Variant report

Variant	nsv1048500
Chromosome Location	chr11:104348766-104548809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:245)
Chromatin interactive
region (count:13)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104539807-104540209	HepG2	liver:	n/a	n/a
2	BACH1	chr11:104404978-104405409	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr11:104451956-104452294	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr11:104452026-104452271	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr11:104520974-104521253	HCT-116	colon:	n/a	n/a
6	CBX3	chr11:104539778-104540232	HCT-116	colon:	n/a	n/a
7	CEBPB	chr11:104365021-104365243	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr11:104539680-104540284	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:104539824-104540164	A549	lung:	n/a	n/a
10	CEBPB	chr11:104418823-104419081	HepG2	liver:	n/a	chr11:104418932-104418943
11	CEBPB	chr11:104539774-104540189	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:104365015-104365286	IMR90	lung:	n/a	n/a
13	CEBPB	chr11:104418796-104419073	Hela-S3	cervix:	n/a	chr11:104418932-104418943
14	CEBPB	chr11:104539817-104540111	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:104508427-104509111	Hela-S3	cervix:	n/a	chr11:104508922-104508933
16	CEBPB	chr11:104539700-104540315	HCT-116	colon:	n/a	n/a
17	CEBPB	chr11:104536453-104536685	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:104537036-104537358	HepG2	liver:	n/a	chr11:104537185-104537196
19	CEBPB	chr11:104452414-104452693	IMR90	lung:	n/a	chr11:104452534-104452547
20	CEBPB	chr11:104494200-104494571	Hela-S3	cervix:	n/a	chr11:104494285-104494296 chr11:104494285-104494296
21	CEBPB	chr11:104481416-104481629	HepG2	liver:	n/a	chr11:104481550-104481558 chr11:104481467-104481478
22	CEBPB	chr11:104365000-104365259	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:104450617-104450780	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:104534113-104534393	IMR90	lung:	n/a	chr11:104534205-104534216
25	CEBPB	chr11:104525013-104525262	A549	lung:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
26	CEBPB	chr11:104489254-104489482	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:104450058-104450309	HepG2	liver:	n/a	chr11:104450182-104450193 chr11:104450182-104450195 chr11:104450183-104450194
28	CEBPB	chr11:104512648-104512834	IMR90	lung:	n/a	chr11:104512746-104512757
29	CEBPB	chr11:104355702-104355911	HepG2	liver:	n/a	chr11:104355849-104355860
30	CEBPB	chr11:104536365-104536737	IMR90	lung:	n/a	n/a
31	CEBPB	chr11:104539759-104540264	A549	lung:	n/a	n/a
32	CEBPB	chr11:104525090-104525327	K562	blood:	n/a	chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
33	CEBPB	chr11:104404965-104405432	IMR90	lung:	n/a	n/a
34	CEBPB	chr11:104525026-104525358	IMR90	lung:	n/a	chr11:104525322-104525333 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525194 chr11:104525181-104525192
35	CEBPB	chr11:104537084-104537209	H1-hESC	embryonic stem cell:	n/a	chr11:104537185-104537196
36	CEBPB	chr11:104474275-104474597	HepG2	liver:	n/a	chr11:104474423-104474434
37	CEBPB	chr11:104474320-104474546	A549	lung:	n/a	chr11:104474423-104474434
38	CEBPB	chr11:104444109-104444452	IMR90	lung:	n/a	chr11:104444139-104444152
39	CEBPB	chr11:104539838-104540124	A549	lung:	n/a	n/a
40	CEBPB	chr11:104474341-104474571	Hela-S3	cervix:	n/a	chr11:104474423-104474434
41	CEBPB	chr11:104440984-104441394	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:104442981-104443405	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr11:104480012-104480256	H1-hESC	embryonic stem cell:	n/a	chr11:104480194-104480207
44	CEBPB	chr11:104494198-104494575	IMR90	lung:	n/a	chr11:104494285-104494296 chr11:104494285-104494296
45	CEBPB	chr11:104489291-104489495	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:104512599-104512892	HepG2	liver:	n/a	chr11:104512746-104512757
47	CEBPB	chr11:104442251-104442397	HepG2	liver:	n/a	chr11:104442293-104442304
48	CEBPB	chr11:104444090-104444528	Hela-S3	cervix:	n/a	chr11:104444139-104444152
49	CEBPB	chr11:104479994-104480282	Hela-S3	cervix:	n/a	chr11:104480194-104480207
50	CEBPB	chr11:104534104-104534298	HepG2	liver:	n/a	chr11:104534205-104534216

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104405198-104405248	AG04449	skin:	fetal
2	chr11:104405198-104405248	AG04449	skin:	fetal
