Variant report

Variant	nsv976274
Chromosome Location	chr13:49655803-49666815
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	ATF2	chr13:49657161-49657765	GM12878	blood:	n/a	n/a
2	ATF2	chr13:49657138-49657805	GM12878	blood:	n/a	n/a
3	BATF	chr13:49657129-49657717	GM12878	blood:	n/a	n/a
4	BATF	chr13:49659061-49659431	GM12878	blood:	n/a	n/a
5	BATF	chr13:49657351-49657609	GM12878	blood:	n/a	n/a
6	BATF	chr13:49662541-49662765	GM12878	blood:	n/a	n/a
7	BCL11A	chr13:49657242-49657727	GM12878	blood:	n/a	n/a
8	BCL3	chr13:49657285-49657665	GM12878	blood:	n/a	n/a
9	BCLAF1	chr13:49657003-49657708	GM12878	blood:	n/a	n/a
10	BCLAF1	chr13:49657192-49657679	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:49659212-49659305	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:49657369-49657608	GM12878	blood:	n/a	n/a
13	CEBPB	chr13:49656956-49657096	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:49661077-49661222	K562	blood:	n/a	chr13:49661102-49661111
15	CEBPB	chr13:49660869-49661351	HCT-116	colon:	n/a	chr13:49661102-49661111
16	CEBPB	chr13:49660885-49661233	A549	lung:	n/a	chr13:49661102-49661111
17	CEBPB	chr13:49656899-49657114	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr13:49660929-49661263	A549	lung:	n/a	chr13:49661102-49661111
19	CEBPB	chr13:49660910-49661295	Hela-S3	cervix:	n/a	chr13:49661102-49661111
20	CEBPB	chr13:49660912-49661284	IMR90	lung:	n/a	chr13:49661102-49661111
21	CEBPB	chr13:49656812-49657214	IMR90	lung:	n/a	n/a
22	CEBPB	chr13:49663159-49663354	IMR90	lung:	n/a	n/a
23	CEBPB	chr13:49657149-49657786	GM12878	blood:	n/a	n/a
24	CEBPB	chr13:49656861-49657106	A549	lung:	n/a	n/a
25	CEBPB	chr13:49660831-49661405	HCT-116	colon:	n/a	chr13:49661102-49661111
26	CHD2	chr13:49657169-49657721	GM12878	blood:	n/a	n/a
27	CTCF	chr13:49658940-49659090	GM12875	blood:	n/a	n/a
28	CTCF	chr13:49658960-49659110	GM12873	blood:	n/a	n/a
29	CTCF	chr13:49658760-49658910	GM06990	blood:	n/a	n/a
30	CTCF	chr13:49658980-49659130	AG10803	skin:	n/a	n/a
31	CTCF	chr13:49657547-49657549	GM12878	blood:	n/a	n/a
32	CTCF	chr13:49656880-49657030	NHEK	skin:	n/a	n/a
33	CTCF	chr13:49658880-49659030	HepG2	liver:	n/a	n/a
34	CUX1	chr13:49657237-49657540	GM12878	blood:	n/a	n/a
35	E2F4	chr13:49656786-49657065	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr13:49660843-49661341	MCF10A-Er-Src	breast:	n/a	n/a
37	EBF1	chr13:49657497-49657602	GM12878	blood:	n/a	n/a
38	ELK1	chr13:49657647-49657650	GM12878	blood:	n/a	n/a
39	EP300	chr13:49657164-49657693	GM12878	blood:	n/a	chr13:49657303-49657312
40	EP300	chr13:49660739-49661379	SK-N-SH	brain:	n/a	chr13:49661004-49661013
41	EP300	chr13:49657271-49657731	GM12878	blood:	n/a	chr13:49657303-49657312
42	EP300	chr13:49660883-49661180	SK-N-SH_RA	brain:	n/a	chr13:49661004-49661013
43	EP300	chr13:49657130-49657736	GM12878	blood:	n/a	chr13:49657303-49657312
44	EP300	chr13:49660705-49661406	SK-N-SH	brain:	n/a	chr13:49661382-49661391 chr13:49661004-49661013
45	EP300	chr13:49660905-49661218	SK-N-SH_RA	brain:	n/a	chr13:49661004-49661013
46	FOS	chr13:49657452-49657628	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr13:49660822-49661277	MCF10A-Er-Src	breast:	n/a	chr13:49661003-49661014 chr13:49661006-49661013 chr13:49661005-49661013 chr13:49661004-49661014
48	FOS	chr13:49656722-49657186	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr13:49656757-49657568	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr13:49656756-49657199	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:49638488..49641005-chr13:49654158..49656722,2	K562	blood:
2	chr13:49657055..49658682-chr13:49662572..49665462,2	MCF-7	breast:
3	chr13:49549529..49551263-chr13:49654719..49657031,2	MCF-7	breast:
4	chr13:49657055..49658682-chr13:49662572..49665462,2	MCF-7	breast:
5	chr13:49649325..49651270-chr13:49659429..49661263,2	K562	blood:
6	chr13:49666571..49669149-chr13:49679481..49681834,2	K562	blood:
7	chr13:49656046..49658921-chr13:49658986..49660902,2	K562	blood:
8	chr13:49660417..49663395-chr13:49676657..49679527,2	MCF-7	breast:
9	chr13:49656046..49658921-chr13:49658986..49660902,2	K562	blood:

Variant related genes	Relation type
RNY3P2	TF binding region
ENSG00000102531	chromatin interactions

Extended variants
information (count: 367 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184952873	chr13:49655821-49655822	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs546037279	chr13:49655853-49655854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs117746234	chr13:49655864-49655865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs573237222	chr13:49655866-49655867	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs369793291	chr13:49655937-49655938	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561959248	chr13:49655940-49655941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11620317	chr13:49655941-49655942	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574029981	chr13:49655944-49655945	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544557317	chr13:49655974-49655975	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564579944	chr13:49655975-49655976	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544386297	chr13:49656018-49656019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189479213	chr13:49656028-49656029	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs180992548	chr13:49656042-49656043	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551628623	chr13:49656044-49656045	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146255153	chr13:49656079-49656080	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11332071	chr13:49656105-49656106	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564722842	chr13:49656106-49656107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs79587094	chr13:49656117-49656118	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs398022708	chr13:49656119-49656120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs369614852	chr13:49656128-49656129	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs371679298	chr13:49656129-49656130	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs553544521	chr13:49656135-49656136	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527606312	chr13:49656155-49656156	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541390998	chr13:49656187-49656188	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs548918001	chr13:49656197-49656198	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372330613	chr13:49656235-49656236	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537888797	chr13:49656242-49656243	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs549462997	chr13:49656296-49656297	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs148458303	chr13:49656297-49656298	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539633316	chr13:49656299-49656300	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557948053	chr13:49656328-49656329	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573169867	chr13:49656361-49656362	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534225450	chr13:49656390-49656391	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185275806	chr13:49656391-49656392	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555691838	chr13:49656415-49656416	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573940278	chr13:49656431-49656432	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564292808	chr13:49656447-49656448	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189626493	chr13:49656481-49656482	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs181924265	chr13:49656511-49656512	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs58426224	chr13:49656528-49656529	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs114690230	chr13:49656541-49656542	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142591872	chr13:49656578-49656579	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs527540237	chr13:49656589-49656590	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546307208	chr13:49656677-49656678	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548998555	chr13:49656679-49656680	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561649627	chr13:49656722-49656723	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530202156	chr13:49656869-49656870	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs561284279	chr13:49656927-49656928	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550361542	chr13:49656963-49656964	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs187004749	chr13:49657017-49657018	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Chronic lymphocytic leukemia	21670202	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
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
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49582200-49659000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr13:49601800-49660600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:49608800-49658800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr13:49627200-49656800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:49627400-49656800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:49627400-49672400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr13:49628600-49656600	Weak transcription	Thymus	Thymus
8	chr13:49628800-49657000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr13:49629000-49665600	Weak transcription	Lung	lung
10	chr13:49629600-49665400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr13:49630200-49656800	Weak transcription	Aorta	Aorta
12	chr13:49630400-49664000	Weak transcription	Fetal Intestine Small	intestine
13	chr13:49632200-49664800	Weak transcription	Fetal Lung	lung
14	chr13:49635000-49664400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr13:49636800-49667800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr13:49637800-49656200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr13:49638800-49656400	Weak transcription	HMEC	breast
18	chr13:49639000-49656400	Weak transcription	NHEK	skin
19	chr13:49639600-49656800	Weak transcription	Gastric	stomach
20	chr13:49639600-49656800	Weak transcription	Ovary	ovary
21	chr13:49639600-49687200	Weak transcription	Pancreas	Pancrea
22	chr13:49640600-49683800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr13:49641200-49663200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr13:49641800-49671600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr13:49643800-49657000	Weak transcription	HSMM	muscle
26	chr13:49645000-49671000	Weak transcription	Small Intestine	intestine
27	chr13:49646400-49660800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr13:49647600-49656200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr13:49648600-49656600	Weak transcription	HSMMtube	muscle
30	chr13:49648800-49659000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr13:49649000-49658600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr13:49649400-49684200	Weak transcription	Right Ventricle	heart
33	chr13:49649600-49656400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr13:49649600-49656800	Weak transcription	NHLF	lung
35	chr13:49649600-49660400	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr13:49649800-49657000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:49649800-49657000	Weak transcription	K562	blood
38	chr13:49649800-49671600	Weak transcription	Brain Hippocampus Middle	brain
39	chr13:49650200-49658000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr13:49650400-49658600	Weak transcription	Colon Smooth Muscle	Colon
41	chr13:49650800-49656600	Weak transcription	NHDF-Ad	bronchial
42	chr13:49651200-49656600	Weak transcription	Primary B cells from cord blood	blood
43	chr13:49651200-49658400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr13:49651400-49656600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr13:49651400-49656600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr13:49651400-49656600	Weak transcription	Left Ventricle	heart
47	chr13:49651400-49656800	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr13:49651400-49656800	Weak transcription	Hela-S3	cervix
49	chr13:49651400-49657000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr13:49651400-49660600	Weak transcription	Adipose Nuclei	Adipose

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