Variant report

Variant	nsv976119
Chromosome Location	chr13:53176029-53218496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1124)
CpG islands
(count:918)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:53183538-53183768	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:53191399-53191692	K562	blood:	n/a	n/a
3	ARID3A	chr13:53191307-53191780	HepG2	liver:	n/a	n/a
4	ATF2	chr13:53191325-53191749	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr13:53191356-53191832	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr13:53191240-53191855	GM12878	blood:	n/a	n/a
7	ATF2	chr13:53191283-53191848	GM12878	blood:	n/a	n/a
8	ATF3	chr13:53190868-53191269	A549	lung:	n/a	n/a
9	ATF3	chr13:53191426-53191696	A549	lung:	n/a	n/a
10	ATF3	chr13:53191126-53191583	A549	lung:	n/a	n/a
11	ATF3	chr13:53190031-53190175	K562	blood:	n/a	n/a
12	ATF3	chr13:53191222-53191681	K562	blood:	n/a	n/a
13	BACH1	chr13:53191461-53191869	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr13:53191419-53191784	GM12878	blood:	n/a	n/a
15	BATF	chr13:53205194-53205499	GM12878	blood:	n/a	n/a
16	BATF	chr13:53197949-53198190	GM12878	blood:	n/a	n/a
17	BCL11A	chr13:53198011-53198210	GM12878	blood:	n/a	n/a
18	BCL3	chr13:53191278-53191797	A549	lung:	n/a	n/a
19	BCLAF1	chr13:53191353-53191822	K562	blood:	n/a	n/a
20	BCLAF1	chr13:53191124-53191910	GM12878	blood:	n/a	n/a
21	BCLAF1	chr13:53191315-53191849	K562	blood:	n/a	n/a
22	BCLAF1	chr13:53191324-53191879	GM12878	blood:	n/a	n/a
23	BHLHE40	chr13:53191383-53191830	K562	blood:	n/a	n/a
24	BHLHE40	chr13:53176718-53176745	HepG2	liver:	n/a	n/a
25	BHLHE40	chr13:53176503-53176777	HepG2	liver:	n/a	n/a
26	BHLHE40	chr13:53191420-53191763	HepG2	liver:	n/a	n/a
27	BHLHE40	chr13:53191334-53191826	GM12878	blood:	n/a	n/a
28	BRCA1	chr13:53183594-53183662	HepG2	liver:	n/a	n/a
29	BRCA1	chr13:53191401-53191762	GM12878	blood:	n/a	n/a
30	BRCA1	chr13:53191469-53191790	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr13:53191402-53191786	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr13:53191415-53191795	K562	blood:	n/a	n/a
33	CBX3	chr13:53191212-53191927	HCT-116	colon:	n/a	n/a
34	CBX3	chr13:53191468-53191712	K562	blood:	n/a	n/a
35	CBX3	chr13:53191167-53191899	HCT-116	colon:	n/a	n/a
36	CCNT2	chr13:53191441-53191776	K562	blood:	n/a	n/a
37	CEBPB	chr13:53189545-53189831	A549	lung:	n/a	chr13:53189741-53189752
38	CEBPB	chr13:53191512-53191755	GM12878	blood:	n/a	n/a
39	CEBPB	chr13:53189551-53189931	IMR90	lung:	n/a	chr13:53189741-53189752
40	CEBPB	chr13:53189556-53190152	HepG2	liver:	n/a	chr13:53189741-53189752
41	CEBPB	chr13:53181067-53181299	K562	blood:	n/a	n/a
42	CEBPB	chr13:53189560-53189897	K562	blood:	n/a	chr13:53189741-53189752
43	CEBPB	chr13:53181063-53181266	K562	blood:	n/a	n/a
44	CEBPB	chr13:53189455-53189961	A549	lung:	n/a	chr13:53189741-53189752
45	CEBPB	chr13:53181003-53181304	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr13:53189557-53189932	H1-hESC	embryonic stem cell:	n/a	chr13:53189741-53189752
47	CEBPB	chr13:53177535-53177725	HepG2	liver:	n/a	chr13:53177633-53177644 chr13:53177631-53177644 chr13:53177628-53177645
48	CEBPB	chr13:53191339-53191861	GM12878	blood:	n/a	chr13:53191369-53191382
49	CEBPB	chr13:53189544-53189826	ECC-1	luminal epithelium:	n/a	chr13:53189741-53189752
50	CEBPB	chr13:53181048-53181301	HepG2	liver:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:53191046-53191096	ProgFib	skin:	n/a
2	chr13:53191537-53191587	GM12878	blood:	n/a
3	chr13:53191650-53191700	ovcar-3	ovarian:	n/a
4	chr13:53191046-53191096	ProgFib	skin:	n/a
5	chr13:53191537-53191587	GM12878	blood:	n/a
6	chr13:53191650-53191700	ovcar-3	ovarian:	n/a
7	chr13:53176723-53176773	AG04450	lung:	fetal
8	chr13:53191650-53191700	HNPCEpiC	eye:	n/a
9	chr13:53176723-53176773	AG09309	skin:	n/a
10	chr13:53191471-53191521	MCF-7	breast:	n/a
11	chr13:53191541-53191591	HAEpiC	amniotic membrane:	n/a
12	chr13:53191491-53191541	PANC-1	pancreas:	n/a
13	chr13:53191537-53191587	HEK293	kidney:	embryo
14	chr13:53191046-53191096	GM12878	blood:	n/a
15	chr13:53191308-53191358	BE2_C	brain:	n/a
16	chr13:53176723-53176773	PFSK-1	brain:	n/a
