Variant report

Variant	rs55680326
Chromosome Location	chr4:97225392-97225393
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 124 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10002816	0.89[ASN][1000 genomes]
rs10006557	0.81[ASN][1000 genomes]
rs10007900	0.89[ASN][1000 genomes]
rs10015613	0.81[ASN][1000 genomes]
rs10021889	0.85[ASN][1000 genomes]
rs10213429	0.87[ASN][1000 genomes]
rs11097501	0.83[ASN][1000 genomes]
rs11097502	0.89[ASN][1000 genomes]
rs11097505	0.87[ASN][1000 genomes]
rs11932384	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12501360	0.87[ASN][1000 genomes]
rs12508802	0.89[ASN][1000 genomes]
rs12509883	0.91[ASN][1000 genomes]
rs12642471	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12644982	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12650441	0.87[ASN][1000 genomes]
rs13104802	0.85[ASN][1000 genomes]
rs13121458	0.83[ASN][1000 genomes]
rs13122821	0.83[ASN][1000 genomes]
rs13122856	0.83[ASN][1000 genomes]
rs13150508	0.87[ASN][1000 genomes]
rs1354704	0.85[ASN][1000 genomes]
rs1354706	0.85[ASN][1000 genomes]
rs1395199	0.87[ASN][1000 genomes]
rs1444021	0.83[ASN][1000 genomes]
rs1506304	0.87[ASN][1000 genomes]
rs1506305	0.85[ASN][1000 genomes]
rs1506306	0.87[ASN][1000 genomes]
rs1506317	0.85[ASN][1000 genomes]
rs1506318	0.89[ASN][1000 genomes]
rs1506319	0.87[ASN][1000 genomes]
rs1506320	0.82[ASN][1000 genomes]
rs1506321	0.81[ASN][1000 genomes]
rs1567036	0.84[ASN][1000 genomes]
rs1605227	0.88[ASN][1000 genomes]
rs17025209	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs17025493	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1847963	0.87[ASN][1000 genomes]
rs1847964	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1847966	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1847967	0.89[ASN][1000 genomes]
rs1847968	0.83[ASN][1000 genomes]
rs1847969	0.89[ASN][1000 genomes]
rs1857889	0.87[ASN][1000 genomes]
rs1867400	0.83[ASN][1000 genomes]
rs1911074	0.82[ASN][1000 genomes]
rs1911076	0.87[ASN][1000 genomes]
rs1911077	0.86[ASN][1000 genomes]
rs1948912	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2048022	0.89[ASN][1000 genomes]
rs2083922	0.89[ASN][1000 genomes]
rs2113973	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2174584	0.85[ASN][1000 genomes]
rs2197322	0.85[ASN][1000 genomes]
rs28407945	0.87[ASN][1000 genomes]
rs28523416	0.87[ASN][1000 genomes]
rs28565871	0.87[ASN][1000 genomes]
rs28633781	0.87[ASN][1000 genomes]
rs2865736	0.82[ASN][1000 genomes]
rs28788633	0.89[ASN][1000 genomes]
rs34198564	0.85[ASN][1000 genomes]
rs35257138	0.84[ASN][1000 genomes]
rs36039803	0.89[ASN][1000 genomes]
rs4146410	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4146411	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4343731	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4414959	0.87[ASN][1000 genomes]
rs4611939	0.82[ASN][1000 genomes]
rs4613576	0.82[ASN][1000 genomes]
rs4619895	0.87[ASN][1000 genomes]
rs4699283	0.89[ASN][1000 genomes]
rs4699285	0.89[ASN][1000 genomes]
rs4699287	0.85[ASN][1000 genomes]
rs4699288	0.81[ASN][1000 genomes]
rs4699483	0.82[ASN][1000 genomes]
rs4699496	0.89[ASN][1000 genomes]
rs4699501	0.82[ASN][1000 genomes]
rs4699503	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4699512	0.81[ASN][1000 genomes]
rs4699513	0.81[ASN][1000 genomes]
rs5017329	0.89[ASN][1000 genomes]
rs55847611	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58334182	0.89[ASN][1000 genomes]
rs60275360	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6532600	0.91[ASN][1000 genomes]
rs6815558	0.91[ASN][1000 genomes]
rs6815743	0.85[ASN][1000 genomes]
rs6816447	0.87[ASN][1000 genomes]
rs6820075	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6830120	0.85[ASN][1000 genomes]
rs6832934	0.87[ASN][1000 genomes]
rs6835808	0.88[ASN][1000 genomes]
rs6837318	0.91[ASN][1000 genomes]
rs6841294	0.82[ASN][1000 genomes]
rs6855768	0.81[ASN][1000 genomes]
rs6857113	0.91[ASN][1000 genomes]
rs72880179	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72880182	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72883800	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72885446	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72885485	0.87[ASN][1000 genomes]
rs7653937	0.87[ASN][1000 genomes]
rs766061	0.87[ASN][1000 genomes]
rs7671604	0.87[ASN][1000 genomes]
rs7673756	0.85[ASN][1000 genomes]
rs7686174	0.85[ASN][1000 genomes]
rs7690397	0.90[ASN][1000 genomes]
rs7698381	0.85[ASN][1000 genomes]
rs9307167	0.91[ASN][1000 genomes]
rs9307168	0.89[ASN][1000 genomes]
rs931841	0.87[ASN][1000 genomes]
rs931842	0.87[ASN][1000 genomes]
rs9884259	0.89[ASN][1000 genomes]
rs9884940	0.89[ASN][1000 genomes]
rs9998383	0.87[ASN][1000 genomes]
rs9999006	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470057	chr4:97104880-97311657	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv461589	chr4:97104881-97311657	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv594916	chr4:97104881-97311657	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv879631	chr4:97114706-97263153	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv879632	chr4:97118539-97308914	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv879633	chr4:97125086-97263153	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv461590	chr4:97197036-97266060	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv594917	chr4:97197036-97266060	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97225200-97226200	Enhancers	Fetal Intestine Large	intestine
2	chr4:97225200-97226200	Enhancers	Fetal Intestine Small	intestine

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