Variant report

Variant	nsv518717
Chromosome Location	chr11:76288937-76310976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:579)
CpG islands
(count:427)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:76290423-76290481	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr11:76309621-76309904	K562	blood:	n/a	n/a
3	BHLHE40	chr11:76290123-76290300	K562	blood:	n/a	n/a
4	BHLHE40	chr11:76309716-76309856	HepG2	liver:	n/a	n/a
5	BHLHE40	chr11:76309619-76309888	GM12878	blood:	n/a	n/a
6	CEBPB	chr11:76288276-76288987	Hela-S3	cervix:	n/a	chr11:76288809-76288820
7	CEBPB	chr11:76288632-76288980	HepG2	liver:	n/a	chr11:76288809-76288820
8	CEBPB	chr11:76291819-76292031	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr11:76302225-76302486	A549	lung:	n/a	n/a
10	CEBPB	chr11:76288479-76289009	MCF-7	breast:	n/a	chr11:76288809-76288820
11	CEBPB	chr11:76298727-76299240	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:76288624-76288989	IMR90	lung:	n/a	chr11:76288809-76288820
13	CEBPB	chr11:76302377-76302495	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:76288639-76288994	K562	blood:	n/a	chr11:76288809-76288820
15	CEBPB	chr11:76288636-76288982	A549	lung:	n/a	chr11:76288809-76288820
16	CTCF	chr11:76309700-76309850	BE2_C	brain:	n/a	n/a
17	CTCF	chr11:76310080-76310230	BJ	skin:	n/a	chr11:76310171-76310180
18	CTCF	chr11:76290040-76290190	GM12875	blood:	n/a	n/a
19	CTCF	chr11:76290033-76290240	GM19238	blood:	n/a	n/a
20	CTCF	chr11:76290079-76290258	GM12891	blood:	n/a	n/a
21	CTCF	chr11:76309600-76309750	SAEC	small airway:	n/a	n/a
22	CTCF	chr11:76309000-76310293	A549	lung:	n/a	chr11:76310171-76310180
23	CTCF	chr11:76290000-76290150	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr11:76309606-76309840	HepG2	liver:	n/a	n/a
25	CTCF	chr11:76309627-76309849	GM13977	blood:	n/a	n/a
26	CTCF	chr11:76309360-76309510	GM12864	blood:	n/a	n/a
27	CTCF	chr11:76290060-76290210	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr11:76309680-76309830	GM12878	blood:	n/a	n/a
29	CTCF	chr11:76310120-76310270	HBMEC	blood vessel:	n/a	chr11:76310171-76310180
30	CTCF	chr11:76310120-76310270	HRPEpiC	eye:	n/a	chr11:76310171-76310180
31	CTCF	chr11:76290099-76290237	MCF-7	breast:	n/a	n/a
32	CTCF	chr11:76309660-76309810	GM12874	blood:	n/a	n/a
33	CTCF	chr11:76309360-76309510	AG09319	gingival:	n/a	n/a
34	CTCF	chr11:76290120-76290270	AG09319	gingival:	n/a	n/a
35	CTCF	chr11:76309340-76309490	GM06990	blood:	n/a	n/a
36	CTCF	chr11:76310060-76310210	HCFaa	heart:	n/a	chr11:76310171-76310180
37	CTCF	chr11:76309525-76309953	MCF-7	breast:	n/a	n/a
38	CTCF	chr11:76309680-76309830	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr11:76309660-76309810	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr11:76309660-76309810	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr11:76309594-76309883	GM19238	blood:	n/a	n/a
42	CTCF	chr11:76309629-76309840	Fibrobl	skin:	n/a	n/a
43	CTCF	chr11:76309680-76309830	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr11:76290020-76290170	GM12874	blood:	n/a	n/a
45	CTCF	chr11:76309700-76309850	GM12875	blood:	n/a	n/a
46	CTCF	chr11:76309680-76309830	HMF	breast:	n/a	n/a
47	CTCF	chr11:76290044-76290279	K562	blood:	n/a	n/a
48	CTCF	chr11:76309600-76309750	HEK293	kidney:	n/a	n/a
49	CTCF	chr11:76309720-76309870	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr11:76299500-76299650	HUVEC	blood vessel:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76299682-76299732	HUVEC	blood vessel:	n/a
2	chr11:76290361-76290411	HIPEpiC	eye:	n/a
3	chr11:76289700-76289750	NB4	blood:	n/a
4	chr11:76289700-76289750	GM19239	blood:	n/a
5	chr11:76294320-76294370	SKMC	muscle:	n/a
6	chr11:76294320-76294370	AG09309	skin:	n/a
7	chr11:76290361-76290411	SK-N-MC	brain:	n/a
8	chr11:76290361-76290411	T-47D	breast:	n/a
9	chr11:76299819-76299869	PrEC	prostate:	n/a
10	chr11:76299819-76299869	PANC-1	pancreas:	n/a
11	chr11:76293719-76293769	HL-60	blood:	n/a
12	chr11:76293719-76293769	SAEC	small airway:	n/a
13	chr11:76299819-76299869	HUVEC	blood vessel:	n/a
14	chr11:76299682-76299732	CMK	blood:	n/a
15	chr11:76293839-76293889	GM12891	blood:	n/a
16	chr11:76289700-76289750	GM06990	blood:	n/a
17	chr11:76294320-76294370	SK-N-SH_RA	brain:	n/a
18	chr11:76299682-76299732	RPTEC	kidney:	n/a
19	chr11:76299682-76299732	HRCEpiC	kidney:	n/a
20	chr11:76294320-76294370	IMR90	lung:	fetal
21	chr11:76293839-76293889	NT2-D1	testis:	n/a
22	chr11:76294320-76294370	AG09319	gingival:	n/a
23	chr11:76289700-76289750	HNPCEpiC	eye:	n/a
24	chr11:76289700-76289750	HEK293	kidney:	embryo
25	chr11:76299819-76299869	A549	lung:	n/a
26	chr11:76299819-76299869	RPTEC	kidney:	n/a
27	chr11:76289700-76289750	HEEpiC	esophagus:	n/a
28	chr11:76293839-76293889	AoSMC	blood vessel:	n/a
29	chr11:76294320-76294370	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:76299819-76299869	HCT-116	colon:	n/a
31	chr11:76289700-76289750	PrEC	prostate:	n/a
32	chr11:76289700-76289750	ovcar-3	ovarian:	n/a
33	chr11:76289700-76289750	NHBE	bronchial:	n/a
34	chr11:76294320-76294370	AG10803	skin:	n/a
35	chr11:76299682-76299732	Hela-S3	cervix:	n/a
