Variant report

Variant	nsv1041207
Chromosome Location	chr13:70347748-70473605
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:383)
CpG islands
(count:123)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:70431391-70431702	HepG2	liver:	n/a	n/a
2	BHLHE40	chr13:70430533-70430835	HepG2	liver:	n/a	chr13:70430691-70430700 chr13:70430688-70430701
3	BRCA1	chr13:70431439-70431586	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr13:70351107-70351445	K562	blood:	n/a	n/a
5	CEBPB	chr13:70431436-70431605	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr13:70430376-70430903	Hela-S3	cervix:	n/a	chr13:70430726-70430738
7	CEBPB	chr13:70440679-70441116	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr13:70368078-70368276	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr13:70431490-70431624	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr13:70431480-70431630	GM06990	blood:	n/a	n/a
11	CTCF	chr13:70381758-70381815	Lung_OC	lung:	n/a	n/a
12	CTCF	chr13:70431520-70431670	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr13:70430480-70430630	AG04450	lung:	n/a	n/a
14	CTCF	chr13:70431354-70431747	IMR90	lung:	n/a	n/a
15	CTCF	chr13:70431300-70431450	HAc	cerebellar:	n/a	n/a
16	CTCF	chr13:70431480-70431630	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr13:70431473-70431707	Lung_OC	lung:	n/a	n/a
18	CTCF	chr13:70377800-70377950	GM12874	blood:	n/a	n/a
19	CTCF	chr13:70431460-70431610	GM12875	blood:	n/a	n/a
20	CTCF	chr13:70459940-70460090	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr13:70431482-70431644	GM20000	blood:	n/a	n/a
22	CTCF	chr13:70431430-70431680	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr13:70431440-70431590	GM12865	blood:	n/a	n/a
24	CTCF	chr13:70431440-70431661	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr13:70431480-70431630	HMF	breast:	n/a	n/a
26	CTCF	chr13:70431500-70431650	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr13:70431500-70431650	GM12869	blood:	n/a	n/a
28	CTCF	chr13:70431440-70431590	GM12878	blood:	n/a	n/a
29	CTCF	chr13:70431460-70431610	GM12864	blood:	n/a	n/a
30	CTCF	chr13:70431440-70431590	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr13:70431325-70431773	HepG2	liver:	n/a	n/a
32	CTCF	chr13:70431440-70431664	GM10266	blood:	n/a	n/a
33	CTCF	chr13:70431396-70431663	A549	lung:	n/a	n/a
34	CTCF	chr13:70431520-70431670	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr13:70431414-70431682	GM12878	blood:	n/a	n/a
36	CTCF	chr13:70431480-70431630	GM12874	blood:	n/a	n/a
37	CTCF	chr13:70454705-70454946	GM12878	blood:	n/a	n/a
38	CTCF	chr13:70431017-70431882	SK-N-SH	brain:	n/a	n/a
39	CTCF	chr13:70432156-70432241	GM20000	blood:	n/a	n/a
40	CTCF	chr13:70431540-70431690	AG09309	skin:	n/a	n/a
41	CTCF	chr13:70431439-70431630	MCF-7	breast:	n/a	n/a
42	CTCF	chr13:70431316-70431789	GM12878	blood:	n/a	n/a
43	CTCF	chr13:70431540-70431690	NB4	blood:	n/a	n/a
44	CTCF	chr13:70431480-70431630	GM12867	blood:	n/a	n/a
45	CTCF	chr13:70431480-70431630	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr13:70431440-70431590	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr13:70431360-70431610	NHLF	lung:	n/a	n/a
48	CTCF	chr13:70431432-70431665	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr13:70431400-70431550	RPTEC	kidney:	n/a	n/a
50	CTCF	chr13:70431440-70431590	AG09319	gingival:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:70431522-70431572	GM06990	blood:	n/a
2	chr13:70431522-70431572	GM06990	blood:	n/a
3	chr13:70369137-70369187	BE2_C	brain:	n/a
4	chr13:70431522-70431572	HRE	kidney:	n/a
5	chr13:70369137-70369187	CMK	blood:	n/a
6	chr13:70369137-70369187	BJ	skin:	n/a
7	chr13:70431522-70431572	GM19239	blood:	n/a
8	chr13:70431522-70431572	LNCaP	prostate:	n/a
9	chr13:70431522-70431572	BE2_C	brain:	n/a
10	chr13:70369137-70369187	IMR90	lung:	fetal
11	chr13:70369137-70369187	SK-N-SH	brain:	n/a
12	chr13:70431522-70431572	ovcar-3	ovarian:	n/a
13	chr13:70431522-70431572	HIPEpiC	eye:	n/a
14	chr13:70431522-70431572	PANC-1	pancreas:	n/a
15	chr13:70431522-70431572	HUVEC	blood vessel:	n/a
16	chr13:70431522-70431572	HRCEpiC	kidney:	n/a
17	chr13:70369137-70369187	HCM	heart:	n/a
18	chr13:70431522-70431572	CMK	blood:	n/a
19	chr13:70369137-70369187	MCF10A-Er-Src	breast:	n/a
20	chr13:70431522-70431572	BJ	skin:	n/a
21	chr13:70431522-70431572	SK-N-MC	brain:	n/a
22	chr13:70369137-70369187	U87	brain:	n/a
23	chr13:70369137-70369187	AG10803	skin:	n/a
24	chr13:70369137-70369187	LNCaP	prostate:	n/a
25	chr13:70431522-70431572	RPTEC	kidney:	n/a
26	chr13:70431522-70431572	NB4	blood:	n/a
27	chr13:70431522-70431572	HPAEpiC	pulmonary alveolar:	n/a
28	chr13:70369137-70369187	AG09319	gingival:	n/a
29	chr13:70431522-70431572	A549	lung:	n/a
30	chr13:70431522-70431572	HNPCEpiC	eye:	n/a
31	chr13:70369137-70369187	ProgFib	skin:	n/a
32	chr13:70431522-70431572	PrEC	prostate:	n/a
33	chr13:70369137-70369187	Caco-2	colon:	n/a
34	chr13:70431522-70431572	HCT-116	colon:	n/a
