Variant report

Variant	nsv968738
Chromosome Location	chr9:102760826-102768041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:102765900-102766050	WI-38	lung:	n/a	n/a
2	CTCF	chr9:102761321-102761395	Fibrobl	skin:	n/a	n/a
3	CTCF	chr9:102760869-102760955	Lung_OC	lung:	n/a	n/a
4	CTCF	chr9:102761384-102761413	MCF-7	breast:	n/a	n/a
5	E2F6	chr9:102760453-102761109	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAFF	chr9:102762128-102762437	K562	blood:	n/a	n/a
7	MAFF	chr9:102762120-102762450	HepG2	liver:	n/a	n/a
8	MAFK	chr9:102762115-102762451	HepG2	liver:	n/a	n/a
9	MAFK	chr9:102762104-102762436	IMR90	lung:	n/a	n/a
10	MAFK	chr9:102762117-102762438	Hela-S3	cervix:	n/a	n/a
11	MAFK	chr9:102762103-102762452	HepG2	liver:	n/a	n/a
12	MAFK	chr9:102762181-102762385	K562	blood:	n/a	n/a
13	MAX	chr9:102760522-102761008	H1-hESC	embryonic stem cell:	n/a	n/a
14	MAX	chr9:102760537-102761061	H1-hESC	embryonic stem cell:	n/a	n/a
15	MXI1	chr9:102760795-102760942	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr9:102766367-102766612	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr9:102766554-102766566	Gliobla	brain:	n/a	n/a
18	POLR2A	chr9:102765981-102766083	MCF-7	breast:	n/a	n/a
19	POLR2A	chr9:102765708-102767027	K562	blood:	n/a	n/a
20	POLR2A	chr9:102766097-102766104	MCF-7	breast:	n/a	n/a
21	POLR2A	chr9:102765907-102766685	GM12878	blood:	n/a	n/a
22	POLR2A	chr9:102761267-102761433	GM12878	blood:	n/a	n/a
23	POLR2A	chr9:102761021-102761713	K562	blood:	n/a	n/a
24	POLR2A	chr9:102761312-102761377	A549	lung:	n/a	n/a
25	POLR2A	chr9:102766361-102766383	GM12878	blood:	n/a	n/a
26	POLR2A	chr9:102766097-102766145	HepG2	liver:	n/a	n/a
27	POLR2A	chr9:102766194-102766286	GM12878	blood:	n/a	n/a
28	POLR2A	chr9:102765856-102765865	MCF-7	breast:	n/a	n/a
29	POLR2A	chr9:102766550-102766732	GM12878	blood:	n/a	n/a
30	POLR2A	chr9:102761344-102761414	MCF-7	breast:	n/a	n/a
31	POLR2A	chr9:102762220-102762887	K562	blood:	n/a	n/a
32	POLR2A	chr9:102766493-102766507	Gliobla	brain:	n/a	n/a
33	POLR2A	chr9:102766393-102766426	GM12878	blood:	n/a	n/a
34	POLR2A	chr9:102766322-102766358	GM12878	blood:	n/a	n/a
35	POLR2A	chr9:102766960-102767068	GM12878	blood:	n/a	n/a
36	POLR2A	chr9:102761246-102761438	GM12878	blood:	n/a	n/a
37	POLR2A	chr9:102766166-102766187	GM12878	blood:	n/a	n/a
38	SETDB1	chr9:102765373-102765815	U2OS	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:102761263-102761313	GM12891	blood:	n/a
2	chr9:102761263-102761313	GM06990	blood:	n/a
3	chr9:102761263-102761313	HEK293	kidney:	embryo
4	chr9:102761263-102761313	T-47D	breast:	n/a
