Variant report

Variant	esv1851738
Chromosome Location	chr13:50474326-50507944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:123)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50479469-50479610	K562	blood:	n/a	n/a
2	BACH1	chr13:50478779-50478905	K562	blood:	n/a	n/a
3	CEBPB	chr13:50481808-50481917	HepG2	liver:	n/a	chr13:50481879-50481890
4	CEBPB	chr13:50481694-50482068	Hela-S3	cervix:	n/a	chr13:50481879-50481890
5	CEBPB	chr13:50481615-50482084	A549	lung:	n/a	chr13:50481879-50481890
6	CEBPB	chr13:50481706-50482074	IMR90	lung:	n/a	chr13:50481879-50481890
7	CEBPB	chr13:50481723-50482020	MCF-7	breast:	n/a	chr13:50481879-50481890
8	CEBPB	chr13:50479556-50479624	K562	blood:	n/a	n/a
9	CEBPB	chr13:50501993-50502358	IMR90	lung:	n/a	n/a
10	CEBPB	chr13:50477757-50477909	HepG2	liver:	n/a	chr13:50477853-50477866
11	CEBPB	chr13:50481766-50482036	A549	lung:	n/a	chr13:50481879-50481890
12	CEBPB	chr13:50477735-50477865	K562	blood:	n/a	n/a
13	CEBPB	chr13:50481640-50482023	HCT-116	colon:	n/a	chr13:50481879-50481890
14	CEBPB	chr13:50481783-50481923	K562	blood:	n/a	chr13:50481879-50481890
15	CEBPB	chr13:50481717-50482046	A549	lung:	n/a	chr13:50481879-50481890
16	CEBPB	chr13:50506251-50506514	IMR90	lung:	n/a	n/a
17	CREB1	chr13:50500147-50500499	GM12878	blood:	n/a	n/a
18	CTCF	chr13:50482900-50483050	HCT-116	colon:	n/a	n/a
19	CTCF	chr13:50482860-50483010	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr13:50482880-50483030	GM12873	blood:	n/a	n/a
21	CTCF	chr13:50482968-50483049	GM19239	blood:	n/a	n/a
22	CTCF	chr13:50482907-50482997	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr13:50482900-50483050	GM12872	blood:	n/a	n/a
24	CTCF	chr13:50482880-50483069	K562	blood:	n/a	n/a
25	CTCF	chr13:50482940-50483090	GM06990	blood:	n/a	n/a
26	CTCF	chr13:50482887-50483087	GM12878	blood:	n/a	n/a
27	CTCF	chr13:50482860-50483010	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr13:50482900-50483050	HAc	cerebellar:	n/a	n/a
29	CTCF	chr13:50490280-50490430	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr13:50482860-50483010	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr13:50482860-50483010	A549	lung:	n/a	n/a
32	CTCF	chr13:50482920-50483070	HEK293	kidney:	n/a	n/a
33	CTCF	chr13:50482890-50483071	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr13:50482840-50482990	GM12873	blood:	n/a	n/a
35	CTCF	chr13:50482860-50483010	HRE	kidney:	n/a	n/a
36	CTCF	chr13:50482800-50482950	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr13:50482885-50483093	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:50482783-50483198	HCT-116	colon:	n/a	n/a
39	CTCF	chr13:50482754-50483213	MCF-7	breast:	n/a	n/a
40	CTCF	chr13:50482860-50483010	HepG2	liver:	n/a	n/a
41	CTCF	chr13:50483026-50483103	GM13976	blood:	n/a	n/a
42	CTCF	chr13:50482926-50483094	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr13:50482948-50483034	NHEK	skin:	n/a	n/a
44	CTCF	chr13:50482904-50483094	MCF-7	breast:	n/a	n/a
45	CTCF	chr13:50482917-50483015	HepG2	liver:	n/a	n/a
46	CTCF	chr13:50482714-50483153	MCF-7	breast:	n/a	n/a
47	CTCF	chr13:50482932-50483085	Gliobla	brain:	n/a	n/a
48	CTCF	chr13:50482840-50482990	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr13:50482860-50483010	K562	blood:	n/a	n/a
50	CTCF	chr13:50482880-50483030	BE2_C	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50487953-50488003	NT2-D1	testis:	n/a
2	chr13:50487953-50488003	NT2-D1	testis:	n/a
3	chr13:50487953-50488003	NH-A	brain:	n/a