35	chr13:70369137-70369187	HPAEpiC	pulmonary alveolar:	n/a
36	chr13:70369137-70369187	NH-A	brain:	n/a
37	chr13:70431522-70431572	H1-hESC	embryonic stem cell:	embryo
38	chr13:70369137-70369187	RPTEC	kidney:	n/a
39	chr13:70431522-70431572	MCF10A-Er-Src	breast:	n/a
40	chr13:70369137-70369187	HNPCEpiC	eye:	n/a
41	chr13:70369137-70369187	HCPEpiC	choroid plexus:	n/a
42	chr13:70369137-70369187	PANC-1	pancreas:	n/a
43	chr13:70431522-70431572	PFSK-1	brain:	n/a
44	chr13:70369137-70369187	H1-hESC	embryonic stem cell:	embryo
45	chr13:70431522-70431572	SK-N-SH_RA	brain:	n/a
46	chr13:70431522-70431572	NHDF-neo	bronchial:	n/a
47	chr13:70431522-70431572	ECC-1	luminal epithelium:	n/a
48	chr13:70369137-70369187	PFSK-1	brain:	n/a
49	chr13:70369137-70369187	HCT-116	colon:	n/a
50	chr13:70369137-70369187	NHBE	bronchial:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:
2	chr13:70111047..70112123-chr13:70431019..70432110,4	MCF-7	breast:
3	chr13:70153553..70154097-chr13:70431151..70432026,2	MCF-7	breast:
4	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:
5	chr13:70111760..70112275-chr13:70431222..70431945,2	K562	blood:
6	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
7	chr13:70139358..70139986-chr13:70431208..70431784,2	MCF-7	breast:
8	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
9	chr13:70444676..70447495-chr17:57919486..57921075,2	MCF-7	breast:
10	chr13:70159894..70160626-chr13:70431095..70431958,2	MCF-7	breast:
11	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:

No data

Variant related genes	Relation type
PSMC1P13	TF binding region
RNY3P10	TF binding region
PSMC1P13	CpG island
RNY3P10	CpG island

Extended variants
information (count: 1124 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72522948	chr13:70367626-70367627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs59126736	chr13:70367627-70367628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200326251	chr13:70367628-70367629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200883126	chr13:70367629-70367630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201851170	chr13:70367630-70367631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs397798632	chr13:70367640-70367641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144386939	chr13:70367678-70367679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138806597	chr13:70367729-70367730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185608971	chr13:70367792-70367793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114628743	chr13:70367800-70367801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs57713566	chr13:70367853-70367854	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs78460984	chr13:70367864-70367865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76458294	chr13:70367906-70367907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs60137040	chr13:70367948-70367949	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs577091439	chr13:70367954-70367955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370485580	chr13:70367955-70367956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75299323	chr13:70367960-70367961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548849583	chr13:70367968-70367969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76677930	chr13:70368024-70368025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs377716482	chr13:70368072-70368073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551394800	chr13:70368097-70368098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73210502	chr13:70368130-70368131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs562961730	chr13:70368168-70368169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556449304	chr13:70368215-70368216	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs151173500	chr13:70368227-70368228	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs536086398	chr13:70368237-70368238	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs139170267	chr13:70368247-70368248	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs368426198	chr13:70368251-70368252	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs572817834	chr13:70368273-70368274	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs541025949	chr13:70368311-70368312	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558135212	chr13:70368313-70368314	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs578012990	chr13:70368326-70368327	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs17085391	chr13:70368382-70368383	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs563474958	chr13:70368403-70368404	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs529030535	chr13:70368438-70368439	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs542459063	chr13:70368448-70368449	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs144034488	chr13:70368449-70368450	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs12583014	