Variant report

Variant	esv3492939
Chromosome Location	chr13:52597220-52599545
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	chr13:52599427-52600756	HepG2	liver:	n/a	n/a
2	CEBPB	chr13:52599470-52600243	HepG2	liver:	n/a	chr13:52599729-52599740 chr13:52599729-52599742
3	CEBPB	chr13:52599505-52600244	HepG2	liver:	n/a	chr13:52599729-52599740 chr13:52599729-52599742
4	CEBPB	chr13:52599526-52600304	HepG2	liver:	n/a	chr13:52599729-52599740 chr13:52599729-52599742
5	CEBPD	chr13:52599545-52599839	HepG2	liver:	n/a	n/a
6	CHD2	chr13:52599491-52600293	HepG2	liver:	n/a	n/a
7	CREB1	chr13:52599377-52600850	HepG2	liver:	n/a	n/a
8	EP300	chr13:52598750-52598751	GM12878	blood:	n/a	n/a
9	EP300	chr13:52599457-52600126	HepG2	liver:	n/a	chr13:52599730-52599744 chr13:52599780-52599790
10	EP300	chr13:52599298-52600362	HepG2	liver:	n/a	chr13:52599730-52599744 chr13:52599780-52599790
11	FOS	chr13:52598847-52598871	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr13:52598752-52598944	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr13:52598597-52598933	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr13:52598677-52599031	MCF10A-Er-Src	breast:	n/a	n/a
15	FOXA1	chr13:52599326-52600301	HepG2	liver:	n/a	chr13:52599775-52599790
16	FOXA1	chr13:52599391-52600250	HepG2	liver:	n/a	chr13:52599775-52599790
17	FOXA1	chr13:52599345-52600283	HepG2	liver:	n/a	chr13:52599775-52599790
18	FOXA1	chr13:52599372-52600154	HepG2	liver:	n/a	chr13:52599775-52599790
19	FOXA2	chr13:52599406-52600303	HepG2	liver:	n/a	n/a
20	FOXA2	chr13:52598270-52598482	HepG2	liver:	n/a	n/a
21	FOXA2	chr13:52598898-52600440	HepG2	liver:	n/a	n/a
22	GATA1	chr13:52596306-52597265	PBDE	blood:	n/a	n/a
23	HDAC2	chr13:52599338-52600264	HepG2	liver:	n/a	n/a
24	HDAC2	chr13:52599437-52600171	HepG2	liver:	n/a	n/a
25	HNF4A	chr13:52599517-52600455	HepG2	liver:	n/a	chr13:52599760-52599778 chr13:52599761-52599776 chr13:52599763-52599775 chr13:52599763-52599775
26	HNF4A	chr13:52599506-52600171	HepG2	liver:	n/a	chr13:52599760-52599778 chr13:52599761-52599776 chr13:52599763-52599775 chr13:52599763-52599775
27	HNF4A	chr13:52599460-52599939	HepG2	liver:	n/a	chr13:52599760-52599778 chr13:52599761-52599776 chr13:52599763-52599775 chr13:52599763-52599775
28	HNF4G	chr13:52599490-52600158	HepG2	liver:	n/a	chr13:52599760-52599778 chr13:52599763-52599775 chr13:52599763-52599775
29	HNF4G	chr13:52599498-52600075	HepG2	liver:	n/a	chr13:52599760-52599778 chr13:52599763-52599775 chr13:52599763-52599775
30	JUN	chr13:52599388-52600042	HepG2	liver:	n/a	chr13:52599730-52599743
31	JUND	chr13:52599534-52600511	HepG2	liver:	n/a	n/a
32	MAX	chr13:52599431-52600920	HepG2	liver:	n/a	chr13:52599732-52599741
33	MBD4	chr13:52599456-52600333	HepG2	liver:	n/a	n/a
34	MBD4	chr13:52599342-52600271	HepG2	liver:	n/a	n/a
35	MXI1	chr13:52599534-52600316	HepG2	liver:	n/a	n/a
36	MYBL2	chr13:52599264-52600394	HepG2	liver:	n/a	n/a
37	MYBL2	chr13:52599310-52600196	HepG2	liver:	n/a	n/a
38	NFIC	chr13:52599417-52600168	HepG2	liver:	n/a	n/a
39	NFIC	chr13:52599426-52600259	HepG2	liver:	n/a	n/a
40	NR2F2	chr13:52599352-52600307	HepG2	liver:	n/a	n/a
41	NR2F2	chr13:52599305-52600863	HepG2	liver:	n/a	n/a
42	POLR2A	chr13:52598004-52598053	HepG2	liver:	n/a	n/a
43	POLR2A	chr13:52598326-52600935	K562	blood:	n/a	n/a
44	POLR2A	chr13:52598659-52599155	HepG2	liver:	n/a	n/a
45	POLR2A	chr13:52597543-52597679	HepG2	liver:	n/a	n/a
46	RAD21	chr13:52599503-52600344	HepG2	liver:	n/a	chr13:52600174-52600193
47	RXRA	chr13:52599488-52600149	HepG2	liver:	n/a	n/a
48	SP1	chr13:52599408-52600192	HepG2	liver:	n/a	n/a
49	STAT3	chr13:52598438-52598720	MCF10A-Er-Src	breast:	n/a	n/a
50	TEAD4	chr13:52599086-52600742	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52598798-52598848	HEEpiC	esophagus:	n/a
2	chr13:52598798-52598848	HEEpiC	esophagus:	n/a
3	chr13:52598175-52598225	Hepatocyte	liver:	n/a
4	chr13:52598902-52598952	CMK	blood:	n/a
5	chr13:52598408-52598458	SKMC	muscle:	n/a
6	chr13:52598902-52598952	NHBE	bronchial:	n/a
7	chr13:52598408-52598458	SK-N-SH	brain:	n/a
8	chr13:52598798-52598848	HEK293	kidney:	embryo
9	chr13:52598798-52598848	U87	brain:	n/a
10	chr13:52598798-52598848	GM19239	blood:	n/a
11	chr13:52598408-52598458	U87	brain:	n/a
12	chr13:52598175-52598225	PANC-1	pancreas:	n/a
13	chr13:52598902-52598952	SK-N-MC	brain:	n/a
14	chr13:52598902-52598952	LNCaP	prostate:	n/a
15	chr13:52598408-52598458	AG10803	skin:	n/a
16	chr13:52598408-52598458	K562	blood:	n/a
17	chr13:52598408-52598458	HRE	kidney:	n/a
18	chr13:52598408-52598458	BJ	skin:	n/a
19	chr13:52598798-52598848	Hela-S3	cervix:	n/a
20	chr13:52598175-52598225	HCPEpiC	choroid plexus:	n/a
21	chr13:52598798-52598848	BJ	skin:	n/a
22	chr13:52598175-52598225	HL-60	blood:	n/a
23	chr13:52598798-52598848	HRPEpiC	eye:	n/a
24	chr13:52598798-52598848	BE2_C	brain:	n/a
25	chr13:52598798-52598848	Hepatocyte	liver:	n/a
26	chr13:52598175-52598225	RPTEC	kidney:	n/a
27	chr13:52598798-52598848	T-47D	breast:	n/a