3	chr11:104435867-104435917	GM12891	blood:	n/a
4	chr11:104501066-104501116	GM06990	blood:	n/a
5	chr11:104405198-104405248	GM12892	blood:	n/a
6	chr11:104508637-104508687	SKMC	muscle:	n/a
7	chr11:104508637-104508687	Caco-2	colon:	n/a
8	chr11:104501066-104501116	BJ	skin:	n/a
9	chr11:104508637-104508687	Jurkat	blood:	n/a
10	chr11:104435867-104435917	CMK	blood:	n/a
11	chr11:104501066-104501116	T-47D	breast:	n/a
12	chr11:104501066-104501116	HUVEC	blood vessel:	n/a
13	chr11:104435867-104435917	RPTEC	kidney:	n/a
14	chr11:104508637-104508687	HCT-116	colon:	n/a
15	chr11:104435867-104435917	HNPCEpiC	eye:	n/a
16	chr11:104508637-104508687	GM06990	blood:	n/a
17	chr11:104435867-104435917	T-47D	breast:	n/a
18	chr11:104501066-104501116	SAEC	small airway:	n/a
19	chr11:104501066-104501116	HCT-116	colon:	n/a
20	chr11:104508637-104508687	Hepatocyte	liver:	n/a
21	chr11:104508637-104508687	PFSK-1	brain:	n/a
22	chr11:104501066-104501116	SK-N-SH	brain:	n/a
23	chr11:104435867-104435917	HCF	heart:	n/a
24	chr11:104405198-104405248	HCT-116	colon:	n/a
25	chr11:104501066-104501116	ECC-1	luminal epithelium:	n/a
26	chr11:104508637-104508687	ProgFib	skin:	n/a
27	chr11:104435867-104435917	NT2-D1	testis:	n/a
28	chr11:104501066-104501116	AG04450	lung:	fetal
29	chr11:104435867-104435917	GM12878	blood:	n/a
30	chr11:104405198-104405248	NB4	blood:	n/a
31	chr11:104435867-104435917	NHDF-neo	bronchial:	n/a
32	chr11:104405198-104405248	HRCEpiC	kidney:	n/a
33	chr11:104435867-104435917	Hepatocyte	liver:	n/a
34	chr11:104405198-104405248	BE2_C	brain:	n/a
35	chr11:104508637-104508687	A549	lung:	n/a
36	chr11:104501066-104501116	CMK	blood:	n/a
37	chr11:104501066-104501116	NHBE	bronchial:	n/a
38	chr11:104435867-104435917	HUVEC	blood vessel:	n/a
39	chr11:104405198-104405248	AG04450	lung:	fetal
40	chr11:104405198-104405248	GM12891	blood:	n/a
41	chr11:104501066-104501116	GM12878	blood:	n/a
42	chr11:104405198-104405248	AG10803	skin:	n/a
43	chr11:104435867-104435917	AG04449	skin:	fetal
44	chr11:104501066-104501116	LNCaP	prostate:	n/a
45	chr11:104508637-104508687	BJ	skin:	n/a
46	chr11:104501066-104501116	IMR90	lung:	fetal
47	chr11:104435867-104435917	NHBE	bronchial:	n/a
48	chr11:104508637-104508687	HRE	kidney:	n/a
49	chr11:104435867-104435917	K562	blood:	n/a
50	chr11:104508637-104508687	AG10803	skin:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:104524242..104527061-chr11:104559725..104562588,2	K562	blood:
2	chr11:104481697..104482494-chr17:63790105..63790828,2	MCF-7	breast:
3	chr11:104481943..104484005-chr11:104508194..104510818,2	K562	blood:
4	chr11:104481943..104484005-chr11:104508194..104510818,2	K562	blood:
5	chr11:104505386..104506145-chr7:1705158..1706031,2	MCF-7	breast:
6	chr11:104380583..104383114-chr11:104384527..104386564,2	K562	blood:
7	chr11:104516723..104519201-chr11:104522234..104524667,2	K562	blood:
8	chr11:104242893..104244741-chr11:104376136..104378191,2	K562	blood:
9	chr11:104380583..104383114-chr11:104384527..104386564,2	K562	blood:
10	chr11:104516723..104519201-chr11:104522234..104524667,2	K562	blood:
11	chr11:104377912..104380713-chr11:104411485..104413500,2	MCF-7	breast:
12	chr11:104372355..104372989-chr5:37799043..37799937,2	MCF-7	breast:
13	chr11:104377912..104380713-chr11:104411485..104413500,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
2	lnc-CASP12-1	chr11:104439083-104439649	XLOC_009538
3	lnc-CASP12-1	chr11:104479965-104480102	NONHSAT023934
4	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422
5	lnc-CASP12-1	chr11:104442804-104443213	NONHSAT023935
6	lnc-CASP12-1	chr11:104479965-104480024	ENSG00000256422
7	lnc-CASP12-1	chr11:104479965-104480030	ENSG00000256422
8	lnc-CASP12-1	chr11:104382877-104382961	ENSG00000256422
9	lnc-CASP12-1	chr11:104415427-104415514	ENSG00000256422
10	lnc-CASP12-1	chr11:104443285-104443325	ENSG00000256422
11	lnc-CASP12-1	chr11:104439776-104439859	ENSG00000256422
12	lnc-CASP12-1	chr11:104439221-104439649	NONHSAT023934
13	lnc-CASP12-1	chr11:104439776-104439859	XLOC_009538
14	lnc-CASP12-1	chr11:104439240-104439649	NONHSAT023935
15	lnc-CASP12-1	chr11:104479965-104480062	XLOC_009538
16	lnc-CASP12-1	chr11:104479965-104480049	ENSG00000256422
17	lnc-CASP12-1	chr11:104415604-104415877	ENSG00000256422
18	lnc-CASP12-1	chr11:104443285-104443325	XLOC_009538
