Variant report

Variant	esv33385
Chromosome Location	chr7:6784757-6840337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:305)
CpG islands
(count:610)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:305 , 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	BHLHE40	chr7:6832293-6832495	HepG2	liver:	n/a	n/a
2	BHLHE40	chr7:6832136-6832415	HepG2	liver:	n/a	n/a
3	CBX3	chr7:6803410-6803703	K562	blood:	n/a	n/a
4	CBX3	chr7:6809662-6809823	K562	blood:	n/a	n/a
5	CEBPB	chr7:6808876-6809289	K562	blood:	n/a	n/a
6	CEBPB	chr7:6808935-6809247	K562	blood:	n/a	n/a
7	CEBPB	chr7:6807101-6807394	K562	blood:	n/a	n/a
8	CEBPD	chr7:6808904-6809347	K562	blood:	n/a	n/a
9	CTCF	chr7:6793081-6793163	GM12892	blood:	n/a	n/a
10	CTCF	chr7:6820971-6821132	K562	blood:	n/a	n/a
11	CTCF	chr7:6826258-6826259	GM10248	blood:	n/a	n/a
12	CTCF	chr7:6804260-6804410	GM12872	blood:	n/a	n/a
13	CTCF	chr7:6834745-6834804	GM10248	blood:	n/a	n/a
14	CTCF	chr7:6826362-6826410	Lung_OC	lung:	n/a	n/a
15	CTCF	chr7:6793084-6793140	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr7:6793102-6793200	K562	blood:	n/a	n/a
17	CTCF	chr7:6793071-6793133	LNCaP	prostate:	n/a	n/a
18	CTCF	chr7:6793050-6793166	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr7:6793082-6793135	NHEK	skin:	n/a	n/a
20	CTCF	chr7:6793092-6793140	HepG2	liver:	n/a	n/a
21	CTCF	chr7:6803622-6803631	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:6803009-6803052	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:6793078-6793165	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:6793060-6793197	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:6793124-6793202	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr7:6803633-6803668	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:6793065-6793163	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:6791433-6791551	LNCaP	prostate:	n/a	n/a
29	CTCF	chr7:6793169-6793184	GM13977	blood:	n/a	n/a
30	CTCF	chr7:6802971-6803048	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:6802974-6803053	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:6793057-6793188	GM10248	blood:	n/a	n/a
33	CTCF	chr7:6802453-6802482	LNCaP	prostate:	n/a	n/a
34	CTCF	chr7:6828519-6828596	LNCaP	prostate:	n/a	n/a
35	CTCF	chr7:6793135-6793190	Medullo	brain:	n/a	n/a
36	CTCF	chr7:6793717-6793774	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr7:6835449-6835560	GM10248	blood:	n/a	n/a
38	CTCF	chr7:6787031-6787131	LNCaP	prostate:	n/a	n/a
39	CTCF	chr7:6793068-6793162	GM12891	blood:	n/a	n/a
40	EBF1	chr7:6831853-6832118	GM12878	blood:	n/a	n/a
41	EBF1	chr7:6829441-6829627	GM12878	blood:	n/a	n/a
42	EBF1	chr7:6829466-6829671	GM12878	blood:	n/a	n/a
43	EGR1	chr7:6833480-6833844	GM12878	blood:	n/a	n/a
44	FOSL2	chr7:6800036-6800661	HepG2	liver:	n/a	n/a
45	FOSL2	chr7:6785052-6785316	HepG2	liver:	n/a	n/a
46	FOSL2	chr7:6792848-6793169	HepG2	liver:	n/a	n/a
