Variant report

Variant	rs4518224
Chromosome Location	chr4:175340477-175340478
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs11725800	0.82[ASN][1000 genomes]
rs11727574	0.80[ASN][1000 genomes]
rs11732586	0.80[ASN][1000 genomes]
rs11735455	0.80[ASN][1000 genomes]
rs13101376	0.80[ASN][1000 genomes]
rs13102962	0.80[ASN][1000 genomes]
rs13107351	0.82[ASN][1000 genomes]
rs13108930	0.82[ASN][1000 genomes]
rs13109756	0.80[ASN][1000 genomes]
rs13112972	0.86[ASN][1000 genomes]
rs13119359	0.87[ASN][1000 genomes]
rs13120534	0.80[ASN][1000 genomes]
rs13122946	0.82[ASN][1000 genomes]
rs13132617	0.82[ASN][1000 genomes]
rs13135662	0.87[ASN][1000 genomes]
rs13140627	0.82[ASN][1000 genomes]
rs13146439	0.82[ASN][1000 genomes]
rs13149585	0.86[ASN][1000 genomes]
rs13149810	0.82[ASN][1000 genomes]
rs13150656	0.82[ASN][1000 genomes]
rs13152348	0.89[ASN][1000 genomes]
rs1922383	0.80[ASN][1000 genomes]
rs28519075	0.80[ASN][1000 genomes]
rs34037587	0.82[ASN][1000 genomes]
rs34054930	0.85[ASN][1000 genomes]
rs34135350	0.85[ASN][1000 genomes]
rs34175211	0.84[ASN][1000 genomes]
rs34572193	0.81[ASN][1000 genomes]
rs34592304	0.85[ASN][1000 genomes]
rs34604934	0.82[ASN][1000 genomes]
rs34674779	0.89[ASN][1000 genomes]
rs34795808	0.80[ASN][1000 genomes]
rs34833822	0.81[ASN][1000 genomes]
rs35078417	0.80[ASN][1000 genomes]
rs35211627	0.85[ASN][1000 genomes]
rs35263478	0.82[ASN][1000 genomes]
rs35295528	0.81[ASN][1000 genomes]
rs35326753	0.84[ASN][1000 genomes]
rs35347093	0.80[ASN][1000 genomes]
rs35423027	0.84[ASN][1000 genomes]
rs35663303	0.81[ASN][1000 genomes]
rs35706347	0.89[ASN][1000 genomes]
rs35760448	0.80[ASN][1000 genomes]
rs35794791	0.83[ASN][1000 genomes]
rs35931018	0.92[ASN][1000 genomes]
rs35978128	0.82[ASN][1000 genomes]
rs36122870	0.82[ASN][1000 genomes]
rs3980460	0.86[ASN][1000 genomes]
rs4273447	0.80[ASN][1000 genomes]
rs4518223	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4568217	0.80[ASN][1000 genomes]
rs4695929	0.86[ASN][1000 genomes]
rs62337061	0.80[ASN][1000 genomes]
rs62337062	0.80[ASN][1000 genomes]
rs62337063	0.80[ASN][1000 genomes]
rs62337086	0.82[ASN][1000 genomes]
rs62337087	0.82[ASN][1000 genomes]
rs6553789	0.80[ASN][1000 genomes]
rs6553790	0.80[ASN][1000 genomes]
rs6553791	0.80[ASN][1000 genomes]
rs67728476	0.80[ASN][1000 genomes]
rs6812366	0.85[ASN][1000 genomes]
rs6827853	0.81[ASN][1000 genomes]
rs6853004	0.80[ASN][1000 genomes]
rs6853166	0.80[ASN][1000 genomes]
rs6853181	0.80[ASN][1000 genomes]
rs7654427	0.80[ASN][1000 genomes]
rs7655606	0.80[ASN][1000 genomes]
rs7665426	0.82[ASN][1000 genomes]
rs7665708	0.80[ASN][1000 genomes]
rs7667325	0.80[ASN][1000 genomes]
rs7667374	0.80[ASN][1000 genomes]
rs7667642	0.80[ASN][1000 genomes]
rs7672838	0.80[ASN][1000 genomes]
rs7677994	0.86[ASN][1000 genomes]
rs7680564	0.80[ASN][1000 genomes]
rs7687802	0.80[ASN][1000 genomes]
rs7688229	0.80[ASN][1000 genomes]
rs7689422	0.80[ASN][1000 genomes]
rs7691061	0.80[ASN][1000 genomes]
rs7693269	0.88[ASN][1000 genomes]
rs7695912	0.80[ASN][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	nsv1016910	chr4:174952788-175349057	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537363	chr4:174952788-175349057	Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv596234	chr4:175053051-175361437	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	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:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175336800-175340600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:175339800-175340600	Enhancers	Hela-S3	cervix
3	chr4:175340000-175340800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:175340200-175344200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:175340400-175340600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr4:175340400-175340800	Enhancers	Placenta	Placenta
7	chr4:175340400-175342200	Enhancers	Fetal Thymus	thymus

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