Variant report

Variant	nsv430397
Chromosome Location	chr11:62852616-63072310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1115)
CpG islands
(count:854)
Chromatin interactive
region (count:41)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:63048505-63048725	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:63013702-63013786	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:63058059-63058071	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:63042279-63042618	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:63006675-63007142	HepG2	liver:	n/a	chr11:63006781-63006797
6	ARID3A	chr11:63017494-63019185	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:63057050-63057851	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:62994277-62994554	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:62980281-62980415	K562	blood:	n/a	n/a
10	ARID3A	chr11:62997354-62997741	HepG2	liver:	n/a	chr11:62997612-62997628
11	ARID3A	chr11:63015225-63015718	HepG2	liver:	n/a	n/a
12	ARID3A	chr11:63008154-63009152	HepG2	liver:	n/a	n/a
13	BACH1	chr11:62910088-62910415	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr11:63008262-63008801	HepG2	liver:	n/a	n/a
15	BHLHE40	chr11:62980280-62980383	K562	blood:	n/a	n/a
16	BRCA1	chr11:62906992-62907098	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr11:62867109-62867352	K562	blood:	n/a	n/a
18	CEBPB	chr11:62861262-62861430	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:63018778-63019222	HepG2	liver:	n/a	chr11:63019015-63019026
20	CEBPB	chr11:62942070-62942393	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:63008163-63008912	HepG2	liver:	n/a	chr11:63008635-63008646
22	CEBPB	chr11:63008500-63008805	HepG2	liver:	n/a	chr11:63008635-63008646
23	CEBPB	chr11:62889471-62889574	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:62942086-62942347	A549	lung:	n/a	n/a
25	CEBPB	chr11:63017650-63017936	HepG2	liver:	n/a	chr11:63017813-63017824
26	CEBPB	chr11:62942183-62942259	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr11:62948109-62948382	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:63070914-63071095	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:63017662-63018061	HepG2	liver:	n/a	chr11:63017813-63017824
30	CEBPB	chr11:62942163-62942345	K562	blood:	n/a	n/a
31	CEBPB	chr11:63008151-63008821	MCF-7	breast:	n/a	chr11:63008635-63008646
32	CEBPB	chr11:63008162-63008869	HepG2	liver:	n/a	chr11:63008635-63008646
33	CEBPB	chr11:63018573-63019219	HepG2	liver:	n/a	chr11:63019015-63019026
34	CEBPB	chr11:63050144-63050310	HepG2	liver:	n/a	chr11:63050171-63050182
35	CEBPB	chr11:63018903-63019138	HepG2	liver:	n/a	chr11:63019015-63019026
36	CEBPB	chr11:62942122-62942392	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:63008634-63008650	Hela-S3	cervix:	n/a	chr11:63008635-63008646
38	CEBPB	chr11:63017642-63018008	HepG2	liver:	n/a	chr11:63017813-63017824
39	CEBPB	chr11:63008165-63008475	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:62981951-62982217	K562	blood:	n/a	n/a
41	CEBPB	chr11:63008109-63008880	MCF-7	breast:	n/a	chr11:63008635-63008646
42	CEBPB	chr11:62947556-62947756	A549	lung:	n/a	n/a
43	CEBPB	chr11:63008296-63008763	A549	lung:	n/a	chr11:63008635-63008646
44	CEBPB	chr11:63008170-63008883	HepG2	liver:	n/a	chr11:63008635-63008646
45	CEBPB	chr11:62942187-62942273	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:63017574-63018211	HepG2	liver:	n/a	chr11:63017813-63017824
47	CEBPD	chr11:63008507-63008820	HepG2	liver:	n/a	n/a
48	CEBPD	chr11:63017665-63017925	HepG2	liver:	n/a	n/a
49	CEBPD	chr11:63008160-63008441	HepG2	liver:	n/a	n/a
50	CTCF	chr11:62895700-62895850	MCF-7	breast:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:62903717-62903767	HRE	kidney:	n/a
2	chr11:62947565-62947615	HNPCEpiC	eye:	n/a
3	chr11:62947565-62947615	HCM	heart:	n/a
4	chr11:62996801-62996851	MCF10A-Er-Src	breast:	n/a
5	chr11:62947565-62947615	AG04449	skin:	fetal
6	chr11:62903717-62903767	HMEC	breast:	n/a
7	chr11:62997285-62997335	RPTEC	kidney:	n/a
8	chr11:63033729-63033779	HMEC	breast:	n/a
9	chr11:62911616-62911666	HepG2	liver:	n/a
10	chr11:62903717-62903767	HCT-116	colon:	n/a
11	chr11:62912823-62912873	HRE	kidney:	n/a
12	chr11:62997285-62997335	HUVEC	blood vessel:	n/a
13	chr11:62903717-62903767	K562	blood:	n/a
14	chr11:62911616-62911666	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:62895811-62895861	Hela-S3	cervix:	n/a
