Variant report

Variant	rs6850695
Chromosome Location	chr4:55185035-55185036
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:55184812..55185387-chr4:55827256..55827776,2	K562	blood:
2	chr4:55184744..55185734-chr4:55306461..55307691,6	MCF-7	breast:
3	chr4:55184927..55185737-chr4:55306931..55307659,2	K562	blood:
4	chr4:55184839..55185711-chr4:55827240..55827767,2	MCF-7	breast:
5	chr4:55184800..55185406-chr4:55706810..55707325,2	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10016845	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10028483	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10029431	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11726309	0.93[ASN][1000 genomes]
rs11728929	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11729535	0.85[ASN][1000 genomes]
rs11732117	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11732388	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11737169	0.85[ASN][1000 genomes]
rs1565665	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1565668	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17084148	0.93[ASN][1000 genomes]
rs1826426	0.87[EUR][1000 genomes]
rs1961871	0.82[EUR][1000 genomes]
rs2087806	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28379127	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28714526	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4583821	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4864510	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4864879	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56342025	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57765231	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs62299407	0.87[ASN][1000 genomes]
rs62299414	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62299416	0.89[ASN][1000 genomes]
rs6554168	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6554170	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6858442	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73234205	0.84[ASN][1000 genomes]
rs9991681	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9994113	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008793	chr4:55060925-55535807	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv537098	chr4:55060925-55535807	Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1001094	chr4:55131860-55189739	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv999400	chr4:55143598-55776995	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv4341	chr4:55172085-55217655	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55182000-55185400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:55183000-55189200	Weak transcription	Brain Anterior Caudate	brain
3	chr4:55183000-55190000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:55184800-55185600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr4:55184800-55185600	Enhancers	GM12878-XiMat	blood

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