Variant report

Variant	rs73007753
Chromosome Location	chr1:152301085-152301086
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16833939	1.00[AFR][1000 genomes]
rs57145409	1.00[AFR][1000 genomes]
rs72999305	1.00[AFR][1000 genomes]
rs72999320	1.00[AFR][1000 genomes]
rs72999351	1.00[AFR][1000 genomes]
rs73001310	1.00[AFR][1000 genomes]
rs73003250	1.00[AFR][1000 genomes]
rs73005434	1.00[AFR][1000 genomes]
rs73005464	1.00[AFR][1000 genomes]
rs73005467	1.00[AFR][1000 genomes]
rs73007748	1.00[AFR][1000 genomes]
rs73007750	1.00[AFR][1000 genomes]
rs73007784	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	nsv1014095	chr1:152104486-152454591	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1005472	chr1:152247763-152443448	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv535161	chr1:152247763-152443448	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv998298	chr1:152288685-152319877	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152286600-152322200	Weak transcription	Ovary	ovary
2	chr1:152298000-152301600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:152298200-152301200	Weak transcription	NHEK	skin
4	chr1:152298200-152301600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:152300000-152303800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:152300400-152302000	Enhancers	HSMM	muscle
7	chr1:152301000-152301800	Enhancers	HSMMtube	muscle
8	chr1:152301000-152302200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:152301000-152302200	Enhancers	HMEC	breast

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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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