Variant report

Variant	esv2757420
Chromosome Location	chr11:5416622-5492033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:793)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:5488057-5488184	K562	blood:	n/a	n/a
2	BACH1	chr11:5479355-5479376	K562	blood:	n/a	n/a
3	CCNT2	chr11:5482271-5482425	K562	blood:	n/a	n/a
4	CEBPB	chr11:5465109-5465384	K562	blood:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
5	CEBPB	chr11:5487417-5487661	K562	blood:	n/a	chr11:5487493-5487504 chr11:5487493-5487504
6	CEBPB	chr11:5465101-5465400	A549	lung:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
7	CEBPB	chr11:5465096-5465433	HepG2	liver:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
8	CEBPB	chr11:5484600-5484903	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:5487995-5488302	K562	blood:	n/a	chr11:5488129-5488140
10	CEBPB	chr11:5488104-5488204	H1-hESC	embryonic stem cell:	n/a	chr11:5488129-5488140
11	CEBPB	chr11:5488047-5488291	HepG2	liver:	n/a	chr11:5488129-5488140
12	CHD2	chr11:5481680-5482514	K562	blood:	n/a	n/a
13	CREB1	chr11:5477763-5479678	K562	blood:	n/a	n/a
14	CREB1	chr11:5481891-5482945	K562	blood:	n/a	n/a
15	CTCF	chr11:5474080-5474230	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr11:5462680-5462830	Caco-2	colon:	n/a	n/a
17	CTCF	chr11:5474080-5474230	MCF-7	breast:	n/a	n/a
18	CTCF	chr11:5474000-5474150	HCT-116	colon:	n/a	n/a
19	CTCF	chr11:5474040-5474330	HCT-116	colon:	n/a	n/a
20	CTCF	chr11:5474060-5474210	Caco-2	colon:	n/a	n/a
21	CTCF	chr11:5433564-5433654	Lung_OC	lung:	n/a	n/a
22	CTCF	chr11:5461880-5461993	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:5473908-5473936	Lung_OC	lung:	n/a	n/a
24	CTCF	chr11:5474080-5474230	HEK293	kidney:	n/a	n/a
25	CTCF	chr11:5474040-5474190	HCFaa	heart:	n/a	n/a
26	CTCF	chr11:5474080-5474230	AG04450	lung:	n/a	n/a
27	CTCF	chr11:5443640-5443790	GM12871	blood:	n/a	n/a
28	CTCF	chr11:5474100-5474250	GM12864	blood:	n/a	n/a
29	CTCF	chr11:5474060-5474210	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr11:5461914-5461956	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr11:5474000-5474150	HMF	breast:	n/a	n/a
32	CTCF	chr11:5488940-5489090	GM12873	blood:	n/a	n/a
33	CTCF	chr11:5474060-5474210	A549	lung:	n/a	n/a
34	CTCF	chr11:5474100-5474250	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr11:5442280-5442430	HepG2	liver:	n/a	n/a
36	CTCF	chr11:5432429-5432471	Medullo	brain:	n/a	n/a
37	CTCF	chr11:5474120-5474270	K562	blood:	n/a	n/a
38	CTCF	chr11:5474134-5474180	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:5461878-5461986	GM12878	blood:	n/a	n/a
40	CTCF	chr11:5442280-5442430	HCT-116	colon:	n/a	n/a
41	CTCF	chr11:5461918-5461964	LNCaP	prostate:	n/a	n/a
42	CTCF	chr11:5474060-5474210	GM12867	blood:	n/a	n/a
43	CTCF	chr11:5474110-5474189	GM12878	blood:	n/a	n/a
44	CTCF	chr11:5461880-5461946	HepG2	liver:	n/a	n/a
45	CTCF	chr11:5461869-5461990	MCF-7	breast:	n/a	n/a
46	CTCF	chr11:5474060-5474210	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr11:5474000-5474150	GM12874	blood:	n/a	n/a
48	CTCF	chr11:5442340-5442490	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr11:5442260-5442410	Caco-2	colon:	n/a	n/a
50	CTCF	chr11:5432422-5432428	Medullo	brain:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5462540-5462590	Jurkat	blood:	n/a
2	chr11:5442443-5442493	HRE	kidney:	n/a
3	chr11:5463768-5463818	HepG2	liver:	n/a
4	chr11:5442434-5442484	Caco-2	colon:	n/a
5	chr11:5442511-5442561	LNCaP	prostate:	n/a
6	chr11:5474584-5474634	CMK	blood:	n/a
7	chr11:5444223-5444273	T-47D	breast:	n/a
8	chr11:5462916-5462966	GM06990	blood:	n/a
9	chr11:5474584-5474634	IMR90	lung:	fetal
10	chr11:5462916-5462966	NH-A	brain:	n/a
