Variant report

Variant	nsv1040190
Chromosome Location	chr11:107045534-107175661
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	chr11:107073929-107074099	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:107125887-107126018	K562	blood:	n/a	n/a
3	ARID3A	chr11:107073226-107073508	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:107114621-107115003	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:107067338-107067971	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:107068416-107069073	HepG2	liver:	n/a	n/a
7	ATF1	chr11:107118328-107118368	K562	blood:	n/a	n/a
8	ATF1	chr11:107119900-107120053	K562	blood:	n/a	n/a
9	BACH1	chr11:107161599-107161648	K562	blood:	n/a	n/a
10	BATF	chr11:107134920-107135143	GM12878	blood:	n/a	chr11:107134970-107134980
11	BHLHE40	chr11:107123579-107123932	K562	blood:	n/a	n/a
12	BHLHE40	chr11:107123612-107123903	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:107125712-107125922	K562	blood:	n/a	n/a
14	BHLHE40	chr11:107130509-107130831	K562	blood:	n/a	n/a
15	BHLHE40	chr11:107120661-107120879	K562	blood:	n/a	n/a
16	CEBPB	chr11:107172562-107172870	IMR90	lung:	n/a	chr11:107172701-107172712
17	CEBPB	chr11:107073000-107073487	HepG2	liver:	n/a	chr11:107073290-107073303
18	CEBPB	chr11:107078552-107078843	HepG2	liver:	n/a	chr11:107078682-107078693
19	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
20	CEBPB	chr11:107088945-107089145	A549	lung:	n/a	n/a
21	CEBPB	chr11:107115611-107115803	K562	blood:	n/a	n/a
22	CEBPB	chr11:107081049-107081357	H1-hESC	embryonic stem cell:	n/a	chr11:107081186-107081197
23	CEBPB	chr11:107172555-107172813	HepG2	liver:	n/a	chr11:107172701-107172712
24	CEBPB	chr11:107092599-107092825	K562	blood:	n/a	chr11:107092693-107092704
25	CEBPB	chr11:107124569-107124744	K562	blood:	n/a	chr11:107124658-107124669
26	CEBPB	chr11:107064765-107064997	HepG2	liver:	n/a	chr11:107064904-107064915
27	CEBPB	chr11:107158345-107158512	A549	lung:	n/a	chr11:107158421-107158434
28	CEBPB	chr11:107092553-107092853	HepG2	liver:	n/a	chr11:107092693-107092704
29	CEBPB	chr11:107119936-107120011	K562	blood:	n/a	n/a
30	CEBPB	chr11:107078519-107078802	IMR90	lung:	n/a	chr11:107078682-107078693
31	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
32	CEBPB	chr11:107074412-107074761	HepG2	liver:	n/a	chr11:107074589-107074602
33	CEBPB	chr11:107115587-107115859	HepG2	liver:	n/a	n/a
34	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
35	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
36	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
37	CEBPB	chr11:107081085-107081330	A549	lung:	n/a	chr11:107081186-107081197
38	CEBPB	chr11:107084550-107084568	K562	blood:	n/a	n/a
39	CEBPB	chr11:107069412-107069724	HepG2	liver:	n/a	chr11:107069594-107069607 chr11:107069594-107069605 chr11:107069594-107069607 chr11:107069594-107069605 chr11:107069595-107069606 chr11:107069594-107069607
40	CEBPB	chr11:107172632-107172925	MCF-7	breast:	n/a	chr11:107172701-107172712
41	CEBPB	chr11:107172543-107172898	Hela-S3	cervix:	n/a	chr11:107172701-107172712
42	CEBPB	chr11:107068363-107068591	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:107172623-107172831	H1-hESC	embryonic stem cell:	n/a	chr11:107172701-107172712
44	CEBPB	chr11:107078638-107078786	K562	blood:	n/a	chr11:107078682-107078693
45	CEBPB	chr11:107050691-107050918	HepG2	liver:	n/a	chr11:107050773-107050784
46	CEBPB	chr11:107172641-107172753	A549	lung:	n/a	chr11:107172701-107172712
47	CEBPB	chr11:107081026-107081331	HepG2	liver:	n/a	chr11:107081186-107081197
48	CEBPB	chr11:107074508-107074643	HepG2	liver:	n/a	chr11:107074589-107074602
49	CEBPB	chr11:107078553-107078815	A549	lung:	n/a	chr11:107078682-107078693
50	CEBPB	chr11:107124645-107124705	HepG2	liver:	n/a	chr11:107124658-107124669

