Variant report

Variant	nsv1035911
Chromosome Location	chr11:107020991-107198181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:107114621-107115003	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:107073226-107073508	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:107028240-107028924	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:107068416-107069073	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:107073929-107074099	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:107067338-107067971	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:107125887-107126018	K562	blood:	n/a	n/a
8	ATF1	chr11:107118328-107118368	K562	blood:	n/a	n/a
9	ATF1	chr11:107119900-107120053	K562	blood:	n/a	n/a
10	BACH1	chr11:107161599-107161648	K562	blood:	n/a	n/a
11	BATF	chr11:107134920-107135143	GM12878	blood:	n/a	chr11:107134970-107134980
12	BHLHE40	chr11:107123579-107123932	K562	blood:	n/a	n/a
13	BHLHE40	chr11:107120661-107120879	K562	blood:	n/a	n/a
14	BHLHE40	chr11:107130509-107130831	K562	blood:	n/a	n/a
15	BHLHE40	chr11:107125712-107125922	K562	blood:	n/a	n/a
16	BHLHE40	chr11:107123612-107123903	GM12878	blood:	n/a	n/a
17	CEBPB	chr11:107119936-107120011	K562	blood:	n/a	n/a
18	CEBPB	chr11:107172641-107172753	A549	lung:	n/a	chr11:107172701-107172712
19	CEBPB	chr11:107172623-107172831	H1-hESC	embryonic stem cell:	n/a	chr11:107172701-107172712
20	CEBPB	chr11:107137114-107137420	HepG2	liver:	n/a	chr11:107137269-107137282 chr11:107137269-107137282 chr11:107137271-107137280 chr11:107137294-107137305 chr11:107137270-107137281 chr11:107137269-107137280
21	CEBPB	chr11:107081026-107081331	HepG2	liver:	n/a	chr11:107081186-107081197
22	CEBPB	chr11:107158345-107158512	A549	lung:	n/a	chr11:107158421-107158434
23	CEBPB	chr11:107073000-107073487	HepG2	liver:	n/a	chr11:107073290-107073303
24	CEBPB	chr11:107078553-107078815	A549	lung:	n/a	chr11:107078682-107078693
25	CEBPB	chr11:107092599-107092825	K562	blood:	n/a	chr11:107092693-107092704
26	CEBPB	chr11:107081085-107081330	A549	lung:	n/a	chr11:107081186-107081197
27	CEBPB	chr11:107137105-107137326	H1-hESC	embryonic stem cell:	n/a	chr11:107137269-107137282 chr11:107137269-107137282 chr11:107137271-107137280 chr11:107137294-107137305 chr11:107137270-107137281 chr11:107137269-107137280
28	CEBPB	chr11:107064765-107064997	HepG2	liver:	n/a	chr11:107064904-107064915
29	CEBPB	chr11:107172632-107172925	MCF-7	breast:	n/a	chr11:107172701-107172712
30	CEBPB	chr11:107074412-107074761	HepG2	liver:	n/a	chr11:107074589-107074602
31	CEBPB	chr11:107050691-107050918	HepG2	liver:	n/a	chr11:107050773-107050784
32	CEBPB	chr11:107115587-107115859	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:107084550-107084568	K562	blood:	n/a	n/a
34	CEBPB	chr11:107172543-107172898	Hela-S3	cervix:	n/a	chr11:107172701-107172712
35	CEBPB	chr11:107028244-107028868	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:107137130-107137427	K562	blood:	n/a	chr11:107137269-107137282 chr11:107137269-107137282 chr11:107137271-107137280 chr11:107137294-107137305 chr11:107137270-107137281 chr11:107137269-107137280
37	CEBPB	chr11:107078552-107078843	HepG2	liver:	n/a	chr11:107078682-107078693
38	CEBPB	chr11:107078638-107078786	K562	blood:	n/a	chr11:107078682-107078693
39	CEBPB	chr11:107069586-107069618	H1-hESC	embryonic stem cell:	n/a	chr11:107069594-107069607 chr11:107069594-107069605 chr11:107069594-107069607 chr11:107069594-107069605 chr11:107069595-107069606 chr11:107069594-107069607
40	CEBPB	chr11:107074508-107074643	HepG2	liver:	n/a	chr11:107074589-107074602
41	CEBPB	chr11:107028331-107028869	A549	lung:	n/a	n/a
42	CEBPB	chr11:107081049-107081357	H1-hESC	embryonic stem cell:	n/a	chr11:107081186-107081197
43	CEBPB	chr11:107172562-107172870	IMR90	lung:	n/a	chr11:107172701-107172712
44	CEBPB	chr11:107115611-107115803	K562	blood:	n/a	n/a
45	CEBPB	chr11:107078519-107078802	IMR90	lung:	n/a	chr11:107078682-107078693
46	CEBPB	chr11:107124645-107124705	HepG2	liver:	n/a	chr11:107124658-107124669
47	CEBPB	chr11:107137126-107137444	IMR90	lung:	n/a	chr11:107137269-107137282 chr11:107137269-107137282 chr11:107137271-107137280 chr11:107137294-107137305 chr11:107137270-107137281 chr11:107137269-107137280
48	CEBPB	chr11:107088945-107089145	A549	lung:	n/a	n/a
49	CEBPB	chr11:107137123-107137343	A549	lung:	n/a	chr11:107137269-107137282 chr11:107137269-107137282 chr11:107137271-107137280 chr11:107137294-107137305 chr11:107137270-107137281 chr11:107137269-107137280
