Variant report

Variant	esv2759829
Chromosome Location	chr11:55689863-55849156
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	ATF1	chr11:55749566-55749730	K562	blood:	n/a	n/a
2	CEBPB	chr11:55828199-55828299	K562	blood:	n/a	n/a
3	CEBPB	chr11:55730195-55730482	IMR90	lung:	n/a	chr11:55730352-55730363
4	CEBPB	chr11:55704335-55704572	HepG2	liver:	n/a	chr11:55704400-55704413 chr11:55704401-55704412
5	CEBPB	chr11:55834333-55834597	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:55730191-55730507	HepG2	liver:	n/a	chr11:55730352-55730363
7	CEBPB	chr11:55698713-55698910	A549	lung:	n/a	n/a
8	CEBPB	chr11:55710296-55710606	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:55807323-55807629	HepG2	liver:	n/a	chr11:55807438-55807449
10	CEBPB	chr11:55741577-55741777	HepG2	liver:	n/a	chr11:55741709-55741720
11	CEBPB	chr11:55823995-55824138	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr11:55824010-55824142	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr11:55710360-55710510	AoAF	blood vessel:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
14	CTCF	chr11:55710400-55710550	WI-38	lung:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
15	CTCF	chr11:55710320-55710470	HRPEpiC	eye:	n/a	chr11:55710457-55710465 chr11:55710452-55710470 chr11:55710453-55710469
16	CTCF	chr11:55768480-55768630	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr11:55710380-55710530	BE2_C	brain:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
18	CTCF	chr11:55716941-55717054	GM12891	blood:	n/a	n/a
19	CTCF	chr11:55710361-55710550	GM13977	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
20	CTCF	chr11:55710380-55710530	HRE	kidney:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
21	CTCF	chr11:55710320-55710470	HEK293	kidney:	n/a	chr11:55710457-55710465 chr11:55710452-55710470 chr11:55710453-55710469
22	CTCF	chr11:55710380-55710530	RPTEC	kidney:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
23	CTCF	chr11:55710440-55710590	AG04449	skin:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
24	CTCF	chr11:55710320-55710470	HVMF	connective:	n/a	chr11:55710457-55710465 chr11:55710452-55710470 chr11:55710453-55710469
25	CTCF	chr11:55710353-55710571	Pancreas_OC	pancreas:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
26	CTCF	chr11:55710360-55710510	HRE	kidney:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
27	CTCF	chr11:55716958-55717014	GM12892	blood:	n/a	n/a
28	CTCF	chr11:55710353-55710528	HepG2	liver:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
29	CTCF	chr11:55710400-55710550	AG10803	skin:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
30	CTCF	chr11:55710460-55710610	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr11:55710213-55710569	MCF-7	breast:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
32	CTCF	chr11:55710316-55710565	HCT-116	colon:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
33	CTCF	chr11:55710360-55710510	NHEK	skin:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
34	CTCF	chr11:55710420-55710570	Hela-S3	cervix:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
35	CTCF	chr11:55710364-55710548	K562	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
36	CTCF	chr11:55710283-55710585	A549	lung:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
37	CTCF	chr11:55716914-55717067	MCF-7	breast:	n/a	n/a
38	CTCF	chr11:55710400-55710550	GM12874	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
39	CTCF	chr11:55710380-55710530	HCPEpiC	choroid plexus:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
40	CTCF	chr11:55710380-55710530	HEEpiC	esophagus:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
41	CTCF	chr11:55710360-55710510	MCF-7	breast:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
42	CTCF	chr11:55830312-55830375	GM13976	blood:	n/a	n/a
43	CTCF	chr11:55710420-55710570	GM12867	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
44	CTCF	chr11:55732338-55732401	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr11:55710400-55710550	MCF-7	breast:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
46	CTCF	chr11:55710343-55710564	LNCaP	prostate:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
47	CTCF	chr11:55710440-55710590	AG09319	gingival:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
48	CTCF	chr11:55710280-55710430	HCT-116	colon:	n/a	n/a
49	CTCF	chr11:55764276-55764363	Lung_OC	lung:	n/a	n/a
50	CTCF	chr11:55716822-55717107	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:55796572-55796622	HMEC	breast:	n/a
2	chr11:55737045-55737095	HMEC	breast:	n/a
3	chr11:55736968-55737018	NHDF-neo	bronchial:	n/a
4	chr11:55735459-55735509	HEK293	kidney:	embryo
5	chr11:55737045-55737095	HCPEpiC	choroid plexus:	n/a
6	chr11:55704601-55704651	HRE	kidney:	n/a
7	chr11:55797628-55797678	BJ	skin:	n/a
8	chr11:55705284-55705334	HNPCEpiC	eye:	n/a
9	chr11:55736968-55737018	HMEC	breast:	n/a
10	chr11:55705284-55705334	K562	blood:	n/a
11	chr11:55735459-55735509	GM06990	blood:	n/a
12	chr11:55753849-55753899	SK-N-SH	brain:	n/a
13	chr11:55737045-55737095	PANC-1	pancreas:	n/a
14	chr11:55737045-55737095	CMK	blood:	n/a
15	chr11:55796572-55796622	SAEC	small airway:	n/a
16	chr11:55796572-55796622	SK-N-SH_RA	brain:	n/a
17	chr11:55737045-55737095	NT2-D1	testis:	n/a
18	chr11:55749739-55749789	HCM	heart:	n/a
19	chr11:55704601-55704651	BE2_C	brain:	n/a
20	chr11:55797626-55797676	NHDF-neo	bronchial:	n/a
