Variant report

Variant	nsv587745
Chromosome Location	chr21:45681769-45682841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EGR1	chr21:45681705-45681972	K562	blood:	n/a	n/a
2	EGR1	chr21:45681580-45681947	K562	blood:	n/a	n/a
3	THAP1	chr21:45681580-45681822	K562	blood:	n/a	n/a
4	ZBTB7A	chr21:45681814-45681932	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45681834-45681884	Jurkat	blood:	n/a
2	chr21:45681834-45681884	LNCaP	prostate:	n/a
3	chr21:45681834-45681884	Hela-S3	cervix:	n/a
4	chr21:45681834-45681884	HCT-116	colon:	n/a
5	chr21:45681834-45681884	HIPEpiC	eye:	n/a
6	chr21:45681834-45681884	NHDF-neo	bronchial:	n/a
7	chr21:45681834-45681884	H1-hESC	embryonic stem cell:	embryo
8	chr21:45681834-45681884	HCF	heart:	n/a
9	chr21:45681834-45681884	T-47D	breast:	n/a
10	chr21:45681834-45681884	GM06990	blood:	n/a
11	chr21:45681834-45681884	PrEC	prostate:	n/a
12	chr21:45681834-45681884	HRPEpiC	eye:	n/a
13	chr21:45681834-45681884	PFSK-1	brain:	n/a
14	chr21:45681834-45681884	PANC-1	pancreas:	n/a
15	chr21:45681834-45681884	HRCEpiC	kidney:	n/a
16	chr21:45681834-45681884	ProgFib	skin:	n/a
17	chr21:45681834-45681884	AG09319	gingival:	n/a
18	chr21:45681834-45681884	AoSMC	blood vessel:	n/a
19	chr21:45681834-45681884	IMR90	lung:	fetal
20	chr21:45681834-45681884	HMEC	breast:	n/a
21	chr21:45681834-45681884	AG10803	skin:	n/a
22	chr21:45681834-45681884	NH-A	brain:	n/a
23	chr21:45681834-45681884	HEK293	kidney:	embryo
24	chr21:45681834-45681884	RPTEC	kidney:	n/a
25	chr21:45681834-45681884	SAEC	small airway:	n/a
26	chr21:45681834-45681884	AG04449	skin:	fetal
27	chr21:45681834-45681884	SK-N-SH	brain:	n/a
28	chr21:45681834-45681884	HAEpiC	amniotic membrane:	n/a
29	chr21:45681834-45681884	SK-N-SH_RA	brain:	n/a
30	chr21:45681834-45681884	HepG2	liver:	n/a
31	chr21:45681834-45681884	HCM	heart:	n/a
32	chr21:45681834-45681884	GM12891	blood:	n/a
33	chr21:45681834-45681884	ECC-1	luminal epithelium:	n/a
34	chr21:45681834-45681884	HEEpiC	esophagus:	n/a
35	chr21:45681834-45681884	AG04450	lung:	fetal
36	chr21:45681834-45681884	NHBE	bronchial:	n/a
37	chr21:45681834-45681884	CMK	blood:	n/a
38	chr21:45681834-45681884	HUVEC	blood vessel:	n/a
39	chr21:45681834-45681884	NT2-D1	testis:	n/a
40	chr21:45681834-45681884	BJ	skin:	n/a
41	chr21:45681834-45681884	HL-60	blood:	n/a
42	chr21:45681834-45681884	A549	lung:	n/a
43	chr21:45681834-45681884	SK-N-MC	brain:	n/a
44	chr21:45681834-45681884	BE2_C	brain:	n/a
45	chr21:45681834-45681884	GM19239	blood:	n/a
46	chr21:45681834-45681884	AG09309	skin:	n/a
47	chr21:45681834-45681884	SKMC	muscle:	n/a
48	chr21:45681834-45681884	HNPCEpiC	eye:	n/a
49	chr21:45681834-45681884	GM12878	blood:	n/a
50	chr21:45681834-45681884	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:45680895..45685107-chr21:45717932..45721130,4	MCF-7	breast:

No data

Variant related genes	Relation type
DNMT3L	TF binding region
DNMT3L	CpG island
ENSG00000141959	chromatin interactions

Extended variants
information (count: 35 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556893816	chr21:45681827-45681828	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181641804	chr21:45681852-45681853	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs542166466	chr21:45681877-45681878	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs113185110	chr21:45681878-45681879	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs62226881	chr21:45681887-45681888	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs560389133	chr21:45681907-45681908	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113544693	chr21:45681981-45681982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572477758	chr21:45682048-45682049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112542439	chr21:45682049-45682050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs59593850	chr21:45682081-45682082	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs59446093	chr21:45682166-45682167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs57918171	chr21:45682167-45682168	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543123444	chr21:45682397-45682398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540055550	chr21:45682403-45682404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147895125	chr21:45682475-45682476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564774130	chr21:45682507-45682508	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532152284	chr21:45682520-45682521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561740650	chr21:45682525-45682526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs56988500	chr21:45682538-45682539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs60296086	chr21:45682544-45682545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs141656595	chr21:45682545-45682546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560497453	chr21:45682568-45682569	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548121635	chr21:45682569-45682570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192493044	chr21:45682570-45682571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377216357	chr21:45682589-45682590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs533837455	chr21:45682593-45682594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs180821595	chr21:45682594-45682595	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571106634	chr21:45682628-45682629	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116458620	chr21:45682652-45682653	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556588549	chr21:45682711-45682712	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145505737	chr21:45682785-45682786	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575033277	chr21:45682791-45682792	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147731811	chr21:45682803-45682804	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149216252	chr21:45682807-45682808	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572335716	chr21:45682813-45682814	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 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
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
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
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	21364760	CNVD
Down syndrome	21154855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45662800-45705600	Weak transcription	Right Atrium	heart
2	chr21:45681000-45681800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr21:45681000-45682600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr21:45681200-45681800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr21:45681400-45681800	Bivalent Enhancer	HepG2	liver
6	chr21:45681400-45682000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr21:45681600-45681800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr21:45681600-45683000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr21:45681800-45683000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr21:45681800-45683000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr21:45681800-45683200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr21:45682000-45682400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr21:45682400-45683800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr21:45682600-45683000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr21:45682600-45684600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr21:45682800-45684000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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