Variant report

Variant	nsv556279
Chromosome Location	chr11:107006900-107186896
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	chr11:107125887-107126018	K562	blood:	n/a	n/a
2	ARID3A	chr11:107073929-107074099	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:107068416-107069073	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:107067338-107067971	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:107073226-107073508	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:107114621-107115003	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:107028240-107028924	HepG2	liver:	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	chr11:107011043-107011106	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:107161599-107161648	K562	blood:	n/a	n/a
12	BATF	chr11:107134920-107135143	GM12878	blood:	n/a	chr11:107134970-107134980
13	BHLHE40	chr11:107130509-107130831	K562	blood:	n/a	n/a
14	BHLHE40	chr11:107125712-107125922	K562	blood:	n/a	n/a
15	BHLHE40	chr11:107123579-107123932	K562	blood:	n/a	n/a
16	BHLHE40	chr11:107120661-107120879	K562	blood:	n/a	n/a
17	BHLHE40	chr11:107123612-107123903	GM12878	blood:	n/a	n/a
18	CEBPB	chr11:107115611-107115803	K562	blood:	n/a	n/a
19	CEBPB	chr11:107073000-107073487	HepG2	liver:	n/a	chr11:107073290-107073303
20	CEBPB	chr11:107078638-107078786	K562	blood:	n/a	chr11:107078682-107078693
21	CEBPB	chr11:107074508-107074643	HepG2	liver:	n/a	chr11:107074589-107074602
22	CEBPB	chr11:107084550-107084568	K562	blood:	n/a	n/a
23	CEBPB	chr11:107092553-107092853	HepG2	liver:	n/a	chr11:107092693-107092704
24	CEBPB	chr11:107081049-107081357	H1-hESC	embryonic stem cell:	n/a	chr11:107081186-107081197
25	CEBPB	chr11:107074412-107074761	HepG2	liver:	n/a	chr11:107074589-107074602
26	CEBPB	chr11:107172623-107172831	H1-hESC	embryonic stem cell:	n/a	chr11:107172701-107172712
27	CEBPB	chr11:107172555-107172813	HepG2	liver:	n/a	chr11:107172701-107172712
28	CEBPB	chr11:107158345-107158512	A549	lung:	n/a	chr11:107158421-107158434
29	CEBPB	chr11:107050691-107050918	HepG2	liver:	n/a	chr11:107050773-107050784
30	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
31	CEBPB	chr11:107078552-107078843	HepG2	liver:	n/a	chr11:107078682-107078693
32	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
33	CEBPB	chr11:107078553-107078815	A549	lung:	n/a	chr11:107078682-107078693
34	CEBPB	chr11:107015417-107015595	A549	lung:	n/a	chr11:107015490-107015501
35	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
36	CEBPB	chr11:107081085-107081330	A549	lung:	n/a	chr11:107081186-107081197
37	CEBPB	chr11:107028244-107028868	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:107028331-107028869	A549	lung:	n/a	n/a
39	CEBPB	chr11:107119936-107120011	K562	blood:	n/a	n/a
40	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
41	CEBPB	chr11:107092599-107092825	K562	blood:	n/a	chr11:107092693-107092704
42	CEBPB	chr11:107124645-107124705	HepG2	liver:	n/a	chr11:107124658-107124669
43	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
44	CEBPB	chr11:107115587-107115859	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:107015451-107015537	H1-hESC	embryonic stem cell:	n/a	chr11:107015490-107015501
46	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
47	CEBPB	chr11:107068363-107068591	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:107081026-107081331	HepG2	liver:	n/a	chr11:107081186-107081197
49	CEBPB	chr11:107172632-107172925	MCF-7	breast:	n/a	chr11:107172701-107172712
50	CEBPB	chr11:107124569-107124744	K562	blood:	n/a	chr11:107124658-107124669

