Variant report

Variant	nsv1023955
Chromosome Location	chr9:14754010-14800259
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	chr9:14768583-14768889	K562	blood:	n/a	n/a
2	ATF1	chr9:14797561-14797747	K562	blood:	n/a	n/a
3	ATF1	chr9:14779539-14779966	K562	blood:	n/a	n/a
4	ATF3	chr9:14779743-14779981	K562	blood:	n/a	n/a
5	BHLHE40	chr9:14779512-14779982	K562	blood:	n/a	n/a
6	BHLHE40	chr9:14770538-14770679	K562	blood:	n/a	n/a
7	CEBPB	chr9:14782789-14783062	MCF-7	breast:	n/a	n/a
8	CEBPB	chr9:14779753-14779973	MCF-7	breast:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
9	CEBPB	chr9:14779747-14779985	A549	lung:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
10	CEBPB	chr9:14777095-14777393	HepG2	liver:	n/a	chr9:14777345-14777356 chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135 chr9:14777345-14777356
11	CEBPB	chr9:14799060-14799419	K562	blood:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
12	CEBPB	chr9:14799051-14799431	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
13	CEBPB	chr9:14782802-14783000	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:14799090-14799366	MCF-7	breast:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
15	CEBPB	chr9:14799137-14799326	Hela-S3	cervix:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
16	CEBPB	chr9:14799070-14799407	IMR90	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
17	CEBPB	chr9:14799109-14799362	H1-hESC	embryonic stem cell:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
18	CEBPB	chr9:14799112-14799348	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
19	CEBPB	chr9:14799005-14799390	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
20	CEBPB	chr9:14782726-14783009	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr9:14779706-14780011	K562	blood:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
22	CEBPB	chr9:14779678-14780012	HepG2	liver:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
23	CEBPB	chr9:14799044-14799407	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
24	CEBPB	chr9:14799087-14799406	A549	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
25	CEBPB	chr9:14779694-14779938	K562	blood:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
26	CEBPB	chr9:14777093-14777293	A549	lung:	n/a	chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135
27	CEBPB	chr9:14756265-14756314	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:14782745-14783078	MCF-7	breast:	n/a	n/a
29	CEBPD	chr9:14799130-14799332	HepG2	liver:	n/a	n/a
30	CTCF	chr9:14769280-14769430	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr9:14769280-14769430	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr9:14768620-14768770	HMF	breast:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
33	CTCF	chr9:14768640-14768790	GM12865	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
34	CTCF	chr9:14768521-14768866	ECC-1	luminal epithelium:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
35	CTCF	chr9:14768620-14768770	GM06990	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
36	CTCF	chr9:14769340-14769490	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr9:14769280-14769430	GM12865	blood:	n/a	n/a
38	CTCF	chr9:14769320-14769470	HPF	lung:	n/a	n/a
39	CTCF	chr9:14768660-14768810	NHEK	skin:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
40	CTCF	chr9:14769320-14769470	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr9:14769320-14769470	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr9:14769040-14769190	AG10803	skin:	n/a	n/a
43	CTCF	chr9:14769320-14769470	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr9:14769210-14769529	A549	lung:	n/a	n/a
45	CTCF	chr9:14769320-14769470	GM12874	blood:	n/a	n/a
46	CTCF	chr9:14768530-14768895	T-47D	breast:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
47	CTCF	chr9:14768640-14768790	HAc	cerebellar:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
48	CTCF	chr9:14768600-14768750	Hela-S3	cervix:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
49	CTCF	chr9:14768287-14769582	SK-N-SH	brain:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
50	CTCF	chr9:14768640-14768790	MCF-7	breast:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714

No.	Distal block	Cell Line	Cell type
1	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
2	chr9:14465013..14466518-chr9:14768250..14769873,6	MCF-7	breast:
3	chr9:14441846..14442823-chr9:14768420..14769609,5	MCF-7	breast:
4	chr9:14692712..14694901-chr9:14767288..14769707,2	MCF-7	breast:
5	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
6	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
7	chr9:14693065..14694740-chr9:14764446..14767133,2	MCF-7	breast:
8	chr9:14692738..14695647-chr9:14753924..14755803,2	MCF-7	breast:
9	chr9:14692067..14693708-chr9:14756273..14757823,2	MCF-7	breast:
10	chr9:14406326..14406836-chr9:14756241..14756794,2	MCF-7	breast:
11	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
12	chr4:48089025..48089740-chr9:14788684..14789184,2	MCF-7	breast:
13	chr9:14785127..14787393-chr9:14791653..14793787,2	MCF-7	breast:

Variant related genes	Relation type
FREM1	TF binding region
ENSG00000164946	chromatin interactions
ENSG00000175893	chromatin interactions

