Variant report

Variant	nsv972574
Chromosome Location	chr8:119634666-119651085
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	BATF	chr8:119650982-119651273	GM12878	blood:	n/a	n/a
2	BATF	chr8:119639827-119640142	GM12878	blood:	n/a	n/a
3	BCL11A	chr8:119639874-119640136	GM12878	blood:	n/a	n/a
4	BHLHE40	chr8:119633139-119634823	GM12878	blood:	n/a	chr8:119634206-119634222
5	BHLHE40	chr8:119639927-119640003	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:119640702-119641204	GM12878	blood:	n/a	n/a
7	CEBPB	chr8:119645778-119645976	H1-hESC	embryonic stem cell:	n/a	chr8:119645848-119645859
8	CEBPB	chr8:119640822-119641003	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:119645690-119646009	HepG2	liver:	n/a	chr8:119645848-119645859
10	CHD1	chr8:119639970-119640010	GM12878	blood:	n/a	n/a
11	CHD1	chr8:119634554-119635171	GM12878	blood:	n/a	chr8:119634634-119634644
12	CHD2	chr8:119632938-119634983	GM12878	blood:	n/a	chr8:119634634-119634644
13	CHD2	chr8:119633834-119634978	Hela-S3	cervix:	n/a	chr8:119634634-119634644
14	CREB1	chr8:119640565-119641118	GM12878	blood:	n/a	n/a
15	CREB1	chr8:119640592-119641088	GM12878	blood:	n/a	n/a
16	CREB1	chr8:119634386-119634741	A549	lung:	n/a	n/a
17	CTCF	chr8:119634568-119634709	GM12878	blood:	n/a	chr8:119634639-119634649
18	CTCF	chr8:119634750-119634835	Lung_OC	lung:	n/a	n/a
19	CUX1	chr8:119634993-119635074	GM12878	blood:	n/a	n/a
20	EBF1	chr8:119639755-119639949	GM12878	blood:	n/a	n/a
21	EBF1	chr8:119645581-119645759	GM12878	blood:	n/a	chr8:119645726-119645735 chr8:119645725-119645735
22	EBF1	chr8:119634645-119635002	GM12878	blood:	n/a	chr8:119634896-119634907
23	EBF1	chr8:119640859-119641243	GM12878	blood:	n/a	n/a
24	EBF1	chr8:119634500-119635105	GM12878	blood:	n/a	chr8:119634896-119634907
25	EBF1	chr8:119634633-119635054	GM12878	blood:	n/a	chr8:119634896-119634907
26	ELF1	chr8:119633250-119634829	GM12878	blood:	n/a	chr8:119633545-119633557 chr8:119634209-119634221 chr8:119633314-119633325 chr8:119633548-119633560
27	ELF1	chr8:119632789-119634771	MCF-7	breast:	n/a	chr8:119633545-119633557 chr8:119634209-119634221 chr8:119633314-119633325 chr8:119633548-119633560
28	ELK1	chr8:119648346-119648361	Hela-S3	cervix:	n/a	n/a
29	EP300	chr8:119639846-119640058	GM12878	blood:	n/a	n/a
30	EP300	chr8:119640619-119641019	GM12878	blood:	n/a	n/a
31	EP300	chr8:119634725-119635013	GM12878	blood:	n/a	n/a
32	EP300	chr8:119634707-119635036	GM12878	blood:	n/a	n/a
33	FOS	chr8:119646439-119646832	HUVEC	blood vessel:	n/a	chr8:119646633-119646643 chr8:119646634-119646642 chr8:119646634-119646642 chr8:119646633-119646643 chr8:119646632-119646643 chr8:119646632-119646644 chr8:119646633-119646643 chr8:119646630-119646641 chr8:119646635-119646642
34	FOS	chr8:119635379-119635385	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:119647289-119647608	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:119647288-119647621	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr8:119647302-119647607	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr8:119647342-119647621	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL2	chr8:119647302-119647755	SK-N-SH	brain:	n/a	n/a
40	GATA2	chr8:119646412-119646802	HUVEC	blood vessel:	n/a	chr8:119646635-119646644 chr8:119646569-119646576 chr8:119646564-119646578 chr8:119646567-119646579
41	GTF2F1	chr8:119634495-119635064	Hela-S3	cervix:	n/a	n/a
42	HCFC1	chr8:119633557-119635458	Hela-S3	cervix:	n/a	n/a
43	HCFC1	chr8:119634031-119634668	K562	blood:	n/a	n/a
44	IKZF1	chr8:119640584-119641023	GM12878	blood:	n/a	n/a
45	JUND	chr8:119647338-119647670	SK-N-SH	brain:	n/a	n/a
46	KAP1	chr8:119649540-119649941	U2OS	brain:	n/a	n/a
47	MAX	chr8:119632804-119634970	MCF-7	breast:	n/a	chr8:119633696-119633706 chr8:119634122-119634132
48	MAX	chr8:119634040-119635000	Hela-S3	cervix:	n/a	chr8:119634122-119634132
49	MAX	chr8:119634422-119634879	ECC-1	luminal epithelium:	n/a	n/a
50	MAX	chr8:119634492-119634738	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:119638289-119638339	MCF10A-Er-Src	breast:	n/a
2	chr8:119634634-119634684	HepG2	liver:	n/a
3	chr8:119634634-119634684	K562	blood:	n/a
4	chr8:119638289-119638339	BJ	skin:	n/a
5	chr8:119638289-119638339	HL-60	blood:	n/a
6	chr8:119638289-119638339	AG04449	skin:	fetal
7	chr8:119638289-119638339	HRPEpiC	eye:	n/a
8	chr8:119638289-119638339	SK-N-SH_RA	brain:	n/a
9	chr8:119634634-119634684	A549	lung:	n/a
10	chr8:119634634-119634684	Jurkat	blood:	n/a
11	chr8:119638289-119638339	HCT-116	colon:	n/a
12	chr8:119634634-119634684	Hela-S3	cervix:	n/a
13	chr8:119634634-119634684	HMEC	breast:	n/a
14	chr8:119638289-119638339	A549	lung:	n/a
15	chr8:119638289-119638339	Jurkat	blood:	n/a
16	chr8:119634634-119634684	AG09319	gingival:	n/a
17	chr8:119638289-119638339	Hela-S3	cervix:	n/a
18	chr8:119638289-119638339	U87	brain:	n/a
19	chr8:119638289-119638339	T-47D	breast:	n/a
20	chr8:119638289-119638339	AG09319	gingival:	n/a
21	chr8:119638289-119638339	GM19239	blood:	n/a