4	chr13:50507883-50507933	HRPEpiC	eye:	n/a
5	chr13:50507883-50507933	HepG2	liver:	n/a
6	chr13:50487953-50488003	HRE	kidney:	n/a
7	chr13:50507883-50507933	K562	blood:	n/a
8	chr13:50507883-50507933	NHDF-neo	bronchial:	n/a
9	chr13:50507883-50507933	PFSK-1	brain:	n/a
10	chr13:50507883-50507933	IMR90	lung:	fetal
11	chr13:50507883-50507933	GM12878	blood:	n/a
12	chr13:50487953-50488003	HEK293	kidney:	embryo
13	chr13:50507883-50507933	ECC-1	luminal epithelium:	n/a
14	chr13:50487953-50488003	HL-60	blood:	n/a
15	chr13:50507883-50507933	GM12891	blood:	n/a
16	chr13:50487953-50488003	HRCEpiC	kidney:	n/a
17	chr13:50487953-50488003	PrEC	prostate:	n/a
18	chr13:50507883-50507933	AG04450	lung:	fetal
19	chr13:50507883-50507933	HMEC	breast:	n/a
20	chr13:50507883-50507933	AG04449	skin:	fetal
21	chr13:50487953-50488003	GM12891	blood:	n/a
22	chr13:50487953-50488003	NHDF-neo	bronchial:	n/a
23	chr13:50507883-50507933	GM12892	blood:	n/a
24	chr13:50507883-50507933	GM06990	blood:	n/a
25	chr13:50507883-50507933	HCM	heart:	n/a
26	chr13:50507883-50507933	HAEpiC	amniotic membrane:	n/a
27	chr13:50507883-50507933	HCPEpiC	choroid plexus:	n/a
28	chr13:50507883-50507933	HUVEC	blood vessel:	n/a
29	chr13:50487953-50488003	Caco-2	colon:	n/a
30	chr13:50487953-50488003	H1-hESC	embryonic stem cell:	embryo
31	chr13:50507883-50507933	AoSMC	blood vessel:	n/a
32	chr13:50487953-50488003	HCF	heart:	n/a
33	chr13:50487953-50488003	SK-N-MC	brain:	n/a
34	chr13:50487953-50488003	NHBE	bronchial:	n/a
35	chr13:50487953-50488003	HRPEpiC	eye:	n/a
36	chr13:50507883-50507933	Jurkat	blood:	n/a
37	chr13:50487953-50488003	MCF10A-Er-Src	breast:	n/a
38	chr13:50487953-50488003	MCF-7	breast:	n/a
39	chr13:50507883-50507933	HEK293	kidney:	embryo
40	chr13:50507883-50507933	Hela-S3	cervix:	n/a
41	chr13:50487953-50488003	SK-N-SH	brain:	n/a
42	chr13:50487953-50488003	PANC-1	pancreas:	n/a
43	chr13:50507883-50507933	SKMC	muscle:	n/a
44	chr13:50507883-50507933	ovcar-3	ovarian:	n/a
45	chr13:50487953-50488003	U87	brain:	n/a
46	chr13:50507883-50507933	A549	lung:	n/a
47	chr13:50487953-50488003	CMK	blood:	n/a
48	chr13:50507883-50507933	HRCEpiC	kidney:	n/a
49	chr13:50487953-50488003	HIPEpiC	eye:	n/a
50	chr13:50507883-50507933	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50495816..50497958-chr13:50500274..50502867,2	K562	blood:
2	chr13:50507293..50510312-chr13:50568081..50571220,3	MCF-7	breast:
3	chr13:50495816..50497958-chr13:50500274..50502867,2	K562	blood:
4	chr13:50494914..50497363-chr13:50507125..50509301,2	MCF-7	breast:
5	chr13:50486918..50489140-chr13:50503061..50505201,2	K562	blood:
6	chr13:50494914..50497363-chr13:50507125..50509301,2	MCF-7	breast:
7	chr13:50504120..50506142-chr19:54703000..54704992,2	K562	blood:
8	chr13:50472956..50475084-chr13:50475360..50476987,2	MCF-7	breast:
9	chr13:50474382..50476998-chr13:50509261..50512069,3	MCF-7	breast:
10	chr13:50472956..50475084-chr13:50475360..50476987,2	MCF-7	breast:
11	chr13:50505920..50507836-chr13:50548605..50550830,2	K562	blood:
12	chr13:50486918..50489140-chr13:50503061..50505201,2	K562	blood:
13	chr13:50503267..50506681-chr13:50507802..50511782,3	K562	blood:
14	chr13:50503635..50507616-chr13:50508303..50511854,6	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRYD7-3	chr13:50479127-50479278	NONHSAT033764
2	lnc-SPRYD7-3	chr13:50476390-50476491	NONHSAT033764
3	lnc-SPRYD7-3	chr13:50479931-50479997	NONHSAT033764
4	lnc-SPRYD7-3	chr13:50478837-50479046	NONHSAT033764

