Variant report

Variant	rs11759127
Chromosome Location	chr6:101343118-101343119
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:101328331..101330007-chr6:101341794..101343997,2	K562	blood:
2	chr6:101337316..101339556-chr6:101341141..101344086,2	K562	blood:
3	chr6:101341802..101344010-chr6:101345674..101348065,2	K562	blood:
4	chr6:101328507..101330711-chr6:101341226..101343294,2	K562	blood:

Variant related genes	Relation type
ENSG00000260000	Chromatin interaction
ENSG00000270987	Chromatin interaction
ENSG00000112249	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11755579	0.88[JPT][hapmap]
rs11758174	0.94[JPT][hapmap];1.00[YRI][hapmap]
rs13205402	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs13212730	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs13220881	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1361072	0.91[ASN][1000 genomes]
rs1813223	0.94[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2004276	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2024842	0.87[ASN][1000 genomes]
rs2398247	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs35748724	0.97[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs3811078	0.84[CHB][hapmap]
rs4840157	0.93[JPT][hapmap];0.81[AFR][1000 genomes]
rs4840160	0.94[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4840161	0.97[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4840164	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4840169	0.87[ASN][1000 genomes]
rs4840170	0.87[ASN][1000 genomes]
rs599934	1.00[JPT][hapmap]
rs62419249	0.87[ASN][1000 genomes]
rs62420689	0.85[AFR][1000 genomes]
rs652335	1.00[JPT][hapmap]
rs669543	0.81[ASN][1000 genomes]
rs672437	0.99[ASN][1000 genomes]
rs694418	0.81[ASN][1000 genomes]
rs7758630	0.82[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7769142	0.87[ASN][1000 genomes]
rs9322212	0.84[CHB][hapmap]
rs9322270	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9322271	0.94[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9322276	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9322279	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9377241	0.94[JPT][hapmap]
rs9390698	0.93[JPT][hapmap];0.83[AFR][1000 genomes]
rs9390701	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9390702	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9404060	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs979122	0.80[CEU][hapmap];0.93[JPT][hapmap]
rs9791225	0.94[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs998254	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS 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	nsv1020692	chr6:101136992-101426071	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	esv2763587	chr6:101277874-101510491	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr6:101340800-101345400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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