50	CEBPB	chr11:107068363-107068591	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107047888-107047938	PANC-1	pancreas:	n/a
2	chr11:107047888-107047938	SK-N-SH	brain:	n/a
3	chr11:107044383-107044433	GM12878	blood:	n/a
4	chr11:107044383-107044433	SKMC	muscle:	n/a
5	chr11:107047494-107047544	ovcar-3	ovarian:	n/a
6	chr11:107044383-107044433	PANC-1	pancreas:	n/a
7	chr11:107047888-107047938	Caco-2	colon:	n/a
8	chr11:107048184-107048234	HRPEpiC	eye:	n/a
9	chr11:107047494-107047544	NHDF-neo	bronchial:	n/a
10	chr11:107047888-107047938	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:107048184-107048234	AG04449	skin:	fetal
12	chr11:107044383-107044433	Hela-S3	cervix:	n/a
13	chr11:107047888-107047938	AG04450	lung:	fetal
14	chr11:107047888-107047938	AG04449	skin:	fetal
15	chr11:107047888-107047938	SKMC	muscle:	n/a
16	chr11:107048184-107048234	NB4	blood:	n/a
17	chr11:107044383-107044433	AG09319	gingival:	n/a
18	chr11:107048184-107048234	HNPCEpiC	eye:	n/a
19	chr11:107048184-107048234	A549	lung:	n/a
20	chr11:107047494-107047544	PrEC	prostate:	n/a
21	chr11:107047888-107047938	ECC-1	luminal epithelium:	n/a
22	chr11:107048184-107048234	GM12878	blood:	n/a
23	chr11:107044383-107044433	HEEpiC	esophagus:	n/a
24	chr11:107044383-107044433	U87	brain:	n/a
25	chr11:107048184-107048234	PFSK-1	brain:	n/a
26	chr11:107047494-107047544	AG09319	gingival:	n/a
27	chr11:107048184-107048234	PANC-1	pancreas:	n/a
28	chr11:107047888-107047938	HRPEpiC	eye:	n/a
29	chr11:107047888-107047938	HRE	kidney:	n/a
30	chr11:107048184-107048234	T-47D	breast:	n/a
31	chr11:107047888-107047938	BE2_C	brain:	n/a
32	chr11:107047888-107047938	HRCEpiC	kidney:	n/a
33	chr11:107048184-107048234	HCM	heart:	n/a
34	chr11:107048184-107048234	HRE	kidney:	n/a
35	chr11:107044383-107044433	NH-A	brain:	n/a
36	chr11:107048184-107048234	HRCEpiC	kidney:	n/a
37	chr11:107044383-107044433	LNCaP	prostate:	n/a
38	chr11:107047888-107047938	GM06990	blood:	n/a
39	chr11:107048184-107048234	IMR90	lung:	fetal
40	chr11:107048184-107048234	HCPEpiC	choroid plexus:	n/a
41	chr11:107047494-107047544	AG04449	skin:	fetal
42	chr11:107044383-107044433	ECC-1	luminal epithelium:	n/a
43	chr11:107048184-107048234	HEEpiC	esophagus:	n/a
44	chr11:107048184-107048234	GM19239	blood:	n/a
45	chr11:107047888-107047938	T-47D	breast:	n/a
46	chr11:107047888-107047938	CMK	blood:	n/a
47	chr11:107048184-107048234	HAEpiC	amniotic membrane:	n/a
48	chr11:107048184-107048234	AoSMC	blood vessel:	n/a
49	chr11:107047494-107047544	GM12891	blood:	n/a
50	chr11:107047494-107047544	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:107173736..107175485-chr11:107175928..107178317,2	K562	blood:
2	chr11:107081384..107083481-chr11:107086943..107088953,2	K562	blood:
3	chr11:107131927..107134128-chr11:107134135..107136466,2	K562	blood:
4	chr11:107096224..107098662-chr11:107099428..107101008,2	K562	blood:
5	chr11:107123368..107125286-chr11:107129770..107131910,2	K562	blood:
6	chr11:107121227..107123059-chr11:107129085..107131752,2	K562	blood:
7	chr11:107173992..107176253-chr11:107193691..107195884,2	K562	blood:
8	chr11:107146912..107148719-chr11:107151854..107154613,2	MCF-7	breast:
9	chr11:107096224..107098662-chr11:107099428..107101008,2	K562	blood:
10	chr11:107173992..107176253-chr11:107193691..107195884,2	K562	blood:
11	chr11:107123368..107125286-chr11:107129770..107131910,2	K562	blood:
12	chr11:107173736..107175485-chr11:107175928..107178317,2	K562	blood:
13	chr11:107114259..107116985-chr11:107121608..107123484,2	K562	blood:
14	chr11:107131927..107134128-chr11:107134135..107136466,2	K562	blood:
15	chr11:107108368..107111074-chr11:107113381..107114991,2	K562	blood:
16	chr11:107114259..107116985-chr11:107121608..107123484,2	K562	blood:
17	chr11:107069683..107071743-chr11:107086703..107088900,2	K562	blood:
18	chr11:107108368..107111074-chr11:107113381..107114991,2	K562	blood:
19	chr11:107121227..107123059-chr11:107129085..107131752,2	K562	blood:
20	chr11:107146912..107148719-chr11:107151854..107154613,2	MCF-7	breast:
21	chr11:107069683..107071743-chr11:107086703..107088900,2	K562	blood:
22	chr11:107081384..107083481-chr11:107086943..107088953,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CWF19L2-1	chr11:107184094-107184136	NONHSAT023993
2	lnc-CWF19L2-1	chr11:107183057-107184045	NONHSAT023993
