Variant report

Variant	rs60736029
Chromosome Location	chr8:62661804-62661805
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs4374988	1.00[ASN][1000 genomes]
rs58595833	1.00[AMR][1000 genomes]
rs60456313	1.00[AMR][1000 genomes]
rs61243363	1.00[AMR][1000 genomes]
rs73263149	1.00[AMR][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	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv932198	chr8:62336705-62914562	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv2761430	chr8:62517980-62873803	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1015216	chr8:62517980-62873803	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 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	chr8:62658000-62662600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:62658000-62662800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr8:62658200-62662600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr8:62658600-62666800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:62659200-62663600	Enhancers	Primary B cells from cord blood	blood
6	chr8:62660400-62662800	Enhancers	Primary B cells from peripheral blood	blood
7	chr8:62661200-62662600	Weak transcription	K562	blood
8	chr8:62661400-62662600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr8:62661400-62664200	Enhancers	HepG2	liver
10	chr8:62661400-62666800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:62661600-62662600	Weak transcription	Stomach Mucosa	stomach
12	chr8:62661600-62664400	Enhancers	A549	lung
13	chr8:62661800-62662600	Weak transcription	Monocytes-CD14+_RO01746	blood

Quick Search:

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

what's new

Quick links