Variant report

Variant	nsv523430
Chromosome Location	chr1:94582249-94591481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94591083-94592179	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94586990-94587278	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94581863-94582438	HepG2	liver:	n/a	chr1:94582390-94582406 chr1:94582322-94582338
4	BHLHE40	chr1:94591375-94592066	HepG2	liver:	n/a	n/a
5	BRCA1	chr1:94591448-94591557	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:94591162-94591482	Hela-S3	cervix:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
7	CEBPB	chr1:94581959-94582348	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:94591138-94591496	IMR90	lung:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
9	CEBPB	chr1:94591139-94591429	K562	blood:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
10	CEBPB	chr1:94591189-94591473	H1-hESC	embryonic stem cell:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
11	CEBPB	chr1:94582021-94582349	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:94591132-94591851	HepG2	liver:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
13	CEBPB	chr1:94581974-94582341	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:94591070-94591576	ECC-1	luminal epithelium:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
15	CEBPB	chr1:94591165-94591692	A549	lung:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
16	CEBPB	chr1:94585460-94585744	HepG2	liver:	n/a	chr1:94585587-94585598 chr1:94585667-94585680
17	CEBPB	chr1:94591151-94591510	ECC-1	luminal epithelium:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
18	CEBPB	chr1:94588266-94588381	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:94591405-94591827	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:94591024-94591600	A549	lung:	n/a	chr1:94591311-94591320 chr1:94591257-94591266 chr1:94591311-94591320 chr1:94591311-94591320
21	CEBPB	chr1:94591475-94591752	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:94591363-94591854	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:94581945-94582380	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:94585448-94585741	IMR90	lung:	n/a	chr1:94585587-94585598 chr1:94585667-94585680
25	CEBPD	chr1:94581976-94582286	HepG2	liver:	n/a	n/a
26	CEBPZ	chr1:94591401-94591676	HepG2	liver:	n/a	n/a
27	CHD2	chr1:94591392-94591760	HepG2	liver:	n/a	n/a
28	CHD2	chr1:94581957-94582347	HepG2	liver:	n/a	n/a
29	CHD2	chr1:94586092-94586250	HepG2	liver:	n/a	n/a
30	CREB1	chr1:94581796-94582445	HepG2	liver:	n/a	n/a
31	CREB1	chr1:94581760-94582545	HepG2	liver:	n/a	n/a
32	CTCF	chr1:94585180-94585330	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr1:94585160-94585310	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr1:94585220-94585370	HMF	breast:	n/a	n/a
35	CTCF	chr1:94585180-94585330	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr1:94585140-94585290	GM12873	blood:	n/a	n/a
37	CTCF	chr1:94584880-94585030	GM12873	blood:	n/a	n/a
38	CTCF	chr1:94585080-94585230	HepG2	liver:	n/a	n/a
39	CTCF	chr1:94585080-94585230	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:94585120-94585270	HCT-116	colon:	n/a	n/a
41	CTCF	chr1:94587180-94587330	HepG2	liver:	n/a	n/a
42	CTCF	chr1:94585120-94585270	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr1:94585100-94585250	HEK293	kidney:	n/a	n/a
44	CTCF	chr1:94585180-94585330	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr1:94585120-94585270	HAc	cerebellar:	n/a	n/a
46	CTCF	chr1:94585120-94585270	BJ	skin:	n/a	n/a
47	CTCF	chr1:94585140-94585290	HCM	heart:	n/a	n/a
48	CTCF	chr1:94585160-94585310	GM12866	blood:	n/a	n/a
49	CTCF	chr1:94585120-94585270	HEK293	kidney:	n/a	n/a
50	CTCF	chr1:94585140-94585290	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94585452-94585502	HRCEpiC	kidney:	n/a
2	chr1:94586670-94586720	SK-N-SH_RA	brain:	n/a
3	chr1:94587872-94587922	SKMC	muscle:	n/a
4	chr1:94587872-94587922	HIPEpiC	eye:	n/a
5	chr1:94587076-94587126	NH-A	brain:	n/a
6	chr1:94587031-94587081	HUVEC	blood vessel:	n/a
7	chr1:94587031-94587081	U87	brain:	n/a
8	chr1:94587589-94587639	HEEpiC	esophagus:	n/a
9	chr1:94586592-94586642	NH-A	brain:	n/a
10	chr1:94585452-94585502	MCF10A-Er-Src	breast:	n/a
11	chr1:94587031-94587081	NH-A	brain:	n/a
12	chr1:94585452-94585502	HNPCEpiC	eye:	n/a
13	chr1:94585452-94585502	SK-N-SH_RA	brain:	n/a
14	chr1:94585452-94585502	LNCaP	prostate:	n/a
15	chr1:94586592-94586642	HRPEpiC	eye:	n/a
16	chr1:94585452-94585502	SKMC	muscle:	n/a
17	chr1:94585452-94585502	HEK293	kidney:	embryo
18	chr1:94587031-94587081	NHDF-neo	bronchial:	n/a
19	chr1:94587905-94587955	K562	blood:	n/a
20	chr1:94587031-94587081	H1-hESC	embryonic stem cell:	embryo
21	chr1:94586670-94586720	GM12878	blood:	n/a
22	chr1:94587076-94587126	HCM	heart:	n/a
23	chr1:94586592-94586642	Hepatocyte	liver:	n/a
24	chr1:94586670-94586720	HNPCEpiC	eye:	n/a
25	chr1:94587031-94587081	GM19239	blood:	n/a
