Variant report

Variant	nsv983059
Chromosome Location	chr11:104914933-104916043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:124)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:104915949-104916196	GM12878	blood:	n/a	n/a
2	CEBPB	chr11:104915430-104916328	IMR90	lung:	n/a	chr11:104915784-104915797
3	CEBPB	chr11:104914457-104916305	Hela-S3	cervix:	n/a	chr11:104915784-104915797
4	CTCF	chr11:104915481-104915558	Spleen_OC	spleen:	n/a	n/a
5	E2F4	chr11:104915974-104916280	MCF10A-Er-Src	breast:	n/a	n/a
6	EBF1	chr11:104915907-104916477	GM12878	blood:	n/a	n/a
7	EP300	chr11:104914850-104915159	Hela-S3	cervix:	n/a	n/a
8	EP300	chr11:104915934-104916072	GM12878	blood:	n/a	n/a
9	EP300	chr11:104915957-104916127	GM12878	blood:	n/a	n/a
10	EP300	chr11:104915951-104916258	Hela-S3	cervix:	n/a	n/a
11	FOS	chr11:104916034-104916245	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr11:104915938-104916278	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr11:104915927-104916246	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr11:104914949-104915170	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104915099-104915109
15	FOS	chr11:104914860-104915222	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104914879-104914888 chr11:104915099-104915109
16	FOS	chr11:104915931-104916250	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr11:104914969-104915169	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104915099-104915109
18	FOS	chr11:104914952-104915225	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104915099-104915109
19	IKZF1	chr11:104915870-104916108	GM12878	blood:	n/a	n/a
20	IRF4	chr11:104915923-104916270	GM12878	blood:	n/a	chr11:104916055-104916069
21	MAZ	chr11:104915920-104916116	GM12878	blood:	n/a	n/a
22	MXI1	chr11:104915914-104916254	GM12878	blood:	n/a	n/a
23	MXI1	chr11:104915447-104916126	Hela-S3	cervix:	n/a	n/a
24	MYC	chr11:104915938-104916269	MCF10A-Er-Src	breast:	n/a	n/a
25	MYC	chr11:104915927-104916324	MCF10A-Er-Src	breast:	n/a	n/a
26	MYC	chr11:104915885-104916133	NB4	blood:	n/a	n/a
27	POLR2A	chr11:104915766-104916641	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr11:104915912-104916234	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:104915034-104915053	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr11:104915810-104916256	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:104915782-104916329	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr11:104915088-104915169	HepG2	liver:	n/a	n/a
33	POLR2A	chr11:104915946-104916118	GM12878	blood:	n/a	n/a
34	POLR2A	chr11:104915943-104916249	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr11:104915792-104916183	GM12892	blood:	n/a	n/a
36	POLR2A	chr11:104915646-104916222	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr11:104915764-104916208	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr11:104915382-104915402	ProgFib	skin:	n/a	n/a
39	POLR2A	chr11:104915836-104916140	GM12891	blood:	n/a	n/a
40	POLR2A	chr11:104915825-104916334	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr11:104915706-104916257	GM12878	blood:	n/a	n/a