3	lnc-CWF19L2-1	chr11:107181806-107181958	XLOC_009544
4	lnc-CWF19L2-1	chr11:107182073-107186290	XLOC_009544
5	lnc-CWF19L2-1	chr11:107182858-107186997	ENSG00000261098.1
6	lnc-CWF19L2-1	chr11:107184592-107184806	NONHSAT023993

Variant related genes	Relation type
ENSG00000261098	TF binding region
ENSG00000255353	TF binding region
ENSG00000261098	CpG island
ENSG00000255353	CpG island

Extended variants
information (count: 5466 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5466 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11212045	chr11:107020991-107020992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567847497	chr11:107020992-107020993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567636557	chr11:107021016-107021017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113149489	chr11:107021026-107021027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556618506	chr11:107021090-107021091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578120144	chr11:107021096-107021097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545529826	chr11:107021115-107021116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113102099	chr11:107021131-107021132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374998835	chr11:107021136-107021137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557940877	chr11:107021154-107021155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370331832	chr11:107021162-107021163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73544874	chr11:107021199-107021200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs561866420	chr11:107021252-107021253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573557565	chr11:107021262-107021263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114595555	chr11:107021323-107021324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146384719	chr11:107021346-107021347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532822225	chr11:107021351-107021352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148589401	chr11:107021355-107021356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183845417	chr11:107021445-107021446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527913731	chr11:107021448-107021449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549630231	chr11:107021450-107021451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189163917	chr11:107021452-107021453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538547846	chr11:107021516-107021517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561257969	chr11:107021529-107021530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571673949	chr11:107021536-107021537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574512780	chr11:107021578-107021579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192259633	chr11:107021617-107021618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182919018	chr11:107021633-107021634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78253524	chr11:107021719-107021720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533772689	chr11:107021721-107021722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555556766	chr11:107021759-107021760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186903279	chr11:107021796-107021797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377592061	chr11:107021865-107021866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544107868	chr11:107021890-107021891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191696683	chr11:107021891-107021892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577264602	chr11:107021934-107021935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544688248	chr11:107021947-107021948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560018659	chr11:107021987-107021988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527404495	chr11:107021993-107021994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549277924	chr11:107022002-107022003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531890090	chr11:107022016-107022017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551792179	chr11:107022034-107022035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370715983	chr11:107022047-107022048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543586665	chr11:107022064-107022065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561542817	chr11:107022084-107022085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531997917	chr11:107022104-107022105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35095526	chr11:107022121-107022122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550543901	chr11:107022135-107022136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368434718	chr11:107022145-107022146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571661824	chr11:107022177-107022178	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