22	chr8:119638289-119638339	BE2_C	brain:	n/a
23	chr8:119634634-119634684	HNPCEpiC	eye:	n/a
24	chr8:119638289-119638339	AoSMC	blood vessel:	n/a
25	chr8:119634634-119634684	ovcar-3	ovarian:	n/a
26	chr8:119634634-119634684	HL-60	blood:	n/a
27	chr8:119634634-119634684	GM12892	blood:	n/a
28	chr8:119638289-119638339	K562	blood:	n/a
29	chr8:119634634-119634684	ECC-1	luminal epithelium:	n/a
30	chr8:119634634-119634684	Caco-2	colon:	n/a
31	chr8:119634634-119634684	GM06990	blood:	n/a
32	chr8:119638289-119638339	GM12892	blood:	n/a
33	chr8:119634634-119634684	MCF10A-Er-Src	breast:	n/a
34	chr8:119638289-119638339	HCF	heart:	n/a
35	chr8:119634634-119634684	HCF	heart:	n/a
36	chr8:119634634-119634684	SK-N-SH_RA	brain:	n/a
37	chr8:119634634-119634684	HRE	kidney:	n/a
38	chr8:119634634-119634684	GM12878	blood:	n/a
39	chr8:119634634-119634684	HUVEC	blood vessel:	n/a
40	chr8:119634634-119634684	MCF-7	breast:	n/a
41	chr8:119638289-119638339	HRE	kidney:	n/a
42	chr8:119638289-119638339	H1-hESC	embryonic stem cell:	embryo
43	chr8:119638289-119638339	LNCaP	prostate:	n/a
44	chr8:119634634-119634684	HEK293	kidney:	embryo
45	chr8:119638289-119638339	MCF-7	breast:	n/a
46	chr8:119634634-119634684	AG04450	lung:	fetal
47	chr8:119634634-119634684	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:119634634-119634684	HCM	heart:	n/a
49	chr8:119634634-119634684	AG09309	skin:	n/a
50	chr8:119634634-119634684	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:119633322..119635580-chr8:119639291..119641315,2	MCF-7	breast:
2	chr8:119633762..119636095-chr8:119645506..119648099,2	MCF-7	breast:

Variant related genes	Relation type
SAMD12	TF binding region
SAMD12	CpG island
ENSG00000177570	chromatin interactions

Extended variants
information (count: 630 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559374656	chr8:119634674-119634675	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs191518260	chr8:119634679-119634680	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs183831556	chr8:119634706-119634707	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563616677	chr8:119634759-119634760	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs188772638	chr8:119634771-119634772	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs551957526	chr8:119634820-119634821	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs374308839	chr8:119634823-119634824	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs376110787	chr8:119634857-119634858	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs140509381	chr8:119634863-119634864	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs563989914	chr8:119634875-119634876	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs532744066	chr8:119635017-119635018	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs370789543	chr8:119635027-119635028	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs146018064	chr8:119635034-119635035	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs547521229	chr8:119635044-119635045	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs111519945	chr8:119635047-119635048	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs79112892	chr8:119635106-119635107	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs546108499	chr8:119635114-119635115	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs559580452	chr8:119635128-119635129	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs570329084	chr8:119635167-119635168	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs537388452	chr8:119635240-119635241	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs559186120	chr8:119635242-119635243	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs571088976	chr8:119635337-119635338	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs372057229	chr8:119635347-119635348	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs139970115	chr8:119635392-119635393	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs192519284	chr8:119635394-119635395	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs5894445	chr8:119635434-119635435	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs80135985	chr8:119635445-119635446	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs398009564	chr8:119635446-119635447	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs368602016	chr8:119635499-119635500	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs528694846	chr8:119635605-119635606	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371870846	chr8:119635724-119635725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574318535	chr8:119635775-119635776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73709148	chr8:119635777-119635778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs149755793	chr8:119635816-119635817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34556307	chr8:119635819-119635820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145557346	