Extended variants
information (count: 2319 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2035987	chr9:14754010-14754011	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374676038	chr9:14754030-14754031	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556951482	chr9:14754045-14754046	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567154937	chr9:14754058-14754059	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs533064077	chr9:14754154-14754155	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543145141	chr9:14754162-14754163	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552696239	chr9:14754168-14754169	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559445716	chr9:14754171-14754172	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs572605700	chr9:14754196-14754197	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115164757	chr9:14754239-14754240	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563524859	chr9:14754290-14754291	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558546808	chr9:14754301-14754302	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575109599	chr9:14754323-14754324	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113136501	chr9:14754324-14754325	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573191327	chr9:14754369-14754370	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs180974617	chr9:14754373-14754374	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186003504	chr9:14754402-14754403	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529561963	chr9:14754405-14754406	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs16932258	chr9:14754428-14754429	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559948572	chr9:14754433-14754434	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs528610842	chr9:14754469-14754470	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs377345847	chr9:14754491-14754492	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551555295	chr9:14754492-14754493	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372437661	chr9:14754493-14754494	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147246117	chr9:14754597-14754598	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530794462	chr9:14754598-14754599	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192042359	chr9:14754622-14754623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567220207	chr9:14754732-14754733	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs537241618	chr9:14754775-14754776	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs536768506	chr9:14754783-14754784	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536093696	chr9:14754795-14754796	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552757077	chr9:14754797-14754798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566303150	chr9:14754804-14754805	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182261193	chr9:14754805-14754806	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7023573	chr9:14754864-14754865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs186795653	chr9:14754895-14754896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543863763	chr9:14754903-14754904	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373849311	chr9:14754913-14754914	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554561159	chr9:14754918-14754919	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564849887	chr9:14754919-14754920	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574398041	chr9:14754980-14754981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543310643	chr9:14754986-14754987	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190455153	chr9:14755079-14755080	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs141409084	chr9:14755080-14755081	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114172975	chr9:14755084-14755085	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183033277	chr9:14755090-14755091	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187323051	chr9:14755118-14755119	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs377588282	chr9:14755136-14755137	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550339657	chr9:14755176-14755177	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs386732939	chr9:14755182-14755183	Enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14730800-14764400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:14732600-14755200	Weak transcription	Fetal Intestine Large	intestine
3	chr9:14745000-14809800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:14748800-14775600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:14748800-14775800	Weak transcription	Fetal Muscle Trunk	muscle
6	chr9:14748800-14790000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:14749400-14755000	Weak transcription	Colon Smooth Muscle	Colon
8	chr9:14750200-14754800	Weak transcription	Aorta	Aorta
9	chr9:14750200-14755000	Weak transcription	Pancreas	Pancrea
10	chr9:14750600-14756200	Weak transcription	Fetal Brain Male	brain
11	chr9:14750800-14755400	Weak transcription	Fetal Stomach	stomach
12	chr9:14751400-14754600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr9:14751600-14754400	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:14751800-14754800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr9:14752200-14759400	Strong transcription	HepG2	liver
16	chr9:14752600-14756000	Strong transcription	Fetal Kidney	kidney
17	chr9:14752800-14754600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr9:14752800-14759800	Weak transcription	Fetal Heart	heart
19	chr9:14752800-14775800	Weak transcription	Duodenum Mucosa	Duodenum
20	chr9:14753800-14754200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:14754000-14755600	Strong transcription	Adipose Nuclei	Adipose
22	chr9:14754000-14755800	Strong transcription	Fetal Lung	lung
23	chr9:14754200-14754400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:14754400-14754600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:14754400-14756400	Strong transcription	Fetal Muscle Leg	muscle
26	chr9:14754600-14755000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr9:14754600-14755400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:14754600-14755800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr9:14754800-14755800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr9:14754800-14755800	Strong transcription	Aorta	Aorta
31	chr9:14755000-14755400	Strong transcription	Colon Smooth Muscle	Colon
32	chr9:14755000-14755600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr9:14755000-14755800	Strong transcription	Pancreas	Pancrea
34	chr9:14755200-14755800	Strong transcription	Fetal Intestine Large	intestine
35	chr9:14755400-14755800	Strong transcription	Fetal Stomach	stomach
36	chr9:14755400-14756200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:14755400-14768400	Weak transcription	Colon Smooth Muscle	Colon
38	chr9:14755600-14759800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr9:14755600-14765200	Weak transcription	Adipose Nuclei	Adipose
40	chr9:14755800-14756800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:14755800-14757000	Weak transcription	Fetal Lung	lung
42	chr9:14755800-14758000	Weak transcription	Aorta	Aorta
43	chr9:14755800-14759600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr9:14755800-14766000	Weak transcription	Fetal Intestine Large	intestine
45	chr9:14755800-14775600	Weak transcription	Fetal Stomach	stomach
46	chr9:14755800-14812400	Weak transcription	Pancreas	Pancrea
47	chr9:14756000-14757000	Weak transcription	Fetal Kidney	kidney
48	chr9:14756200-14759600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:14756400-14766400	Weak transcription	Fetal Muscle Leg	muscle
50	chr9:14756800-14757600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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