Variant report

Variant	rs17446807
Chromosome Location	chr5:151730104-151730105
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11950114	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11950281	0.91[EUR][1000 genomes]
rs17112995	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17113236	0.82[CEU][hapmap]
rs4958527	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55664233	0.95[EUR][1000 genomes]
rs55696736	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56237127	0.95[EUR][1000 genomes]
rs62394469	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62394473	0.95[EUR][1000 genomes]
rs62394474	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62394476	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62394478	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62394495	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62394501	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62394506	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62396630	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7447179	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023828	chr5:151522149-151956217	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830519	chr5:151588627-151800192	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv883048	chr5:151682439-151846236	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv432814	chr5:151682807-151852807	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv432815	chr5:151682807-151875807	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv432816	chr5:151691807-151875807	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151728800-151731200	Enhancers	Stomach Mucosa	stomach
2	chr5:151729000-151730200	Enhancers	Fetal Stomach	stomach
3	chr5:151729000-151730400	Enhancers	Fetal Lung	lung
4	chr5:151729600-151730200	Enhancers	Fetal Heart	heart
5	chr5:151729600-151730200	Enhancers	Fetal Intestine Large	intestine
6	chr5:151729600-151730400	Enhancers	Left Ventricle	heart
7	chr5:151729600-151730400	Enhancers	Pancreas	Pancrea
8	chr5:151729600-151731600	Enhancers	Gastric	stomach
9	chr5:151729800-151730200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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