Variant report

Variant	rs713732
Chromosome Location	chr22:33833853-33833854
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1807547	0.82[ASN][1000 genomes]
rs2267206	1.00[CEU][hapmap];1.00[CHB][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2267207	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9619347	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948523	chr22:33414164-34098417	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
2	nsv1067068	chr22:33452180-33851033	Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
3	nsv933455	chr22:33532697-33915429	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1059927	chr22:33615699-33904339	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv544682	chr22:33615699-33904339	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1061485	chr22:33670971-33885169	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
7	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
8	nsv1062127	chr22:33755479-34085278	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
9	nsv544683	chr22:33755479-34085278	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1064026	chr22:33767185-33902059	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
11	nsv531588	chr22:33776857-34150188	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
12	nsv914983	chr22:33800119-34035034	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1060666	chr22:33800218-33841525	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
14	nsv1060283	chr22:33809137-34043739	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
15	nsv544684	chr22:33809137-34043739	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
16	nsv1060862	chr22:33810445-33891296	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
17	nsv1057547	chr22:33810445-33939474	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
18	nsv1055791	chr22:33822226-34159536	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
19	nsv1065417	chr22:33823850-34053325	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
20	nsv933309	chr22:33825232-34053000	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
21	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

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33778600-33852000	Weak transcription	Pancreas	Pancrea
2	chr22:33780600-33834000	Weak transcription	Gastric	stomach
3	chr22:33812400-33834000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr22:33817200-33834000	Weak transcription	Brain Anterior Caudate	brain
5	chr22:33818400-33834000	Weak transcription	HSMMtube	muscle
6	chr22:33819200-33839800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr22:33823000-33836000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr22:33823400-33836800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr22:33823400-33839400	Weak transcription	Fetal Muscle Leg	muscle
10	chr22:33824400-33834000	Weak transcription	Lung	lung
11	chr22:33826000-33837800	Weak transcription	GM12878-XiMat	blood
12	chr22:33826800-33844600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr22:33827600-33834000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr22:33827600-33838000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr22:33828200-33834000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr22:33828200-33834200	Weak transcription	Colon Smooth Muscle	Colon
17	chr22:33828200-33834200	Weak transcription	Stomach Smooth Muscle	stomach
18	chr22:33828200-33834400	Weak transcription	Brain Hippocampus Middle	brain
19	chr22:33828200-33837400	Weak transcription	Ovary	ovary
20	chr22:33828200-33848200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr22:33828200-33855000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr22:33828400-33834000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr22:33828400-33834000	Weak transcription	Fetal Stomach	stomach
24	chr22:33828400-33836200	Weak transcription	Adipose Nuclei	Adipose
25	chr22:33828800-33836000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr22:33828800-33857800	Weak transcription	Primary B cells from peripheral blood	blood
27	chr22:33831800-33834000	Enhancers	Fetal Heart	heart
28	chr22:33832200-33834000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr22:33832400-33834200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr22:33832600-33834200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr22:33832600-33834400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr22:33832600-33834800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr22:33832800-33834200	Weak transcription	Left Ventricle	heart
34	chr22:33832800-33839200	Weak transcription	Right Ventricle	heart
35	chr22:33833200-33834200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr22:33833400-33834200	Enhancers	Fetal Thymus	thymus
37	chr22:33833400-33835000	Enhancers	NHEK	skin
38	chr22:33833400-33835400	Enhancers	HMEC	breast
39	chr22:33833600-33834000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr22:33833600-33834200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr22:33833600-33835000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr22:33833600-33835400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr22:33833600-33835600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr22:33833600-33835600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr22:33833800-33834000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr22:33833800-33834200	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr22:33833800-33834600	Enhancers	Primary hematopoietic stem cells	blood
48	chr22:33833800-33834600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr22:33833800-33834600	Flanking Active TSS	A549	lung
50	chr22:33833800-33834800	Enhancers	NH-A	brain

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