chr8:119635867-119635868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116350350	chr8:119635884-119635885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559109473	chr8:119635916-119635917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577411681	chr8:119636018-119636019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183492453	chr8:119636065-119636066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528300055	chr8:119636074-119636075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111961009	chr8:119636124-119636125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73709149	chr8:119636164-119636165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs148883994	chr8:119636178-119636179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531023485	chr8:119636214-119636215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548557493	chr8:119636333-119636334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569991371	chr8:119636343-119636344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528121584	chr8:119636349-119636350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78306852	chr8:119636350-119636351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201203123	chr8:119636351-119636352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:143)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119632600-119635200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr8:119632800-119635000	Active TSS	Colonic Mucosa	Colon
3	chr8:119632800-119635000	Active TSS	Rectal Smooth Muscle	rectum
4	chr8:119633000-119634800	Active TSS	H9 Cell Line	embryonic stem cell
5	chr8:119633000-119634800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
6	chr8:119633000-119634800	Flanking Active TSS	Primary hematopoietic stem cells	blood
7	chr8:119633000-119634800	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr8:119633000-119634800	Active TSS	Brain Germinal Matrix	brain
9	chr8:119633000-119634800	Active TSS	Fetal Intestine Large	intestine
10	chr8:119633000-119634800	Active TSS	Gastric	stomach
11	chr8:119633000-119635000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr8:119633000-119635000	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr8:119633000-119635200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
14	chr8:119633200-119634800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr8:119633200-119634800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
16	chr8:119633200-119635000	Active TSS	Duodenum Smooth Muscle	Duodenum
17	chr8:119633200-119635200	Active TSS	Sigmoid Colon	Sigmoid Colon
18	chr8:119633400-119634800	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr8:119633400-119634800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
20	chr8:119633400-119634800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr8:119633400-119634800	Active TSS	Aorta	Aorta
22	chr8:119633400-119634800	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr8:119633400-119635000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:119633400-119635000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr8:119633400-119635000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:119633400-119635000	Active TSS	Psoas Muscle	Psoas
27	chr8:119633400-119635200	Active TSS	Fetal Kidney	kidney
28	chr8:119633600-119634800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:119633600-119634800	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr8:119633600-119634800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
31	chr8:119633600-119634800	Active TSS	A549	lung
32	chr8:119633600-119634800	Active TSS	HSMMtube	muscle
33	chr8:119633600-119635000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr8:119633600-119635000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr8:119633600-119635200	Active TSS	Brain Hippocampus Middle	brain
36	chr8:119633800-119634800	Active TSS	Primary T cells from cord blood	blood
37	chr8:119633800-119634800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr8:119633800-119634800	Flanking Active TSS	Placenta	Placenta
39	chr8:119633800-119634800	Active TSS	K562	blood
40	chr8:119633800-119635000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:119633800-119635000	Active TSS	Fetal Brain Male	brain
42	chr8:119633800-119635000	Active TSS	HMEC	breast
43	chr8:119634000-119634800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:119634000-119634800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:119634000-119634800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:119634000-119634800	Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr8:119634000-119634800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
48	chr8:119634000-119634800	Active TSS	Placenta Amnion	Placenta Amnion
49	chr8:119634000-119635000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr8:119634000-119635000	Active TSS	Fetal Brain Female	brain

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