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C13orf1	hsa-let-7b-5p	chr13:50487339-50487361
2	C13orf1	hsa-let-7b-5p	chr13:50486965-50486985

Variant related genes	Relation type
RNY4P9	TF binding region
RNY4P9	CpG island
ENSG00000264864	chromatin interactions
ENSG00000204977	chromatin interactions
ENSG00000170889	chromatin interactions
ENSG00000123178	chromatin interactions
ENSG00000223660	chromatin interactions

Extended variants
information (count: 1188 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:1188 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9562939	chr13:50474326-50474327	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560356286	chr13:50474327-50474328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376538807	chr13:50474348-50474349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139869404	chr13:50474349-50474350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568804290	chr13:50474364-50474365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs57911688	chr13:50474366-50474367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527509469	chr13:50474434-50474435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540517471	chr13:50474435-50474436	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561207991	chr13:50474449-50474450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531639608	chr13:50474450-50474451	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs150760757	chr13:50474454-50474455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112821631	chr13:50474469-50474470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571236239	chr13:50474471-50474472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374398708	chr13:50474497-50474498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538227705	chr13:50474505-50474506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547495368	chr13:50474509-50474510	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565621596	chr13:50474510-50474511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560411211	chr13:50474514-50474515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs529931372	chr13:50474516-50474517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534161172	chr13:50474551-50474552	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs377181578	chr13:50474559-50474560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573851013	chr13:50474571-50474572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538160666	chr13:50474585-50474586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs529066233	chr13:50474591-50474592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556408391	chr13:50474592-50474593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577989519	chr13:50474595-50474596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545053277	chr13:50474601-50474602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560671478	chr13:50474615-50474616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572440332	chr13:50474621-50474622	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542892313	chr13:50474627-50474628	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561071308	chr13:50474628-50474629	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531498788	chr13:50474652-50474653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs200221277	chr13:50474684-50474685	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs142609136	chr13:50474692-50474693	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs78199720	chr13:50474704-50474705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75028415	chr13:50474711-50474712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187185348	chr13:50474722-50474723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190463851	chr13:50474723-50474724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200635572	chr13:50474727-50474728	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547842576	chr13:50474745-50474746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201975955	chr13:50474746-50474747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200177674	chr13:50474750-50474751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201479283	chr13:50474751-50474752	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs59514064	chr13:50474863-50474864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs57104849	chr13:50474867-50474868	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs56279204	chr13:50474880-50474881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs57307396	chr13:50474882-50474883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs55750930	chr13:50474899-50474900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs59216997	chr13:50474905-50474906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539066890	chr13:50474906-50474907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:124)

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	17899364	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
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	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
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	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
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	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
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50468600-50486000	Weak transcription	Liver	Liver
2	chr13:50473000-50476600	Weak transcription	HepG2	liver
3	chr13:50476400-50497400	Weak transcription	Pancreas	Pancrea
4	chr13:50476600-50477000	Enhancers	HepG2	liver
5	chr13:50477000-50479000	Weak transcription	HepG2	liver
6	chr13:50477800-50499600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr13:50478000-50487200	Weak transcription	Ovary	ovary
8	chr13:50478000-50495200	Weak transcription	Brain Hippocampus Middle	brain
9	chr13:50478600-50491400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:50479000-50479200	Enhancers	HepG2	liver
11	chr13:50479000-50479400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:50479000-50479400	Enhancers	Esophagus	oesophagus
13	chr13:50479200-50479600	Enhancers	K562	blood
14	chr13:50479200-50489600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr13:50479400-50482200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr13:50479400-50490600	Weak transcription	Esophagus	oesophagus
17	chr13:50479600-50508600	Weak transcription	K562	blood
18	chr13:50479800-50500000	Weak transcription	Colon Smooth Muscle	Colon
19	chr13:50480800-50508800	Weak transcription	Fetal Brain Male	brain
20	chr13:50481200-50482800	Enhancers	Placenta	Placenta
21	chr13:50481400-50482200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:50481400-50486200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr13:50481400-50489600	Weak transcription	Fetal Intestine Large	intestine
24	chr13:50481800-50482000	Enhancers	A549	lung
25	chr13:50481800-50482600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr13:50481800-50509600	Weak transcription	Right Ventricle	heart
27	chr13:50482000-50482200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr13:50482000-50482200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:50482000-50482400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr13:50482000-50482400	Enhancers	HMEC	breast
31	chr13:50482000-50488000	Weak transcription	A549	lung
32	chr13:50482200-50482800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:50482200-50486000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr13:50482200-50486000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr13:50482200-50486200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr13:50482200-50486200	Weak transcription	Osteobl	bone
37	chr13:50482200-50488000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr13:50482200-50490400	Weak transcription	Fetal Muscle Leg	muscle
39	chr13:50482400-50486000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr13:50482400-50486000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr13:50482400-50488000	Weak transcription	HMEC	breast
42	chr13:50482400-50489600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr13:50482600-50486000	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr13:50482600-50488000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr13:50482600-50490200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr13:50482600-50490400	Weak transcription	NHLF	lung
47	chr13:50482600-50509600	Weak transcription	Primary B cells from cord blood	blood
48	chr13:50482800-50485800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:50482800-50488000	Weak transcription	Placenta	Placenta
50	chr13:50483000-50492200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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