Variant report

Variant	nsv606195
Chromosome Location	chr7:11140383-11216782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:0)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:11175371-11175473	K562	blood:	n/a	n/a
2	BATF	chr7:11160374-11160600	GM12878	blood:	n/a	n/a
3	BCL3	chr7:11195043-11195271	GM12878	blood:	n/a	n/a
4	BHLHE40	chr7:11215693-11215816	K562	blood:	n/a	n/a
5	BHLHE40	chr7:11210726-11210891	GM12878	blood:	n/a	n/a
6	BRCA1	chr7:11167087-11167179	GM12878	blood:	n/a	n/a
7	CEBPB	chr7:11210550-11210871	HepG2	liver:	n/a	chr7:11210690-11210701
8	CEBPB	chr7:11210526-11210841	IMR90	lung:	n/a	chr7:11210690-11210701
9	CEBPB	chr7:11210530-11210811	Hela-S3	cervix:	n/a	chr7:11210690-11210701
10	CEBPB	chr7:11169609-11170090	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:11210548-11210824	A549	lung:	n/a	chr7:11210690-11210701
12	CREB1	chr7:11160285-11160708	GM12878	blood:	n/a	n/a
13	CREB1	chr7:11210819-11211347	GM12878	blood:	n/a	n/a
14	CTCF	chr7:11193420-11193570	AG09319	gingival:	n/a	n/a
15	CTCF	chr7:11205495-11205611	GM12878	blood:	n/a	chr7:11205529-11205550
16	CTCF	chr7:11193245-11193764	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:11201882-11201973	Lung_OC	lung:	n/a	n/a
18	CTCF	chr7:11205460-11205610	HEEpiC	esophagus:	n/a	chr7:11205529-11205550
19	CTCF	chr7:11193348-11193541	GM12878	blood:	n/a	n/a
20	CTCF	chr7:11193460-11193610	Caco-2	colon:	n/a	n/a
21	CTCF	chr7:11205527-11205585	LNCaP	prostate:	n/a	chr7:11205529-11205550
22	CTCF	chr7:11193340-11193490	AG10803	skin:	n/a	n/a
23	CTCF	chr7:11211560-11211710	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr7:11193426-11193560	Gliobla	brain:	n/a	n/a
25	CTCF	chr7:11193400-11193550	HAc	cerebellar:	n/a	n/a
26	CTCF	chr7:11193400-11193621	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:11193420-11193527	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr7:11205512-11205612	LNCaP	prostate:	n/a	chr7:11205529-11205550
29	CTCF	chr7:11193400-11193550	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:11193323-11193632	K562	blood:	n/a	n/a
31	CTCF	chr7:11193400-11193550	RPTEC	kidney:	n/a	n/a
32	CTCF	chr7:11193380-11193530	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:11205503-11205584	GM10266	blood:	n/a	chr7:11205529-11205550
34	CTCF	chr7:11205369-11205742	GM12878	blood:	n/a	chr7:11205529-11205550
35	CTCF	chr7:11193451-11193552	HepG2	liver:	n/a	n/a
36	CTCF	chr7:11193400-11193550	BE2_C	brain:	n/a	n/a
37	CTCF	chr7:11193426-11193535	K562	blood:	n/a	n/a
38	CTCF	chr7:11193420-11193570	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr7:11193364-11193594	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:11205503-11205565	GM10248	blood:	n/a	chr7:11205529-11205550
41	CTCF	chr7:11193398-11193606	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:11169973-11169981	K562	blood:	n/a	n/a
43	CTCF	chr7:11193382-11193624	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:11193255-11193758	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:11193420-11193570	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr7:11205490-11205605	Hela-S3	cervix:	n/a	chr7:11205529-11205550
47	CUX1	chr7:11168345-11168348	K562	blood:	n/a	n/a
48	E2F4	chr7:11216210-11216391	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr7:11167092-11167334	GM12878	blood:	n/a	chr7:11167213-11167224
50	EBF1	chr7:11210613-11210807	GM12878	blood:	n/a	n/a

