Variant report

Variant	esv33330
Chromosome Location	chr11:71404311-71427551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:510)
CpG islands
(count:488)
Chromatin interactive
region (count:0)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
2	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
3	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
4	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
5	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
6	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
7	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
8	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
10	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
11	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
12	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
13	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
14	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
15	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
16	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
17	BCL11A	chr11:71425414-71425925	GM12878	blood:	n/a	n/a
18	BCL11A	chr11:71406992-71407565	GM12878	blood:	n/a	n/a
19	BCL11A	chr11:71426893-71427066	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:71421456-71421625	GM12878	blood:	n/a	n/a
21	BCL11A	chr11:71423022-71423248	GM12878	blood:	n/a	n/a
22	BCL11A	chr11:71425028-71425302	GM12878	blood:	n/a	n/a
23	BCL11A	chr11:71407051-71407260	GM12878	blood:	n/a	n/a
24	BCL11A	chr11:71425402-71425946	GM12878	blood:	n/a	n/a
25	BCL11A	chr11:71421911-71422277	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:71422007-71422279	GM12878	blood:	n/a	n/a
27	CBX3	chr11:71407215-71407600	K562	blood:	n/a	n/a
28	CBX3	chr11:71416054-71416848	K562	blood:	n/a	n/a
29	CBX3	chr11:71427417-71428015	K562	blood:	n/a	chr11:71427545-71427556
30	CBX3	chr11:71412681-71413317	K562	blood:	n/a	n/a
31	CBX3	chr11:71416099-71416860	K562	blood:	n/a	n/a
32	CEBPB	chr11:71417107-71417265	K562	blood:	n/a	n/a
33	CEBPB	chr11:71416396-71416836	K562	blood:	n/a	n/a
34	CEBPB	chr11:71416985-71417411	K562	blood:	n/a	n/a
35	CEBPB	chr11:71410232-71410343	A549	lung:	n/a	n/a
36	CEBPB	chr11:71415991-71416919	K562	blood:	n/a	n/a
37	CEBPB	chr11:71410037-71410373	K562	blood:	n/a	n/a
38	CEBPB	chr11:71410234-71410354	K562	blood:	n/a	n/a
39	CEBPB	chr11:71423993-71424152	K562	blood:	n/a	n/a
40	CEBPB	chr11:71416448-71416822	K562	blood:	n/a	n/a
41	CEBPB	chr11:71412457-71412469	A549	lung:	n/a	n/a
42	CEBPB	chr11:71410128-71410324	MCF-7	breast:	n/a	n/a
43	CEBPB	chr11:71417048-71417357	K562	blood:	n/a	n/a
44	CEBPD	chr11:71423953-71424424	K562	blood:	n/a	n/a
45	CEBPD	chr11:71416336-71417381	K562	blood:	n/a	n/a
