Variant report

Variant	rs7947035
Chromosome Location	chr11:35290312-35290313
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:35290304-35290589	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:35289687..35293483-chr11:35296744..35298908,3	MCF-7	breast:

Variant related genes	Relation type
SLC1A2	TF binding region

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10488814	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs16927196	1.00[TSI][hapmap]
rs16927209	0.82[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];1.00[EUR][1000 genomes]
rs16927212	0.86[ASW][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16927214	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16927220	1.00[EUR][1000 genomes]
rs16927255	1.00[EUR][1000 genomes]
rs16927281	1.00[EUR][1000 genomes]
rs6484773	1.00[EUR][1000 genomes]
rs6484777	1.00[EUR][1000 genomes]
rs7102949	0.85[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7106060	1.00[EUR][1000 genomes]
rs7109108	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7125980	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7130500	1.00[EUR][1000 genomes]
rs73439144	1.00[EUR][1000 genomes]
rs7941569	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv541004	chr11:35122694-35297414	Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv832120	chr11:35277410-35490304	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35265800-35305800	Weak transcription	HepG2	liver
2	chr11:35270200-35292600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:35270400-35296400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:35270400-35307000	Weak transcription	Fetal Brain Male	brain
5	chr11:35282200-35297000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:35282200-35297000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:35282400-35296600	Weak transcription	Aorta	Aorta
8	chr11:35282600-35296800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr11:35283000-35302000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr11:35284600-35296600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr11:35284600-35300800	Weak transcription	Brain Angular Gyrus	brain
12	chr11:35284800-35296600	Weak transcription	Brain Hippocampus Middle	brain
13	chr11:35285800-35308800	Weak transcription	Gastric	stomach
14	chr11:35286400-35293800	Weak transcription	Brain Anterior Caudate	brain
15	chr11:35287600-35296200	Weak transcription	Liver	Liver
16	chr11:35287800-35293000	Weak transcription	Fetal Brain Female	brain
17	chr11:35288000-35290400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr11:35288000-35293000	Weak transcription	Primary B cells from peripheral blood	blood
19	chr11:35288200-35295600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:35288400-35290600	Enhancers	NHLF	lung
21	chr11:35288400-35293600	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr11:35288600-35293600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr11:35288800-35293600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:35288800-35297000	Weak transcription	Brain Germinal Matrix	brain
25	chr11:35289200-35290400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr11:35289600-35291800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:35289600-35293200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr11:35289600-35293200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr11:35289600-35296600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:35289800-35290800	Enhancers	Pancreas	Pancrea
31	chr11:35289800-35293000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:35289800-35296600	Weak transcription	NHDF-Ad	bronchial
33	chr11:35290000-35296800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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