Variant report

Variant	rs61667592
Chromosome Location	chr7:121450698-121450699
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs61732004	1.00[AMR][1000 genomes]
rs73433081	1.00[AMR][1000 genomes]
rs73717711	1.00[AMR][1000 genomes]
rs73717727	1.00[AMR][1000 genomes]
rs73717739	1.00[AMR][1000 genomes]
rs73717744	1.00[AMR][1000 genomes]
rs73717746	1.00[AMR][1000 genomes]
rs73717750	1.00[AMR][1000 genomes]
rs73717752	1.00[AMR][1000 genomes]
rs73717779	1.00[AMR][1000 genomes]
rs7778337	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429808	chr7:121384049-121600049	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121443200-121458800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:121447600-121451200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:121448200-121451200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:121448200-121452200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:121450000-121451600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:121450200-121451600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:121450400-121451000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:121450400-121451600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:121450400-121451800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:121450400-121451800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:121450600-121451600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:121450600-121451800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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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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