26	chr1:94586670-94586720	PANC-1	pancreas:	n/a
27	chr1:94587031-94587081	AG09319	gingival:	n/a
28	chr1:94587872-94587922	HEEpiC	esophagus:	n/a
29	chr1:94586592-94586642	NT2-D1	testis:	n/a
30	chr1:94587905-94587955	AG09319	gingival:	n/a
31	chr1:94585452-94585502	Jurkat	blood:	n/a
32	chr1:94587905-94587955	NH-A	brain:	n/a
33	chr1:94586592-94586642	BE2_C	brain:	n/a
34	chr1:94586592-94586642	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:94587872-94587922	PrEC	prostate:	n/a
36	chr1:94586592-94586642	AoSMC	blood vessel:	n/a
37	chr1:94587905-94587955	HL-60	blood:	n/a
38	chr1:94587031-94587081	HEEpiC	esophagus:	n/a
39	chr1:94586592-94586642	HRE	kidney:	n/a
40	chr1:94587031-94587081	GM06990	blood:	n/a
41	chr1:94586670-94586720	HEEpiC	esophagus:	n/a
42	chr1:94587031-94587081	SK-N-SH	brain:	n/a
43	chr1:94587905-94587955	GM19239	blood:	n/a
44	chr1:94586592-94586642	AG04450	lung:	fetal
45	chr1:94587872-94587922	CMK	blood:	n/a
46	chr1:94587076-94587126	H1-hESC	embryonic stem cell:	embryo
47	chr1:94587872-94587922	PANC-1	pancreas:	n/a
48	chr1:94587076-94587126	MCF-7	breast:	n/a
49	chr1:94585452-94585502	BE2_C	brain:	n/a
50	chr1:94585452-94585502	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:94532482..94534156-chr1:94582374..94584202,2	MCF-7	breast:
2	chr1:94571469..94574892-chr1:94577789..94583222,4	K562	blood:
3	chr1:94567017..94567580-chr1:94583611..94584143,2	MCF-7	breast:
4	chr1:94561960..94563528-chr1:94582281..94584718,2	MCF-7	breast:
5	chr1:94532251..94537168-chr1:94582958..94586481,4	MCF-7	breast:
6	chr1:94564934..94567258-chr1:94582385..94584556,2	MCF-7	breast:
7	chr1:94526939..94529383-chr1:94580613..94583165,2	MCF-7	breast:
8	chr1:94567418..94570803-chr1:94581520..94584135,4	MCF-7	breast:

Variant related genes	Relation type
ABCA4	TF binding region
ABCA4	CpG island
ENSG00000198691	chromatin interactions

Extended variants
information (count: 394 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:394 , 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	rs3789445	chr1:94582249-94582250	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs4147803	chr1:94582293-94582294	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs145618578	chr1:94582358-94582359	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566914028	chr1:94582364-94582365	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11576368	chr1:94582401-94582402	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555916556	chr1:94582406-94582407	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372115719	chr1:94582418-94582419	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187514648	chr1:94582461-94582462	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538439707	chr1:94582472-94582473	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373126321	chr1:94582488-94582489	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11165075	chr1:94582492-94582493	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs139755424	chr1:94582494-94582495	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs60321670	chr1:94582500-94582501	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201094316	chr1:94582512-94582513	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369304462	chr1:94582519-94582520	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs199937387	chr1:94582522-94582523	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs60374748	chr1:94582523-94582524	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201011120	chr1:94582524-94582525	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs59559890	chr1:94582525-94582526	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540610252	chr1:94582534-94582535	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182541690	chr1:94582554-94582555	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150464572	chr1:94582563-94582564	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534271809	chr1:94582567-94582568	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs200297582	chr1:94582568-94582569	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs60160516	chr1:94582575-94582576	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs57665252	chr1:94582582-94582583	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376145866	chr1:94582583-94582584	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs71652552	chr1:94582628-94582629	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs541498234	chr1:94582631-94582632	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554994719	chr1:94582632-94582633	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35108354	chr1:94582639-94582640	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192391644	chr1:94582643-94582644	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575306092	chr1:94582714-94582715	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544401583	