19	lnc-CASP12-1	chr11:104410659-104410753	ENSG00000256422
20	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023934
21	lnc-CASP12-1	chr11:104439776-104439859	NONHSAT023935
22	lnc-CASP12-1	chr11:104439258-104439649	ENSG00000256422

No data

Variant related genes	Relation type
ENSG00000256422	TF binding region
ENSG00000256422	CpG island

Extended variants
information (count: 5513 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5513 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76684245	chr11:104348769-104348770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72974744	chr11:104348773-104348774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570442421	chr11:104348796-104348797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532823783	chr11:104348849-104348850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74386037	chr11:104348863-104348864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs58182768	chr11:104348878-104348879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150379403	chr11:104348889-104348890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7121679	chr11:104348915-104348916	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554750422	chr11:104348934-104348935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11374753	chr11:104348940-104348941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs55886647	chr11:104348952-104348953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34339525	chr11:104348992-104348993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541992221	chr11:104349000-104349001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7122709	chr11:104349012-104349013	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs534046785	chr11:104349030-104349031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553875725	chr11:104349072-104349073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11226380	chr11:104349125-104349126	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs545915257	chr11:104349160-104349161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566490474	chr11:104349214-104349215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551252142	chr11:104349246-104349247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542013521	chr11:104349259-104349260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561888040	chr11:104349280-104349281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563952370	chr11:104349325-104349326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527511803	chr11:104349366-104349367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182184791	chr11:104349385-104349386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564210802	chr11:104349412-104349413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532940032	chr11:104349476-104349477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369618236	chr11:104349522-104349523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149934212	chr11:104349523-104349524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34479910	chr11:104349534-104349535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549514382	chr11:104349566-104349567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376122024	chr11:104349610-104349611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569493401	chr11:104349620-104349621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115751491	chr11:104349744-104349745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79736170	chr11:104349770-104349771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187577531	chr11:104349857-104349858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1487692	chr11:104349863-104349864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs553837185	chr11:104349902-104349903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529103028	chr11:104349936-104349937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570862159	chr11:104349951-104349952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539783316	chr11:104349959-104349960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556300921	chr11:104349963-104349964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368817489	chr11:104349989-104349990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191856511	