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107044383-107044433	IMR90	lung:	fetal
2	chr11:107048184-107048234	HEK293	kidney:	embryo
3	chr11:107044383-107044433	K562	blood:	n/a
4	chr11:107047494-107047544	AG10803	skin:	n/a
5	chr11:107047494-107047544	LNCaP	prostate:	n/a
6	chr11:107047494-107047544	HCF	heart:	n/a
7	chr11:107044383-107044433	AG04450	lung:	fetal
8	chr11:107044383-107044433	Hela-S3	cervix:	n/a
9	chr11:107047494-107047544	HAEpiC	amniotic membrane:	n/a
10	chr11:107047888-107047938	PANC-1	pancreas:	n/a
11	chr11:107047494-107047544	U87	brain:	n/a
12	chr11:107044383-107044433	HEEpiC	esophagus:	n/a
13	chr11:107047494-107047544	AG04449	skin:	fetal
14	chr11:107044383-107044433	AG09319	gingival:	n/a
15	chr11:107047494-107047544	HNPCEpiC	eye:	n/a
16	chr11:107044383-107044433	MCF-7	breast:	n/a
17	chr11:107047888-107047938	GM19239	blood:	n/a
18	chr11:107047494-107047544	HCPEpiC	choroid plexus:	n/a
19	chr11:107047888-107047938	NHBE	bronchial:	n/a
20	chr11:107047494-107047544	SK-N-SH	brain:	n/a
21	chr11:107044383-107044433	ECC-1	luminal epithelium:	n/a
22	chr11:107048184-107048234	ovcar-3	ovarian:	n/a
23	chr11:107047494-107047544	PrEC	prostate:	n/a
24	chr11:107047888-107047938	T-47D	breast:	n/a
25	chr11:107047494-107047544	Caco-2	colon:	n/a
26	chr11:107047494-107047544	ovcar-3	ovarian:	n/a
27	chr11:107044383-107044433	A549	lung:	n/a
28	chr11:107047494-107047544	AG09319	gingival:	n/a
29	chr11:107048184-107048234	PANC-1	pancreas:	n/a
30	chr11:107048184-107048234	HNPCEpiC	eye:	n/a
31	chr11:107047888-107047938	H1-hESC	embryonic stem cell:	embryo
32	chr11:107044383-107044433	HRCEpiC	kidney:	n/a
33	chr11:107044383-107044433	ProgFib	skin:	n/a
34	chr11:107047888-107047938	SK-N-SH	brain:	n/a
35	chr11:107044383-107044433	GM12892	blood:	n/a
36	chr11:107047494-107047544	K562	blood:	n/a
37	chr11:107047494-107047544	NHBE	bronchial:	n/a
38	chr11:107047494-107047544	ProgFib	skin:	n/a
39	chr11:107044383-107044433	HUVEC	blood vessel:	n/a
40	chr11:107047888-107047938	Hepatocyte	liver:	n/a
41	chr11:107047888-107047938	AG09319	gingival:	n/a
42	chr11:107047494-107047544	HL-60	blood:	n/a
43	chr11:107047494-107047544	HCM	heart:	n/a
44	chr11:107047888-107047938	GM12891	blood:	n/a
45	chr11:107047888-107047938	AG10803	skin:	n/a
46	chr11:107048184-107048234	A549	lung:	n/a
47	chr11:107044383-107044433	AoSMC	blood vessel:	n/a
48	chr11:107044383-107044433	SK-N-MC	brain:	n/a
49	chr11:107044383-107044433	AG09309	skin:	n/a
50	chr11:107047888-107047938	ProgFib	skin:	n/a

