Variant report

Variant	nsv971285
Chromosome Location	chr8:11181086-11184863
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:11181267-11181696	GM12878	blood:	n/a	n/a
2	BHLHE40	chr8:11181454-11181536	GM12878	blood:	n/a	n/a
3	EBF1	chr8:11181483-11181534	GM12878	blood:	n/a	n/a
4	EP300	chr8:11181423-11181623	GM12878	blood:	n/a	n/a
5	EP300	chr8:11181320-11181594	GM12878	blood:	n/a	n/a
6	FOXA1	chr8:11181175-11181508	HepG2	liver:	n/a	n/a
7	FOXA2	chr8:11181164-11181475	HepG2	liver:	n/a	n/a
8	FOXM1	chr8:11181294-11181684	GM12878	blood:	n/a	n/a
9	IKZF1	chr8:11181333-11181610	GM12878	blood:	n/a	n/a
10	JUN	chr8:11183847-11184013	K562	blood:	n/a	n/a
11	MAZ	chr8:11183733-11183825	HepG2	liver:	n/a	n/a
12	NFIC	chr8:11181226-11181695	GM12878	blood:	n/a	n/a
13	PAX5	chr8:11181377-11181552	GM12878	blood:	n/a	n/a
14	POLR2A	chr8:11182549-11182586	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr8:11183643-11183723	HepG2	liver:	n/a	n/a
16	POLR2A	chr8:11182467-11182544	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr8:11182293-11182294	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr8:11182384-11182395	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr8:11182324-11182343	A549	lung:	n/a	n/a
20	RFX5	chr8:11181424-11181580	GM12878	blood:	n/a	n/a
21	RUNX3	chr8:11181234-11181755	GM12878	blood:	n/a	n/a
22	RUNX3	chr8:11181289-11181664	GM12878	blood:	n/a	n/a
23	STAT3	chr8:11181424-11181605	GM12878	blood:	n/a	n/a
24	TBP	chr8:11181450-11181542	GM12878	blood:	n/a	n/a
25	TCF7L2	chr8:11184726-11185039	HepG2	liver:	n/a	n/a
26	ZNF143	chr8:11181378-11181557	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11182979-11183029	HNPCEpiC	eye:	n/a
2	chr8:11182979-11183029	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:11183844-11183894	IMR90	lung:	fetal
4	chr8:11184217-11184267	NT2-D1	testis:	n/a
5	chr8:11182979-11183029	HCPEpiC	choroid plexus:	n/a
6	chr8:11184217-11184267	HIPEpiC	eye:	n/a
7	chr8:11183844-11183894	AG04449	skin:	fetal
8	chr8:11182979-11183029	GM12891	blood:	n/a
9	chr8:11182979-11183029	MCF10A-Er-Src	breast:	n/a
10	chr8:11183844-11183894	HEK293	kidney:	embryo
11	chr8:11183844-11183894	SK-N-SH_RA	brain:	n/a
12	chr8:11184217-11184267	Hela-S3	cervix:	n/a
13	chr8:11183014-11183064	SK-N-SH	brain:	n/a
14	chr8:11184217-11184267	SK-N-SH_RA	brain:	n/a
15	chr8:11182872-11182922	HEEpiC	esophagus:	n/a
16	chr8:11184217-11184267	HMEC	breast:	n/a
17	chr8:11182872-11182922	NHDF-neo	bronchial:	n/a
18	chr8:11182872-11182922	HCPEpiC	choroid plexus:	n/a
19	chr8:11183844-11183894	ovcar-3	ovarian:	n/a
20	chr8:11182872-11182922	ProgFib	skin:	n/a
21	chr8:11182872-11182922	NHBE	bronchial:	n/a
22	chr8:11183014-11183064	ovcar-3	ovarian:	n/a
23	chr8:11182979-11183029	SAEC	small airway:	n/a
24	chr8:11184217-11184267	Hepatocyte	liver:	n/a
25	chr8:11182979-11183029	K562	blood:	n/a
26	chr8:11182872-11182922	ECC-1	luminal epithelium:	n/a
27	chr8:11182872-11182922	GM12891	blood:	n/a
28	chr8:11182979-11183029	HL-60	blood:	n/a
29	chr8:11183844-11183894	HCM	heart:	n/a
30	chr8:11183844-11183894	SK-N-SH	brain:	n/a
31	chr8:11182979-11183029	AG10803	skin:	n/a
32	chr8:11183014-11183064	HCT-116	colon:	n/a
33	chr8:11182979-11183029	HRE	kidney:	n/a
34	chr8:11183014-11183064	HNPCEpiC	eye:	n/a
35	chr8:11183844-11183894	H1-hESC	embryonic stem cell:	embryo
36	chr8:11184217-11184267	CMK	blood:	n/a
37	chr8:11183014-11183064	A549	lung:	n/a
38	chr8:11183844-11183894	AoSMC	blood vessel:	n/a
39	chr8:11182979-11183029	NH-A	brain:	n/a
40	chr8:11184217-11184267	ovcar-3	ovarian:	n/a
41	chr8:11183844-11183894	HRPEpiC	eye:	n/a
42	chr8:11184217-11184267	HEK293	kidney:	embryo
43	chr8:11182979-11183029	NB4	blood:	n/a
44	chr8:11184217-11184267	AoSMC	blood vessel:	n/a
45	chr8:11183844-11183894	U87	brain:	n/a
46	chr8:11182979-11183029	HCM	heart:	n/a
47	chr8:11182872-11182922	HMEC	breast:	n/a
48	chr8:11182872-11182922	GM19239	blood:	n/a
49	chr8:11182872-11182922	PrEC	prostate:	n/a
50	chr8:11183844-11183894	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:11170423..11173089-chr8:11183633..11185692,2	K562	blood:
2	chr8:11177843..11179564-chr8:11181108..11182895,2	K562	blood:
3	chr8:11140705..11143665-chr8:11184811..11187065,2	K562	blood:
4	chr8:11160652..11163561-chr8:11179931..11182609,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF131216.6.1-2	chr8:11181416-11182018	NONHSAT125048

