Variant report

Variant	nsv587743
Chromosome Location	chr21:45675877-45683350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:41)
CpG islands
(count:550)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:41 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr21:45678920-45679198	K562	blood:	n/a	n/a
2	CEBPB	chr21:45678940-45679276	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr21:45678946-45679248	IMR90	lung:	n/a	n/a
4	CHD2	chr21:45681498-45681620	HepG2	liver:	n/a	n/a
5	CTCF	chr21:45680565-45680603	Lung_OC	lung:	n/a	n/a
6	CTCF	chr21:45679320-45679470	WERI-Rb-1	eye:	n/a	n/a
7	E2F4	chr21:45679052-45679252	MCF10A-Er-Src	breast:	n/a	n/a
8	EGR1	chr21:45681705-45681972	K562	blood:	n/a	n/a
9	EGR1	chr21:45681580-45681947	K562	blood:	n/a	n/a
10	ELF1	chr21:45683096-45683404	GM12878	blood:	n/a	chr21:45683380-45683392
11	FOS	chr21:45676487-45676627	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr21:45679023-45679327	MCF10A-Er-Src	breast:	n/a	chr21:45679144-45679153
13	FOS	chr21:45679065-45679299	MCF10A-Er-Src	breast:	n/a	chr21:45679144-45679153
14	FOS	chr21:45679144-45679320	MCF10A-Er-Src	breast:	n/a	chr21:45679144-45679153
15	FOS	chr21:45679042-45679321	MCF10A-Er-Src	breast:	n/a	chr21:45679144-45679153
16	MAZ	chr21:45683341-45683375	K562	blood:	n/a	n/a
17	MYC	chr21:45679129-45679302	MCF10A-Er-Src	breast:	n/a	n/a
18	NFE2	chr21:45680094-45680101	GM12878	blood:	n/a	n/a
19	POLR2A	chr21:45681258-45681302	MCF-7	breast:	n/a	n/a
20	POLR2A	chr21:45678463-45679350	HepG2	liver:	n/a	n/a
21	POLR2A	chr21:45676059-45676145	HepG2	liver:	n/a	n/a
22	POLR2A	chr21:45677076-45677166	HepG2	liver:	n/a	n/a
23	POLR2A	chr21:45678956-45678996	HepG2	liver:	n/a	n/a
24	POLR2A	chr21:45681032-45681217	HepG2	liver:	n/a	n/a
25	POLR2A	chr21:45676620-45677023	HepG2	liver:	n/a	n/a
26	POLR2A	chr21:45677901-45678199	HepG2	liver:	n/a	n/a
27	RUNX3	chr21:45680038-45680282	GM12878	blood:	n/a	n/a
28	STAT3	chr21:45679002-45679346	MCF10A-Er-Src	breast:	n/a	n/a
29	STAT3	chr21:45678982-45679314	MCF10A-Er-Src	breast:	n/a	n/a
30	STAT3	chr21:45679067-45679355	MCF10A-Er-Src	breast:	n/a	n/a
31	STAT3	chr21:45676554-45676585	MCF10A-Er-Src	breast:	n/a	n/a
32	THAP1	chr21:45681580-45681822	K562	blood:	n/a	n/a
33	UBTF	chr21:45678452-45678533	K562	blood:	n/a	n/a
34	USF1	chr21:45683349-45683657	H1-hESC	embryonic stem cell:	n/a	n/a
35	USF1	chr21:45683292-45683656	H1-hESC	embryonic stem cell:	n/a	n/a
36	ZBTB7A	chr21:45681814-45681932	K562	blood:	n/a	n/a
37	ZBTB7A	chr21:45683090-45683659	K562	blood:	n/a	n/a
38	ZBTB7A	chr21:45683093-45683338	K562	blood:	n/a	n/a
