Variant report

Variant	esv3436432
Chromosome Location	chr21:46398024-46399372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46368902..46370547-chr21:46397253..46400112,2	MCF-7	breast:
2	chr21:46398242..46400941-chr21:46419716..46421408,2	K562	blood:
3	chr21:46394940..46396856-chr21:46398540..46400419,2	MCF-7	breast:
4	chr21:46395684..46402043-chr21:46492415..46498561,16	K562	blood:
5	chr21:46398645..46400991-chr21:46405366..46407936,3	K562	blood:
6	chr21:46397240..46399857-chr21:46414261..46417239,2	K562	blood:
7	chr21:46399144..46400887-chr21:46402281..46403943,2	MCF-7	breast:
8	chr21:46398654..46417262-chr21:46491498..46498908,48	K562	blood:
9	chr21:46318143..46320481-chr21:46398627..46400161,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000261706	chromatin interactions
ENSG00000197381	chromatin interactions
ENSG00000268856	chromatin interactions
ENSG00000235374	chromatin interactions

Extended variants
information (count: 118 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:118 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138913723	chr21:46398069-46398070	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs560504280	chr21:46398090-46398091	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs527666091	chr21:46398102-46398103	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs73909911	chr21:46398116-46398117	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs571580588	chr21:46398121-46398122	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs538886598	chr21:46398137-46398138	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs550508237	chr21:46398141-46398142	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs569033693	chr21:46398175-46398176	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs536006080	chr21:46398177-46398178	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs554230895	chr21:46398187-46398188	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs560487010	chr21:46398197-46398198	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs533556246	chr21:46398221-46398222	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs369227529	chr21:46398230-46398231	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs577469083	chr21:46398262-46398263	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs141933963	chr21:46398267-46398268	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs112369083	chr21:46398287-46398288	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs552194076	chr21:46398288-46398289	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs183908591	chr21:46398290-46398291	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs402183	chr21:46398302-46398303	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs140166443	chr21:46398309-46398310	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs363936	chr21:46398313-46398314	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs411754	chr21:46398314-46398315	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs67175262	chr21:46398320-46398321	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs200296664	chr21:46398321-46398322	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs11702266	chr21:46398324-46398325	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs75484286	chr21:46398331-46398332	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs530542885	chr21:46398332-46398333	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs574960163	chr21:46398333-46398334	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs79879260	chr21:46398335-46398336	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs74336782	chr21:46398342-46398343	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs75259285	chr21:46398343-46398344	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs201181285	chr21:46398346-46398347	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs74532800	chr21:46398353-46398354	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs199817169	chr21:46398354-46398355	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs527753610	chr21:46398355-46398356	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs77080757	chr21:46398357-46398358	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs62214519	chr21:46398368-46398369	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs71317717	chr21:46398412-46398413	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs552613415	chr21:46398430-46398431	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs564426275	chr21:46398431-46398432	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs71322600	chr21:46398466-46398467	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs532352235	chr21:46398467-46398468	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs550846074	chr21:46398471-46398472	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs71322601	chr21:46398477-46398478	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs71317718	chr21:46398478-46398479	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs71199648	chr21:46398488-46398489	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs70940591	chr21:46398499-46398500	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs71317719	chr21:46398500-46398501	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs188410487	chr21:46398510-46398511	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs568993321	chr21:46398519-46398520	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	17426248	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Congenital heart defects	20877625	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46380200-46402600	Weak transcription	Aorta	Aorta
2	chr21:46382800-46404800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr21:46384200-46399600	Strong transcription	Fetal Intestine Small	intestine
4	chr21:46385000-46401400	Strong transcription	Thymus	Thymus
5	chr21:46386400-46400600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr21:46386800-46400600	Weak transcription	Small Intestine	intestine
7	chr21:46387800-46399000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr21:46388600-46398200	Strong transcription	Gastric	stomach
9	chr21:46388600-46398400	Weak transcription	Brain Angular Gyrus	brain
10	chr21:46388600-46399800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr21:46390000-46398600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr21:46390000-46399400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr21:46390200-46399000	Weak transcription	GM12878-XiMat	blood
14	chr21:46390200-46399400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr21:46390200-46400400	Weak transcription	Right Atrium	heart
16	chr21:46390200-46403200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr21:46390200-46406400	Weak transcription	Brain Anterior Caudate	brain
18	chr21:46390400-46400600	Weak transcription	Fetal Lung	lung
19	chr21:46390400-46402600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr21:46390400-46402600	Weak transcription	HUVEC	blood vessel
21	chr21:46390400-46402800	Weak transcription	Osteobl	bone
22	chr21:46390400-46408600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr21:46390600-46402800	Weak transcription	NHLF	lung
24	chr21:46390800-46398200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr21:46391000-46399800	Strong transcription	Right Ventricle	heart
26	chr21:46391000-46402600	Weak transcription	A549	lung
27	chr21:46391000-46403600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr21:46391200-46398400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr21:46391200-46399800	Strong transcription	Fetal Stomach	stomach
30	chr21:46391200-46400000	Weak transcription	Fetal Heart	heart
31	chr21:46391200-46402800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr21:46391400-46399400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr21:46391800-46402600	Weak transcription	Fetal Brain Male	brain
34	chr21:46392000-46398200	Strong transcription	Stomach Smooth Muscle	stomach
35	chr21:46392200-46398200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr21:46392200-46398200	Strong transcription	Dnd41	blood
37	chr21:46392200-46398400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr21:46392200-46402600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr21:46392600-46398400	Strong transcription	Esophagus	oesophagus
40	chr21:46393000-46399600	Strong transcription	Lung	lung
41	chr21:46393000-46399800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr21:46393000-46402600	Weak transcription	Ovary	ovary
43	chr21:46393000-46409200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr21:46393200-46398200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr21:46393200-46400400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr21:46393200-46401200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr21:46393200-46402400	Weak transcription	NH-A	brain
48	chr21:46393600-46399600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr21:46394000-46398200	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr21:46394200-46398200	Strong transcription	Brain Germinal Matrix	brain

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