Variant report

Variant	nsv900576
Chromosome Location	chr13:76132484-76176680
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	chr13:76140823-76141209	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76140888-76140979	K562	blood:	n/a	n/a
3	ATF2	chr13:76161743-76162267	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr13:76161744-76162155	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:76152548-76152550	K562	blood:	n/a	n/a
6	BATF	chr13:76153753-76153938	GM12878	blood:	n/a	n/a
7	BATF	chr13:76153723-76153987	GM12878	blood:	n/a	n/a
8	BRCA1	chr13:76153639-76153677	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr13:76159335-76159585	K562	blood:	n/a	n/a
10	CBX3	chr13:76159288-76159637	K562	blood:	n/a	n/a
11	CEBPB	chr13:76140742-76141072	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:76161789-76162201	HepG2	liver:	n/a	n/a
13	CEBPB	chr13:76164903-76165196	HepG2	liver:	n/a	chr13:76165016-76165027
14	CEBPB	chr13:76133589-76133901	A549	lung:	n/a	n/a
15	CEBPB	chr13:76140781-76141013	K562	blood:	n/a	n/a
16	CEBPB	chr13:76140760-76141096	A549	lung:	n/a	n/a
17	CEBPB	chr13:76164885-76165156	K562	blood:	n/a	chr13:76165016-76165027
18	CEBPB	chr13:76133569-76133925	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:76133530-76133960	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:76161851-76162197	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr13:76140756-76141122	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr13:76133595-76133998	A549	lung:	n/a	n/a
23	CEBPB	chr13:76164922-76165193	IMR90	lung:	n/a	chr13:76165016-76165027
24	CEBPB	chr13:76140737-76141073	IMR90	lung:	n/a	n/a
25	CEBPB	chr13:76133555-76133921	HepG2	liver:	n/a	n/a
26	CHD2	chr13:76173934-76173966	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr13:76141020-76141170	MCF-7	breast:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
28	CTCF	chr13:76140980-76141130	AG10803	skin:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
29	CTCF	chr13:76140940-76141090	HFF	foreskin:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
30	CTCF	chr13:76140932-76141166	H1-hESC	embryonic stem cell:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
31	CTCF	chr13:76140860-76141010	MCF-7	breast:	n/a	n/a
32	CTCF	chr13:76140886-76141169	A549	lung:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
33	CTCF	chr13:76140980-76141130	AG09319	gingival:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
34	CTCF	chr13:76165775-76165828	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr13:76141120-76141270	NHEK	skin:	n/a	n/a
36	CTCF	chr13:76140980-76141130	AG04450	lung:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
37	CTCF	chr13:76140930-76141235	A549	lung:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
38	CTCF	chr13:76164111-76164206	ProgFib	skin:	n/a	n/a
39	CTCF	chr13:76140960-76141110	HL-60	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
40	CTCF	chr13:76140940-76141090	HBMEC	blood vessel:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
41	CTCF	chr13:76140980-76141130	RPTEC	kidney:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
42	CTCF	chr13:76160331-76160405	Lung_OC	lung:	n/a	n/a
43	CTCF	chr13:76140980-76141130	HPAF	blood vessel:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
44	CTCF	chr13:76140943-76141135	LNCaP	prostate:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
45	CTCF	chr13:76140920-76141070	HUVEC	blood vessel:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
46	CTCF	chr13:76140952-76141103	HepG2	liver:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
47	CTCF	chr13:76140923-76141153	Medullo	brain:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
48	CTCF	chr13:76140980-76141130	Caco-2	colon:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
49	CTCF	chr13:76140945-76141133	GM13977	blood:	n/a	chr13:76141046-76141067 chr13:76141044-76141062
50	CTCF	chr13:76141020-76141170	HMF	breast:	n/a	chr13:76141046-76141067 chr13:76141044-76141062

No.	Distal block	Cell Line	Cell type
1	chr13:76123286..76125327-chr13:76160450..76162067,2	K562	blood:
2	chr13:76160277..76161808-chr13:76162172..76164407,2	K562	blood:
3	chr13:76143405..76146053-chr13:76147700..76149492,2	K562	blood:
4	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
5	chr13:76124376..76126025-chr13:76132730..76134454,2	K562	blood:
6	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
7	chr13:76160277..76161808-chr13:76162172..76164407,2	K562	blood:
8	chr13:76153049..76155664-chr13:76161169..76162949,2	K562	blood:
9	chr13:76153049..76155664-chr13:76161169..76162949,2	K562	blood:
10	chr13:76141660..76144515-chr13:76144732..76146608,2	MCF-7	breast:
11	chr13:76143405..76146053-chr13:76147700..76149492,2	K562	blood:
12	chr13:76123475..76126296-chr13:76136199..76138617,2	MCF-7	breast:
13	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
14	chr13:76124076..76125593-chr13:76162284..76165016,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LMO7-2	chr13:76140968-76140987	ENSG00000261553.1
2	lnc-LMO7-2	chr13:76143596-76143643	ENSG00000261553.1
3	lnc-LMO7-2	chr13:76169051-76169126	ENSG00000261553.1
4	lnc-COMMD6-4	chr13:76161358-76161715	l_873_chr13:76072523-76201534_testes
5	lnc-COMMD6-4	chr13:76140115-76140230	l_873_chr13:76072523-76201534_testes
6	lnc-LMO7-2	chr13:76141363-76141448	ENSG00000261553.1