36	chr11:76293839-76293889	HAEpiC	amniotic membrane:	n/a
37	chr11:76299819-76299869	NH-A	brain:	n/a
38	chr11:76293839-76293889	K562	blood:	n/a
39	chr11:76293839-76293889	GM12878	blood:	n/a
40	chr11:76299819-76299869	PFSK-1	brain:	n/a
41	chr11:76293839-76293889	GM19239	blood:	n/a
42	chr11:76294320-76294370	ECC-1	luminal epithelium:	n/a
43	chr11:76299682-76299732	HCF	heart:	n/a
44	chr11:76294320-76294370	HEEpiC	esophagus:	n/a
45	chr11:76293719-76293769	HepG2	liver:	n/a
46	chr11:76293719-76293769	NB4	blood:	n/a
47	chr11:76290361-76290411	Jurkat	blood:	n/a
48	chr11:76294320-76294370	HL-60	blood:	n/a
49	chr11:76299819-76299869	HRCEpiC	kidney:	n/a
50	chr11:76299819-76299869	AG10803	skin:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76278010..76280644-chr11:76290119..76292118,2	MCF-7	breast:
2	chr11:76301219..76303049-chr11:76308621..76311229,3	K562	blood:
3	chr11:76290103..76291705-chr11:76300211..76301911,2	MCF-7	breast:
4	chr11:76309441..76311518-chr11:76311642..76314549,3	K562	blood:
5	chr11:76282655..76284320-chr11:76288646..76291233,2	MCF-7	breast:
6	chr11:76309744..76311546-chr11:76315205..76316740,2	K562	blood:
7	chr11:76309665..76310190-chr11:76388826..76389418,2	MCF-7	breast:
8	chr11:76304158..76306221-chr11:76306296..76307989,2	K562	blood:
9	chr11:76309253..76310227-chr11:76391621..76392159,2	K562	blood:
10	chr11:76289446..76290623-chr11:76391607..76392461,4	MCF-7	breast:
11	chr11:76290103..76291705-chr11:76300211..76301911,2	MCF-7	breast:
12	chr11:76262034..76262940-chr11:76309241..76310049,2	K562	blood:
13	chr11:76310504..76312351-chr11:76321930..76323768,2	K562	blood:
14	chr11:76263076..76264727-chr11:76289911..76291686,2	K562	blood:
15	chr11:76309452..76310726-chr11:76391627..76392625,9	MCF-7	breast:
16	chr11:76304158..76306221-chr11:76306296..76307989,2	K562	blood:
17	chr11:76289419..76290667-chr11:76391568..76392518,9	MCF-7	breast:
18	chr11:76300424..76303049-chr11:76308365..76310172,3	K562	blood:
19	chr11:76154912..76157253-chr11:76299607..76302337,2	K562	blood:
20	chr11:76309431..76311546-chr11:76315205..76316981,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254755	TF binding region
ENSG00000254755	CpG island
ENSG00000255135	chromatin interactions
ENSG00000254755	chromatin interactions
ENSG00000158636	chromatin interactions

Extended variants
information (count: 889 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:889 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10899234	chr11:76288937-76288938	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs150910923	chr11:76288939-76288940	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs576654844	chr11:76288979-76288980	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs545578069	chr11:76289016-76289017	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs556263780	chr11:76289030-76289031	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs567597654	chr11:76289031-76289032	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs576051376	chr11:76289061-76289062	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs139403677	chr11:76289086-76289087	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189639408	chr11:76289087-76289088	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116511538	chr11:76289093-76289094	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs117275177	chr11:76289104-76289105	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs564750690	chr11:76289112-76289113	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs369021536	chr11:76289248-76289249	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs72934310	chr11:76289261-76289262	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs145035944	chr11:76289326-76289327	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs563853429	chr11:76289335-76289336	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs115790742	chr11:76289337-76289338	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs549417576	chr11:76289344-76289345	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs116294490	chr11:76289345-76289346	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs534671782	chr11:76289448-76289449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547321934	chr11:76289493-76289494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28559296	chr11:76289541-76289542	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539294844	chr11:76289578-76289579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180760951	chr11:76289581-76289582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115489765	chr11:76289659-76289660	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs147586159	chr11:76289678-76289679	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs184461957	chr11:76289680-76289681	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs572102632	chr11:76289707-76289708	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs541014487	chr11:76289723-76289724	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs189393269	chr11:76289777-76289778	