Variant report

Variant	rs527822465
Chromosome Location	chr22:30283929-30283930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064081	chr22:29826745-30623965	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv544677	chr22:29826745-30623965	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	esv1829662	chr22:30171725-30304390	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	esv1829425	chr22:30184378-30297376	Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	esv1851082	chr22:30253256-30294744	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv1833221	chr22:30274129-30297376	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv829161	chr22:30276811-30298332	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv829162	chr22:30276811-30298761	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv11554	chr22:30280400-30298271	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv1825528	chr22:30282800-30295577	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3426601	chr22:30283554-30284187	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30280000-30286200	Weak transcription	Gastric	stomach
2	chr22:30280200-30284000	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr22:30280200-30293600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr22:30280200-30303800	Weak transcription	Aorta	Aorta
5	chr22:30280400-30284000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr22:30280400-30297400	Weak transcription	K562	blood
7	chr22:30280600-30284000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr22:30280800-30291600	Weak transcription	Lung	lung
9	chr22:30280800-30303600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr22:30281000-30284000	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr22:30281000-30287600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr22:30281000-30303000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr22:30281000-30303200	Weak transcription	Fetal Muscle Leg	muscle
14	chr22:30281400-30312200	Weak transcription	Primary B cells from peripheral blood	blood
15	chr22:30281600-30303400	Weak transcription	Fetal Intestine Small	intestine
16	chr22:30281800-30286200	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr22:30281800-30299000	Weak transcription	Spleen	Spleen
18	chr22:30281800-30300200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr22:30282000-30297600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr22:30282200-30284800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr22:30282200-30286800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr22:30282200-30287600	Weak transcription	Right Atrium	heart
23	chr22:30282200-30290400	Weak transcription	Fetal Stomach	stomach
24	chr22:30282200-30303000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr22:30282200-30303200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr22:30282200-30310200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr22:30282600-30284600	Enhancers	Fetal Brain Female	brain
28	chr22:30282600-30290200	Weak transcription	Fetal Brain Male	brain
29	chr22:30282600-30300000	Weak transcription	Small Intestine	intestine
30	chr22:30282600-30303400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr22:30283000-30284000	Enhancers	Brain Hippocampus Middle	brain
32	chr22:30283000-30284000	Enhancers	Colon Smooth Muscle	Colon
33	chr22:30283000-30284400	Enhancers	Liver	Liver
34	chr22:30283000-30284600	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr22:30283200-30284000	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr22:30283200-30284000	Enhancers	Brain Angular Gyrus	brain
37	chr22:30283200-30284000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr22:30283200-30284600	Enhancers	Brain Substantia Nigra	brain
39	chr22:30283200-30284600	Enhancers	Rectal Smooth Muscle	rectum
40	chr22:30283400-30284200	Enhancers	Ovary	ovary
41	chr22:30283400-30284400	Enhancers	Left Ventricle	heart
42	chr22:30283400-30284400	Enhancers	Pancreas	Pancrea
43	chr22:30283400-30286800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr22:30283600-30284000	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr22:30283600-30284600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr22:30283600-30285800	Weak transcription	Duodenum Mucosa	Duodenum
47	chr22:30283600-30286400	Weak transcription	Right Ventricle	heart
48	chr22:30283600-30287600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr22:30283600-30287800	Weak transcription	Primary hematopoietic stem cells	blood
50	chr22:30283800-30284000	Enhancers	Primary B cells from cord blood	blood

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