Variant report

Variant	nsv892183
Chromosome Location	chr9:6811507-6855838
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	chr9:6845117-6845374	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6819233-6819386	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6845932-6846244	HepG2	liver:	n/a	n/a
4	BACH1	chr9:6854906-6854915	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr9:6816627-6816816	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:6845885-6846304	HepG2	liver:	n/a	n/a
7	CEBPB	chr9:6845155-6845343	HepG2	liver:	n/a	chr9:6845269-6845280
8	CEBPB	chr9:6845142-6845308	Hela-S3	cervix:	n/a	chr9:6845269-6845280
9	CEBPB	chr9:6845120-6845326	A549	lung:	n/a	chr9:6845269-6845280
10	CEBPB	chr9:6845100-6845379	IMR90	lung:	n/a	chr9:6845269-6845280
11	CEBPB	chr9:6855320-6855457	HepG2	liver:	n/a	chr9:6855409-6855420
12	CEBPB	chr9:6845072-6845462	HepG2	liver:	n/a	chr9:6845269-6845280
13	CEBPB	chr9:6833914-6834218	A549	lung:	n/a	n/a
14	CEBPB	chr9:6845149-6845367	K562	blood:	n/a	chr9:6845269-6845280
15	CEBPB	chr9:6833935-6834181	K562	blood:	n/a	n/a
16	CEBPB	chr9:6855379-6855455	A549	lung:	n/a	chr9:6855409-6855420
17	CEBPB	chr9:6833910-6834257	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:6845142-6845388	H1-hESC	embryonic stem cell:	n/a	chr9:6845269-6845280
19	CEBPB	chr9:6837930-6837971	A549	lung:	n/a	chr9:6837935-6837946
20	CEBPB	chr9:6837817-6838082	HepG2	liver:	n/a	chr9:6837935-6837946
21	CEBPB	chr9:6845080-6845466	HepG2	liver:	n/a	chr9:6845269-6845280
22	CEBPB	chr9:6845058-6845486	HepG2	liver:	n/a	chr9:6845269-6845280
23	CEBPB	chr9:6827408-6827673	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPD	chr9:6845083-6845422	HepG2	liver:	n/a	n/a
25	CEBPD	chr9:6845166-6845369	HepG2	liver:	n/a	n/a
26	CHD1	chr9:6827620-6827645	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:6846000-6846150	HBMEC	blood vessel:	n/a	chr9:6846078-6846087
28	CTCF	chr9:6845980-6846130	HCM	heart:	n/a	chr9:6846078-6846087
29	CTCF	chr9:6845960-6846110	HCM	heart:	n/a	chr9:6846078-6846087
30	CTCF	chr9:6845940-6846090	BJ	skin:	n/a	chr9:6846078-6846087
31	CTCF	chr9:6845980-6846130	WI-38	lung:	n/a	chr9:6846078-6846087
32	CTCF	chr9:6827497-6827591	A549	lung:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
33	CTCF	chr9:6827500-6827650	Hela-S3	cervix:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
34	CTCF	chr9:6827460-6827610	HMEC	breast:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
35	CTCF	chr9:6827440-6827590	HEK293	kidney:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
36	CTCF	chr9:6827520-6827670	MCF-7	breast:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
37	CTCF	chr9:6845960-6846110	RPTEC	kidney:	n/a	chr9:6846078-6846087
38	CTCF	chr9:6845999-6846176	ProgFib	skin:	n/a	chr9:6846078-6846087
39	CTCF	chr9:6827962-6828001	GM13976	blood:	n/a	n/a
40	CTCF	chr9:6829080-6829230	A549	lung:	n/a	n/a
41	CTCF	chr9:6846009-6846172	Hela-S3	cervix:	n/a	chr9:6846078-6846087
42	CTCF	chr9:6846020-6846170	HPAF	blood vessel:	n/a	chr9:6846078-6846087
43	CTCF	chr9:6827300-6827743	A549	lung:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
44	CTCF	chr9:6827480-6827630	Caco-2	colon:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
45	CTCF	chr9:6845960-6846110	BJ	skin:	n/a	chr9:6846078-6846087
46	CTCF	chr9:6827440-6827590	NHEK	skin:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
47	CTCF	chr9:6827460-6827610	GM12864	blood:	n/a	chr9:6827536-6827557 chr9:6827537-6827550 chr9:6827534-6827552
48	CTCF	chr9:6846000-6846150	Hela-S3	cervix:	n/a	chr9:6846078-6846087
49	CTCF	chr9:6829060-6829210	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr9:6846000-6846150	HMEC	breast:	n/a	chr9:6846078-6846087

