Variant report

Variant	rs6536298
Chromosome Location	chr4:159012365-159012366
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:158912447..158914519-chr4:159011128..159013827,2	MCF-7	breast:
2	chr4:159011423..159013282-chr4:159081920..159084638,2	MCF-7	breast:
3	chr4:159010029..159020346-chr4:159088735..159099117,18	MCF-7	breast:
4	chr4:159010781..159012395-chr4:159090900..159093537,2	MCF-7	breast:
5	chr4:159010502..159012661-chr4:159014631..159016735,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164125	Chromatin interaction
ENSG00000248429	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10003459	0.85[CEU][hapmap];0.82[CHD][hapmap];0.83[EUR][1000 genomes]
rs10003566	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10005547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10027000	0.85[CEU][hapmap];0.86[CHD][hapmap];0.83[TSI][hapmap]
rs10049927	0.81[CEU][hapmap]
rs10517684	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs10517688	0.85[CHB][hapmap]
rs10857307	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs10857308	1.00[JPT][hapmap]
rs11100149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12503001	0.80[EUR][1000 genomes]
rs12504989	1.00[JPT][hapmap]
rs12506818	0.81[ASN][1000 genomes]
rs12511578	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs12645318	0.85[ASN][1000 genomes]
rs12650454	0.93[JPT][hapmap]
rs13106004	0.80[EUR][1000 genomes]
rs13106234	0.80[EUR][1000 genomes]
rs17036918	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs17036921	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs17037241	0.85[CHB][hapmap]
rs2245735	0.85[CHB][hapmap];0.84[CHD][hapmap];0.87[JPT][hapmap]
rs28477319	0.83[EUR][1000 genomes]
rs28514324	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4077776	0.81[CEU][hapmap]
rs4129400	1.00[JPT][hapmap]
rs4362869	0.84[EUR][1000 genomes]
rs4388135	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs4398571	0.84[CHD][hapmap]
rs4460050	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs4513617	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4574459	0.85[CHD][hapmap];0.83[TSI][hapmap]
rs4691449	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs4691452	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6814979	0.80[CEU][hapmap];0.80[JPT][hapmap]
rs6843728	0.85[CEU][hapmap];0.82[CHD][hapmap];0.83[EUR][1000 genomes]
rs6844184	0.83[EUR][1000 genomes]
rs7384	0.85[CHB][hapmap];0.84[CHD][hapmap];0.87[JPT][hapmap]
rs7656059	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7657303	0.81[CEU][hapmap];0.82[CHD][hapmap];0.83[TSI][hapmap]
rs7692254	0.80[JPT][hapmap]
rs9968557	0.80[CEU][hapmap];0.82[CHD][hapmap];0.80[EUR][1000 genomes]
rs9993747	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];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	nsv993476	chr4:158550643-159202015	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers 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	16 gene(s)	inside rSNPs	diseases
2	nsv1030124	chr4:158758675-159251140	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv881288	chr4:158891733-159028080	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1021067	chr4:158972282-159175475	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv880293	chr4:159012365-159049020	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:159011800-159014200	Weak transcription	Ovary	ovary
2	chr4:159011800-159014600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr4:159011800-159015000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:159011800-159015400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:159011800-159015400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:159011800-159015800	Weak transcription	HSMMtube	muscle
7	chr4:159012000-159015000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:159012000-159015200	Weak transcription	Osteobl	bone
9	chr4:159012000-159015400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:159012200-159015600	Weak transcription	A549	lung

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