5	chr9:102761263-102761313	HIPEpiC	eye:	n/a
6	chr9:102761263-102761313	Hela-S3	cervix:	n/a
7	chr9:102761263-102761313	ProgFib	skin:	n/a
8	chr9:102761263-102761313	HepG2	liver:	n/a
9	chr9:102761263-102761313	H1-hESC	embryonic stem cell:	embryo
10	chr9:102761263-102761313	GM12892	blood:	n/a
11	chr9:102761263-102761313	NT2-D1	testis:	n/a
12	chr9:102761263-102761313	HPAEpiC	pulmonary alveolar:	n/a
13	chr9:102761263-102761313	Jurkat	blood:	n/a
14	chr9:102761263-102761313	ovcar-3	ovarian:	n/a
15	chr9:102761263-102761313	NH-A	brain:	n/a
16	chr9:102761263-102761313	AG09319	gingival:	n/a
17	chr9:102761263-102761313	PANC-1	pancreas:	n/a
18	chr9:102761263-102761313	LNCaP	prostate:	n/a
19	chr9:102761263-102761313	GM12878	blood:	n/a
20	chr9:102761263-102761313	HRPEpiC	eye:	n/a
21	chr9:102761263-102761313	PrEC	prostate:	n/a
22	chr9:102761263-102761313	HRCEpiC	kidney:	n/a
23	chr9:102761263-102761313	AoSMC	blood vessel:	n/a
24	chr9:102761263-102761313	IMR90	lung:	fetal
25	chr9:102761263-102761313	SAEC	small airway:	n/a
26	chr9:102761263-102761313	A549	lung:	n/a
27	chr9:102761263-102761313	HMEC	breast:	n/a
28	chr9:102761263-102761313	AG04450	lung:	fetal
29	chr9:102761263-102761313	SKMC	muscle:	n/a
30	chr9:102761263-102761313	HCPEpiC	choroid plexus:	n/a
31	chr9:102761263-102761313	CMK	blood:	n/a
32	chr9:102761263-102761313	K562	blood:	n/a
33	chr9:102761263-102761313	RPTEC	kidney:	n/a
34	chr9:102761263-102761313	NHBE	bronchial:	n/a
35	chr9:102761263-102761313	HCF	heart:	n/a
36	chr9:102761263-102761313	BE2_C	brain:	n/a
37	chr9:102761263-102761313	SK-N-SH_RA	brain:	n/a
38	chr9:102761263-102761313	NHDF-neo	bronchial:	n/a
39	chr9:102761263-102761313	U87	brain:	n/a
40	chr9:102761263-102761313	HL-60	blood:	n/a
41	chr9:102761263-102761313	AG09309	skin:	n/a
42	chr9:102761263-102761313	GM19239	blood:	n/a
43	chr9:102761263-102761313	ECC-1	luminal epithelium:	n/a
44	chr9:102761263-102761313	AG10803	skin:	n/a
45	chr9:102761263-102761313	HNPCEpiC	eye:	n/a
46	chr9:102761263-102761313	NB4	blood:	n/a
47	chr9:102761263-102761313	HCM	heart:	n/a
48	chr9:102761263-102761313	HCT-116	colon:	n/a
49	chr9:102761263-102761313	AG04449	skin:	fetal
50	chr9:102761263-102761313	HUVEC	blood vessel:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:102711128..102712717-chr9:102764359..102766420,2	MCF-7	breast:
2	chr9:102725264..102726847-chr9:102764305..102766386,2	K562	blood:
3	chr9:102767086..102769713-chr9:102770531..102773622,3	K562	blood:
4	chr9:102765208..102767665-chr9:102771829..102774715,3	MCF-7	breast:
5	chr9:102767086..102769925-chr9:102772122..102773628,2	K562	blood:

No data

Variant related genes	Relation type
UPF3AP3	TF binding region
UPF3AP3	CpG island

Extended variants
information (count: 211 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:211 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577279938	chr9:102760931-102760932	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546235360	chr9:102760933-102760934	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559844011	chr9:102760981-102760982	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528596841	chr9:102760990-102760991	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113923847	chr9:102760996-102760997	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144598898	chr9:102761033-102761034	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560964314	chr9:102761060-102761061	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529984439	chr9:102761069-102761070	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141103772	chr9:102761071-102761072	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563625205	chr9:102761102-102761103	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531950767	chr9:102761129-102761130	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373112563	chr9:102761131-102761132	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551765833	chr9:102761139-102761140	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565390803	chr9:102761140-102761141	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534459478	chr9:102761149-102761150	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377654220	chr9:102761159-102761160	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181594203	chr9:102761166-102761167	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537673410	chr9:102761243-102761244	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557335981	chr9:102761253-102761254	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369760708	chr9:102761288-102761289	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144840806	chr9:102761291-102761292	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539794651	chr9:102761292-102761293	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553448572	chr9:102761305-102761306	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573363743	chr9:102761318-102761319	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541991453	chr9:102761335-102761336	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112108489	chr9:102761364-102761365	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs574520864	chr9:102761382-102761383	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs543620790	chr9:102761386-102761387	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs563204667	chr9:102761392-102761393	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs532277801	chr9:102761393-102761394	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs551753587	chr9:102761396-102761397	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558964986	chr9:102761435-102761436	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs4495492	chr9:102761448-102761449	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs571714195	chr9:102761469-102761470	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373175942	chr9:102761511-102761512	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs76345285	chr9:102761514-102761515	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs568161659	chr9:102761542-102761543	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs1881752	chr9:102761603-102761604	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs551156981	chr9:102761610-102761611	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs145565980	chr9:102761615-102761616	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs187390200	chr9:102761617-102761618	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs557028353	chr9:102761620-102761621	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs538989147	chr9:102761649-102761650	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs56332470	chr9:102761661-102761662	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs553385356	chr9:102761682-102761683	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs190221730	chr9:102761698-102761699	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs180967347	chr9:102761747-102761748	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555546122	chr9:102761752-102761753	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148868743	chr9:102761778-102761779	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143504864	chr9:102761833-102761834	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102699800-102765800	Weak transcription	Psoas Muscle	Psoas
2	chr9:102711400-102765800	Weak transcription	Right Ventricle	heart
3	chr9:102711400-102769200	Weak transcription	Osteobl	bone
4	chr9:102712200-102765600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr9:102713200-102765600	Weak transcription	HSMMtube	muscle
6	chr9:102718000-102777600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr9:102719000-102765400	Weak transcription	HepG2	liver
8	chr9:102729400-102764600	Weak transcription	HSMM	muscle
9	chr9:102729600-102765600	Weak transcription	NHEK	skin
10	chr9:102729600-102826800	Weak transcription	HMEC	breast
11	chr9:102730200-102765600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr9:102731000-102765600	Weak transcription	NHLF	lung
13	chr9:102731000-102778200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr9:102731800-102765600	Weak transcription	Small Intestine	intestine
15	chr9:102732600-102765600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr9:102733000-102765600	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:102733200-102765000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr9:102735800-102764600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr9:102740600-102765600	Weak transcription	A549	lung
20	chr9:102740800-102765400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:102740800-102765600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr9:102743400-102765600	Weak transcription	K562	blood
23	chr9:102744800-102765600	Weak transcription	NHDF-Ad	bronchial
24	chr9:102745200-102765600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr9:102745400-102765200	Weak transcription	Hela-S3	cervix
26	chr9:102746200-102765000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr9:102747000-102765400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr9:102747600-102765600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr9:102749400-102764600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr9:102749400-102765600	Weak transcription	Brain Hippocampus Middle	brain
31	chr9:102751400-102763400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr9:102751400-102765600	Weak transcription	Aorta	Aorta
33	chr9:102751400-102765600	Weak transcription	Left Ventricle	heart
34	chr9:102751600-102765600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:102751600-102765600	Weak transcription	Esophagus	oesophagus
36	chr9:102751600-102765600	Weak transcription	Fetal Thymus	thymus
37	chr9:102751600-102765600	Weak transcription	Gastric	stomach
38	chr9:102751600-102765600	Weak transcription	Dnd41	blood
39	chr9:102751600-102765800	Weak transcription	Colonic Mucosa	Colon
40	chr9:102751800-102765600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr9:102751800-102765800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr9:102751800-102765800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr9:102752000-102763200	Weak transcription	Placenta	Placenta
44	chr9:102752000-102765600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr9:102752000-102765600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr9:102752000-102765600	Weak transcription	Brain Angular Gyrus	brain
47	chr9:102752200-102761200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr9:102752200-102764000	Weak transcription	Fetal Lung	lung
49	chr9:102752200-102765400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr9:102752200-102765400	Weak transcription	Skeletal Muscle Female	skeletal muscle

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