Variant report

Variant	esv3330095
Chromosome Location	chr13:96281000-96297421
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:1160)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:96296108-96296371	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr13:96297114-96297296	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPD	chr13:96296812-96297098	HepG2	liver:	n/a	n/a
4	CHD1	chr13:96296008-96296219	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr13:96295049-96295238	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr13:96297013-96297346	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr13:96294401-96294502	HepG2	liver:	n/a	n/a
8	CHD2	chr13:96296773-96297196	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr13:96296109-96296419	A549	lung:	n/a	n/a
10	CREB1	chr13:96296762-96297128	A549	lung:	n/a	n/a
11	CREB1	chr13:96296560-96297273	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr13:96295809-96296699	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr13:96296140-96296290	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr13:96294520-96294670	BJ	skin:	n/a	n/a
15	CTCF	chr13:96294220-96294370	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr13:96296840-96296990	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr13:96296813-96296848	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr13:96293580-96293730	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr13:96296740-96296890	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr13:96296238-96296311	Fibrobl	skin:	n/a	n/a
21	CTCF	chr13:96293760-96293910	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr13:96295980-96296130	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr13:96293380-96293530	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr13:96293620-96293770	AG09319	gingival:	n/a	n/a
25	CTCF	chr13:96293860-96294010	BJ	skin:	n/a	n/a
26	CTCF	chr13:96293881-96293886	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr13:96293660-96293810	BE2_C	brain:	n/a	n/a
28	CTCF	chr13:96294420-96294570	HCM	heart:	n/a	n/a
29	CTCF	chr13:96293620-96293770	BJ	skin:	n/a	n/a
30	CTCF	chr13:96294420-96294570	GM12865	blood:	n/a	n/a
31	CTCF	chr13:96294200-96294350	AG10803	skin:	n/a	n/a
32	CTCF	chr13:96293887-96293969	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr13:96296200-96296350	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr13:96293740-96293890	HCM	heart:	n/a	n/a
35	CTCF	chr13:96296240-96296390	AG04449	skin:	n/a	n/a
36	CTCF	chr13:96295980-96296130	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr13:96293620-96293770	HRE	kidney:	n/a	n/a
38	CTCF	chr13:96295860-96296010	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr13:96296800-96296950	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr13:96293860-96294010	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr13:96294480-96294630	HBMEC	blood vessel:	n/a	n/a
42	E2F4	chr13:96296009-96296023	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr13:96296877-96297218	MCF10A-Er-Src	breast:	n/a	chr13:96297046-96297055
44	E2F6	chr13:96293840-96294602	H1-hESC	embryonic stem cell:	n/a	n/a
45	E2F6	chr13:96295905-96296693	A549	lung:	n/a	chr13:96296158-96296167
46	E2F6	chr13:96295831-96297286	H1-hESC	embryonic stem cell:	n/a	chr13:96297046-96297055 chr13:96296158-96296167
47	E2F6	chr13:96296905-96297219	A549	lung:	n/a	chr13:96297046-96297055
48	E2F6	chr13:96296710-96297350	A549	lung:	n/a	chr13:96297046-96297055
49	E2F6	chr13:96296924-96297107	K562	blood:	n/a	chr13:96297046-96297055
50	E2F6	chr13:96293655-96294542	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96294131-96294181	A549	lung:	n/a
2	chr13:96294131-96294181	A549	lung:	n/a
3	chr13:96294131-96294181	HCT-116	colon:	n/a
4	chr13:96297197-96297247	GM12891	blood:	n/a
5	chr13:96296144-96296194	Hepatocyte	liver:	n/a
6	chr13:96294468-96294518	HRE	kidney:	n/a
7	chr13:96293572-96293622	HRE	kidney:	n/a
8	chr13:96297281-96297331	HUVEC	blood vessel:	n/a
9	chr13:96294468-96294518	HRCEpiC	kidney:	n/a
10	chr13:96296979-96297029	HCM	heart:	n/a
11	chr13:96296997-96297047	GM06990	blood:	n/a
12	chr13:96294131-96294181	HRPEpiC	eye:	n/a
13	chr13:96296983-96297033	HRE	kidney:	n/a
14	chr13:96294131-96294181	HNPCEpiC	eye:	n/a
15	chr13:96293572-96293622	GM06990	blood:	n/a
16	chr13:96294863-96294913	Caco-2	colon:	n/a
17	chr13:96297051-96297101	AG09319	gingival:	n/a
18	chr13:96296144-96296194	HNPCEpiC	eye:	n/a
19	chr13:96294131-96294181	AG10803	skin:	n/a
20	chr13:96296983-96297033	NB4	blood:	n/a
21	chr13:96294863-96294913	BJ	skin:	n/a
22	chr13:96293882-96293932	NHBE	bronchial:	n/a
23	chr13:96297053-96297103	Caco-2	colon:	n/a
24	chr13:96296844-96296894	SAEC	small airway:	n/a
25	chr13:96294468-96294518	HCM	heart:	n/a
26	chr13:96296708-96296758	AoSMC	blood vessel:	n/a
27	chr13:96296997-96297047	NHBE	bronchial:	n/a
28	chr13:96297338-96297388	NH-A	brain:	n/a
29	chr13:96297051-96297101	SK-N-MC	brain:	n/a
30	chr13:96296983-96297033	HCPEpiC	choroid plexus:	n/a
31	chr13:96294468-96294518	AG04450	lung:	fetal
32	chr13:96297224-96297274	GM19239	blood:	n/a
33	chr13:96296844-96296894	HRPEpiC	eye:	n/a
34	chr13:96294468-96294518	RPTEC	kidney:	n/a
35	chr13:96291582-96291632	HL-60	blood:	n/a
36	chr13:96296708-96296758	HRCEpiC	kidney:	n/a
37	chr13:96297197-96297247	IMR90	lung:	fetal
38	chr13:96296708-96296758	NH-A	brain:	n/a
39	chr13:96297224-96297274	RPTEC	kidney:	n/a
40	chr13:96296708-96296758	NHDF-neo	bronchial:	n/a
41	chr13:96297197-96297247	ProgFib	skin:	n/a
42	chr13:96296997-96297047	BE2_C	brain:	n/a
43	chr13:96296144-96296194	SAEC	small airway:	n/a
44	chr13:96294131-96294181	U87	brain:	n/a
45	chr13:96296983-96297033	HEK293	kidney:	embryo
46	chr13:96297058-96297108	Hepatocyte	liver:	n/a
47	chr13:96294863-96294913	SK-N-SH_RA	brain:	n/a
48	chr13:96293882-96293932	Caco-2	colon:	n/a
49	chr13:96296997-96297047	AG04449	skin:	fetal
50	chr13:96291582-96291632	HCM	heart:	n/a

