Variant report

Variant	rs6553795
Chromosome Location	chr4:175367701-175367702
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1035804	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11133039	0.85[ASN][1000 genomes]
rs11725050	0.91[ASN][1000 genomes]
rs11930740	0.82[ASN][1000 genomes]
rs12642478	0.90[ASN][1000 genomes]
rs12643801	0.95[ASN][1000 genomes]
rs12644593	0.90[ASN][1000 genomes]
rs12645224	0.89[ASN][1000 genomes]
rs12646844	0.95[ASN][1000 genomes]
rs1365611	0.90[ASN][1000 genomes]
rs1365612	0.90[ASN][1000 genomes]
rs1426941	0.95[ASN][1000 genomes]
rs17293172	0.90[ASN][1000 genomes]
rs17293403	0.89[ASN][1000 genomes]
rs1820520	0.90[ASN][1000 genomes]
rs2244093	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2244289	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2332897	0.90[ASN][1000 genomes]
rs2555622	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2555623	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2612662	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2612663	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2612679	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4613542	0.91[ASN][1000 genomes]
rs56808147	0.82[ASN][1000 genomes]
rs58959177	0.95[ASN][1000 genomes]
rs62337117	0.88[ASN][1000 genomes]
rs62337119	0.94[ASN][1000 genomes]
rs6553794	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6553796	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6813684	0.90[ASN][1000 genomes]
rs6814296	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7673142	0.90[ASN][1000 genomes]
rs930025	0.90[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	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175356000-175370800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:175367400-175368000	Weak transcription	A549	lung
3	chr4:175367600-175368800	Enhancers	Stomach Mucosa	stomach

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