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6836634-6836684	HRE	kidney:	n/a
2	chr9:6836634-6836684	GM06990	blood:	n/a
3	chr9:6836634-6836684	PANC-1	pancreas:	n/a
4	chr9:6836634-6836684	NH-A	brain:	n/a
5	chr9:6836634-6836684	PrEC	prostate:	n/a
6	chr9:6836634-6836684	NB4	blood:	n/a
7	chr9:6836634-6836684	HL-60	blood:	n/a
8	chr9:6836634-6836684	HCPEpiC	choroid plexus:	n/a
9	chr9:6836634-6836684	K562	blood:	n/a
10	chr9:6835001-6835051	SAEC	small airway:	n/a
11	chr9:6836634-6836684	SK-N-SH	brain:	n/a
12	chr9:6835001-6835051	PFSK-1	brain:	n/a
13	chr9:6836634-6836684	ProgFib	skin:	n/a
14	chr9:6835001-6835051	H1-hESC	embryonic stem cell:	embryo
15	chr9:6836634-6836684	GM12892	blood:	n/a
16	chr9:6835001-6835051	HNPCEpiC	eye:	n/a
17	chr9:6835001-6835051	HCT-116	colon:	n/a
18	chr9:6836634-6836684	LNCaP	prostate:	n/a
19	chr9:6835001-6835051	HAEpiC	amniotic membrane:	n/a
20	chr9:6836634-6836684	HEEpiC	esophagus:	n/a
21	chr9:6836634-6836684	HRPEpiC	eye:	n/a
22	chr9:6836634-6836684	NT2-D1	testis:	n/a
23	chr9:6835001-6835051	HepG2	liver:	n/a
24	chr9:6835001-6835051	ovcar-3	ovarian:	n/a
25	chr9:6835001-6835051	Caco-2	colon:	n/a
26	chr9:6836634-6836684	SK-N-SH_RA	brain:	n/a
27	chr9:6836634-6836684	BE2_C	brain:	n/a
28	chr9:6835001-6835051	Hela-S3	cervix:	n/a
29	chr9:6836634-6836684	GM12878	blood:	n/a
30	chr9:6835001-6835051	GM19239	blood:	n/a
31	chr9:6836634-6836684	H1-hESC	embryonic stem cell:	embryo
32	chr9:6835001-6835051	HL-60	blood:	n/a
33	chr9:6836634-6836684	HRCEpiC	kidney:	n/a
34	chr9:6835001-6835051	HRPEpiC	eye:	n/a
35	chr9:6835001-6835051	T-47D	breast:	n/a
36	chr9:6835001-6835051	SK-N-SH_RA	brain:	n/a
37	chr9:6836634-6836684	Hepatocyte	liver:	n/a
38	chr9:6836634-6836684	HIPEpiC	eye:	n/a
39	chr9:6835001-6835051	MCF-7	breast:	n/a
40	chr9:6835001-6835051	ProgFib	skin:	n/a
41	chr9:6835001-6835051	HCPEpiC	choroid plexus:	n/a
42	chr9:6836634-6836684	NHBE	bronchial:	n/a
43	chr9:6836634-6836684	GM19239	blood:	n/a
44	chr9:6836634-6836684	MCF10A-Er-Src	breast:	n/a
45	chr9:6836634-6836684	AG04449	skin:	fetal
46	chr9:6835001-6835051	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:6835001-6835051	NT2-D1	testis:	n/a
48	chr9:6835001-6835051	NH-A	brain:	n/a
49	chr9:6835001-6835051	SK-N-MC	brain:	n/a
50	chr9:6835001-6835051	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
2	chr9:6757938..6759489-chr9:6817335..6820629,3	MCF-7	breast:
3	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
4	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
5	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
6	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:
7	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:
8	chr9:6845574..6847293-chr9:6858590..6860659,2	K562	blood:

Variant related genes	Relation type
ENSG00000230581	TF binding region
ENSG00000230581	CpG island
ENSG00000107077	chromatin interactions