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107048184-107048234	K562	blood:	n/a
2	chr11:107047888-107047938	HCF	heart:	n/a
3	chr11:107047494-107047544	GM06990	blood:	n/a
4	chr11:107047888-107047938	AG09319	gingival:	n/a
5	chr11:107048184-107048234	GM12878	blood:	n/a
6	chr11:107047494-107047544	HMEC	breast:	n/a
7	chr11:107047888-107047938	GM12891	blood:	n/a
8	chr11:107047494-107047544	HIPEpiC	eye:	n/a
9	chr11:107047494-107047544	NT2-D1	testis:	n/a
10	chr11:107047888-107047938	AG04449	skin:	fetal
11	chr11:107048184-107048234	GM12891	blood:	n/a
12	chr11:107047494-107047544	ProgFib	skin:	n/a
13	chr11:107047888-107047938	HCPEpiC	choroid plexus:	n/a
14	chr11:107047888-107047938	BJ	skin:	n/a
15	chr11:107048184-107048234	HCT-116	colon:	n/a
16	chr11:107047888-107047938	HNPCEpiC	eye:	n/a
17	chr11:107047888-107047938	AG10803	skin:	n/a
18	chr11:107047494-107047544	AoSMC	blood vessel:	n/a
19	chr11:107047888-107047938	HL-60	blood:	n/a
20	chr11:107047494-107047544	NH-A	brain:	n/a
21	chr11:107048184-107048234	RPTEC	kidney:	n/a
22	chr11:107048184-107048234	HNPCEpiC	eye:	n/a
23	chr11:107048184-107048234	PFSK-1	brain:	n/a
24	chr11:107047494-107047544	NHDF-neo	bronchial:	n/a
25	chr11:107047494-107047544	HAEpiC	amniotic membrane:	n/a
26	chr11:107047494-107047544	HCF	heart:	n/a
27	chr11:107048184-107048234	Hela-S3	cervix:	n/a
28	chr11:107047494-107047544	HNPCEpiC	eye:	n/a
29	chr11:107047494-107047544	HL-60	blood:	n/a
30	chr11:107048184-107048234	PANC-1	pancreas:	n/a
31	chr11:107048184-107048234	NT2-D1	testis:	n/a
32	chr11:107047888-107047938	HEK293	kidney:	embryo
33	chr11:107048184-107048234	GM19239	blood:	n/a
34	chr11:107047888-107047938	T-47D	breast:	n/a
35	chr11:107047494-107047544	K562	blood:	n/a
36	chr11:107047494-107047544	AG09309	skin:	n/a
37	chr11:107047888-107047938	SKMC	muscle:	n/a
38	chr11:107047494-107047544	Hepatocyte	liver:	n/a
39	chr11:107047888-107047938	HEEpiC	esophagus:	n/a
40	chr11:107047494-107047544	Hela-S3	cervix:	n/a
41	chr11:107047494-107047544	HRPEpiC	eye:	n/a
42	chr11:107048184-107048234	HIPEpiC	eye:	n/a
43	chr11:107048184-107048234	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:107047494-107047544	NHBE	bronchial:	n/a
45	chr11:107048184-107048234	AG09309	skin:	n/a
46	chr11:107047494-107047544	HUVEC	blood vessel:	n/a
47	chr11:107048184-107048234	HUVEC	blood vessel:	n/a
48	chr11:107047888-107047938	AoSMC	blood vessel:	n/a
49	chr11:107047494-107047544	AG04450	lung:	fetal
50	chr11:107047888-107047938	HIPEpiC	eye:	n/a