46	CTCF	chr11:71410140-71410290	GM12865	blood:	n/a	n/a
47	CTCF	chr11:71410100-71410250	AG09319	gingival:	n/a	n/a
48	CTCF	chr11:71407583-71407630	GM20000	blood:	n/a	n/a
49	CTCF	chr11:71422636-71422702	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr11:71418120-71418270	RPTEC	kidney:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71417713-71417763	HepG2	liver:	n/a
2	chr11:71420947-71420997	SK-N-MC	brain:	n/a
3	chr11:71420485-71420535	CMK	blood:	n/a
4	chr11:71420485-71420535	AoSMC	blood vessel:	n/a
5	chr11:71420485-71420535	AG09319	gingival:	n/a
6	chr11:71421380-71421430	HNPCEpiC	eye:	n/a
7	chr11:71421380-71421430	A549	lung:	n/a
8	chr11:71418204-71418254	IMR90	lung:	fetal
9	chr11:71420485-71420535	Hela-S3	cervix:	n/a
10	chr11:71421380-71421430	NH-A	brain:	n/a
11	chr11:71417713-71417763	SAEC	small airway:	n/a
12	chr11:71420947-71420997	H1-hESC	embryonic stem cell:	embryo
13	chr11:71420467-71420517	U87	brain:	n/a
14	chr11:71417713-71417763	HRPEpiC	eye:	n/a
15	chr11:71421279-71421329	GM12892	blood:	n/a
16	chr11:71421279-71421329	HMEC	breast:	n/a
17	chr11:71421279-71421329	GM06990	blood:	n/a
18	chr11:71417657-71417707	CMK	blood:	n/a
19	chr11:71417657-71417707	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:71421279-71421329	IMR90	lung:	fetal
21	chr11:71418204-71418254	AG04450	lung:	fetal
22	chr11:71421380-71421430	HRCEpiC	kidney:	n/a
23	chr11:71421279-71421329	HCPEpiC	choroid plexus:	n/a
24	chr11:71417657-71417707	NHBE	bronchial:	n/a
25	chr11:71421279-71421329	HL-60	blood:	n/a
26	chr11:71417713-71417763	NB4	blood:	n/a
27	chr11:71421380-71421430	BE2_C	brain:	n/a
28	chr11:71420947-71420997	ECC-1	luminal epithelium:	n/a
29	chr11:71418204-71418254	HCT-116	colon:	n/a
30	chr11:71421279-71421329	GM19239	blood:	n/a
31	chr11:71420467-71420517	HEEpiC	esophagus:	n/a
32	chr11:71417713-71417763	PANC-1	pancreas:	n/a
33	chr11:71421380-71421430	HepG2	liver:	n/a
34	chr11:71420467-71420517	NHBE	bronchial:	n/a
35	chr11:71417657-71417707	HNPCEpiC	eye:	n/a
36	chr11:71421279-71421329	HPAEpiC	pulmonary alveolar:	n/a
37	chr11:71417713-71417763	GM12878	blood:	n/a
38	chr11:71420947-71420997	T-47D	breast:	n/a
39	chr11:71418204-71418254	HL-60	blood:	n/a
40	chr11:71420467-71420517	H1-hESC	embryonic stem cell:	embryo
41	chr11:71420467-71420517	GM12892	blood:	n/a
42	chr11:71421279-71421329	SKMC	muscle:	n/a
43	chr11:71421380-71421430	MCF10A-Er-Src	breast:	n/a
44	chr11:71421380-71421430	PFSK-1	brain:	n/a
45	chr11:71421380-71421430	HEK293	kidney:	embryo
46	chr11:71418204-71418254	Jurkat	blood:	n/a
47	chr11:71421380-71421430	NHBE	bronchial:	n/a
48	chr11:71421279-71421329	NHDF-neo	bronchial:	n/a
49	chr11:71420467-71420517	RPTEC	kidney:	n/a
50	chr11:71420467-71420517	GM19239	blood:	n/a