17	chr13:53191387-53191437	HCPEpiC	choroid plexus:	n/a
18	chr13:53191541-53191591	Jurkat	blood:	n/a
19	chr13:53216641-53216691	RPTEC	kidney:	n/a
20	chr13:53191387-53191437	K562	blood:	n/a
21	chr13:53191387-53191437	ovcar-3	ovarian:	n/a
22	chr13:53191650-53191700	HRCEpiC	kidney:	n/a
23	chr13:53191387-53191437	Jurkat	blood:	n/a
24	chr13:53191547-53191597	PrEC	prostate:	n/a
25	chr13:53191387-53191437	AG09309	skin:	n/a
26	chr13:53194212-53194262	NHDF-neo	bronchial:	n/a
27	chr13:53191308-53191358	HEEpiC	esophagus:	n/a
28	chr13:53191491-53191541	SKMC	muscle:	n/a
29	chr13:53191909-53191959	HCF	heart:	n/a
30	chr13:53194212-53194262	NB4	blood:	n/a
31	chr13:53191643-53191693	GM12891	blood:	n/a
32	chr13:53191650-53191700	PFSK-1	brain:	n/a
33	chr13:53191308-53191358	HMEC	breast:	n/a
34	chr13:53191541-53191591	T-47D	breast:	n/a
35	chr13:53191387-53191437	IMR90	lung:	fetal
36	chr13:53176723-53176773	Hepatocyte	liver:	n/a
37	chr13:53191541-53191591	SAEC	small airway:	n/a
38	chr13:53194212-53194262	SAEC	small airway:	n/a
39	chr13:53176723-53176773	GM12878	blood:	n/a
40	chr13:53191046-53191096	PFSK-1	brain:	n/a
41	chr13:53191541-53191591	CMK	blood:	n/a
42	chr13:53191541-53191591	AG09309	skin:	n/a
43	chr13:53191537-53191587	Jurkat	blood:	n/a
44	chr13:53191547-53191597	SKMC	muscle:	n/a
45	chr13:53191046-53191096	SK-N-MC	brain:	n/a
46	chr13:53194212-53194262	MCF10A-Er-Src	breast:	n/a
47	chr13:53191909-53191959	IMR90	lung:	fetal
48	chr13:53191471-53191521	Caco-2	colon:	n/a
49	chr13:53191643-53191693	PANC-1	pancreas:	n/a
50	chr13:53191537-53191587	GM06990	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:53207158..53209023-chr13:53213230..53214955,2	K562	blood:
2	chr13:53199936..53201723-chr13:53223791..53226214,2	K562	blood:
3	chr13:53190401..53192261-chr13:53196338..53199090,3	MCF-7	breast:
4	chr13:53215652..53217319-chr13:53217527..53219580,2	K562	blood:
5	chr13:53217144..53219904-chr13:53245859..53248065,2	K562	blood:
6	chr13:52768173..52768983-chr13:53191222..53192131,3	NB4	blood:
7	chr13:53186017..53187839-chr13:53226485..53228736,2	MCF-7	breast:
8	chr13:53207158..53209023-chr13:53213230..53214955,2	K562	blood:
9	chr13:53028109..53029845-chr13:53190052..53193351,3	MCF-7	breast:
10	chr13:53197627..53200441-chr13:53224440..53227074,2	K562	blood:
11	chr13:53184666..53187320-chr13:53188643..53190811,2	K562	blood:
12	chr13:53201490..53204133-chr13:53204662..53206494,2	K562	blood:
13	chr13:53213837..53216389-chr13:53220135..53222271,3	MCF-7	breast:
14	chr13:53217025..53220829-chr13:53221987..53226213,6	K562	blood:
15	chr13:53190930..53191973-chr13:53226605..53227465,3	MCF-7	breast:
16	chr13:53184666..53187320-chr13:53188643..53190811,2	K562	blood:
17	chr13:53176767..53178427-chr13:53183717..53185389,2	MCF-7	breast:
18	chr13:53189348..53193688-chr13:53225267..53228139,8	MCF-7	breast:
19	chr13:53201490..53204133-chr13:53204662..53206494,2	K562	blood:
20	chr13:53215104..53218356-chr13:53226198..53228845,3	K562	blood:
21	chr13:53183231..53184124-chr13:53542318..53542852,2	MCF-7	breast:
22	chr13:53191451..53193324-chr13:53224550..53227605,3	MCF-7	breast:
23	chr13:53215104..53217509-chr13:53226480..53228845,2	K562	blood:
24	chr13:53202759..53205661-chr13:53225651..53228135,2	MCF-7	breast:
25	chr13:53190995..53193647-chr13:53195298..53197430,2	K562	blood:
26	chr13:53212411..53216541-chr13:53222004..53227678,9	MCF-7	breast:
27	chr13:53176767..53178427-chr13:53183717..53185389,2	MCF-7	breast:
28	chr13:53199898..53201820-chr13:53204717..53207641,2	K562	blood:
29	chr13:53199898..53201820-chr13:53204717..53207641,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUGT1-2	chr13:53206555-53206624	NONHSAT033997
2	lnc-SUGT1-2	chr13:53196121-53196400	NONHSAT033997
3	lnc-SUGT1-2	chr13:53191693-53191840	NONHSAT033997
4	lnc-SUGT1-2	chr13:53211436-53211581	NONHSAT033997
5	lnc-SUGT1-2	chr13:53203352-53203490	NONHSAT033997
6	lnc-SUGT1-2	chr13:53201575-53201710	NONHSAT033997

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HNRNPA1L2	hsa-miR-1	chr13:53217806-53217827

Variant related genes	Relation type
MRPS31P4	TF binding region