chr13:70368598-70368599	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs574220457	chr13:70368603-70368604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75346116	chr13:70368643-70368644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146498671	chr13:70368661-70368662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80120512	chr13:70368676-70368677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9572290	chr13:70368689-70368690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs58800073	chr13:70368696-70368697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs397965183	chr13:70368705-70368706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530460644	chr13:70368713-70368714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189349184	chr13:70368754-70368755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181680946	chr13:70368792-70368793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141006158	chr13:70368793-70368794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556006321	chr13:70368812-70368813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	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
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70367600-70368200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr13:70367800-70368200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:70367800-70368600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:70367800-70368600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr13:70367800-70368600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr13:70367800-70368800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:70368000-70368200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr13:70368000-70368600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr13:70368000-70368600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr13:70368000-70368600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:70368000-70368600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:70368000-70368600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr13:70368000-70368800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr13:70368200-70368600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr13:70368200-70368600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr13:70368200-70369000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr13:70368600-70368800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr13:70368600-70369000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:70368600-70370400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:70370400-70371000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr13:70377400-70383200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr13:70383000-70383600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:70383200-70383600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr13:70383600-70383800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr13:70383800-70384000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr13:70393200-70395000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr13:70394200-70394600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:70399800-70400200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:70399800-70400400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr13:70399800-70400600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr13:70400000-70400600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr13:70400000-70400800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr13:70400200-70402200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr13:70402000-70403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr13:70402200-70403200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr13:70402200-70403400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr13:70402600-70403200	Enhancers	Adipose Nuclei	Adipose
38	chr13:70402600-70403200	Enhancers	Placenta Amnion	Placenta Amnion
39	chr13:70402800-70403000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr13:70402800-70403200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr13:70426000-70430400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr13:70428600-70430200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr13:70430200-70430600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr13:70430200-70430600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr13:70430200-70431200	Enhancers	Fetal Intestine Small	intestine
46	chr13:70430200-70431400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr13:70430200-70431400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr13:70430400-70431000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr13:70430400-70431200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr13:70430400-70431200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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