42	POLR2A	chr11:104915879-104916135	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:104915864-104916242	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr11:104915687-104916248	GM12892	blood:	n/a	n/a
45	POLR2A	chr11:104914870-104915025	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr11:104914799-104915032	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr11:104915821-104916199	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr11:104915834-104916114	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr11:104915853-104916122	GM12891	blood:	n/a	n/a
50	POLR2A	chr11:104915793-104916186	GM12891	blood:	n/a	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104916018-104916068	GM12891	blood:	n/a
2	chr11:104916018-104916068	HEEpiC	esophagus:	n/a
3	chr11:104916018-104916068	GM12891	blood:	n/a
4	chr11:104916018-104916068	HEEpiC	esophagus:	n/a
5	chr11:104915759-104915809	Jurkat	blood:	n/a
6	chr11:104916018-104916068	AG04450	lung:	fetal
7	chr11:104916018-104916068	NB4	blood:	n/a
8	chr11:104916018-104916068	GM06990	blood:	n/a
9	chr11:104916018-104916068	MCF-7	breast:	n/a
10	chr11:104915759-104915809	HepG2	liver:	n/a
11	chr11:104916018-104916068	SKMC	muscle:	n/a
12	chr11:104915759-104915809	HL-60	blood:	n/a
13	chr11:104916018-104916068	HRPEpiC	eye:	n/a
14	chr11:104916018-104916068	H1-hESC	embryonic stem cell:	embryo
15	chr11:104916018-104916068	HCT-116	colon:	n/a
16	chr11:104915759-104915809	ovcar-3	ovarian:	n/a
17	chr11:104915759-104915809	AG10803	skin:	n/a
18	chr11:104915759-104915809	PANC-1	pancreas:	n/a
19	chr11:104915759-104915809	BE2_C	brain:	n/a
20	chr11:104915759-104915809	NT2-D1	testis:	n/a
21	chr11:104915759-104915809	LNCaP	prostate:	n/a
22	chr11:104916018-104916068	MCF10A-Er-Src	breast:	n/a
23	chr11:104915759-104915809	Hela-S3	cervix:	n/a
24	chr11:104915759-104915809	GM06990	blood:	n/a
25	chr11:104915759-104915809	HEK293	kidney:	embryo
26	chr11:104916018-104916068	HRE	kidney:	n/a
27	chr11:104916018-104916068	ECC-1	luminal epithelium:	n/a
28	chr11:104915759-104915809	HRCEpiC	kidney:	n/a
29	chr11:104916018-104916068	HCM	heart:	n/a
30	chr11:104915759-104915809	U87	brain:	n/a
31	chr11:104916018-104916068	HCF	heart:	n/a
32	chr11:104915759-104915809	K562	blood:	n/a
33	chr11:104915759-104915809	HRPEpiC	eye:	n/a
34	chr11:104916018-104916068	NH-A	brain:	n/a
35	chr11:104915759-104915809	ProgFib	skin:	n/a
36	chr11:104915759-104915809	AG09319	gingival:	n/a
37	chr11:104915759-104915809	BJ	skin:	n/a
38	chr11:104915759-104915809	AG04449	skin:	fetal
39	chr11:104916018-104916068	HNPCEpiC	eye:	n/a
40	chr11:104916018-104916068	GM12892	blood:	n/a
41	chr11:104916018-104916068	Caco-2	colon:	n/a
42	chr11:104916018-104916068	AoSMC	blood vessel:	n/a
43	chr11:104916018-104916068	K562	blood:	n/a
44	chr11:104915759-104915809	HNPCEpiC	eye:	n/a
45	chr11:104915759-104915809	H1-hESC	embryonic stem cell:	embryo
46	chr11:104915759-104915809	AG04450	lung:	fetal
47	chr11:104916018-104916068	GM12878	blood:	n/a
48	chr11:104916018-104916068	AG04449	skin:	fetal
49	chr11:104916018-104916068	SK-N-SH_RA	brain:	n/a
50	chr11:104916018-104916068	BE2_C	brain:	n/a