39	ZBTB7A	chr21:45683266-45683648	ECC-1	luminal epithelium:	n/a	n/a
40	ZBTB7A	chr21:45683323-45683739	ECC-1	luminal epithelium:	n/a	n/a
41	ZBTB7A	chr21:45679228-45679370	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45678303-45678353	CMK	blood:	n/a
2	chr21:45678303-45678353	CMK	blood:	n/a
3	chr21:45681834-45681884	K562	blood:	n/a
4	chr21:45678406-45678456	HRCEpiC	kidney:	n/a
5	chr21:45678543-45678593	Hepatocyte	liver:	n/a
6	chr21:45683146-45683196	HCM	heart:	n/a
7	chr21:45678303-45678353	NHBE	bronchial:	n/a
8	chr21:45678137-45678187	AG10803	skin:	n/a
9	chr21:45678137-45678187	AG09319	gingival:	n/a
10	chr21:45678406-45678456	NHBE	bronchial:	n/a
11	chr21:45681834-45681884	Jurkat	blood:	n/a
12	chr21:45683146-45683196	PANC-1	pancreas:	n/a
13	chr21:45678406-45678456	HPAEpiC	pulmonary alveolar:	n/a
14	chr21:45681834-45681884	LNCaP	prostate:	n/a
15	chr21:45678543-45678593	AoSMC	blood vessel:	n/a
16	chr21:45681834-45681884	PrEC	prostate:	n/a
17	chr21:45675982-45676032	K562	blood:	n/a
18	chr21:45675982-45676032	HUVEC	blood vessel:	n/a
19	chr21:45683146-45683196	SAEC	small airway:	n/a
20	chr21:45678543-45678593	HRE	kidney:	n/a
21	chr21:45683146-45683196	GM19239	blood:	n/a
22	chr21:45678543-45678593	HEK293	kidney:	embryo
23	chr21:45678303-45678353	MCF-7	breast:	n/a
24	chr21:45678137-45678187	SK-N-MC	brain:	n/a
25	chr21:45678406-45678456	NB4	blood:	n/a
26	chr21:45678406-45678456	HepG2	liver:	n/a
27	chr21:45679577-45679627	HCT-116	colon:	n/a
28	chr21:45678406-45678456	BE2_C	brain:	n/a
29	chr21:45678303-45678353	HUVEC	blood vessel:	n/a
30	chr21:45683302-45683352	Hela-S3	cervix:	n/a
31	chr21:45683146-45683196	GM12891	blood:	n/a
32	chr21:45683302-45683352	HMEC	breast:	n/a
33	chr21:45679577-45679627	GM06990	blood:	n/a
34	chr21:45681834-45681884	PANC-1	pancreas:	n/a
35	chr21:45679577-45679627	U87	brain:	n/a
36	chr21:45678303-45678353	GM19239	blood:	n/a
37	chr21:45678543-45678593	SAEC	small airway:	n/a
38	chr21:45678543-45678593	ProgFib	skin:	n/a
39	chr21:45678137-45678187	HEK293	kidney:	embryo
40	chr21:45679577-45679627	NH-A	brain:	n/a
41	chr21:45675982-45676032	HCM	heart:	n/a
42	chr21:45675982-45676032	SK-N-SH	brain:	n/a
43	chr21:45678406-45678456	HCPEpiC	choroid plexus:	n/a
44	chr21:45678406-45678456	Hepatocyte	liver:	n/a
45	chr21:45678406-45678456	ProgFib	skin:	n/a
46	chr21:45675982-45676032	PANC-1	pancreas:	n/a
47	chr21:45678137-45678187	AG04450	lung:	fetal
48	chr21:45681834-45681884	AG10803	skin:	n/a
49	chr21:45683146-45683196	SK-N-SH	brain:	n/a
50	chr21:45678406-45678456	AG04449	skin:	fetal