21	chr11:55737045-55737095	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:55753849-55753899	T-47D	breast:	n/a
23	chr11:55704601-55704651	HepG2	liver:	n/a
24	chr11:55735459-55735509	HRPEpiC	eye:	n/a
25	chr11:55796572-55796622	SK-N-SH	brain:	n/a
26	chr11:55797626-55797676	AG10803	skin:	n/a
27	chr11:55735459-55735509	SAEC	small airway:	n/a
28	chr11:55737072-55737122	U87	brain:	n/a
29	chr11:55737072-55737122	AoSMC	blood vessel:	n/a
30	chr11:55797626-55797676	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:55737072-55737122	GM19239	blood:	n/a
32	chr11:55753849-55753899	HEEpiC	esophagus:	n/a
33	chr11:55797628-55797678	MCF10A-Er-Src	breast:	n/a
34	chr11:55796572-55796622	HepG2	liver:	n/a
35	chr11:55749739-55749789	HAEpiC	amniotic membrane:	n/a
36	chr11:55797628-55797678	HEK293	kidney:	embryo
37	chr11:55737045-55737095	RPTEC	kidney:	n/a
38	chr11:55735459-55735509	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:55737045-55737095	H1-hESC	embryonic stem cell:	embryo
40	chr11:55797626-55797676	SK-N-MC	brain:	n/a
41	chr11:55705284-55705334	NHBE	bronchial:	n/a
42	chr11:55796572-55796622	MCF10A-Er-Src	breast:	n/a
43	chr11:55703443-55703493	NHDF-neo	bronchial:	n/a
44	chr11:55798206-55798256	PANC-1	pancreas:	n/a
45	chr11:55737045-55737095	ECC-1	luminal epithelium:	n/a
46	chr11:55753849-55753899	HRE	kidney:	n/a
47	chr11:55735459-55735509	BJ	skin:	n/a
48	chr11:55703443-55703493	AG10803	skin:	n/a
49	chr11:55704364-55704414	Hepatocyte	liver:	n/a
50	chr11:55735459-55735509	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:55702690..55706471-chr11:55707075..55709513,3	MCF-7	breast:
2	chr11:55726290..55727933-chr11:55735253..55737882,2	K562	blood:
3	chr11:55698028..55700897-chr11:55714005..55716618,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10AG1-1	chr11:55724692-55725106	NONHSAT021375

Variant related genes	Relation type
OR10AF1P	TF binding region
OR7E5P	TF binding region
OR5AQ1P	TF binding region
OR10AK1P	TF binding region
OR5I1	TF binding region
OR5J1P	TF binding region
OR5AS1	TF binding region
OR5F2P	TF binding region
OR10AG1	TF binding region
OR5F1	TF binding region
OR5BE1P	TF binding region
OR10AF1P	CpG island
OR7E5P	CpG island
OR5AQ1P	CpG island
OR10AK1P	CpG island
OR5I1	CpG island
OR5J1P	CpG island
OR5AS1	CpG island
OR5F2P	CpG island
OR10AG1	CpG island
OR5F1	CpG island
OR5BE1P	CpG island
ENSG00000167825	chromatin interactions
ENSG00000174970	chromatin interactions
ENSG00000255416	chromatin interactions

Extended variants
information (count: 2142 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2142 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577017087	chr11:55698033-55698034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs570542629	chr11:55698040-55698041	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539514588	chr11:55698041-55698042	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs140177020	chr11:55698042-55698043	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs7941718	chr11:55698048-55698049	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs559576107	chr11:55698076-55698077	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs138222239	chr11:55698099-55698100	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs36088468	chr11:55698107-55698108	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192574287	chr11:55698126-55698127	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs61894170	chr11:55698164-55698165	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546319335	chr11:55698235-55698236	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565117221	chr11:55698258-55698259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs532306918	chr11:55698268-55698269	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149579300	chr11:55698284-55698285	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77113517	chr11:55698352-55698353	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574809667	chr11:55698354-55698355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529706762	chr11:55698358-55698359	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs9667319	chr11:55698444-55698445	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs74780821	chr11:55698494-55698495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536792311	chr11:55698499-55698500	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558217894	chr11:55698519-55698520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9667699	chr11:55698587-55698588	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs113926518	chr11:55698597-55698598	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553272242	chr11:55698604-55698605	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575065811	chr11:55698605-55698606	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542490129	chr11:55698614-55698615	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189000396	chr11:55698616-55698617	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145180212	chr11:55698629-55698630	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201226343	chr11:55698640-55698641	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs193143790	chr11:55698661-55698662	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9666864	chr11:55698689-55698690	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs9667335	chr11:55698707-55698708	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs9667708	