chr11:104350041-104350042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535725427	chr11:104350110-104350111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555734526	chr11:104350139-104350140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79136121	chr11:104350161-104350162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549156438	chr11:104350222-104350223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555510631	chr11:104350262-104350263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541274334	chr11:104350275-104350276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Renal cell carcinoma	18194544	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
low-grade B-cell lymphoma tumor	18367492	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
Melanoma	17363583	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
Obesity	19966786	CNVD
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104347200-104357800	Weak transcription	Ovary	ovary
2	chr11:104348400-104349200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:104355600-104355800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:104355600-104357000	Enhancers	Fetal Lung	lung
5	chr11:104355600-104358400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:104356000-104356200	Enhancers	Brain Germinal Matrix	brain
7	chr11:104356400-104356800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:104356400-104357400	Weak transcription	Brain Germinal Matrix	brain
9	chr11:104356600-104358200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr11:104356800-104357200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:104357000-104357800	Weak transcription	Fetal Lung	lung
12	chr11:104357200-104358400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:104357200-104358400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr11:104357400-104358400	Enhancers	Brain Germinal Matrix	brain
15	chr11:104357600-104358000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:104357600-104359600	Enhancers	Fetal Heart	heart
17	chr11:104357800-104358000	Enhancers	Ovary	ovary
18	chr11:104357800-104358400	Enhancers	Fetal Lung	lung
19	chr11:104357800-104358600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr11:104358200-104358600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:104358200-104358600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:104358400-104358800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:104358800-104362200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:104361000-104362400	ZNF genes & repeats	Adipose Nuclei	Adipose
25	chr11:104363400-104364800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:104364400-104365400	Weak transcription	Aorta	Aorta
27	chr11:104365400-104365600	Enhancers	Aorta	Aorta
28	chr11:104374400-104375200	Enhancers	Dnd41	blood
29	chr11:104378000-104388400	Weak transcription	Pancreas	Pancrea
30	chr11:104380800-104381200	Enhancers	Stomach Mucosa	stomach
31	chr11:104382600-104383000	Enhancers	Placenta	Placenta
32	chr11:104384600-104393600	Weak transcription	Aorta	Aorta
33	chr11:104388400-104388600	Enhancers	Pancreas	Pancrea
34	chr11:104388600-104393000	Weak transcription	Pancreas	Pancrea
35	chr11:104393000-104393800	Enhancers	Pancreas	Pancrea
36	chr11:104393000-104393800	Enhancers	Stomach Smooth Muscle	stomach
37	chr11:104393000-104394000	Enhancers	Adipose Nuclei	Adipose
38	chr11:104393000-104394000	Enhancers	Brain Germinal Matrix	brain
39	chr11:104393000-104395600	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr11:104393200-104393600	Enhancers	Fetal Brain Female	brain
41	chr11:104393400-104393800	Enhancers	Brain Cingulate Gyrus	brain
42	chr11:104393400-104393800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr11:104393400-104393800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr11:104393400-104393800	Enhancers	Colon Smooth Muscle	Colon
45	chr11:104393400-104393800	Enhancers	Fetal Heart	heart
46	chr11:104393400-104393800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr11:104393400-104393800	Enhancers	Rectal Smooth Muscle	rectum
48	chr11:104393400-104394000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr11:104393400-104394600	Enhancers	Brain Angular Gyrus	brain
50	chr11:104393400-104395200	Enhancers	Ovary	ovary

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