Variant report

Variant	rs912456
Chromosome Location	chr6:37731102-37731103
allele	A/G
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:7)

rs_ID	r²[population]
rs13437039	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13437447	0.85[ASN][1000 genomes]
rs16890159	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs912454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9470691	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9470695	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9470696	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1024016	chr6:37567651-37981590	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37728200-37732600	Enhancers	HepG2	liver
2	chr6:37729000-37734000	Enhancers	Stomach Mucosa	stomach
3	chr6:37730200-37731600	Enhancers	Fetal Brain Male	brain
4	chr6:37730200-37733600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:37730400-37731200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr6:37730600-37731200	Enhancers	Fetal Brain Female	brain
7	chr6:37730600-37732400	Weak transcription	Placenta	Placenta
8	chr6:37730800-37731600	Enhancers	Duodenum Mucosa	Duodenum
9	chr6:37730800-37733200	Weak transcription	Gastric	stomach
10	chr6:37730800-37735200	Enhancers	Liver	Liver
11	chr6:37731000-37731200	Flanking Active TSS	HSMMtube	muscle

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