chr11:55698751-55698752	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs532370142	chr11:55698777-55698778	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541192191	chr11:55698816-55698817	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs61894171	chr11:55698844-55698845	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs529972647	chr11:55698867-55698868	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77521421	chr11:55698891-55698892	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs569588921	chr11:55698977-55698978	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530383525	chr11:55698995-55698996	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs9667688	chr11:55698998-55698999	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs61894172	chr11:55699031-55699032	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs372810307	chr11:55699065-55699066	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553321854	chr11:55699096-55699097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568639057	chr11:55699154-55699155	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144297074	chr11:55699159-55699160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557592728	chr11:55699165-55699166	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112862462	chr11:55699174-55699175	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115814191	chr11:55699179-55699180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552350354	chr11:55699186-55699187	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Glioblastoma multiforme	22286061	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
Multiple myeloma	16616336	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:55698800-55699000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:55717000-55717400	Enhancers	Pancreas	Pancrea
3	chr11:55730000-55734000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:55733400-55734800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:55734000-55734200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:55734000-55734400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr11:55741000-55741400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr11:55741200-55742000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr11:55741400-55746000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr11:55742000-55742400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:55742400-55742600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr11:55742600-55745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr11:55745600-55747000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr11:55745800-55747000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr11:55746000-55746800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr11:55746000-55746800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:55746000-55746800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:55746200-55747200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr11:55746200-55747400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:55746600-55747400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:55746800-55747400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:55747400-55753000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr11:55753000-55754000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr11:55753400-55753600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr11:55753400-55753800	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr11:55753600-55754000	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr11:55761200-55761400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr11:55761400-55762600	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr11:55762600-55763600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr11:55762800-55764200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr11:55798200-55798800	Enhancers	Pancreas	Pancrea
32	chr11:55800400-55800600	Enhancers	Pancreas	Pancrea
33	chr11:55822200-55824800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr11:55822600-55822800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr11:55822600-55823600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:55822600-55823800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:55822800-55824800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:55822800-55834000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr11:55823000-55823800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr11:55823400-55824000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr11:55823400-55824600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr11:55823400-55825400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr11:55823600-55824000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr11:55823800-55824000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr11:55823800-55824400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr11:55823800-55826000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr11:55824000-55824200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr11:55824000-55824200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr11:55824000-55824800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr11:55824000-55825000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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