47	FOSL2	chr7:6800150-6800626	HepG2	liver:	n/a	n/a
48	FOSL2	chr7:6831707-6832497	HepG2	liver:	n/a	chr7:6831940-6831952 chr7:6831943-6831954 chr7:6831941-6831951 chr7:6831941-6831951 chr7:6831941-6831951 chr7:6831941-6831951
49	FOSL2	chr7:6831747-6832440	HepG2	liver:	n/a	chr7:6831940-6831952 chr7:6831943-6831954 chr7:6831941-6831951 chr7:6831941-6831951 chr7:6831941-6831951 chr7:6831941-6831951
50	FOSL2	chr7:6793491-6794248	HepG2	liver:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6817550-6817600	NHBE	bronchial:	n/a
2	chr7:6838775-6838825	GM06990	blood:	n/a
3	chr7:6817550-6817600	HEEpiC	esophagus:	n/a
4	chr7:6793823-6793873	HMEC	breast:	n/a
5	chr7:6803522-6803572	HRE	kidney:	n/a
6	chr7:6819532-6819582	Caco-2	colon:	n/a
7	chr7:6800488-6800538	HRE	kidney:	n/a
8	chr7:6836436-6836486	Hepatocyte	liver:	n/a
9	chr7:6836436-6836486	AG10803	skin:	n/a
10	chr7:6838775-6838825	AG09309	skin:	n/a
11	chr7:6800488-6800538	HL-60	blood:	n/a
12	chr7:6803522-6803572	AG09309	skin:	n/a
13	chr7:6790012-6790062	HCT-116	colon:	n/a
14	chr7:6800488-6800538	ovcar-3	ovarian:	n/a
15	chr7:6790012-6790062	PrEC	prostate:	n/a
16	chr7:6800488-6800538	HAEpiC	amniotic membrane:	n/a
17	chr7:6793977-6794027	NB4	blood:	n/a
18	chr7:6797497-6797547	NHBE	bronchial:	n/a
19	chr7:6838775-6838825	Hepatocyte	liver:	n/a
20	chr7:6793823-6793873	SK-N-MC	brain:	n/a
21	chr7:6790012-6790062	HEK293	kidney:	embryo
22	chr7:6819532-6819582	ProgFib	skin:	n/a
23	chr7:6790012-6790062	HCF	heart:	n/a
24	chr7:6838775-6838825	U87	brain:	n/a
25	chr7:6793977-6794027	BJ	skin:	n/a
26	chr7:6793823-6793873	Hela-S3	cervix:	n/a
27	chr7:6819532-6819582	BJ	skin:	n/a
28	chr7:6817550-6817600	PrEC	prostate:	n/a
29	chr7:6817550-6817600	IMR90	lung:	fetal
30	chr7:6836436-6836486	HRCEpiC	kidney:	n/a
31	chr7:6803522-6803572	NB4	blood:	n/a
32	chr7:6819532-6819582	PANC-1	pancreas:	n/a
33	chr7:6800488-6800538	AG10803	skin:	n/a
34	chr7:6790012-6790062	NB4	blood:	n/a
35	chr7:6797497-6797547	AG04449	skin:	fetal
36	chr7:6838775-6838825	NHDF-neo	bronchial:	n/a
37	chr7:6817550-6817600	CMK	blood:	n/a
38	chr7:6817550-6817600	BJ	skin:	n/a
39	chr7:6838775-6838825	ECC-1	luminal epithelium:	n/a
40	chr7:6819532-6819582	MCF10A-Er-Src	breast:	n/a
41	chr7:6793977-6794027	PFSK-1	brain:	n/a
42	chr7:6803522-6803572	T-47D	breast:	n/a
43	chr7:6803522-6803572	SK-N-MC	brain:	n/a
44	chr7:6790012-6790062	Caco-2	colon:	n/a
45	chr7:6793823-6793873	RPTEC	kidney:	n/a
46	chr7:6797497-6797547	PrEC	prostate:	n/a
47	chr7:6793823-6793873	Jurkat	blood:	n/a
48	chr7:6838775-6838825	HUVEC	blood vessel:	n/a
49	chr7:6797497-6797547	NT2-D1	testis:	n/a
50	chr7:6836436-6836486	Hela-S3	cervix:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCZ1B-1	chr7:6833772-6834166	NONHSAT119073
2	lnc-RSPH10B2-1	chr7:6792653-6793492	NONHSAT119063
3	lnc-CCZ1B-1	chr7:6836407-6836567	NONHSAT119073
4	lnc-CCZ1B-1	chr7:6836264-6836309	NONHSAT119073