chr1:94582726-94582727	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185563842	chr1:94582737-94582738	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188677069	chr1:94582739-94582740	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs546952325	chr1:94582762-94582763	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs35758710	chr1:94582763-94582764	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141122431	chr1:94582790-94582791	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs115845770	chr1:94582829-94582830	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs549455800	chr1:94582927-94582928	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs569335064	chr1:94582930-94582931	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112981179	chr1:94582978-94582979	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs111628058	chr1:94582979-94582980	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571781389	chr1:94583006-94583007	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34305112	chr1:94583031-94583032	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs386633550	chr1:94583037-94583038	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs113395890	chr1:94583038-94583039	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs3789448	chr1:94583074-94583075	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs201986410	chr1:94583082-94583083	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94564600-94591800	Weak transcription	Right Atrium	heart
2	chr1:94567400-94585400	Weak transcription	Brain Anterior Caudate	brain
3	chr1:94571000-94583000	Weak transcription	Pancreas	Pancrea
4	chr1:94574600-94583000	Weak transcription	Brain Substantia Nigra	brain
5	chr1:94575800-94583000	Weak transcription	Left Ventricle	heart
6	chr1:94579200-94582400	Weak transcription	Fetal Heart	heart
7	chr1:94580200-94587600	Enhancers	Placenta	Placenta
8	chr1:94580400-94587600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:94580600-94583400	Enhancers	Fetal Kidney	kidney
10	chr1:94580800-94582600	Weak transcription	Fetal Lung	lung
11	chr1:94581000-94585200	Enhancers	Ovary	ovary
12	chr1:94581200-94583000	Enhancers	Brain Cingulate Gyrus	brain
13	chr1:94581200-94583200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:94581200-94584200	Enhancers	NHDF-Ad	bronchial
15	chr1:94581200-94584400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:94581400-94583000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
17	chr1:94581400-94583000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:94581400-94583600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:94581400-94583800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr1:94581400-94584200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr1:94581400-94585200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr1:94581400-94587600	Enhancers	Fetal Muscle Leg	muscle
23	chr1:94581400-94588000	Enhancers	Placenta Amnion	Placenta Amnion
24	chr1:94581600-94582600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
25	chr1:94581600-94582800	Enhancers	Fetal Brain Male	brain
26	chr1:94581600-94582800	Enhancers	Osteobl	bone
27	chr1:94581600-94583200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr1:94581600-94583600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr1:94581600-94583600	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr1:94581600-94583800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:94581600-94585000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:94581600-94586200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:94581600-94588600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:94581800-94582400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr1:94581800-94582800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr1:94581800-94582800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:94581800-94582800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:94581800-94583000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
39	chr1:94581800-94583000	Weak transcription	Spleen	Spleen
40	chr1:94581800-94583400	Enhancers	Adipose Nuclei	Adipose
41	chr1:94582000-94582600	Enhancers	HepG2	liver
42	chr1:94582000-94583000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:94582000-94583000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
44	chr1:94582000-94583000	Bivalent Enhancer	Fetal Intestine Large	intestine
45	chr1:94582000-94583800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr1:94582000-94583800	Enhancers	Fetal Stomach	stomach
47	chr1:94582000-94583800	Weak transcription	A549	lung
48	chr1:94582000-94585600	Enhancers	Fetal Muscle Trunk	muscle
49	chr1:94582200-94582400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:94582200-94582400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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