Variant report

Variant	rs17487632
Chromosome Location	chr4:16287640-16287641
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1018126	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11721872	0.88[ASN][1000 genomes]
rs11731242	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11731731	0.88[ASN][1000 genomes]
rs11733994	0.88[ASN][1000 genomes]
rs11736183	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1501130	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16893213	0.83[ASN][1000 genomes]
rs16893270	0.92[ASN][1000 genomes]
rs17308524	0.80[ASN][1000 genomes]
rs1801072	0.82[ASN][1000 genomes]
rs1909915	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1987773	0.80[ASN][1000 genomes]
rs2041538	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2058424	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2191955	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2312942	0.82[ASN][1000 genomes]
rs2312945	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28399788	0.80[ASN][1000 genomes]
rs28608599	0.83[ASN][1000 genomes]
rs41531449	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4577575	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55823457	0.80[ASN][1000 genomes]
rs56127222	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57499215	0.92[ASN][1000 genomes]
rs59179944	0.80[ASN][1000 genomes]
rs6449226	0.80[ASN][1000 genomes]
rs6449228	0.80[ASN][1000 genomes]
rs6449229	0.80[ASN][1000 genomes]
rs67487480	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67965240	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6817116	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6821068	0.80[ASN][1000 genomes]
rs6826508	0.80[ASN][1000 genomes]
rs6826788	0.80[ASN][1000 genomes]
rs6834803	0.80[ASN][1000 genomes]
rs6837983	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6843493	0.82[ASN][1000 genomes]
rs73235992	0.80[ASN][1000 genomes]
rs929557	0.92[ASN][1000 genomes]
rs929558	0.92[ASN][1000 genomes]
rs975668	0.80[ASN][1000 genomes]
rs975669	0.80[ASN][1000 genomes]
rs975777	0.80[ASN][1000 genomes]
rs975778	0.80[ASN][1000 genomes]
rs990782	0.81[AMR][1000 genomes];0.94[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	nsv1004821	chr4:16055996-16830629	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537046	chr4:16055996-16830629	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv537047	chr4:16182060-16375787	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv537048	chr4:16226406-16375787	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16286400-16291800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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