16	chr11:63033729-63033779	PANC-1	pancreas:	n/a
17	chr11:62912823-62912873	Jurkat	blood:	n/a
18	chr11:62895811-62895861	K562	blood:	n/a
19	chr11:63057592-63057642	Caco-2	colon:	n/a
20	chr11:62996801-62996851	AG04449	skin:	fetal
21	chr11:62895811-62895861	SK-N-SH	brain:	n/a
22	chr11:63035103-63035153	HRE	kidney:	n/a
23	chr11:62996801-62996851	GM06990	blood:	n/a
24	chr11:62912823-62912873	SK-N-SH	brain:	n/a
25	chr11:62997004-62997054	NT2-D1	testis:	n/a
26	chr11:63033729-63033779	RPTEC	kidney:	n/a
27	chr11:62997983-62998033	PFSK-1	brain:	n/a
28	chr11:63066471-63066521	SK-N-SH	brain:	n/a
29	chr11:63035103-63035153	HL-60	blood:	n/a
30	chr11:63066471-63066521	MCF-7	breast:	n/a
31	chr11:62996801-62996851	AG04450	lung:	fetal
32	chr11:63035103-63035153	MCF-7	breast:	n/a
33	chr11:63057478-63057528	IMR90	lung:	fetal
34	chr11:62996801-62996851	RPTEC	kidney:	n/a
35	chr11:63057478-63057528	T-47D	breast:	n/a
36	chr11:62997285-62997335	SK-N-SH_RA	brain:	n/a
37	chr11:62947565-62947615	Hepatocyte	liver:	n/a
38	chr11:62911616-62911666	GM06990	blood:	n/a
39	chr11:62997285-62997335	GM12892	blood:	n/a
40	chr11:63035103-63035153	HEK293	kidney:	embryo
41	chr11:62997004-62997054	IMR90	lung:	fetal
42	chr11:63057478-63057528	NH-A	brain:	n/a
43	chr11:62996801-62996851	SKMC	muscle:	n/a
44	chr11:63066471-63066521	HRE	kidney:	n/a
45	chr11:62996801-62996851	Caco-2	colon:	n/a
46	chr11:62996801-62996851	PANC-1	pancreas:	n/a
47	chr11:63033729-63033779	HRCEpiC	kidney:	n/a
48	chr11:62911616-62911666	GM19239	blood:	n/a
49	chr11:63035103-63035153	HRCEpiC	kidney:	n/a
50	chr11:62895811-62895861	NHBE	bronchial:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63005254..63007411-chr11:63010336..63012960,2	K562	blood:
2	chr11:62990724..62992823-chr11:63013955..63016825,2	MCF-7	breast:
3	chr11:62885732..62888321-chr11:62888957..62891249,2	MCF-7	breast:
4	chr11:62885732..62888321-chr11:62888957..62891249,2	MCF-7	breast:
5	chr11:62802829..62803373-chr11:62979825..62980365,2	MCF-7	breast:
6	chr11:62673078..62674101-chr11:62979871..62981035,3	K562	blood:
7	chr11:62913836..62916578-chr11:62923107..62925108,2	MCF-7	breast:
8	chr11:63036813..63039630-chr11:63043025..63045856,2	K562	blood:
9	chr11:63044723..63045242-chr11:63275245..63276140,2	MCF-7	breast:
10	chr11:62997179..62998138-chr13:34015248..34015801,2	MCF-7	breast:
11	chr11:63042850..63045277-chr11:63045866..63048411,2	MCF-7	breast:
12	chr11:63044561..63045230-chr11:63246286..63246902,2	MCF-7	breast:
13	chr11:62885383..62887108-chr11:62890801..62892716,2	K562	blood:
14	chr11:62851942..62854202-chr11:62871987..62874309,2	K562	blood:
15	chr11:63042013..63042918-chr11:63403002..63403779,2	MCF-7	breast:
16	chr11:63057865..63060126-chr11:63074539..63077166,2	MCF-7	breast:
17	chr11:62885255..62885775-chr3:160939134..160940048,2	HCT-116	colon:
18	chr11:62980374..62982290-chr11:62983906..62985581,2	K562	blood:
19	chr11:62895693..62896269-chr11:62979891..62980787,2	MCF-7	breast:
20	chr11:63072177..63073810-chr11:63074201..63076770,2	MCF-7	breast:
21	chr11:62851942..62854202-chr11:62871987..62874309,2	K562	blood:
22	chr11:62992812..62995599-chr11:63006882..63009821,2	MCF-7	breast:
23	chr11:62676265..62676873-chr11:62979808..62980394,3	K562	blood:
24	chr11:62990724..62992823-chr11:63013955..63016825,2	MCF-7	breast:
25	chr11:62992812..62995599-chr11:63006882..63009821,2	MCF-7	breast:
26	chr11:63065508..63067181-chr11:63068021..63070968,2	MCF-7	breast:
27	chr11:62980374..62982290-chr11:62983906..62985581,2	K562	blood:
28	chr11:62939715..62942669-chr11:62943076..62946010,2	K562	blood:
29	chr11:62802846..62803791-chr11:62980023..62980911,6	MCF-7	breast:
30	chr11:63044665..63045444-chr11:63402967..63403950,3	MCF-7	breast:
31	chr11:62939715..62942669-chr11:62943076..62946010,2	K562	blood:
32	chr11:63044746..63045474-chr11:63275562..63276187,3	MCF-7	breast:
33	chr11:62885383..62887108-chr11:62890801..62892716,2	K562	blood:
34	chr11:63005254..63007411-chr11:63010336..63012960,2	K562	blood:
35	chr11:63036813..63039630-chr11:63043025..63045856,2	K562	blood:
36	chr11:62913836..62916578-chr11:62923107..62925108,2	MCF-7	breast:
37	chr11:62848664..62851040-chr11:62854770..62857085,2	MCF-7	breast:
38	chr11:62802803..62803858-chr11:63041979..63043067,8	MCF-7	breast:
39	chr11:63042850..63045277-chr11:63045866..63048411,2	MCF-7	breast:
40	chr11:63065508..63067181-chr11:63068021..63070968,2	MCF-7	breast:
41	chr11:62895693..62896269-chr11:62979891..62980787,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC22A9-2	chr11:63024450-63024659	l_487_chr11:63018728-63024659_testes
2	lnc-SLC22A9-2	chr11:63018729-63019657	l_487_chr11:63018728-63024659_testes

No data

Variant related genes	Relation type
ENSG00000256863	TF binding region
SLC22A24	TF binding region
CCND2P1	TF binding region
SLC22A25	TF binding region
RPL29P22	TF binding region
ENSG00000256181	TF binding region
SLC22A10	TF binding region
ENSG00000256863	CpG island
SLC22A24	CpG island
CCND2P1	CpG island
SLC22A25	CpG island
RPL29P22	CpG island
ENSG00000256181	CpG island
SLC22A10	CpG island
ENSG00000169251	chromatin interactions
ENSG00000133317	chromatin interactions
ENSG00000256863	chromatin interactions
ENSG00000256847	chromatin interactions

Extended variants
information (count: 6186 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:6186 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537781152	chr11:62854861-62854862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs117311387	chr11:62854917-62854918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374039638	chr11:62854925-62854926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186137346	chr11:62854936-62854937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557195624	chr11:62854990-62854991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140977572	chr11:62855023-62855024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547374736	chr11:62855025-62855026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7927104	chr11:62855031-62855032	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs536266635	chr11:62855066-62855067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548957476	chr11:62855105-62855106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11231347	chr11:62855111-62855112	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs537634051	chr11:62855209-62855210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375519686	chr11:62855219-62855220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557977371	chr11:62855224-62855225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150211619	chr11:62855225-62855226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138727273	chr11:62855284-62855285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533909364	chr11:62855374-62855375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs61355084	chr11:62855376-62855377	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs142762522	chr11:62863405-62863406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552962380	chr11:62863427-62863428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184268615	chr11:62863432-62863433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554854763	chr11:62863468-62863469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574508599	chr11:62863469-62863470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543256896	chr11:62863479-62863480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147369451	chr11:62863492-62863493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532105556	chr11:62863493-62863494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374095536	chr11:62863494-62863495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559053081	chr11:62863502-62863503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528111522	chr11:62863509-62863510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7113279	chr11:62863518-62863519	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs189467728	chr11:62863519-62863520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370535827	chr11:62863526-62863527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371518525	chr11:62863538-62863539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551224216	chr11:62863565-62863566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374808719	chr11:62863570-62863571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376030248	chr11:62863575-62863576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527306932	chr11:62863597-62863598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539905445	chr11:62863612-62863613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76405384	chr11:62863620-62863621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566708196	chr11:62863624-62863625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535852110	