No data

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:11140028..11142682-chr7:11145035..11146787,2	K562	blood:
2	chr7:11162789..11165137-chr7:11166828..11168631,2	K562	blood:
3	chr7:11162789..11165137-chr7:11166828..11168631,2	K562	blood:
4	chr7:11192916..11193961-chr7:11251567..11252421,4	MCF-7	breast:
5	chr7:11196790..11199546-chr7:11202946..11205522,2	K562	blood:
6	chr7:11179754..11182412-chr7:11187476..11189973,2	K562	blood:
7	chr7:11193091..11193870-chr7:11383205..11383845,2	MCF-7	breast:
8	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
9	chr7:5013239..5014028-chr7:11185489..11186384,2	NB4	blood:
10	chr7:11187936..11191247-chr7:11191383..11194500,4	K562	blood:
11	chr7:11187936..11191247-chr7:11191383..11194500,4	K562	blood:
12	chr7:11175308..11177163-chr7:11367863..11369367,2	MCF-7	breast:
13	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
14	chr7:11141677..11144293-chr7:11222755..11224742,2	K562	blood:
15	chr7:11149421..11151035-chr7:11153801..11157843,3	K562	blood:
16	chr7:11012606..11015240-chr7:11166727..11169294,2	MCF-7	breast:
17	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
18	chr7:11140028..11142682-chr7:11145035..11146787,2	K562	blood:
19	chr7:11140028..11142682-chr7:11145035..11147597,3	K562	blood:
20	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
21	chr7:11193379..11193920-chr7:11380707..11381612,2	MCF-7	breast:
22	chr7:11169416..11171057-chr7:11171117..11173550,2	K562	blood:
23	chr7:11193047..11193912-chr7:11250807..11251473,2	MCF-7	breast:
24	chr7:11196790..11199292-chr7:11202946..11205439,2	K562	blood:
25	chr7:11196790..11199546-chr7:11202946..11205522,2	K562	blood:
26	chr7:11196790..11199292-chr7:11202946..11205439,2	K562	blood:
27	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
28	chr7:11197789..11199466-chr7:11199534..11202480,2	K562	blood:
29	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
30	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
31	chr7:11197789..11199466-chr7:11199534..11202480,2	K562	blood:
32	chr7:11140028..11142682-chr7:11145035..11147597,3	K562	blood:
33	chr7:11146142..11148658-chr7:11151256..11153162,2	K562	blood:
34	chr7:11169416..11171057-chr7:11171117..11173550,2	K562	blood:
35	chr7:11205391..11208108-chr7:11211440..11214054,2	MCF-7	breast:
36	chr7:11205391..11208108-chr7:11211440..11214054,2	MCF-7	breast:
37	chr7:11193309..11193972-chr7:11380975..11381751,3	MCF-7	breast:
38	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
39	chr7:11179754..11182412-chr7:11187476..11189973,2	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF14	hsa-miR-155-5p	chr7:11142799-11142820
2	PHF14	hsa-miR-155-5p	chr7:11142813-11142835
3	PHF14	hsa-miR-155-5p	chr7:11148709-11148731

Variant related genes	Relation type
PHF14	TF binding region
ENSG00000230333	TF binding region
ENSG00000196204	chromatin interactions
ENSG00000106443	chromatin interactions