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	MTMR9	hsa-miR-148a-3p	chr8:11181198-11181204
2	MTMR9	hsa-miR-130b-3p	chr8:11181184-11181204
3	MTMR9	hsa-miR-148a-3p	chr8:11181171-11181177
4	MTMR9	hsa-miR-34a-5p	chr8:11181173-11181179
5	MTMR9	hsa-miR-148a-3p	chr8:11181185-11181205

Variant related genes	Relation type
SLC35G5	TF binding region
ENSG00000246477	TF binding region
SLC35G5	CpG island
ENSG00000246477	CpG island
ENSG00000104643	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546099412	chr8:11181121-11181122	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560536103	chr8:11181161-11181162	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138332448	chr8:11181175-11181176	Weak transcription Strong transcription Enhancers Genic enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
4	rs182928895	chr8:11181200-11181201	Weak transcription Strong transcription Enhancers Genic enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
5	rs141889352	chr8:11181211-11181212	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150653850	chr8:11181233-11181234	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139780862	chr8:11181257-11181258	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186201539	chr8:11181289-11181290	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548161007	chr8:11181309-11181310	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200437726	chr8:11181357-11181358	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201453624	chr8:11181359-11181360	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377024504	chr8:11181391-11181392	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1046510	chr8:11181418-11181419	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs149392497	chr8:11181462-11181463	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs111691498	chr8:11181495-11181496	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs146368940	chr8:11181496-11181497	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs543720883	chr8:11181516-11181517	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs537113318	chr8:11181577-11181578	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs552107779	chr8:11181655-11181656	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs529331734	chr8:11181657-11181658	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs12682265	chr8:11181679-11181680	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs190869080	chr8:11181689-11181690	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs534492277	chr8:11181711-11181712	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs372968053	chr8:11181716-11181717	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs552886356	chr8:11181744-11181745	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs574385649	chr8:11181782-11181783	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs535469492	chr8:11181788-11181789	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs139742019	chr8:11181822-11181823	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs371402438	chr8:11181837-11181838	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs182672482	chr8:11181839-11181840	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs564409251	chr8:11181841-11181842	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs188813014	chr8:11181849-11181850	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs531115859	chr8:11181908-11181909	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs74391833	chr8:11181956-11181957	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs34270001	chr8:11182019-11182020	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74876306	chr8:11182037-11182038	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200474295	chr8:11182039-11182040	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539612398	chr8:11182051-11182052	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529570773	chr8:11182053-11182054	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548223698	chr8:11182067-11182068	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557921838	chr8:11182108-11182109	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74984782	chr8:11182137-11182138	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6995404	chr8:11182148-11182149	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs2736261	chr8:11182183-11182184	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs534550823	chr8:11182218-11182219	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192356734	chr8:11182225-11182226	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79618563	chr8:11182230-11182231	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531911195	chr8:11182264-11182265	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374147050	chr8:11182265-11182266	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546122029	chr8:11182294-11182295	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11154200-11181400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr8:11154200-11183800	Strong transcription	Liver	Liver
3	chr8:11154600-11183000	Strong transcription	Fetal Muscle Trunk	muscle
4	chr8:11155000-11184000	Strong transcription	Dnd41	blood
5	chr8:11155600-11183200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr8:11157400-11182600	Strong transcription	Skeletal Muscle Female	skeletal muscle
7	chr8:11157600-11183000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr8:11161600-11183200	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr8:11161800-11182600	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr8:11162000-11181200	Strong transcription	HSMM	muscle
11	chr8:11162000-11182600	Strong transcription	Duodenum Mucosa	Duodenum
12	chr8:11162000-11183400	Strong transcription	Primary T cells from cord blood	blood
13	chr8:11162200-11181600	Strong transcription	Primary B cells from peripheral blood	blood
14	chr8:11162200-11183200	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr8:11162400-11182600	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:11162400-11183000	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr8:11162400-11183000	Strong transcription	Adipose Nuclei	Adipose
18	chr8:11162400-11183200	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr8:11162400-11183600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr8:11162400-11183800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr8:11162400-11184000	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr8:11162400-11184000	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr8:11162400-11184200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:11162600-11182800	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr8:11162600-11184000	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:11165400-11181200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr8:11167400-11185200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr8:11167800-11184600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr8:11170600-11185400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:11170800-11183800	Strong transcription	Primary hematopoietic stem cells	blood
31	chr8:11171000-11183000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:11171000-11184200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:11171000-11184200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr8:11171200-11183200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr8:11171200-11183400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:11171600-11191400	Weak transcription	Psoas Muscle	Psoas
37	chr8:11172200-11183600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr8:11173800-11183200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr8:11174000-11183800	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr8:11174400-11182000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr8:11175400-11185000	Weak transcription	Small Intestine	intestine
42	chr8:11175800-11183800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr8:11176000-11184200	Weak transcription	Right Ventricle	heart
44	chr8:11176000-11184400	Weak transcription	K562	blood
45	chr8:11176000-11185600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:11176000-11187800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr8:11176000-11189000	Weak transcription	Gastric	stomach
48	chr8:11176600-11187000	Weak transcription	Colonic Mucosa	Colon
49	chr8:11177000-11182200	Strong transcription	Fetal Brain Female	brain
50	chr8:11177000-11182600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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