Variant report

Variant	rs9621790
Chromosome Location	chr22:34268515-34268516
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:34259639..34261419-chr22:34267116..34269181,2	MCF-7	breast:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12169279	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12169322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12169356	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13433559	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1894426	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4821190	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62227813	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62227814	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs737726	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7410607	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9621781	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9621786	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9621787	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9621788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9621789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9621791	0.98[AFR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9621792	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934109	chr22:33722066-34339500	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	esv2763261	chr22:33831348-34288389	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1057450	chr22:33928913-34849012	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv914990	chr22:34090440-34373293	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv914991	chr22:34106384-34293516	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1056553	chr22:34116979-34286191	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv914992	chr22:34135007-34283144	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1061736	chr22:34178034-34394918	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv544689	chr22:34178034-34394918	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1066419	chr22:34231732-34553006	Active TSS Genic enhancers Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv544690	chr22:34231732-34553006	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	esv3343210	chr22:34236744-34404210	Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34251000-34269200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr22:34254600-34269200	Weak transcription	Fetal Stomach	stomach
3	chr22:34256200-34269600	Enhancers	Fetal Heart	heart
4	chr22:34257200-34269200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr22:34257200-34269600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr22:34257600-34269600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr22:34260200-34269000	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr22:34261200-34269400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr22:34261800-34270400	Weak transcription	Liver	Liver
10	chr22:34262200-34269200	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr22:34263600-34269200	Weak transcription	Small Intestine	intestine
12	chr22:34263800-34269800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr22:34264000-34269000	Weak transcription	Adipose Nuclei	Adipose
14	chr22:34264000-34271200	Weak transcription	HSMM	muscle
15	chr22:34264200-34269000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr22:34264200-34269000	Weak transcription	Colonic Mucosa	Colon
17	chr22:34264600-34269200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr22:34264600-34269200	Weak transcription	Fetal Brain Male	brain
19	chr22:34264600-34269400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr22:34264800-34279400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr22:34265000-34269000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr22:34265400-34269000	Weak transcription	Fetal Brain Female	brain
23	chr22:34265600-34271400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr22:34265800-34269400	Weak transcription	Aorta	Aorta
25	chr22:34265800-34269600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr22:34266000-34269200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr22:34266200-34269200	Weak transcription	Brain Angular Gyrus	brain
28	chr22:34266400-34268600	Weak transcription	NHLF	lung
29	chr22:34266400-34269000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr22:34266400-34269000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr22:34266400-34269000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr22:34266400-34269000	Weak transcription	Stomach Smooth Muscle	stomach
33	chr22:34266400-34269000	Weak transcription	HSMMtube	muscle
34	chr22:34266400-34269200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr22:34266400-34269200	Weak transcription	Brain Anterior Caudate	brain
36	chr22:34266400-34269200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr22:34266600-34269000	Weak transcription	Brain Hippocampus Middle	brain
38	chr22:34266600-34269000	Weak transcription	Colon Smooth Muscle	Colon
39	chr22:34266600-34269000	Weak transcription	NHDF-Ad	bronchial
40	chr22:34266600-34269200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr22:34266600-34269200	Weak transcription	Brain Substantia Nigra	brain
42	chr22:34266800-34269400	Weak transcription	Psoas Muscle	Psoas
43	chr22:34266800-34270000	Enhancers	GM12878-XiMat	blood
44	chr22:34267000-34269000	Weak transcription	Right Ventricle	heart
45	chr22:34267400-34268600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr22:34267600-34270600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr22:34267600-34271000	Enhancers	Primary B cells from peripheral blood	blood
48	chr22:34268000-34268600	Flanking Active TSS	Left Ventricle	heart
49	chr22:34268000-34268600	Enhancers	Ovary	ovary
50	chr22:34268000-34268800	Enhancers	Pancreas	Pancrea

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