Extended variants
information (count: 2368 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2368 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11998950	chr9:6811507-6811508	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377356869	chr9:6811512-6811513	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561857595	chr9:6811568-6811569	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145732200	chr9:6811618-6811619	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112356508	chr9:6811624-6811625	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568691374	chr9:6811629-6811630	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182145108	chr9:6811636-6811637	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186746199	chr9:6811650-6811651	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563760803	chr9:6811661-6811662	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531186181	chr9:6811672-6811673	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113351391	chr9:6811678-6811679	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537668148	chr9:6811705-6811706	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78020970	chr9:6811722-6811723	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191954275	chr9:6811726-6811727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564029535	chr9:6811747-6811748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547682531	chr9:6811769-6811770	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566227836	chr9:6811781-6811782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533477251	chr9:6811795-6811796	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533683203	chr9:6811796-6811797	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552026554	chr9:6811798-6811799	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570102126	chr9:6811804-6811805	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537435622	chr9:6811818-6811819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555945169	chr9:6811837-6811838	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117438377	chr9:6811855-6811856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12682800	chr9:6811856-6811857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555642805	chr9:6811871-6811872	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148952638	chr9:6811886-6811887	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572178291	chr9:6811964-6811965	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143687893	chr9:6812004-6812005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575679161	chr9:6812041-6812042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184208162	chr9:6812064-6812065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570340268	chr9:6812078-6812079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543015731	chr9:6812112-6812113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368429656	chr9:6812124-6812125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561306714	chr9:6812127-6812128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs151063785	chr9:6812139-6812140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541090813	chr9:6812177-6812178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559721860	chr9:6812199-6812200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141334583	chr9:6812205-6812206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188790063	chr9:6812223-6812224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570364239	chr9:6812232-6812233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113265335	chr9:6812233-6812234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368478796	chr9:6812240-6812241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112239939	chr9:6812325-6812326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549410274	chr9:6812326-6812327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115197669	chr9:6812327-6812328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549300278	chr9:6812359-6812360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534830496	chr9:6812419-6812420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547049957	chr9:6812420-6812421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112955264	chr9:6812450-6812451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6788200-6819400	Weak transcription	K562	blood
2	chr9:6789000-6831800	Weak transcription	Osteobl	bone
3	chr9:6789200-6823400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr9:6789200-6834200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:6789200-6834400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr9:6791400-6818400	Weak transcription	Pancreas	Pancrea
7	chr9:6792000-6831400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr9:6793200-6834400	Weak transcription	Ovary	ovary
9	chr9:6793800-6818600	Weak transcription	Colonic Mucosa	Colon
10	chr9:6793800-6827200	Weak transcription	Fetal Kidney	kidney
11	chr9:6794400-6815600	Weak transcription	Colon Smooth Muscle	Colon
12	chr9:6794400-6834600	Weak transcription	Right Ventricle	heart
13	chr9:6794600-6815400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr9:6794600-6815400	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr9:6794600-6823200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr9:6794600-6823400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr9:6794600-6823400	Weak transcription	Placenta	Placenta
18	chr9:6794600-6823400	Weak transcription	Hela-S3	cervix
19	chr9:6794600-6827800	Weak transcription	HSMM	muscle
20	chr9:6794600-6831600	Weak transcription	HSMMtube	muscle
21	chr9:6794800-6815400	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr9:6794800-6818800	Weak transcription	Brain Substantia Nigra	brain
23	chr9:6794800-6821800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr9:6794800-6823000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr9:6794800-6823000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr9:6794800-6823200	Weak transcription	NHEK	skin
27	chr9:6794800-6834200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr9:6795000-6823400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr9:6795000-6863800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr9:6795200-6818400	Weak transcription	Right Atrium	heart
31	chr9:6795400-6849600	Weak transcription	HMEC	breast
32	chr9:6795600-6823200	Weak transcription	Left Ventricle	heart
33	chr9:6796000-6818400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr9:6796600-6817800	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr9:6798000-6814400	Weak transcription	Dnd41	blood
36	chr9:6799600-6823200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:6799600-6834400	Weak transcription	Spleen	Spleen
38	chr9:6802400-6814200	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr9:6805800-6814600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr9:6806000-6814600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:6806000-6815400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr9:6806000-6816000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:6806000-6818400	Weak transcription	HepG2	liver
44	chr9:6806000-6822800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr9:6806000-6823400	Weak transcription	Brain Anterior Caudate	brain
46	chr9:6806000-6831600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:6806000-6834600	Weak transcription	Brain Angular Gyrus	brain
48	chr9:6806200-6822800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:6806200-6823400	Weak transcription	Brain Cingulate Gyrus	brain
50	chr9:6806200-6823400	Weak transcription	Brain Hippocampus Middle	brain

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