No data

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
2	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
3	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
4	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
5	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
6	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1

No data

Variant related genes	Relation type
ENSG00000254805	TF binding region
ENPP7P8	TF binding region
ENSG00000223235	TF binding region
ENSG00000254972	TF binding region
ENSG00000254805	CpG island
ENPP7P8	CpG island
ENSG00000223235	CpG island
ENSG00000254972	CpG island

Extended variants
information (count: 1351 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56796099	chr11:71404318-71404319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377365755	chr11:71404320-71404321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571349442	chr11:71404328-71404329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538745885	chr11:71404357-71404358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557180029	chr11:71404374-71404375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575358823	chr11:71404421-71404422	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188531205	chr11:71404422-71404423	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs76914949	chr11:71404423-71404424	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs77526943	chr11:71404441-71404442	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs7118449	chr11:71404489-71404490	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181673608	chr11:71404492-71404493	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs200761039	chr11:71404494-71404495	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs560445382	chr11:71404499-71404500	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs540572378	chr11:71404502-71404503	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs564868969	chr11:71404506-71404507	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs138127615	chr11:71404516-71404517	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs542858082	chr11:71404540-71404541	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs78438416	chr11:71404550-71404551	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs185795429	chr11:71404563-71404564	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs562459167	chr11:71404650-71404651	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs531105216	chr11:71404676-71404677	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs113371726	chr11:71404692-71404693	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7118742	chr11:71404708-71404709	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs567883435	chr11:71404813-71404814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528752169	chr11:71404834-71404835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546937429	chr11:71404849-71404850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199541472	chr11:71404856-71404857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571263041	chr11:71404891-71404892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538658475	chr11:71404960-71404961	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs528993245	chr11:71404986-71404987	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs557395268	chr11:71404999-71405000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs145545861	chr11:71405000-71405001	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs536785327	chr11:71405006-71405007	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs554457229	chr11:71405026-71405027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573120050	chr11:71405051-71405052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534031793	chr11:71405062-71405063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558899872	chr11:71405064-71405065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576873121	chr11:71405065-71405066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543886694	chr11:71405073-71405074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562533073	chr11:71405093-71405094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192045688	chr11:71405103-71405104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541949909	chr11:71405134-71405135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138153546	chr11:71405136-71405137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568854987	chr11:71405168-71405169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528666775	chr11:71405181-71405182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546851617	chr11:71405228-71405229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371140796	chr11:71405237-71405238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182265756	chr11:71405239-71405240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375066941	chr11:71405275-71405276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550681629	chr11:71405279-71405280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71403400-71404400	Enhancers	K562	blood
2	chr11:71404000-71404800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:71404200-71404400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:71404200-71404600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr11:71404200-71405000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr11:71404400-71404800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr11:71404800-71409200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:71406400-71411400	Weak transcription	Fetal Intestine Small	intestine
9	chr11:71409200-71409800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:71409800-71411400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:71411400-71412400	Enhancers	Fetal Intestine Small	intestine
12	chr11:71411400-71412600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:71411400-71412600	Enhancers	Fetal Intestine Large	intestine
14	chr11:71412400-71413200	Weak transcription	Fetal Intestine Small	intestine
15	chr11:71413200-71415800	ZNF genes & repeats	Fetal Intestine Small	intestine
16	chr11:71414800-71416000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:71415400-71415600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr11:71415400-71416000	Enhancers	K562	blood
19	chr11:71415400-71416400	Enhancers	Fetal Intestine Large	intestine
20	chr11:71415600-71416200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr11:71415800-71416000	Weak transcription	Fetal Intestine Small	intestine
22	chr11:71416000-71416400	Flanking Active TSS	K562	blood
23	chr11:71416000-71416600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:71416000-71417000	Enhancers	Fetal Intestine Small	intestine
25	chr11:71416200-71416400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr11:71416400-71417400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr11:71416400-71417400	Weak transcription	Fetal Intestine Large	intestine
28	chr11:71416400-71417400	Enhancers	K562	blood
29	chr11:71416600-71417400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:71417000-71417400	Weak transcription	Fetal Intestine Small	intestine
31	chr11:71417000-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:71417200-71417600	Enhancers	Fetal Lung	lung
33	chr11:71417200-71417800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr11:71417200-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:71417400-71417600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:71417400-71417800	Flanking Active TSS	K562	blood
37	chr11:71417400-71418000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr11:71417400-71418000	Genic enhancers	Fetal Intestine Small	intestine
39	chr11:71417400-71421000	Enhancers	Fetal Intestine Large	intestine
40	chr11:71417600-71417800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:71417600-71419400	Weak transcription	Fetal Lung	lung
42	chr11:71417800-71418000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:71417800-71418600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr11:71417800-71419000	Enhancers	K562	blood
45	chr11:71417800-71421800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr11:71418000-71418400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:71418000-71419600	Enhancers	Fetal Intestine Small	intestine
48	chr11:71418000-71421000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:71418400-71419200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr11:71418400-71419400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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