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs578249682	chr11:76289779-76289780	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs368824413	chr11:76289818-76289819	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs544048050	chr11:76289860-76289861	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs372823305	chr11:76289914-76289915	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs182043059	chr11:76289958-76289959	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs549232912	chr11:76289968-76289969	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs186074017	chr11:76289976-76289977	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs528506884	chr11:76289996-76289997	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs190448601	chr11:76290006-76290007	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149712753	chr11:76290069-76290070	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539359823	chr11:76290088-76290089	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550013307	chr11:76290098-76290099	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369554140	chr11:76290110-76290111	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535614302	chr11:76290130-76290131	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555207331	chr11:76290142-76290143	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572165482	chr11:76290152-76290153	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577112201	chr11:76290170-76290171	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74498650	chr11:76290294-76290295	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs557791858	chr11:76290396-76290397	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs181761356	chr11:76290445-76290446	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76282800-76291000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:76285200-76290000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr11:76285600-76291600	Enhancers	Placenta	Placenta
4	chr11:76285800-76292200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr11:76286000-76289800	Weak transcription	Ovary	ovary
6	chr11:76287000-76289000	Enhancers	Colon Smooth Muscle	Colon
7	chr11:76287000-76289800	Weak transcription	Aorta	Aorta
8	chr11:76287000-76291000	Enhancers	Fetal Stomach	stomach
9	chr11:76287000-76291400	Enhancers	Placenta Amnion	Placenta Amnion
10	chr11:76287400-76291200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:76287800-76289400	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr11:76287800-76289600	Enhancers	HUVEC	blood vessel
13	chr11:76287800-76289600	Enhancers	Osteobl	bone
14	chr11:76287800-76291000	Enhancers	Muscle Satellite Cultured Cells	--
15	chr11:76287800-76291200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:76287800-76291200	Enhancers	Left Ventricle	heart
17	chr11:76288000-76289000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:76288000-76289000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:76288000-76289000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:76288000-76289000	Enhancers	Rectal Smooth Muscle	rectum
21	chr11:76288000-76289200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:76288000-76289200	Enhancers	HSMM	muscle
23	chr11:76288000-76289600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr11:76288000-76289600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:76288000-76289600	Enhancers	Spleen	Spleen
26	chr11:76288000-76290000	Enhancers	HMEC	breast
27	chr11:76288000-76290400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:76288000-76290600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:76288000-76290600	Enhancers	Stomach Smooth Muscle	stomach
30	chr11:76288000-76290800	Enhancers	NH-A	brain
31	chr11:76288000-76291000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:76288000-76291200	Enhancers	NHDF-Ad	bronchial
33	chr11:76288000-76291600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr11:76288200-76289000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr11:76288200-76289000	Enhancers	Fetal Lung	lung
36	chr11:76288200-76289000	Enhancers	Lung	lung
37	chr11:76288200-76289000	Enhancers	A549	lung
38	chr11:76288200-76289200	Flanking Active TSS	Hela-S3	cervix
39	chr11:76288200-76289600	Enhancers	Fetal Intestine Large	intestine
40	chr11:76288200-76289800	Enhancers	Adipose Nuclei	Adipose
41	chr11:76288200-76291000	Enhancers	Fetal Kidney	kidney
42	chr11:76288200-76291000	Enhancers	NHLF	lung
43	chr11:76288200-76291200	Enhancers	Fetal Muscle Trunk	muscle
44	chr11:76288200-76291200	Enhancers	Fetal Muscle Leg	muscle
45	chr11:76288200-76291400	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr11:76288200-76291600	Enhancers	Right Atrium	heart
47	chr11:76288400-76289400	Enhancers	Fetal Intestine Small	intestine
48	chr11:76288400-76289800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:76288400-76290000	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr11:76288400-76290400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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