28	chr13:52598408-52598458	H1-hESC	embryonic stem cell:	embryo
29	chr13:52598408-52598458	Hepatocyte	liver:	n/a
30	chr13:52598902-52598952	Hela-S3	cervix:	n/a
31	chr13:52598902-52598952	AG09309	skin:	n/a
32	chr13:52598408-52598458	ovcar-3	ovarian:	n/a
33	chr13:52598175-52598225	HepG2	liver:	n/a
34	chr13:52598902-52598952	Hepatocyte	liver:	n/a
35	chr13:52598175-52598225	PrEC	prostate:	n/a
36	chr13:52598798-52598848	HRCEpiC	kidney:	n/a
37	chr13:52598902-52598952	HEEpiC	esophagus:	n/a
38	chr13:52598902-52598952	T-47D	breast:	n/a
39	chr13:52598408-52598458	ECC-1	luminal epithelium:	n/a
40	chr13:52598798-52598848	HCT-116	colon:	n/a
41	chr13:52598175-52598225	HIPEpiC	eye:	n/a
42	chr13:52598902-52598952	Caco-2	colon:	n/a
43	chr13:52598175-52598225	GM12878	blood:	n/a
44	chr13:52598902-52598952	BJ	skin:	n/a
45	chr13:52598798-52598848	ovcar-3	ovarian:	n/a
46	chr13:52598798-52598848	GM06990	blood:	n/a
47	chr13:52598408-52598458	Caco-2	colon:	n/a
48	chr13:52598408-52598458	HCT-116	colon:	n/a
49	chr13:52598408-52598458	HCPEpiC	choroid plexus:	n/a
50	chr13:52598175-52598225	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:52570761..52572532-chr13:52599540..52601096,2	K562	blood:
2	chr13:52596842..52598775-chr13:52613940..52616833,2	K562	blood:
3	chr13:52585087..52587899-chr13:52598320..52601537,3	MCF-7	breast:
4	chr13:52584551..52590049-chr13:52591418..52597330,6	K562	blood:
5	chr13:52592255..52594860-chr13:52597501..52600884,3	K562	blood:
6	chr13:52584543..52591722-chr13:52593134..52598355,11	K562	blood:

Variant related genes	Relation type
UTP14C	TF binding region
UTP14C	CpG island
ENSG00000253710	chromatin interactions
ENSG00000123191	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528464226	chr13:52597291-52597292	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs186952574	chr13:52597324-52597325	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs544036796	chr13:52597344-52597345	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs546708778	chr13:52597373-52597374	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs143351974	chr13:52597411-52597412	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531069754	chr13:52597594-52597595	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs368473635	chr13:52597626-52597627	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs191391712	chr13:52597650-52597651	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs564688181	chr13:52597658-52597659	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs147505359	chr13:52597678-52597679	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs539679566	chr13:52597683-52597684	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs139384473	chr13:52597687-52597688	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183711680	chr13:52597797-52597798	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187049208	chr13:52597799-52597800	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139964015	chr13:52597814-52597815	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs148964037	chr13:52597817-52597818	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs201037813	chr13:52597820-52597821	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201819653	chr13:52597821-52597822	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs80174229	chr13:52597826-52597827	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs201110418	chr13:52597832-52597833	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376057068	chr13:52597838-52597839	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574381172	chr13:52597843-52597844	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111881531	chr13:52597850-52597851	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs557330881	chr13:52597851-52597852	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs372643204	chr13:52597853-52597854	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs6561656	chr13:52597888-52597889	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs556678313	chr13:52597916-52597917	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112372712	chr13:52597927-52597928	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs376943099	chr13:52597928-52597929	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576927254	chr13:52597961-52597962	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573221442	chr13:52597978-52597979	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545681972	chr13:52597987-52597988	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs553202580	chr13:52598000-52598001	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369640424	chr13:52598016-52598017	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs530855133	chr13:52598034-52598035	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs544488061	chr13:52598059-52598060	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs564468615	