Variant related genes	Relation type
ENSG00000261553	TF binding region
UCHL3	TF binding region
ENSG00000118939	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000261553	chromatin interactions

Extended variants
information (count: 1554 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1554 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7319441	chr13:76132484-76132485	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568354364	chr13:76132555-76132556	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535849899	chr13:76132565-76132566	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550944938	chr13:76132583-76132584	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569228612	chr13:76132610-76132611	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369104383	chr13:76132625-76132626	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373627785	chr13:76132626-76132627	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146075577	chr13:76132666-76132667	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373998104	chr13:76132685-76132686	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138712100	chr13:76132686-76132687	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566647780	chr13:76132690-76132691	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149339495	chr13:76132696-76132697	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555481021	chr13:76132706-76132707	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573519320	chr13:76132753-76132754	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144840383	chr13:76132788-76132789	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4885311	chr13:76132843-76132844	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181454602	chr13:76132847-76132848	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545357929	chr13:76132893-76132894	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9573585	chr13:76132912-76132913	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560368188	chr13:76133000-76133001	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552274409	chr13:76133051-76133052	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117730948	chr13:76133081-76133082	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377111693	chr13:76133167-76133168	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34100020	chr13:76133182-76133183	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185989728	chr13:76133197-76133198	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547534721	chr13:76133214-76133215	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564260056	chr13:76133215-76133216	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573149133	chr13:76133234-76133235	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570530353	chr13:76133237-76133238	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371178269	chr13:76133256-76133257	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550965009	chr13:76133257-76133258	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568941444	chr13:76133261-76133262	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145569551	chr13:76133314-76133315	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556174116	chr13:76133342-76133343	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575260083	chr13:76133378-76133379	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551702126	chr13:76133409-76133410	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533192329	chr13:76133418-76133419	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9543975	chr13:76133419-76133420	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs555125331	chr13:76133465-76133466	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573702373	chr13:76133514-76133515	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529765541	chr13:76133543-76133544	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13378810	chr13:76133598-76133599	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs556110092	chr13:76133611-76133612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141254050	chr13:76133676-76133677	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115651477	chr13:76133813-76133814	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554130452	chr13:76133832-76133833	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183348122	chr13:76133859-76133860	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185801041	chr13:76133886-76133887	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114010115	chr13:76133910-76133911	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs8192741	chr13:76133923-76133924	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:95)

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
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
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	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
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1073 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76124600-76183000	Weak transcription	Small Intestine	intestine
2	chr13:76124800-76135200	Weak transcription	Pancreas	Pancrea
3	chr13:76124800-76146400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr13:76124800-76146600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr13:76124800-76146600	Weak transcription	Lung	lung
6	chr13:76124800-76147600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:76124800-76164000	Weak transcription	Spleen	Spleen
8	chr13:76124800-76167600	Weak transcription	Gastric	stomach
9	chr13:76124800-76170600	Weak transcription	Colonic Mucosa	Colon
10	chr13:76125000-76141400	Weak transcription	Fetal Lung	lung
11	chr13:76125000-76143400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr13:76125000-76147600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr13:76125000-76156200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr13:76125000-76158000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr13:76125000-76192800	Weak transcription	Brain Substantia Nigra	brain
16	chr13:76125000-76209600	Weak transcription	Right Ventricle	heart
17	chr13:76125200-76141000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr13:76125200-76147200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr13:76125200-76147200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr13:76125200-76147600	Weak transcription	Brain Angular Gyrus	brain
21	chr13:76125200-76173800	Weak transcription	Fetal Heart	heart
22	chr13:76125200-76177800	Weak transcription	Stomach Mucosa	stomach
23	chr13:76125400-76132800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr13:76125400-76136600	Weak transcription	Hela-S3	cervix
25	chr13:76125400-76138800	Weak transcription	Fetal Intestine Small	intestine
26	chr13:76125400-76143000	Weak transcription	Brain Hippocampus Middle	brain
27	chr13:76125400-76143000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr13:76125400-76143200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr13:76125400-76147000	Weak transcription	Brain Germinal Matrix	brain
30	chr13:76125400-76147600	Weak transcription	Brain Anterior Caudate	brain
31	chr13:76125400-76191000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr13:76125600-76158000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr13:76125600-76182000	Weak transcription	Fetal Brain Male	brain
34	chr13:76126400-76136800	Strong transcription	HSMM	muscle
35	chr13:76126600-76132600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr13:76126600-76140200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr13:76126800-76134800	Weak transcription	HepG2	liver
38	chr13:76128200-76143800	Weak transcription	NHLF	lung
39	chr13:76129200-76135000	Weak transcription	Psoas Muscle	Psoas
40	chr13:76129400-76133400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr13:76129400-76134800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr13:76129400-76134800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr13:76129400-76135000	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr13:76129400-76143800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr13:76129400-76145000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr13:76129400-76145800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr13:76129400-76147200	Weak transcription	Aorta	Aorta
48	chr13:76129400-76147200	Weak transcription	Left Ventricle	heart
49	chr13:76129400-76147600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr13:76129400-76151400	Weak transcription	Brain Inferior Temporal Lobe	brain

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