Variant report

Variant	rs11755079
Chromosome Location	chr6:150411758-150411759
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:150410116..150412744-chr6:150428842..150431815,2	K562	blood:
2	chr6:150410347..150413118-chr6:150413236..150416818,3	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11754434	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11754488	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11756904	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11756945	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11759611	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13201209	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13216978	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1748295	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2010259	0.81[CEU][hapmap]
rs35742354	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs489664	0.81[ASN][1000 genomes]
rs491336	0.84[ASN][1000 genomes]
rs67804438	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs682942	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs683002	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7738164	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7753353	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7765587	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7767719	0.80[EUR][1000 genomes]
rs789819	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs789820	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs789821	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs789822	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs789823	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs789824	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs789825	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs789826	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs789827	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs789828	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs789829	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs806072	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9322242	0.80[EUR][1000 genomes]
rs9322243	0.80[EUR][1000 genomes]
rs9371701	0.80[EUR][1000 genomes]
rs9383663	0.80[EUR][1000 genomes]
rs9397624	0.80[EUR][1000 genomes]
rs9479622	0.80[EUR][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	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv886770	chr6:150395424-150499889	Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1016239	chr6:150407607-150424171	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv1024915	chr6:150407607-150425510	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv886771	chr6:150411442-150437749	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150408800-150412400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:150409000-150412400	Weak transcription	HMEC	breast
3	chr6:150409000-150412600	Weak transcription	NHEK	skin
4	chr6:150409000-150413800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:150410000-150412400	Weak transcription	Brain Angular Gyrus	brain
6	chr6:150410200-150412400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr6:150410200-150412600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:150410400-150412400	Weak transcription	Brain Anterior Caudate	brain
9	chr6:150410400-150421800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:150410600-150412400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr6:150410600-150414400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:150411400-150413000	Enhancers	Brain Substantia Nigra	brain
13	chr6:150411600-150411800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:150411600-150411800	Enhancers	Brain Hippocampus Middle	brain
15	chr6:150411600-150411800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr6:150411600-150413200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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