Variant report

Variant	nsv900083
Chromosome Location	chr13:52783120-52885838
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:424)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr13:52853509-52853730	GM12878	blood:	n/a	chr13:52853641-52853652
2	BATF	chr13:52809172-52809423	GM12878	blood:	n/a	n/a
3	BATF	chr13:52810391-52810616	GM12878	blood:	n/a	n/a
4	BATF	chr13:52797274-52797490	GM12878	blood:	n/a	n/a
5	CBX3	chr13:52884107-52884381	K562	blood:	n/a	n/a
6	CBX3	chr13:52874759-52875007	K562	blood:	n/a	n/a
7	CBX3	chr13:52884093-52884361	K562	blood:	n/a	n/a
8	CBX3	chr13:52874658-52875125	K562	blood:	n/a	n/a
9	CEBPB	chr13:52834731-52834822	H1-hESC	embryonic stem cell:	n/a	chr13:52834737-52834748
10	CEBPB	chr13:52834731-52834765	IMR90	lung:	n/a	chr13:52834737-52834748
11	CEBPB	chr13:52834570-52834812	K562	blood:	n/a	chr13:52834737-52834748
12	CEBPB	chr13:52834561-52834763	HepG2	liver:	n/a	chr13:52834737-52834748
13	CEBPB	chr13:52864873-52864902	HepG2	liver:	n/a	n/a
14	CEBPD	chr13:52855570-52855946	K562	blood:	n/a	n/a
15	CTCF	chr13:52810460-52810610	Caco-2	colon:	n/a	n/a
16	CTCF	chr13:52810520-52810670	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr13:52810500-52810650	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr13:52810284-52810286	Gliobla	brain:	n/a	n/a
19	CTCF	chr13:52810520-52810670	AG09319	gingival:	n/a	n/a
20	CTCF	chr13:52810520-52810670	HMEC	breast:	n/a	n/a
21	CTCF	chr13:52810520-52810670	HRE	kidney:	n/a	n/a
22	CTCF	chr13:52810383-52810642	K562	blood:	n/a	n/a
23	CTCF	chr13:52877300-52877339	GM10266	blood:	n/a	n/a
24	CTCF	chr13:52853493-52853534	GM19239	blood:	n/a	n/a
25	CTCF	chr13:52810500-52810650	GM12866	blood:	n/a	n/a
26	CTCF	chr13:52810480-52810630	GM12875	blood:	n/a	n/a
27	CTCF	chr13:52796480-52796562	ProgFib	skin:	n/a	n/a
28	CTCF	chr13:52785269-52785383	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:52819327-52819390	GM10266	blood:	n/a	n/a
30	CTCF	chr13:52810540-52810690	GM12878	blood:	n/a	n/a
31	CTCF	chr13:52823566-52823616	GM10266	blood:	n/a	n/a
32	CTCF	chr13:52810287-52810665	ProgFib	skin:	n/a	n/a
33	CTCF	chr13:52810480-52810630	HepG2	liver:	n/a	n/a
34	CTCF	chr13:52810500-52810650	GM12870	blood:	n/a	n/a
35	CTCF	chr13:52810500-52810650	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr13:52810520-52810670	HL-60	blood:	n/a	n/a
37	CTCF	chr13:52810467-52810623	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr13:52810500-52810650	HFF	foreskin:	n/a	n/a
39	CTCF	chr13:52810143-52810150	A549	lung:	n/a	n/a
40	CTCF	chr13:52836705-52836769	MCF-7	breast:	n/a	chr13:52836720-52836741 chr13:52836725-52836743
41	CTCF	chr13:52810436-52810676	GM10266	blood:	n/a	n/a
42	CTCF	chr13:52815600-52815701	Fibrobl	skin:	n/a	n/a
43	CTCF	chr13:52810287-52810678	Gliobla	brain:	n/a	n/a
44	CTCF	chr13:52810365-52810684	Medullo	brain:	n/a	n/a
45	CTCF	chr13:52810426-52810854	A549	lung:	n/a	n/a