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45675362..45678242-chr21:45707030..45708929,2	K562	blood:
2	chr21:45555238..45556922-chr21:45675752..45678028,2	K562	blood:
3	chr21:45679421..45681484-chr21:45691729..45694649,2	MCF-7	breast:
4	chr21:45676552..45678534-chr21:45719639..45721347,2	MCF-7	breast:
5	chr21:45659396..45661208-chr21:45675575..45677572,2	K562	blood:
6	chr21:45678302..45680831-chr21:45686072..45687676,2	MCF-7	breast:
7	chr21:45675362..45677457-chr21:45707030..45709484,2	K562	blood:
8	chr21:45677174..45681552-chr21:45685520..45688325,5	K562	blood:
9	chr21:45668918..45671490-chr21:45672484..45676954,6	MCF-7	breast:
10	chr21:45677975..45679719-chr21:45719083..45722045,2	K562	blood:
11	chr21:45675133..45677330-chr21:45753304..45755141,2	K562	blood:
12	chr21:45680895..45685107-chr21:45717932..45721130,4	MCF-7	breast:
13	chr21:45668732..45670990-chr21:45677363..45679329,2	K562	blood:
14	chr21:45671627..45673914-chr21:45675329..45677455,2	K562	blood:

No data

Variant related genes	Relation type
DNMT3L	TF binding region
DNMT3L	CpG island
ENSG00000141959	chromatin interactions
ENSG00000232010	chromatin interactions
ENSG00000142182	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000160226	chromatin interactions

Extended variants
information (count: 374 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2070563	chr21:45675877-45675878	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73366550	chr21:45675904-45675905	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs377424986	chr21:45675907-45675908	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs75141318	chr21:45675920-45675921	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs192362607	chr21:45675972-45675973	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs200231352	chr21:45675973-45675974	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs199990417	chr21:45675974-45675975	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs148594562	chr21:45675981-45675982	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs142917827	chr21:45675997-45675998	Enhancers Weak transcription	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs373613659	chr21:45676003-45676004	Enhancers Weak transcription	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs151101964	chr21:45676010-45676011	Enhancers Weak transcription	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs376070394	chr21:45676011-45676012	Enhancers Weak transcription	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs370394403	chr21:45676022-45676023	Enhancers Weak transcription	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs373942735	chr21:45676055-45676056	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs181037394	chr21:45676072-45676073	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs577798956	chr21:45676130-45676131	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs184673535	chr21:45676135-45676136	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs114438986	chr21:45676145-45676146	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs535841113	chr21:45676164-45676165	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs554284038	chr21:45676176-45676177	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs57964258	chr21:45676210-45676211	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs12483008	chr21:45676226-45676227	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs75546846	chr21:45676230-45676231	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs112248290	chr21:45676255-45676256	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs540823171	chr21:45676272-45676273	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs565306281	chr21:45676293-45676294	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs370220695	chr21:45676347-45676348	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs372304625	chr21:45676363-45676364	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs377174187	chr21:45676371-45676372	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs577480450	chr21:45676396-45676397	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs190039356	chr21:45676400-45676401	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs148417229	chr21:45676414-45676415	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs181538516	chr21:45676432-45676433	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs185698516	chr21:45676438-45676439	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs560641090	chr21:45676457-45676458	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs113096304	chr21:45676464-45676465	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs546789335	chr21:45676465-45676466	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs79768851	chr21:45676496-45676497	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs75203607	chr21:45676497-45676498	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs551213197	chr21:45676508-45676509	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs571388004	chr21:45676563-45676564	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs569352304	chr21:45676586-45676587	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs190506191	chr21:45676625-45676626	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs73907135	chr21:45676630-45676631	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs568800750	chr21:45676695-45676696	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs12482693	chr21:45676698-45676699	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs554096223	chr21:45676700-45676701	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs566580517	chr21:45676716-45676717	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs554733637	chr21:45676794-45676795	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs533615212	chr21:45676795-45676796	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 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:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45662800-45705600	Weak transcription	Right Atrium	heart
2	chr21:45666200-45681000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr21:45668600-45677000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr21:45671800-45681400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr21:45672000-45678000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr21:45674200-45676800	Enhancers	Hela-S3	cervix
7	chr21:45675600-45676800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr21:45675800-45676800	Weak transcription	Placenta	Placenta
9	chr21:45676600-45677000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr21:45676800-45677000	Enhancers	Placenta	Placenta
11	chr21:45676800-45679000	Weak transcription	Hela-S3	cervix
12	chr21:45677600-45677800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr21:45677800-45678200	Enhancers	HepG2	liver
14	chr21:45678000-45678400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr21:45678200-45678400	Flanking Active TSS	HepG2	liver
16	chr21:45678400-45678600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr21:45678400-45678600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr21:45678800-45679000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr21:45679000-45679800	Enhancers	Hela-S3	cervix
20	chr21:45679200-45679400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr21:45679200-45679600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr21:45679600-45681000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr21:45681000-45681200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr21:45681000-45681600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr21:45681000-45681800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr21:45681000-45682600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr21:45681200-45681800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr21:45681400-45681800	Bivalent Enhancer	HepG2	liver
29	chr21:45681400-45682000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr21:45681600-45681800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr21:45681600-45683000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr21:45681800-45683000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr21:45681800-45683000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr21:45681800-45683200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr21:45682000-45682400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr21:45682400-45683800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr21:45682600-45683000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr21:45682600-45684600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr21:45682800-45684000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr21:45683000-45683200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr21:45683000-45683400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr21:45683000-45683600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr21:45683000-45683600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr21:45683000-45683800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr21:45683000-45683800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr21:45683000-45683800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr21:45683000-45684000	Enhancers	H1 Cell Line	embryonic stem cell
48	chr21:45683000-45684000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr21:45683000-45684000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr21:45683000-45684200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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