chr13:52598078-52598079	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs533469509	chr13:52598085-52598086	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs546846944	chr13:52598088-52598089	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373497332	chr13:52598094-52598095	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs116901370	chr13:52598095-52598096	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs373209186	chr13:52598096-52598097	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs76231456	chr13:52598114-52598115	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs149690619	chr13:52598171-52598172	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs141164575	chr13:52598184-52598185	Strong transcription Weak transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs17480245	chr13:52598189-52598190	Strong transcription Weak transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs113000928	chr13:52598200-52598201	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs377575937	chr13:52598219-52598220	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs572298072	chr13:52598242-52598243	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs147971217	chr13:52598248-52598249	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52587000-52598200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:52587000-52598800	Weak transcription	Small Intestine	intestine
3	chr13:52587000-52600000	Weak transcription	Esophagus	oesophagus
4	chr13:52587200-52600000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr13:52587400-52598200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:52587400-52598200	Weak transcription	Right Ventricle	heart
7	chr13:52587400-52598400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr13:52587400-52598800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr13:52587400-52600000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr13:52587600-52598000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr13:52587600-52598000	Weak transcription	Fetal Kidney	kidney
12	chr13:52587600-52598400	Weak transcription	Brain Substantia Nigra	brain
13	chr13:52587600-52599400	Weak transcription	Stomach Mucosa	stomach
14	chr13:52587800-52598200	Weak transcription	Fetal Heart	heart
15	chr13:52588000-52598000	Weak transcription	Rectal Smooth Muscle	rectum
16	chr13:52588000-52609200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr13:52588000-52617400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr13:52588200-52598000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr13:52588200-52598200	Weak transcription	NHDF-Ad	bronchial
20	chr13:52588200-52602200	Weak transcription	Hela-S3	cervix
21	chr13:52589400-52605200	Strong transcription	Fetal Muscle Trunk	muscle
22	chr13:52589800-52603400	Strong transcription	Placenta	Placenta
23	chr13:52589800-52605400	Strong transcription	Fetal Thymus	thymus
24	chr13:52590000-52604400	Strong transcription	Primary T cells from cord blood	blood
25	chr13:52590200-52600400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr13:52590200-52603400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr13:52590400-52598800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:52590400-52599200	Strong transcription	Fetal Muscle Leg	muscle
29	chr13:52590400-52602000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr13:52590600-52601400	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr13:52590600-52604200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr13:52590800-52599000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr13:52591000-52599400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr13:52591000-52599400	Weak transcription	Pancreas	Pancrea
35	chr13:52591000-52599800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:52591000-52604600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr13:52591400-52598200	Weak transcription	Aorta	Aorta
38	chr13:52591600-52603400	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr13:52591600-52603400	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr13:52591600-52604000	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr13:52591800-52599400	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr13:52591800-52599800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr13:52591800-52603600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr13:52591800-52603800	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr13:52592000-52599800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr13:52592400-52598200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr13:52592400-52600000	Weak transcription	Gastric	stomach
48	chr13:52592600-52601000	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr13:52593000-52598600	Strong transcription	Liver	Liver
50	chr13:52593200-52598200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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