No data

Variant related genes	Relation type
RSPH10B2	TF binding region
CCZ1B	TF binding region
RSPH10B2	CpG island
CCZ1B	CpG island

Extended variants
information (count: 610 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:610 , 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	rs2692546	chr7:6784766-6784767	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2692545	chr7:6784787-6784788	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs397834136	chr7:6784816-6784817	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371038596	chr7:6784860-6784861	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs62439746	chr7:6784871-6784872	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2711199	chr7:6784877-6784878	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574273704	chr7:6784889-6784890	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2711198	chr7:6784890-6784891	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs193184740	chr7:6784934-6784935	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184704032	chr7:6784939-6784940	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2692543	chr7:6785000-6785001	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs60946336	chr7:6785023-6785024	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187923247	chr7:6785158-6785159	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545784155	chr7:6785184-6785185	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557865001	chr7:6785185-6785186	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559152344	chr7:6785186-6785187	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs57520146	chr7:6785198-6785199	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs58207919	chr7:6785213-6785214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59660422	chr7:6785229-6785230	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548048382	chr7:6785230-6785231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139448912	chr7:6785234-6785235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539578888	chr7:6785235-6785236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60841922	chr7:6785236-6785237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs60549286	chr7:6785250-6785251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537463576	chr7:6785254-6785255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60645856	chr7:6785256-6785257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577973654	chr7:6785267-6785268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59205069	chr7:6785270-6785271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60640514	chr7:6785275-6785276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368409541	chr7:6785285-6785286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548060462	chr7:6785290-6785291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs58353394	chr7:6785312-6785313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs57608899	chr7:6785376-6785377	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs370694812	chr7:6785394-6785395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146430524	chr7:6785399-6785400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140755443	chr7:6785400-6785401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183633639	chr7:6785416-6785417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572227233	chr7:6785448-6785449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369257157	chr7:6785455-6785456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372267083	chr7:6785457-6785458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145536798	chr7:6785460-6785461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564215598	chr7:6785463-6785464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188436572	chr7:6785466-6785467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543486913	chr7:6785484-6785485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562357777	chr7:6785494-6785495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529651767	chr7:6785501-6785502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148847587	chr7:6785511-6785512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181331054	chr7:6785515-6785516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185019240	chr7:6785527-6785528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143359496	chr7:6785533-6785534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6770400-6784800	Weak transcription	NHLF	lung
2	chr7:6770800-6786400	Weak transcription	Fetal Brain Male	brain
3	chr7:6771000-6786200	Weak transcription	HUVEC	blood vessel
4	chr7:6771000-6786400	Weak transcription	Primary B cells from cord blood	blood
5	chr7:6771200-6792400	Weak transcription	NHEK	skin
6	chr7:6772800-6787000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr7:6773000-6786400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:6773400-6788200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr7:6775800-6785000	Weak transcription	NH-A	brain
10	chr7:6777200-6784800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:6777200-6785000	Weak transcription	HSMM	muscle
12	chr7:6777200-6786600	Weak transcription	HSMMtube	muscle
13	chr7:6777400-6784800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:6777400-6784800	Weak transcription	Fetal Lung	lung
15	chr7:6777400-6786400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr7:6777400-6786400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr7:6777400-6786600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr7:6777400-6787000	Weak transcription	Fetal Kidney	kidney
19	chr7:6777400-6788200	Weak transcription	Brain Substantia Nigra	brain
20	chr7:6777400-6790600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr7:6777400-6791600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr7:6777400-6792000	Weak transcription	Colonic Mucosa	Colon
23	chr7:6777400-6792200	Weak transcription	Fetal Brain Female	brain
24	chr7:6777400-6793000	Weak transcription	Left Ventricle	heart
25	chr7:6777400-6793000	Weak transcription	Ovary	ovary
26	chr7:6777400-6793000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr7:6777400-6793800	Weak transcription	Brain Anterior Caudate	brain
28	chr7:6777600-6786400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr7:6777600-6786400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr7:6777600-6786400	Weak transcription	NHDF-Ad	bronchial
31	chr7:6777600-6792200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr7:6777600-6792200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr7:6777600-6792200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:6777600-6793000	Weak transcription	Gastric	stomach
35	chr7:6777600-6793000	Weak transcription	Spleen	Spleen
36	chr7:6777600-6793800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr7:6777600-6793800	Weak transcription	Brain Germinal Matrix	brain
38	chr7:6777800-6791400	Weak transcription	Esophagus	oesophagus
39	chr7:6777800-6793000	Weak transcription	Fetal Intestine Large	intestine
40	chr7:6779200-6784800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:6779200-6788200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr7:6780200-6787800	Weak transcription	Brain Hippocampus Middle	brain
43	chr7:6780200-6792200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:6780200-6793000	Weak transcription	Lung	lung
45	chr7:6780400-6784800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:6780400-6784800	Weak transcription	Primary T cells from cord blood	blood
47	chr7:6780400-6784800	Weak transcription	Liver	Liver
48	chr7:6780400-6784800	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr7:6780400-6785000	Weak transcription	Brain Angular Gyrus	brain
50	chr7:6780400-6785800	Weak transcription	A549	lung

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