Variant report

Variant	esv16654
Chromosome Location	chr21:44699610-44706185
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:44693342..44695440-chr21:44702341..44704314,2	K562	blood:
2	chr21:44697464..44700056-chr21:44712355..44714854,2	K562	blood:
3	chr21:44699022..44704261-chr21:44706186..44710615,5	MCF-7	breast:
4	chr21:44591547..44593428-chr21:44700375..44702844,2	K562	blood:
5	chr21:44699112..44702350-chr21:44708742..44712038,3	K562	blood:
6	chr21:44702803..44705781-chr21:44760517..44763058,2	MCF-7	breast:
7	chr21:44705161..44709100-chr21:44718607..44720548,3	MCF-7	breast:
8	chr21:44613209..44615263-chr21:44702537..44704678,2	MCF-7	breast:

No data

Extended variants
information (count: 206 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:206 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533198434	chr21:44699685-44699686	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs200451123	chr21:44699800-44699801	Weak transcription ZNF genes & repeats Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs201754258	chr21:44699802-44699803	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs201261617	chr21:44699803-44699804	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs202140601	chr21:44699838-44699839	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs112579851	chr21:44699890-44699891	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs113509434	chr21:44699911-44699912	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs189307186	chr21:44699951-44699952	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs111220579	chr21:44699974-44699975	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs201221055	chr21:44699975-44699976	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs566784575	chr21:44699990-44699991	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs534239088	chr21:44699991-44699992	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181286370	chr21:44699996-44699997	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs186521992	chr21:44700002-44700003	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs111220591	chr21:44700004-44700005	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs191635103	chr21:44700019-44700020	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs111220600	chr21:44700094-44700095	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs182940648	chr21:44700138-44700139	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs186150769	chr21:44700140-44700141	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs190809116	chr21:44700317-44700318	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs188334318	chr21:44700325-44700326	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs111220510	chr21:44700368-44700369	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs200945855	chr21:44700372-44700373	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs200614015	chr21:44700376-44700377	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552478704	chr21:44700470-44700471	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs570695365	chr21:44700474-44700475	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs201342204	chr21:44700490-44700491	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs183414845	chr21:44700491-44700492	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs538470320	chr21:44700560-44700561	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs556774058	chr21:44700562-44700563	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs575300712	chr21:44700568-44700569	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs535832338	chr21:44700570-44700571	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs201322444	chr21:44700600-44700601	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs201796124	chr21:44700705-44700706	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs187841850	chr21:44700745-44700746	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs192517870	chr21:44700747-44700748	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs200333431	chr21:44700764-44700765	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs201924169	chr21:44700769-44700770	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs199904033	chr21:44700798-44700799	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs554620267	chr21:44700826-44700827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573144936	chr21:44700829-44700830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201222293	chr21:44700846-44700847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199542021	chr21:44700860-44700861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373852478	chr21:44700904-44700905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7280617	chr21:44700912-44700913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533471068	chr21:44700913-44700914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546709718	chr21:44700930-44700931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565213922	chr21:44700974-44700975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576954415	chr21:44700991-44700992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544441894	chr21:44701018-44701019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	21364760	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Prostate cancer	18632612	CNVD
Neuroblastoma	20406844	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 cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44694000-44701200	Weak transcription	GM12878-XiMat	blood
2	chr21:44695200-44701000	Weak transcription	A549	lung
3	chr21:44696600-44699800	Enhancers	Spleen	Spleen
4	chr21:44696800-44709000	Weak transcription	Gastric	stomach
5	chr21:44697200-44700000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr21:44697800-44702800	Weak transcription	Right Atrium	heart
7	chr21:44698400-44707200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr21:44699200-44701400	Weak transcription	HepG2	liver
9	chr21:44699200-44702200	Weak transcription	Right Ventricle	heart
10	chr21:44699400-44699800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr21:44699400-44701400	Weak transcription	Brain Germinal Matrix	brain
12	chr21:44699400-44707200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr21:44699800-44700800	Active TSS	HSMM	muscle
14	chr21:44699800-44701200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr21:44700800-44701600	Enhancers	Fetal Thymus	thymus
16	chr21:44701000-44701200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr21:44701000-44701400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr21:44701000-44701600	Enhancers	A549	lung
19	chr21:44701200-44702400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr21:44701200-44702400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr21:44701400-44702400	Enhancers	HepG2	liver
22	chr21:44701400-44703000	Enhancers	Brain Germinal Matrix	brain
23	chr21:44701600-44701800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr21:44701600-44701800	Enhancers	Thymus	Thymus
25	chr21:44701600-44706000	Weak transcription	Fetal Thymus	thymus
26	chr21:44701600-44706800	Weak transcription	A549	lung
27	chr21:44702000-44702200	Enhancers	Stomach Mucosa	stomach
28	chr21:44702200-44702400	Enhancers	Right Ventricle	heart
29	chr21:44702200-44703200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr21:44702400-44702800	Weak transcription	Right Ventricle	heart
31	chr21:44702400-44703000	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr21:44702400-44706200	Weak transcription	HepG2	liver
33	chr21:44702400-44707000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr21:44702800-44703200	Enhancers	Right Ventricle	heart
35	chr21:44703000-44708000	Weak transcription	Brain Germinal Matrix	brain
36	chr21:44705400-44706200	Enhancers	Dnd41	blood
37	chr21:44705800-44707200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr21:44706000-44706200	Enhancers	Pancreas	Pancrea
39	chr21:44706000-44706400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr21:44706000-44708800	Enhancers	Fetal Thymus	thymus

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