46	CTCF	chr13:52810431-52810664	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr13:52810520-52810670	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr13:52810520-52810670	HMF	breast:	n/a	n/a
49	CTCF	chr13:52810520-52810670	GM12878	blood:	n/a	n/a
50	CTCF	chr13:52810410-52810662	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52866820-52866870	IMR90	lung:	fetal
2	chr13:52866820-52866870	BE2_C	brain:	n/a
3	chr13:52866820-52866870	U87	brain:	n/a
4	chr13:52866820-52866870	GM12892	blood:	n/a
5	chr13:52866820-52866870	K562	blood:	n/a
6	chr13:52866820-52866870	HepG2	liver:	n/a
7	chr13:52866820-52866870	GM12878	blood:	n/a
8	chr13:52866820-52866870	ovcar-3	ovarian:	n/a
9	chr13:52866820-52866870	HCM	heart:	n/a
10	chr13:52866820-52866870	MCF10A-Er-Src	breast:	n/a
11	chr13:52866820-52866870	NB4	blood:	n/a
12	chr13:52866820-52866870	HPAEpiC	pulmonary alveolar:	n/a
13	chr13:52866820-52866870	PFSK-1	brain:	n/a
14	chr13:52866820-52866870	AG10803	skin:	n/a
15	chr13:52866820-52866870	NHBE	bronchial:	n/a
16	chr13:52866820-52866870	RPTEC	kidney:	n/a
17	chr13:52866820-52866870	AG04449	skin:	fetal
18	chr13:52866820-52866870	SKMC	muscle:	n/a
19	chr13:52866820-52866870	BJ	skin:	n/a
20	chr13:52866820-52866870	HIPEpiC	eye:	n/a
21	chr13:52866820-52866870	HCT-116	colon:	n/a
22	chr13:52866820-52866870	HUVEC	blood vessel:	n/a
23	chr13:52866820-52866870	SK-N-SH	brain:	n/a
24	chr13:52866820-52866870	MCF-7	breast:	n/a
25	chr13:52866820-52866870	HCPEpiC	choroid plexus:	n/a
26	chr13:52866820-52866870	Jurkat	blood:	n/a
27	chr13:52866820-52866870	HCF	heart:	n/a
28	chr13:52866820-52866870	HMEC	breast:	n/a
29	chr13:52866820-52866870	CMK	blood:	n/a
30	chr13:52866820-52866870	NT2-D1	testis:	n/a
31	chr13:52866820-52866870	Hepatocyte	liver:	n/a
32	chr13:52866820-52866870	GM06990	blood:	n/a
33	chr13:52866820-52866870	HAEpiC	amniotic membrane:	n/a
34	chr13:52866820-52866870	HNPCEpiC	eye:	n/a
35	chr13:52866820-52866870	NHDF-neo	bronchial:	n/a
36	chr13:52866820-52866870	T-47D	breast:	n/a
37	chr13:52866820-52866870	SK-N-SH_RA	brain:	n/a
38	chr13:52866820-52866870	H1-hESC	embryonic stem cell:	embryo
39	chr13:52866820-52866870	SK-N-MC	brain:	n/a
40	chr13:52866820-52866870	HEK293	kidney:	embryo
41	chr13:52866820-52866870	Caco-2	colon:	n/a
42	chr13:52866820-52866870	LNCaP	prostate:	n/a
43	chr13:52866820-52866870	Hela-S3	cervix:	n/a
44	chr13:52866820-52866870	AoSMC	blood vessel:	n/a
45	chr13:52866820-52866870	ProgFib	skin:	n/a
46	chr13:52866820-52866870	HRE	kidney:	n/a
47	chr13:52866820-52866870	HEEpiC	esophagus:	n/a
48	chr13:52866820-52866870	GM12891	blood:	n/a
49	chr13:52866820-52866870	GM19239	blood:	n/a
50	chr13:52866820-52866870	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:52768256..52771397-chr13:52784460..52787312,3	MCF-7	breast:
2	chr13:52885798..52888785-chr13:52889900..52891955,2	MCF-7	breast:

No data

Variant related genes	Relation type
TPTE2P2	TF binding region
ENSG00000217576	TF binding region
TPTE2P2	CpG island
ENSG00000217576	CpG island
ENSG00000243406	chromatin interactions

Extended variants
information (count: 788 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1815348	chr13:52783120-52783121	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139660052	chr13:52783167-52783168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9535905	chr13:52783192-52783193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2768196	chr13:52783216-52783217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189102093	chr13:52783235-52783236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552683692	chr13:52783264-52783265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2094355	chr13:52783283-52783284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375433937	chr13:52783296-52783297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190715774	chr13:52783328-52783329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555070056	chr13:52783330-52783331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200060873	chr13:52783343-52783344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147130209	chr13:52783345-52783346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2094356	chr13:52783346-52783347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575452786	chr13:52783359-52783360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs57648048	chr13:52783382-52783383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs58598740	chr13:52783427-52783428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555425736	chr13:52783445-52783446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557909510	chr13:52783494-52783495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577942961	chr13:52783521-52783522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546056379	chr13:52783578-52783579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183235234	chr13:52783602-52783603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73184380	chr13:52783681-52783682	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs529302575	chr13:52783683-52783684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145504418	chr13:52783690-52783691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562748095	chr13:52783698-52783699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186806497	chr13:52783699-52783700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551814249	chr13:52783702-52783703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571492195	chr13:52783709-52783710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111407232	chr13:52783774-52783775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553646546	chr13:52783788-52783789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546285852	chr13:52783803-52783804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566181751	chr13:52783853-52783854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535184013	chr13:52783857-52783858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111797732	chr13:52783874-52783875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200120073	chr13:52783893-52783894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568784022	chr13:52783921-52783922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141971733	chr13:52783951-52783952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146091517	chr13:52783957-52783958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147856708	chr13:52783987-52783988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540480610	chr13:52784026-52784027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554013919	chr13:52784040-52784041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368755955	chr13:52784054-52784055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530104066	chr13:52784074-52784075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs59209617	chr13:52784142-52784143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562878621	chr13:52784235-52784236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201195716	chr13:52784240-52784241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191210624	chr13:52784256-52784257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545673223	chr13:52784323-52784324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565282543	chr13:52784342-52784343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527980243	chr13:52784357-52784358	Weak transcription	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
Breast cancer	22522925	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52776200-52783400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:52779000-52785200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr13:52779600-52784600	Weak transcription	Placenta	Placenta
4	chr13:52782600-52783600	Enhancers	HepG2	liver
5	chr13:52783400-52783800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:52783600-52784800	Weak transcription	HepG2	liver
7	chr13:52783800-52784600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr13:52784200-52784600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr13:52784600-52786200	Enhancers	Placenta	Placenta
10	chr13:52784600-52786400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:52784800-52785600	Enhancers	HepG2	liver
12	chr13:52784800-52786000	Enhancers	Placenta Amnion	Placenta Amnion
13	chr13:52785200-52785400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:52785200-52785800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr13:52785200-52786200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:52785200-52786200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr13:52785400-52785800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr13:52785400-52786000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr13:52785600-52786000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr13:52785600-52786200	Flanking Active TSS	HepG2	liver
21	chr13:52785600-52786200	Enhancers	NHEK	skin
22	chr13:52786000-52786200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr13:52786000-52786800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr13:52786200-52786400	Active TSS	HepG2	liver
25	chr13:52786800-52787000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr13:52787200-52787600	Enhancers	Fetal Heart	heart
27	chr13:52787600-52793600	Weak transcription	Fetal Heart	heart
28	chr13:52792000-52792800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr13:52792000-52792800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr13:52792200-52792800	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr13:52792400-52792600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr13:52792600-52792800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr13:52792600-52793000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr13:52792800-52793000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:52793600-52794800	Enhancers	Fetal Heart	heart
36	chr13:52793800-52794600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:52803200-52803600	Enhancers	HUVEC	blood vessel
38	chr13:52810000-52810200	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr13:52810000-52810400	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr13:52810000-52810400	Active TSS	H1 Cell Line	embryonic stem cell
41	chr13:52810000-52810400	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr13:52810000-52810400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr13:52810000-52810400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr13:52810000-52810400	Active TSS	Right Atrium	heart
45	chr13:52810200-52810400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr13:52810200-52810600	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr13:52810200-52810600	Active TSS	Brain Anterior Caudate	brain
48	chr13:52815000-52815400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:52815000-52815400	Enhancers	NHEK	skin
50	chr13:52849200-52849600	Active TSS	ES-I3 Cell Line	embryonic stem cell

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