HNRNPA1L2	TF binding region
MRPS31P4	CpG island
HNRNPA1L2	CpG island
ENSG00000139675	chromatin interactions
ENSG00000250299	chromatin interactions
ENSG00000165416	chromatin interactions
ENSG00000136108	chromatin interactions
ENSG00000243406	chromatin interactions

Extended variants
information (count: 1588 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568654744	chr13:53176053-53176054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542064562	chr13:53176060-53176061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192040497	chr13:53176065-53176066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183872718	chr13:53176070-53176071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376696833	chr13:53176093-53176094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs56012743	chr13:53176189-53176190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2768195	chr13:53176201-53176202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369423342	chr13:53176220-53176221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538263970	chr13:53176258-53176259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs61958123	chr13:53176266-53176267	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs558480592	chr13:53176299-53176300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2257325	chr13:53176308-53176309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs563574299	chr13:53176346-53176347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74581183	chr13:53176352-53176353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554375996	chr13:53176366-53176367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574291579	chr13:53176370-53176371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs61958124	chr13:53176415-53176416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144561583	chr13:53176420-53176421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs61958125	chr13:53176438-53176439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557046352	chr13:53176520-53176521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs60607989	chr13:53176540-53176541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs80002597	chr13:53176547-53176548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74263293	chr13:53176551-53176552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545900816	chr13:53176557-53176558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1865879	chr13:53176562-53176563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559665654	chr13:53176610-53176611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528817186	chr13:53176624-53176625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199853408	chr13:53176662-53176663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562315160	chr13:53176738-53176739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111415670	chr13:53176746-53176747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2082979	chr13:53176755-53176756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113429288	chr13:53176765-53176766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111402066	chr13:53176770-53176771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531118839	chr13:53176821-53176822	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs61958126	chr13:53176868-53176869	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs569653185	chr13:53176875-53176876	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs2575954	chr13:53176932-53176933	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs532202076	chr13:53176970-53176971	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs141718949	chr13:53176976-53176977	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs186833559	chr13:53176987-53176988	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs374480570	chr13:53177029-53177030	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs61958127	chr13:53177047-53177048	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs554437291	chr13:53177054-53177055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs567976491	