No data

Variant related genes	Relation type
DZIP1	TF binding region
DZIP1	CpG island

Extended variants
information (count: 647 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532031184	chr13:96281031-96281032	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144156755	chr13:96281079-96281080	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188141918	chr13:96281081-96281082	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370390794	chr13:96281121-96281122	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574144757	chr13:96281122-96281123	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145045056	chr13:96281123-96281124	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149098488	chr13:96281264-96281265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541001121	chr13:96281267-96281268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111990359	chr13:96281299-96281300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113855461	chr13:96281334-96281335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548429672	chr13:96281362-96281363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552694789	chr13:96281417-96281418	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs375682298	chr13:96281435-96281436	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs371095089	chr13:96281453-96281454	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs568426260	chr13:96281526-96281527	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs78764051	chr13:96281571-96281572	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs568378795	chr13:96281573-96281574	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs148333505	chr13:96281603-96281604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547713775	chr13:96281642-96281643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34769361	chr13:96281653-96281654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570711236	chr13:96281660-96281661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539687614	chr13:96281685-96281686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12583161	chr13:96281696-96281697	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs141625152	chr13:96281718-96281719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535210748	chr13:96281745-96281746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570903492	chr13:96281751-96281752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555326080	chr13:96281829-96281830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192675597	chr13:96281835-96281836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147054351	chr13:96281865-96281866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555648058	chr13:96281898-96281899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541314695	chr13:96281909-96281910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184477035	chr13:96281984-96281985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187791075	chr13:96282008-96282009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114353261	chr13:96282022-96282023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377143312	chr13:96282075-96282076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563496244	chr13:96282083-96282084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531798594	chr13:96282096-96282097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541995510	chr13:96282110-96282111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562094632	chr13:96282152-96282153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4551888	chr13:96282199-96282200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192574737	chr13:96282225-96282226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs45564232	chr13:96282229-96282230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371040629	chr13:96282235-96282236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544403768	chr13:96282253-96282254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374150185	chr13:96282257-96282258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371734867	chr13:96282259-96282260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369405143	chr13:96282261-96282262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184350900	chr13:96282268-96282269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533465385	chr13:96282302-96282303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200033665	chr13:96282320-96282321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:922 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96235600-96284200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr13:96247800-96293600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:96251400-96294400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr13:96256400-96295200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr13:96256800-96294200	Weak transcription	Placenta	Placenta
6	chr13:96260200-96293400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr13:96261200-96288400	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr13:96263600-96290000	Weak transcription	Adipose Nuclei	Adipose
9	chr13:96265800-96293400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr13:96266400-96286000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr13:96267600-96293000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr13:96268400-96286400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr13:96268400-96291600	Strong transcription	Osteobl	bone
14	chr13:96268800-96281400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr13:96270200-96293400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr13:96271600-96284800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr13:96272400-96292000	Weak transcription	Colonic Mucosa	Colon
18	chr13:96272600-96284000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:96273000-96287400	Strong transcription	Fetal Lung	lung
20	chr13:96273400-96281400	Weak transcription	Brain Hippocampus Middle	brain
21	chr13:96273400-96284000	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr13:96273600-96293400	Weak transcription	Brain Substantia Nigra	brain
23	chr13:96273600-96293600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr13:96273600-96293600	Weak transcription	Left Ventricle	heart
25	chr13:96273800-96293600	Weak transcription	Gastric	stomach
26	chr13:96273800-96293600	Weak transcription	Pancreas	Pancrea
27	chr13:96274000-96281400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:96275800-96281000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr13:96275800-96281200	Weak transcription	HSMMtube	muscle
30	chr13:96276800-96281400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr13:96276800-96286800	Weak transcription	Fetal Intestine Small	intestine
32	chr13:96276800-96293400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr13:96278400-96285800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:96278800-96290000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr13:96279000-96285200	Strong transcription	Fetal Kidney	kidney
36	chr13:96279000-96285400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr13:96279200-96281000	ZNF genes & repeats	Fetal Brain Female	brain
38	chr13:96279200-96285400	Strong transcription	Fetal Brain Male	brain
39	chr13:96279200-96286000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr13:96279200-96293800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
41	chr13:96279400-96285400	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr13:96279400-96285800	Strong transcription	Brain Inferior Temporal Lobe	brain
43	chr13:96279400-96292000	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr13:96279400-96293800	Weak transcription	Liver	Liver
45	chr13:96279600-96285400	Strong transcription	A549	lung
46	chr13:96279600-96285600	Strong transcription	Brain Angular Gyrus	brain
47	chr13:96279600-96286600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr13:96279600-96290200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr13:96279600-96292000	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr13:96279800-96282000	Strong transcription	Colon Smooth Muscle	Colon

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