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

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

Extended variants
information (count: 3905 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3905 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78055069	chr11:107046942-107046943	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs56188450	chr11:107046989-107046990	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs533337889	chr11:107047004-107047005	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs534417731	chr11:107047005-107047006	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186783041	chr11:107047009-107047010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs12271804	chr11:107048408-107048409	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs560909851	chr11:107048422-107048423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191297607	chr11:107048423-107048424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549871495	chr11:107048425-107048426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571389476	chr11:107048426-107048427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538811772	chr11:107048431-107048432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547980582	chr11:107048457-107048458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115021263	chr11:107048466-107048467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56128282	chr11:107048469-107048470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537001136	chr11:107048487-107048488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115471326	chr11:107048499-107048500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569750444	chr11:107048511-107048512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183883850	chr11:107048512-107048513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189677632	chr11:107048527-107048528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558598027	chr11:107048532-107048533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181235869	chr11:107048538-107048539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369276542	chr11:107048618-107048619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185060635	chr11:107048624-107048625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143370763	chr11:107048628-107048629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572246135	chr11:107048634-107048635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs151332312	chr11:107048635-107048636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552068386	chr11:107048651-107048652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189895937	chr11:107048677-107048678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531308415	chr11:107048682-107048683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140477298	chr11:107048712-107048713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74996249	chr11:107048747-107048748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532276374	chr11:107048808-107048809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547672382	chr11:107048815-107048816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181643228	chr11:107048817-107048818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566291765	chr11:107048818-107048819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527752073	chr11:107048826-107048827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34786943	chr11:107048837-107048838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186119513	chr11:107048861-107048862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7108684	chr11:107048880-107048881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201385252	chr11:107048882-107048883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145631654	chr11:107048890-107048891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534108532	chr11:107048905-107048906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111859717	chr11:107048916-107048917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180681259	chr11:107048961-107048962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs6588946	chr11:107049000-107049001	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs552733374	chr11:107050658-107050659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78699502	chr11:107050660-107050661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112682865	chr11:107050672-107050673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183532409	chr11:107050682-107050683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563523388	chr11:107050693-107050694	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107048400-107049000	Enhancers	H1 Cell Line	embryonic stem cell
2	chr11:107050600-107051400	Enhancers	Adipose Nuclei	Adipose
3	chr11:107050600-107051800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr11:107053400-107053800	Enhancers	NH-A	brain
5	chr11:107053800-107055000	Weak transcription	NH-A	brain
6	chr11:107054600-107055400	Enhancers	Fetal Brain Female	brain
7	chr11:107054600-107056400	Enhancers	Fetal Brain Male	brain
8	chr11:107054800-107055200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr11:107054800-107056000	Enhancers	Fetal Lung	lung
10	chr11:107055000-107055200	Enhancers	NH-A	brain
11	chr11:107063800-107064000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:107063800-107064000	ZNF genes & repeats	Left Ventricle	heart
13	chr11:107067000-107069400	Enhancers	HepG2	liver
14	chr11:107067200-107067400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:107067200-107069200	Enhancers	A549	lung
16	chr11:107067600-107068000	Enhancers	Fetal Intestine Large	intestine
17	chr11:107067600-107068200	Enhancers	Liver	Liver
18	chr11:107068200-107072400	Weak transcription	Liver	Liver
19	chr11:107069000-107072800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:107069200-107069800	Enhancers	Adipose Nuclei	Adipose
21	chr11:107069200-107070000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:107069400-107072600	Weak transcription	HepG2	liver
23	chr11:107070000-107072600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:107072200-107073200	Enhancers	Fetal Brain Male	brain
25	chr11:107072200-107074600	Enhancers	Fetal Brain Female	brain
26	chr11:107072400-107073600	Enhancers	Liver	Liver
27	chr11:107072600-107073200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:107072600-107074800	Enhancers	HepG2	liver
29	chr11:107072800-107073000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:107072800-107073200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:107073000-107073800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:107073200-107073600	Weak transcription	Fetal Brain Male	brain
33	chr11:107073600-107074800	Enhancers	Fetal Brain Male	brain
34	chr11:107073800-107074000	Enhancers	Fetal Intestine Large	intestine
35	chr11:107073800-107074600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:107074400-107074800	Enhancers	Fetal Intestine Large	intestine
37	chr11:107076000-107076600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:107076200-107076600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr11:107079000-107081000	Enhancers	Fetal Brain Male	brain
40	chr11:107079800-107081000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:107081000-107085800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:107081000-107089200	Weak transcription	Fetal Brain Male	brain
43	chr11:107084400-107084800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:107085600-107085800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr11:107085600-107085800	Enhancers	Fetal Kidney	kidney
46	chr11:107085800-107086400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:107085800-107089000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr11:107086400-107089400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:107088200-107089800	Enhancers	Fetal Intestine Small	intestine
50	chr11:107088400-107090200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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