chr13:53177056-53177057	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs386771055	chr13:53177081-53177082	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs550536234	chr13:53177082-53177083	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs577284098	chr13:53177083-53177084	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs539908179	chr13:53177093-53177094	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs553121457	chr13:53177115-53177116	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs573271548	chr13:53177121-53177122	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:1164 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53173800-53182400	Weak transcription	Fetal Heart	heart
2	chr13:53175000-53191000	Weak transcription	Fetal Stomach	stomach
3	chr13:53175200-53176600	Weak transcription	Hela-S3	cervix
4	chr13:53175200-53179200	Weak transcription	NH-A	brain
5	chr13:53175200-53180000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr13:53175200-53183200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:53175200-53183200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr13:53175400-53177800	Enhancers	HUVEC	blood vessel
9	chr13:53175400-53179800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr13:53175400-53180000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr13:53175800-53176800	Enhancers	HepG2	liver
12	chr13:53176000-53179800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr13:53176600-53177200	Enhancers	Hela-S3	cervix
14	chr13:53176800-53177200	Flanking Active TSS	HepG2	liver
15	chr13:53177200-53177600	Enhancers	HepG2	liver
16	chr13:53177200-53180000	Weak transcription	Hela-S3	cervix
17	chr13:53177600-53182400	Weak transcription	HepG2	liver
18	chr13:53177800-53182200	Weak transcription	HUVEC	blood vessel
19	chr13:53179600-53179800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr13:53179800-53180400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr13:53179800-53180600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr13:53179800-53180600	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr13:53180000-53180200	Enhancers	Hela-S3	cervix
24	chr13:53180000-53180800	Enhancers	Placenta	Placenta
25	chr13:53180000-53181800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr13:53180000-53182600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr13:53180400-53182200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr13:53180600-53181200	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr13:53180600-53181200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr13:53181200-53190000	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr13:53181800-53183000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr13:53182000-53182200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr13:53182200-53182400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr13:53182200-53183200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr13:53182200-53183800	Enhancers	HUVEC	blood vessel
36	chr13:53182400-53182800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr13:53182400-53183200	Enhancers	HepG2	liver
38	chr13:53182400-53183600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr13:53182400-53186000	Enhancers	Fetal Heart	heart
40	chr13:53182600-53183400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr13:53182800-53184400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr13:53183000-53183200	Enhancers	Lung	lung
43	chr13:53183000-53183400	Enhancers	Fetal Intestine Large	intestine
44	chr13:53183000-53183600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr13:53183000-53183800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr13:53183200-53183600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr13:53183200-53183600	Enhancers	Brain Cingulate Gyrus	brain
48	chr13:53183200-53183600	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr13:53183200-53183600	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr13:53183200-53183600	Enhancers	Skeletal Muscle Female	skeletal muscle

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