No data

Variant related genes	Relation type
CARD16	TF binding region
CARD16	CpG island

Extended variants
information (count: 101 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144816877	chr11:104914940-104914941	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs530492114	chr11:104914953-104914954	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs559064305	chr11:104914958-104914959	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs9326349	chr11:104914969-104914970	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs182957768	chr11:104915004-104915005	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs187474278	chr11:104915031-104915032	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs530394997	chr11:104915033-104915034	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs550449745	chr11:104915058-104915059	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs368940697	chr11:104915072-104915073	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs200328492	chr11:104915102-104915103	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs539257762	chr11:104915130-104915131	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs148140246	chr11:104915136-104915137	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs1126876	chr11:104915139-104915140	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs566205624	chr11:104915146-104915147	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs61733761	chr11:104915150-104915151	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs375916476	chr11:104915152-104915153	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs199566346	chr11:104915155-104915156	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs367937905	chr11:104915180-104915181	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs558248194	chr11:104915193-104915194	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs577987861	chr11:104915196-104915197	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs146931452	chr11:104915199-104915200	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs536998270	chr11:104915204-104915205	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs139318583	chr11:104915208-104915209	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs557231889	chr11:104915212-104915213	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs201870366	chr11:104915223-104915224	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs34534919	chr11:104915226-104915227	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs143331896	chr11:104915230-104915231	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs199997208	chr11:104915231-104915232	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs377353282	chr11:104915232-104915233	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs372103546	chr11:104915240-104915241	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs201107738	chr11:104915244-104915245	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs142951802	chr11:104915257-104915258	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs192024074	chr11:104915260-104915261	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs61739406	chr11:104915268-104915269	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs148134489	chr11:104915270-104915271	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs61739403	chr11:104915273-104915274	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs61739404	chr11:104915274-104915275	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs377015648	chr11:104915275-104915276	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs61739405	chr11:104915276-104915277	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs141971448	chr11:104915278-104915279	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs1042744	chr11:104915284-104915285	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs188243534	chr11:104915288-104915289	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs35966314	chr11:104915294-104915295	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs536110507	chr11:104915300-104915301	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs111637952	chr11:104915301-104915302	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs61739396	chr11:104915303-104915304	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs184275239	chr11:104915314-104915315	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs61739387	chr11:104915344-104915345	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs369586730	chr11:104915346-104915347	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs141911009	chr11:104915349-104915350	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104906600-104915600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr11:104910200-104915800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:104912200-104915600	Weak transcription	Placenta	Placenta
4	chr11:104912400-104915800	Weak transcription	HepG2	liver
5	chr11:104912600-104917800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr11:104912600-104920800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:104913000-104915000	Flanking Active TSS	Primary T cells from cord blood	blood
8	chr11:104913000-104916200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr11:104913600-104915200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr11:104913600-104915600	Flanking Active TSS	Dnd41	blood
11	chr11:104913600-104916200	Active TSS	Hela-S3	cervix
12	chr11:104913600-104916400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:104913600-104916600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:104913800-104915000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
15	chr11:104913800-104915200	Flanking Active TSS	Primary hematopoietic stem cells	blood
16	chr11:104913800-104915600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr11:104913800-104916000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:104913800-104916200	Active TSS	Primary T cells fromperipheralblood	blood
19	chr11:104914000-104916200	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr11:104914000-104916600	Active TSS	Duodenum Smooth Muscle	Duodenum
21	chr11:104914200-104915200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
22	chr11:104914200-104915600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:104914200-104915800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr11:104914200-104916000	Active TSS	Lung	lung
25	chr11:104914200-104916000	Active TSS	Right Ventricle	heart
26	chr11:104914200-104916000	Active TSS	GM12878-XiMat	blood
27	chr11:104914200-104916200	Active TSS	Colonic Mucosa	Colon
28	chr11:104914200-104916400	Active TSS	Ovary	ovary
29	chr11:104914200-104916400	Flanking Active TSS	HUVEC	blood vessel
30	chr11:104914200-104916600	Active TSS	Rectal Smooth Muscle	rectum
31	chr11:104914400-104915600	Enhancers	NHEK	skin
32	chr11:104914400-104915800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr11:104914400-104916200	Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr11:104914400-104916400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr11:104914400-104916400	Active TSS	Brain Hippocampus Middle	brain
36	chr11:104914400-104916400	Active TSS	Fetal Muscle Leg	muscle
37	chr11:104914400-104916400	Active TSS	Stomach Smooth Muscle	stomach
38	chr11:104914600-104915000	Enhancers	Liver	Liver
39	chr11:104914600-104915000	Enhancers	Colon Smooth Muscle	Colon
40	chr11:104914600-104915000	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr11:104914600-104915400	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr11:104914600-104915600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:104914600-104915600	Weak transcription	Esophagus	oesophagus
44	chr11:104914600-104915600	Weak transcription	Fetal Intestine Large	intestine
45	chr11:104914600-104915600	Weak transcription	Fetal Stomach	stomach
46	chr11:104914600-104915600	Weak transcription	Fetal Thymus	thymus
47	chr11:104914600-104915600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:104914600-104916200	Active TSS	Primary monocytes fromperipheralblood	blood
49	chr11:104914600-104916200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr11:104914600-104916200	Active TSS	Primary T helper naive cells from peripheral blood	blood

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