Variant report

Variant	rs7592163
Chromosome Location	chr2:47725107-47725108
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17036642	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17036644	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61700511	1.00[EUR][1000 genomes]
rs72888255	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888258	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888259	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv531348	chr2:47433147-47827310	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv999576	chr2:47506116-47773960	Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv998314	chr2:47720420-47959168	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr2:47702800-47727000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:47714600-47727200	Weak transcription	Primary T cells from cord blood	blood
3	chr2:47717000-47726200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:47722200-47725200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:47725000-47725400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:47725000-47725400	ZNF genes & repeats	GM12878-XiMat	blood
7	chr2:47725000-47725600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr2:47725000-47725600	Enhancers	HMEC	breast
9	chr2:47725000-47725600	Enhancers	NHEK	skin
10	chr2:47725000-47725800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:47725000-47726600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr2:47725000-47726600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:47725000-47728600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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