Variant report

Variant	rs17113803
Chromosome Location	chr12:74974416-74974417
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10506692	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10506694	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10506695	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1493837	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17113564	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17113637	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17113796	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17113817	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17786070	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55696634	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56236307	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61932696	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61932697	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61932704	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61932713	0.81[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	nsv1039468	chr12:74080586-75000246	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv899293	chr12:74835107-74995760	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv899295	chr12:74854750-74984992	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv899296	chr12:74880668-74974630	Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74973400-74980000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr12:74973800-74974600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr12:74973800-74978400	Weak transcription	Brain Hippocampus Middle	brain
4	chr12:74974000-74974800	Enhancers	Brain Germinal Matrix	brain
5	chr12:74974200-74975400	Enhancers	Stomach Mucosa	stomach
6	chr12:74974400-74974800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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