chr11:62863660-62863661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554561525	chr11:62863678-62863679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs118006559	chr11:62863714-62863715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543191507	chr11:62863814-62863815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376175491	chr11:62863822-62863823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576644437	chr11:62863849-62863850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545465027	chr11:62863860-62863861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1944043	chr11:62863866-62863867	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs560661144	chr11:62863875-62863876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532710519	chr11:62863891-62863892	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20409316	CNVD
Spinal muscular atrophy	17160897	CNVD
Retinitis pigmentosa	17160897	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62854800-62855400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr11:62855000-62855400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:62863400-62864200	Enhancers	Gastric	stomach
4	chr11:62863600-62864000	Enhancers	Fetal Intestine Large	intestine
5	chr11:62873800-62874000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
6	chr11:62900000-62900800	Enhancers	Pancreas	Pancrea
7	chr11:62900200-62900400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr11:62900400-62900800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr11:62900400-62900800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr11:62900600-62900800	Enhancers	Duodenum Mucosa	Duodenum
11	chr11:62908800-62910800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:62909600-62909800	Enhancers	Fetal Intestine Large	intestine
13	chr11:62909600-62910400	Enhancers	HUVEC	blood vessel
14	chr11:62909800-62910800	Weak transcription	Fetal Intestine Large	intestine
15	chr11:62910400-62911800	Weak transcription	HUVEC	blood vessel
16	chr11:62910800-62911400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:62910800-62912600	Enhancers	Fetal Intestine Large	intestine
18	chr11:62911200-62912800	Enhancers	Fetal Intestine Small	intestine
19	chr11:62911400-62914400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:62911800-62913200	Enhancers	HUVEC	blood vessel
21	chr11:62912400-62913400	Enhancers	Left Ventricle	heart
22	chr11:62912600-62913000	Enhancers	Adipose Nuclei	Adipose
23	chr11:62912600-62913600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr11:62913200-62913600	Flanking Active TSS	HUVEC	blood vessel
25	chr11:62913600-62915000	Enhancers	HUVEC	blood vessel
26	chr11:62924800-62925000	Enhancers	Fetal Muscle Trunk	muscle
27	chr11:62927200-62929000	Weak transcription	Liver	Liver
28	chr11:62927600-62928000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr11:62927600-62928000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr11:62927600-62928200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr11:62927800-62928200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr11:62929000-62937200	Strong transcription	Liver	Liver
33	chr11:62932600-62933200	Enhancers	HUVEC	blood vessel
34	chr11:62932800-62933800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:62933000-62933400	Enhancers	NHEK	skin
36	chr11:62933000-62933600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:62933200-62933400	Flanking Active TSS	HUVEC	blood vessel
38	chr11:62933400-62933600	Enhancers	HUVEC	blood vessel
39	chr11:62933400-62934600	Enhancers	Pancreas	Pancrea
40	chr11:62933600-62933800	Flanking Active TSS	HUVEC	blood vessel
41	chr11:62933800-62934000	Enhancers	HUVEC	blood vessel
42	chr11:62937200-62939200	Weak transcription	Liver	Liver
43	chr11:62939200-62952400	Strong transcription	Liver	Liver
44	chr11:62946600-62949600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr11:62946800-62947200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr11:62946800-62947800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr11:62946800-62948400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr11:62946800-62949200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr11:62946800-62949400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr11:62946800-62949400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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