Variant report

Variant	rs73537878
Chromosome Location	chr8:11575685-11575686
allele	C/T
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:7)

rs_ID	r²[population]
rs17153677	1.00[AMR][1000 genomes]
rs59792049	1.00[AMR][1000 genomes]
rs61574109	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73537868	0.95[AFR][1000 genomes]
rs73537875	1.00[AMR][1000 genomes]
rs73537880	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73539809	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1017865	chr8:11377795-11579954	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11568000-11577600	Weak transcription	Gastric	stomach
2	chr8:11572200-11576600	Enhancers	Fetal Intestine Small	intestine
3	chr8:11572400-11577400	Weak transcription	Placenta	Placenta
4	chr8:11573200-11576000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:11574000-11575800	Bivalent Enhancer	Fetal Intestine Large	intestine
6	chr8:11574000-11576000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
7	chr8:11574000-11577800	Enhancers	Stomach Mucosa	stomach
8	chr8:11574000-11578000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:11574000-11578400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:11574400-11576800	Flanking Active TSS	HepG2	liver
11	chr8:11574600-11576800	Enhancers	Ovary	ovary
12	chr8:11575000-11576200	Flanking Active TSS	Liver	Liver
13	chr8:11575200-11575800	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr8:11575200-11576000	Enhancers	Right Atrium	heart
15	chr8:11575200-11576200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
16	chr8:11575200-11576800	Enhancers	Left Ventricle	heart
17	chr8:11575200-11581800	Enhancers	Fetal Heart	heart
18	chr8:11575400-11577400	Weak transcription	Pancreas	Pancrea
19	chr8:11575600-11576600	Weak transcription	Right Ventricle	heart

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