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
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
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	21811512	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164920	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107019600-107021400	Weak transcription	Liver	Liver
2	chr11:107021400-107023000	Enhancers	Liver	Liver
3	chr11:107023000-107027800	Weak transcription	Liver	Liver
4	chr11:107027400-107028400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr11:107027400-107028800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr11:107027400-107029000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr11:107027400-107029600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr11:107027800-107028400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr11:107027800-107028600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr11:107027800-107028800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr11:107027800-107029200	Enhancers	HepG2	liver
12	chr11:107027800-107030200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:107027800-107030200	Enhancers	Liver	Liver
14	chr11:107028000-107028400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:107028000-107032200	Enhancers	Adipose Nuclei	Adipose
16	chr11:107028400-107029000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:107028600-107030000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr11:107029000-107029600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:107029600-107030400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:107029600-107030600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr11:107030000-107030600	Enhancers	HMEC	breast
22	chr11:107030800-107031000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr11:107039400-107043400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr11:107043200-107044600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:107043400-107043800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr11:107043400-107044000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr11:107043400-107044000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:107043400-107044000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr11:107043400-107044000	Enhancers	Placenta Amnion	Placenta Amnion
30	chr11:107043400-107044200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr11:107043400-107044600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:107043600-107044000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr11:107043600-107044000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr11:107043600-107044000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:107048400-107049000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr11:107050600-107051400	Enhancers	Adipose Nuclei	Adipose
37	chr11:107050600-107051800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:107053400-107053800	Enhancers	NH-A	brain
39	chr11:107053800-107055000	Weak transcription	NH-A	brain
40	chr11:107054600-107055400	Enhancers	Fetal Brain Female	brain
41	chr11:107054600-107056400	Enhancers	Fetal Brain Male	brain
42	chr11:107054800-107055200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr11:107054800-107056000	Enhancers	Fetal Lung	lung
44	chr11:107055000-107055200	Enhancers	NH-A	brain
45	chr11:107063800-107064000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr11:107063800-107064000	ZNF genes & repeats	Left Ventricle	heart
47	chr11:107067000-107069400	Enhancers	HepG2	liver
48	chr11:107067200-107067400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:107067200-107069200	Enhancers	A549	lung
50	chr11:107067600-107068000	Enhancers	Fetal Intestine Large	intestine

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