Variant report

Variant	rs4077754
Chromosome Location	chr4:122698983-122698984
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:122698782..122701612-chr4:122704636..122706518,3	K562	blood:
2	chr4:122672244..122674867-chr4:122697032..122699058,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10001422	0.83[EUR][1000 genomes]
rs10011665	0.83[EUR][1000 genomes]
rs10470915	0.85[EUR][1000 genomes]
rs10471016	0.85[EUR][1000 genomes]
rs1051881	0.91[ASN][1000 genomes]
rs11930525	0.85[EUR][1000 genomes]
rs11937861	0.85[EUR][1000 genomes]
rs11947643	0.96[EUR][1000 genomes]
rs1574283	0.85[EUR][1000 genomes]
rs1803183	1.00[ASN][1000 genomes]
rs2621219	0.81[EUR][1000 genomes]
rs2706786	0.81[EUR][1000 genomes]
rs28515183	0.85[EUR][1000 genomes]
rs28676474	0.85[EUR][1000 genomes]
rs3217767	1.00[ASN][1000 genomes]
rs3903026	0.85[EUR][1000 genomes]
rs4309856	0.85[EUR][1000 genomes]
rs4508913	0.85[EUR][1000 genomes]
rs4571354	0.85[EUR][1000 genomes]
rs55685419	1.00[ASN][1000 genomes]
rs55803709	1.00[ASN][1000 genomes]
rs55936221	1.00[ASN][1000 genomes]
rs56030020	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56221685	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56300111	1.00[ASN][1000 genomes]
rs57312551	0.81[EUR][1000 genomes]
rs57779372	1.00[ASN][1000 genomes]
rs58127039	0.83[EUR][1000 genomes]
rs58745264	1.00[ASN][1000 genomes]
rs58921436	0.90[ASN][1000 genomes]
rs59268194	1.00[ASN][1000 genomes]
rs60240575	1.00[ASN][1000 genomes]
rs61180375	1.00[ASN][1000 genomes]
rs61434837	0.91[ASN][1000 genomes]
rs61665948	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6534322	0.89[EUR][1000 genomes]
rs6823340	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6825926	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6830453	1.00[ASN][1000 genomes]
rs6836544	1.00[ASN][1000 genomes]
rs6854295	1.00[ASN][1000 genomes]
rs6858061	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72913994	0.85[EUR][1000 genomes]
rs72915905	0.96[EUR][1000 genomes]
rs73844293	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73844294	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73844297	1.00[ASN][1000 genomes]
rs73844298	1.00[ASN][1000 genomes]
rs73847203	1.00[ASN][1000 genomes]
rs73847204	1.00[ASN][1000 genomes]
rs73847205	0.91[ASN][1000 genomes]
rs73847206	1.00[ASN][1000 genomes]
rs7661218	0.94[EUR][1000 genomes]
rs7684547	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs769243	1.00[ASN][1000 genomes]
rs7694815	1.00[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	nsv817261	chr4:122085173-123020068	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv997539	chr4:122544104-123274266	Genic enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv530157	chr4:122557302-123248756	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv461635	chr4:122633535-122720999	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv595357	chr4:122633535-122720999	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122695400-122705800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:122697400-122699600	Enhancers	GM12878-XiMat	blood
3	chr4:122697600-122705600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:122697800-122700600	Enhancers	NHDF-Ad	bronchial
5	chr4:122697800-122701400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:122698000-122700800	Enhancers	HSMM	muscle
7	chr4:122698200-122699000	Enhancers	Fetal Muscle Leg	muscle
8	chr4:122698200-122699200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:122698200-122702000	Enhancers	Fetal Heart	heart
10	chr4:122698600-122699200	Enhancers	NH-A	brain
11	chr4:122698800-122699200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:122698800-122699200	Enhancers	Primary T cells fromperipheralblood	blood
13	chr4:122698800-122699400	Enhancers	K562	blood
14	chr4:122698800-122699600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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