Variant report

Variant	rs17747516
Chromosome Location	chr2:180353392-180353393
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11884249	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11885574	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11901927	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12471789	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12479252	0.81[CHB][hapmap]
rs12620539	0.91[CHB][hapmap]
rs13003114	0.95[CHB][hapmap];0.91[YRI][hapmap]
rs13006274	0.88[CEU][hapmap];0.91[CHB][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs13016735	0.90[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1400819	0.90[CHB][hapmap];0.96[YRI][hapmap]
rs1400822	0.83[CEU][hapmap];0.95[CHB][hapmap]
rs16866761	0.91[CHB][hapmap];0.84[YRI][hapmap]
rs17285077	0.91[CHB][hapmap]
rs17747613	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2138877	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2271759	0.87[CEU][hapmap];0.91[CHB][hapmap];0.94[EUR][1000 genomes]
rs4893875	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4894100	0.87[CEU][hapmap];0.91[CHB][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs6433794	0.83[CHB][hapmap]
rs6708300	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6715181	0.91[CHB][hapmap]
rs6715297	0.87[CEU][hapmap];0.95[CHB][hapmap]
rs6718486	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7563400	0.98[ASN][1000 genomes]
rs7563476	0.91[CHB][hapmap]
rs9288034	1.00[CHB][hapmap];0.91[JPT][hapmap];0.94[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875468	chr2:180352334-180396869	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180350200-180357800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr2:180350400-180355200	Weak transcription	Right Atrium	heart
3	chr2:180350600-180367200	Weak transcription	Liver	Liver
4	chr2:180352400-180360200	Weak transcription	Gastric	stomach
5	chr2:180352600-180353600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr2:180352600-180360600	Weak transcription	Fetal Intestine Large	intestine
7	chr2:180352800-180378400	Weak transcription	Skeletal Muscle Male	skeletal muscle

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