000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:52647400-52651000	Weak transcription	NHLF	lung
7	chr5:52647400-52651400	Weak transcription	NHDF-Ad	bronchial
8	chr5:52647400-52651600	Weak transcription	HSMM	muscle
9	chr5:52647600-52654800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:52649600-52655000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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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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