Variant report

Variant	nsv892615
Chromosome Location	chr9:14761260-14782367
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	chr9:14779539-14779966	K562	blood:	n/a	n/a
3	ATF3	chr9:14779743-14779981	K562	blood:	n/a	n/a
4	BHLHE40	chr9:14779512-14779982	K562	blood:	n/a	n/a
5	BHLHE40	chr9:14770538-14770679	K562	blood:	n/a	n/a
6	CEBPB	chr9:14779706-14780011	K562	blood:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
7	CEBPB	chr9:14779694-14779938	K562	blood:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
8	CEBPB	chr9:14779753-14779973	MCF-7	breast:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
9	CEBPB	chr9:14777095-14777393	HepG2	liver:	n/a	chr9:14777345-14777356 chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135 chr9:14777345-14777356
10	CEBPB	chr9:14777093-14777293	A549	lung:	n/a	chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135
11	CEBPB	chr9:14779678-14780012	HepG2	liver:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
12	CEBPB	chr9:14779747-14779985	A549	lung:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
13	CTCF	chr9:14769366-14769400	MCF-7	breast:	n/a	n/a
14	CTCF	chr9:14768596-14768844	Pancreas_OC	pancreas:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
15	CTCF	chr9:14769344-14769347	HepG2	liver:	n/a	n/a
16	CTCF	chr9:14769240-14769510	AG04450	lung:	n/a	n/a
17	CTCF	chr9:14768596-14768730	GM19240	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
18	CTCF	chr9:14769300-14769450	GM12872	blood:	n/a	n/a
19	CTCF	chr9:14768640-14768790	GM12869	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
20	CTCF	chr9:14768631-14768809	GM13976	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
21	CTCF	chr9:14768555-14768778	ECC-1	luminal epithelium:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
22	CTCF	chr9:14768471-14768912	A549	lung:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
23	CTCF	chr9:14768600-14768750	HRE	kidney:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
24	CTCF	chr9:14768580-14768730	Hela-S3	cervix:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
25	CTCF	chr9:14769060-14769210	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr9:14768623-14768772	MCF-7	breast:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
27	CTCF	chr9:14769210-14769529	A549	lung:	n/a	n/a
28	CTCF	chr9:14769300-14769449	GM10248	blood:	n/a	n/a
29	CTCF	chr9:14769280-14769430	GM12864	blood:	n/a	n/a
30	CTCF	chr9:14769237-14769498	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr9:14769040-14769190	AG09319	gingival:	n/a	n/a
32	CTCF	chr9:14769012-14769059	GM12878	blood:	n/a	n/a
33	CTCF	chr9:14769280-14769430	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr9:14769281-14769492	LNCaP	prostate:	n/a	n/a
35	CTCF	chr9:14769260-14769410	GM12875	blood:	n/a	n/a
36	CTCF	chr9:14768600-14768750	HFF	foreskin:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
37	CTCF	chr9:14769320-14769470	AG09319	gingival:	n/a	n/a
38	CTCF	chr9:14769380-14769530	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr9:14768600-14768750	GM12868	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
40	CTCF	chr9:14769200-14769350	NHEK	skin:	n/a	n/a
41	CTCF	chr9:14769284-14769483	Gliobla	brain:	n/a	n/a
42	CTCF	chr9:14769320-14769470	AG04450	lung:	n/a	n/a
43	CTCF	chr9:14768620-14768770	NHDF-neo	bronchial:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
44	CTCF	chr9:14766460-14766610	AG10803	skin:	n/a	n/a
45	CTCF	chr9:14768620-14768770	AoAF	blood vessel:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
46	CTCF	chr9:14769040-14769190	AG10803	skin:	n/a	n/a
47	CTCF	chr9:14769260-14769410	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr9:14769060-14769061	GM20000	blood:	n/a	n/a
49	CTCF	chr9:14769300-14769450	AG04449	skin:	n/a	n/a
50	CTCF	chr9:14768640-14768790	GM12870	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714

No.	Distal block	Cell Line	Cell type
1	chr9:14693065..14694740-chr9:14764446..14767133,2	MCF-7	breast:
2	chr9:14441846..14442823-chr9:14768420..14769609,5	MCF-7	breast:
3	chr9:14692712..14694901-chr9:14767288..14769707,2	MCF-7	breast:
4	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
5	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
6	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
7	chr9:14465013..14466518-chr9:14768250..14769873,6	MCF-7	breast:

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

Extended variants
information (count: 1080 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10124839	chr9:14761260-14761261	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547026861	chr9:14761262-14761263	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79207813	chr9:14761285-14761286	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563492331	chr9:14761299-14761300	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538922738	chr9:14761362-14761363	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184698833	chr9:14761364-14761365	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569087639	chr9:14761371-14761372	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538588211	chr9:14761431-14761432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573932426	chr9:14761456-14761457	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117817404	chr9:14761476-14761477	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554633538	chr9:14761503-14761504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574785427	chr9:14761507-14761508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370357758	chr9:14761519-14761520	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369958095	chr9:14761543-14761544	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189560612	chr9:14761562-14761563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539083326	chr9:14761600-14761601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577080034	chr9:14761646-14761647	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140338620	chr9:14761659-14761660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373491382	chr9:14761676-14761677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562703822	chr9:14761679-14761680	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568884553	chr9:14761684-14761685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537868975	chr9:14761685-14761686	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576290961	chr9:14761730-14761731	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541988882	chr9:14761731-14761732	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7858690	chr9:14761788-14761789	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs527350019	chr9:14761803-14761804	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs181058213	chr9:14761805-14761806	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs574657900	chr9:14761828-14761829	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs7874339	chr9:14761877-14761878	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs532867797	chr9:14761916-14761917	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs73644848	chr9:14761978-14761979	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs569147349	chr9:14761979-14761980	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs538045477	chr9:14762012-14762013	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs548325687	chr9:14762057-14762058	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs553888214	chr9:14762101-14762102	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs568547815	chr9:14762116-14762117	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183727881	chr9:14762132-14762133	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs368402936	chr9:14762143-14762144	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs189572501	chr9:14762200-14762201	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572748841	chr9:14762201-14762202	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144184365	chr9:14762219-14762220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539780620	chr9:14762228-14762229	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556489782	chr9:14762246-14762247	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4741428	chr9:14762247-14762248	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs562595903	chr9:14762297-14762298	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542050322	chr9:14762306-14762307	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113208070	chr9:14762307-14762308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs561692518	chr9:14762311-14762312	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114938414	chr9:14762321-14762322	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181831556	chr9:14762327-14762328	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14730800-14764400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:14745000-14809800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:14748800-14775600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:14748800-14775800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:14748800-14790000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:14752800-14775800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr9:14755400-14768400	Weak transcription	Colon Smooth Muscle	Colon
8	chr9:14755600-14765200	Weak transcription	Adipose Nuclei	Adipose
9	chr9:14755800-14766000	Weak transcription	Fetal Intestine Large	intestine
10	chr9:14755800-14775600	Weak transcription	Fetal Stomach	stomach
11	chr9:14755800-14812400	Weak transcription	Pancreas	Pancrea
12	chr9:14756400-14766400	Weak transcription	Fetal Muscle Leg	muscle
13	chr9:14757000-14771800	Strong transcription	Fetal Kidney	kidney
14	chr9:14758200-14766400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr9:14758400-14793400	Weak transcription	Aorta	Aorta
16	chr9:14759400-14765800	Weak transcription	HepG2	liver
17	chr9:14760000-14775200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr9:14760600-14761400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr9:14760800-14761800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:14760800-14763000	Weak transcription	Fetal Lung	lung
21	chr9:14761400-14763000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr9:14761800-14762200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:14762200-14762600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:14762600-14763800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:14763000-14763200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr9:14763000-14770800	Strong transcription	Fetal Lung	lung
27	chr9:14763800-14764200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:14764200-14764400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:14764400-14764800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:14764400-14765200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:14764800-14809600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:14765200-14765400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:14765200-14767200	Strong transcription	Adipose Nuclei	Adipose
34	chr9:14765400-14765600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr9:14765600-14766000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:14765800-14768000	Strong transcription	HepG2	liver
37	chr9:14766000-14766400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:14766000-14766600	Enhancers	Fetal Intestine Large	intestine
39	chr9:14766400-14766800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr9:14766400-14767200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:14766400-14767400	Strong transcription	Fetal Muscle Leg	muscle
42	chr9:14766600-14766800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr9:14766600-14787400	Weak transcription	Fetal Intestine Large	intestine
44	chr9:14766800-14768400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr9:14766800-14775400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:14767200-14769200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:14767200-14779200	Weak transcription	Adipose Nuclei	Adipose
48	chr9:14767400-14779000	Weak transcription	Fetal Muscle Leg	muscle
49	chr9:14768000-14769000	Enhancers	HUVEC	blood vessel
50	chr9:14768000-14773400	Weak transcription	HepG2	liver

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