Extended variants
information (count: 2880 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2880 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7790568	chr7:11140383-11140384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368675415	chr7:11140424-11140425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560382812	chr7:11140457-11140458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs578106390	chr7:11140482-11140483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs193293513	chr7:11140531-11140532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552615190	chr7:11140540-11140541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185153481	chr7:11140551-11140552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553002645	chr7:11140612-11140613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142912264	chr7:11140708-11140709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3801453	chr7:11140783-11140784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs568672060	chr7:11140784-11140785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150641736	chr7:11140807-11140808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3801454	chr7:11140869-11140870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566433878	chr7:11140934-11140935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529392669	chr7:11140937-11140938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538304392	chr7:11140944-11140945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558130101	chr7:11140981-11140982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574864002	chr7:11140987-11140988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544137680	chr7:11140998-11140999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139747238	chr7:11141011-11141012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560749874	chr7:11141022-11141023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574624477	chr7:11141026-11141027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540046429	chr7:11141032-11141033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560255108	chr7:11141050-11141051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149775353	chr7:11141146-11141147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546292435	chr7:11141218-11141219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562886535	chr7:11141235-11141236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531721511	chr7:11141245-11141246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368120919	chr7:11141249-11141250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548927417	chr7:11141305-11141306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562239975	chr7:11141393-11141394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188668438	chr7:11141397-11141398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35619104	chr7:11141434-11141435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547680743	chr7:11141439-11141440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570218643	chr7:11141522-11141523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60453852	chr7:11141547-11141548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538365500	chr7:11141643-11141644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551819007	chr7:11141662-11141663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568543197	chr7:11141703-11141704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34478682	chr7:11141740-11141741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369928890	chr7:11141754-11141755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367914130	chr7:11141781-11141782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145725292	chr7:11141860-11141861	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554891562	chr7:11141898-11141899	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574655299	chr7:11141944-11141945	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534047481	chr7:11141987-11141988	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553707789	chr7:11141994-11141995	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528052284	chr7:11141996-11141997	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546354098	chr7:11142002-11142003	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114607343	chr7:11142041-11142042	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Autism	22495309	CNVD
Cancer	20164919	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11046200-11175000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr7:11046600-11167800	Weak transcription	Thymus	Thymus
3	chr7:11057800-11190200	Weak transcription	Fetal Brain Male	brain
4	chr7:11076400-11193200	Weak transcription	Ovary	ovary
5	chr7:11077000-11162400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr7:11086600-11143800	Weak transcription	HUVEC	blood vessel
7	chr7:11091800-11174200	Weak transcription	Left Ventricle	heart
8	chr7:11094600-11153400	Weak transcription	Hela-S3	cervix
9	chr7:11102200-11189200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr7:11102400-11167800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr7:11102600-11144000	Weak transcription	Liver	Liver
12	chr7:11102600-11161000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr7:11102600-11173200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr7:11102600-11173400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:11102600-11190400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr7:11103000-11189000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr7:11107600-11152800	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr7:11107600-11212200	Weak transcription	Fetal Kidney	kidney
19	chr7:11107800-11161000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr7:11109000-11143800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:11113200-11211800	Weak transcription	Fetal Intestine Large	intestine
22	chr7:11113600-11166600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr7:11113800-11155600	Weak transcription	Brain Germinal Matrix	brain
24	chr7:11114400-11143800	Weak transcription	Fetal Thymus	thymus
25	chr7:11114600-11210000	Weak transcription	Fetal Brain Female	brain
26	chr7:11114800-11142000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:11118000-11199000	Weak transcription	HSMM	muscle
28	chr7:11122800-11153400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr7:11122800-11169800	Weak transcription	Fetal Muscle Leg	muscle
30	chr7:11122800-11173000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr7:11123000-11144200	Weak transcription	GM12878-XiMat	blood
32	chr7:11123000-11161000	Weak transcription	HSMMtube	muscle
33	chr7:11123000-11163000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:11123000-11173200	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr7:11123000-11177800	Weak transcription	HepG2	liver
36	chr7:11123200-11155800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr7:11123400-11169800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr7:11123600-11142000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:11123600-11161000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr7:11124800-11151000	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr7:11125000-11144200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr7:11125000-11162200	Weak transcription	Colon Smooth Muscle	Colon
43	chr7:11125400-11188000	Weak transcription	Small Intestine	intestine
44	chr7:11125800-11167000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:11126200-11142400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:11129000-11142400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:11129200-11142200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:11129600-11154200	Weak transcription	Fetal Lung	lung
49	chr7:11132200-11155800	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr7:11133600-11151000	Weak transcription	Primary hematopoietic stem cells	blood

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