Variant report

Variant	rs61454047
Chromosome Location	chr11:35361912-35361913
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35360058..35364651-chr11:35365186..35370074,5	K562	blood:
2	chr11:35294411..35297300-chr11:35361479..35363731,2	MCF-7	breast:
3	chr11:35360349..35364651-chr11:35366832..35371612,5	K562	blood:
4	chr11:35358795..35361684-chr11:35361699..35364606,3	K562	blood:

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

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11033078	0.99[ASN][1000 genomes]
rs11033085	0.95[ASN][1000 genomes]
rs11033088	0.97[ASN][1000 genomes]
rs11033091	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11033093	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12274790	0.97[ASN][1000 genomes]
rs12290517	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12294219	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1320442	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1320443	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1885344	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3847618	0.99[ASN][1000 genomes]
rs59377579	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7111949	0.97[ASN][1000 genomes]
rs7114489	0.97[ASN][1000 genomes]
rs7127728	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	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
3	esv2758264	chr11:35319320-35480522	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2759819	chr11:35319320-35480522	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35354000-35367800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:35354400-35366000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:35354600-35366000	Weak transcription	Brain Substantia Nigra	brain
4	chr11:35354800-35363200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr11:35357000-35364000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr11:35357800-35362000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:35357800-35362400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:35357800-35362800	Enhancers	NHDF-Ad	bronchial
9	chr11:35358000-35362600	Enhancers	NHLF	lung
10	chr11:35359200-35364600	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr11:35359400-35363400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr11:35359400-35364000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr11:35359600-35362800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:35359800-35362000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr11:35360000-35364000	Weak transcription	K562	blood
16	chr11:35360600-35362200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:35361000-35362200	Enhancers	Brain Anterior Caudate	brain
18	chr11:35361000-35362200	Enhancers	Psoas Muscle	Psoas
19	chr11:35361000-35362600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:35361000-35362800	Enhancers	Pancreas	Pancrea
21	chr11:35361600-35362000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:35361600-35362000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:35361600-35362000	Enhancers	Left Ventricle	heart
24	chr11:35361600-35362000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr11:35361600-35362200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr11:35361600-35362200	Enhancers	Right Atrium	heart
27	chr11:35361600-35362200	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr11:35361600-35362600	Enhancers	Stomach Smooth Muscle	stomach
29	chr11:35361600-35363200	Enhancers	Adipose Nuclei	Adipose
30	chr11:35361600-35363200	Enhancers	Liver	Liver
31	chr11:35361600-35363400	Enhancers	HepG2	liver
32	chr11:35361600-35364400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:35361600-35364600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:35361800-35362000	Enhancers	Brain Cingulate Gyrus	brain
35	chr11:35361800-35365800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr11:35361800-35367800	Weak transcription	Brain Hippocampus Middle	brain
37	chr11:35361800-35368200	Weak transcription	Hela-S3	cervix

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