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

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

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

Extended variants
information (count: 5142 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5142 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561866703	chr11:107010055-107010056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185232501	chr11:107010137-107010138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542853418	chr11:107010234-107010235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541143113	chr11:107010272-107010273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs879295	chr11:107010273-107010274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs139334474	chr11:107010303-107010304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150041863	chr11:107010426-107010427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35666262	chr11:107010468-107010469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563862681	chr11:107010470-107010471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369378785	chr11:107010475-107010476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553057765	chr11:107010500-107010501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572852711	chr11:107010508-107010509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372782323	chr11:107010512-107010513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190534263	chr11:107010537-107010538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs202194048	chr11:107010554-107010555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552263387	chr11:107010587-107010588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529313443	chr11:107010614-107010615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534756640	chr11:107010633-107010634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12797995	chr11:107010695-107010696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs192536130	chr11:107010701-107010702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12293378	chr11:107010738-107010739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs554830507	chr11:107010810-107010811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547470437	chr11:107010885-107010886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145177048	chr11:107010896-107010897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146785936	chr11:107010945-107010946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183648106	chr11:107010955-107010956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576781099	chr11:107010980-107010981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555990839	chr11:107010981-107010982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553146523	chr11:107010992-107010993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188256829	chr11:107011004-107011005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575881725	chr11:107011037-107011038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565025372	chr11:107011048-107011049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2009553	chr11:107011057-107011058	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs563928897	chr11:107011083-107011084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs180966087	chr11:107011098-107011099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12273374	chr11:107011101-107011102	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs1895730	chr11:107011120-107011121	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552267857	chr11:107011127-107011128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528510615	chr11:107011166-107011167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546678259	chr11:107011167-107011168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186437199	chr11:107011180-107011181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189633464	chr11:107011216-107011217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7951809	chr11:107011261-107011262	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs79477412	chr11:107011263-107011264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181671660	chr11:107011287-107011288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376430070	chr11:107011288-107011289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186765422	chr11:107011343-107011344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370268904	chr11:107011373-107011374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373670082	chr11:107011376-107011377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12274812	chr11:107011386-107011387	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:623 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107010000-107010200	Enhancers	Brain Germinal Matrix	brain
2	chr11:107010000-107010200	Enhancers	Fetal Brain Female	brain
3	chr11:107010200-107010400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:107010200-107010400	Enhancers	Fetal Brain Male	brain
5	chr11:107010200-107010800	Weak transcription	Brain Germinal Matrix	brain
6	chr11:107010800-107011600	Enhancers	Brain Germinal Matrix	brain
7	chr11:107011200-107012800	Enhancers	Fetal Muscle Leg	muscle
8	chr11:107011600-107011800	Enhancers	Fetal Brain Male	brain
9	chr11:107012000-107012400	Enhancers	Fetal Brain Female	brain
10	chr11:107012600-107012800	Enhancers	Fetal Brain Male	brain
11	chr11:107019200-107019600	Enhancers	Liver	Liver
12	chr11:107019600-107021400	Weak transcription	Liver	Liver
13	chr11:107021400-107023000	Enhancers	Liver	Liver
14	chr11:107023000-107027800	Weak transcription	Liver	Liver
15	chr11:107027400-107028400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr11:107027400-107028800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr11:107027400-107029000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr11:107027400-107029600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr11:107027800-107028400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr11:107027800-107028600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr11:107027800-107028800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr11:107027800-107029200	Enhancers	HepG2	liver
23	chr11:107027800-107030200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr11:107027800-107030200	Enhancers	Liver	Liver
25	chr11:107028000-107028400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr11:107028000-107032200	Enhancers	Adipose Nuclei	Adipose
27	chr11:107028400-107029000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:107028600-107030000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr11:107029000-107029600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:107029600-107030400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:107029600-107030600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:107030000-107030600	Enhancers	HMEC	breast
33	chr11:107030800-107031000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr11:107039400-107043400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr11:107043200-107044600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr11:107043400-107043800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:107043400-107044000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr11:107043400-107044000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr11:107043400-107044000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr11:107043400-107044000	Enhancers	Placenta Amnion	Placenta Amnion
41	chr11:107043400-107044200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr11:107043400-107044600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:107043600-107044000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr11:107043600-107044000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr11:107043600-107044000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:107048400-107049000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr11:107050600-107051400	Enhancers	Adipose Nuclei	Adipose
48	chr11:107050600-107051800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:107053400-107053800	Enhancers	NH-A	brain
50	chr11:107053800-107055000	Weak transcription	NH-A	brain

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