11	chr11:5474584-5474634	AoSMC	blood vessel:	n/a
12	chr11:5463768-5463818	Hepatocyte	liver:	n/a
13	chr11:5462916-5462966	HEK293	kidney:	embryo
14	chr11:5475082-5475132	HMEC	breast:	n/a
15	chr11:5462916-5462966	AG04450	lung:	fetal
16	chr11:5474965-5475015	ovcar-3	ovarian:	n/a
17	chr11:5462540-5462590	AG04449	skin:	fetal
18	chr11:5442434-5442484	BJ	skin:	n/a
19	chr11:5462916-5462966	PrEC	prostate:	n/a
20	chr11:5474584-5474634	NT2-D1	testis:	n/a
21	chr11:5442443-5442493	BE2_C	brain:	n/a
22	chr11:5475082-5475132	HIPEpiC	eye:	n/a
23	chr11:5462916-5462966	NHDF-neo	bronchial:	n/a
24	chr11:5442434-5442484	HRPEpiC	eye:	n/a
25	chr11:5474612-5474662	K562	blood:	n/a
26	chr11:5444223-5444273	RPTEC	kidney:	n/a
27	chr11:5462540-5462590	HAEpiC	amniotic membrane:	n/a
28	chr11:5474612-5474662	PrEC	prostate:	n/a
29	chr11:5442443-5442493	LNCaP	prostate:	n/a
30	chr11:5474584-5474634	HUVEC	blood vessel:	n/a
31	chr11:5474612-5474662	MCF10A-Er-Src	breast:	n/a
32	chr11:5474001-5474051	CMK	blood:	n/a
33	chr11:5475082-5475132	HRCEpiC	kidney:	n/a
34	chr11:5433817-5433867	H1-hESC	embryonic stem cell:	embryo
35	chr11:5474584-5474634	Caco-2	colon:	n/a
36	chr11:5474965-5475015	GM06990	blood:	n/a
37	chr11:5463768-5463818	SK-N-SH_RA	brain:	n/a
38	chr11:5462916-5462966	IMR90	lung:	fetal
39	chr11:5442511-5442561	Hela-S3	cervix:	n/a
40	chr11:5442443-5442493	NHBE	bronchial:	n/a
41	chr11:5444223-5444273	HIPEpiC	eye:	n/a
42	chr11:5474965-5475015	HL-60	blood:	n/a
43	chr11:5433817-5433867	SK-N-MC	brain:	n/a
44	chr11:5442443-5442493	MCF-7	breast:	n/a
45	chr11:5442511-5442561	Jurkat	blood:	n/a
46	chr11:5433817-5433867	Caco-2	colon:	n/a
47	chr11:5463768-5463818	ECC-1	luminal epithelium:	n/a
48	chr11:5475082-5475132	MCF10A-Er-Src	breast:	n/a
49	chr11:5474001-5474051	PANC-1	pancreas:	n/a
50	chr11:5462916-5462966	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5402054..5402614-chr11:5441811..5442439,2	MCF-7	breast:
2	11:5218976-5222789..11:5425882-5426881	GM12878	blood:
3	chr11:5473913..5477314-chr11:5481378..5484455,3	K562	blood:
4	chr11:5448582..5452295-chr11:5454742..5458081,4	K562	blood:
5	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
6	chr11:5468259..5472386-chr11:5473307..5476028,4	K562	blood:
7	chr11:5448582..5452295-chr11:5454742..5458081,4	K562	blood:
8	11:5482799-5488942..11:5533869-5541626	Hela-S3	cervix:
9	11:5475173-5482799..11:5714465-5718134	H1-hESC	embryonic stem cell:	embryo
10	11:5482799-5488942..11:5707362-5712027	H1-hESC	embryonic stem cell:	embryo
11	11:5146608-5154908..11:5482799-5488942	H1-hESC	embryonic stem cell:	embryo
12	11:5482799-5488942..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
13	11:5475173-5482799..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
14	chr11:5442840..5444659-chr11:5449789..5452716,3	K562	blood:
15	11:5321718-5325668..11:5463864-5469052	K562	blood:
16	11:5482799-5488942..11:5721056-5732713	Hela-S3	cervix:
17	11:4988858-5002113..11:5469844-5475173	Hela-S3	cervix:
18	11:5482799-5488942..11:5566274-5571131	H1-hESC	embryonic stem cell:	embryo
19	11:4778081-4789138..11:5425882-5426881	H1-hESC	embryonic stem cell:	embryo
20	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:
21	11:5250847-5268367..11:5463864-5469052	K562	blood:
22	11:5407716-5412355..11:5482799-5488942	H1-hESC	embryonic stem cell:	embryo
23	chr11:5454190..5457946-chr11:5459430..5461152,3	K562	blood:
24	11:5482799-5488942..11:5714465-5718134	Hela-S3	cervix:
25	chr11:5486296..5490583-chr11:5492213..5495535,7	K562	blood:
26	chr11:5486174..5488915-chr11:5526268..5527984,3	K562	blood:
27	11:5250847-5268367..11:5482799-5488942	Hela-S3	cervix:
28	11:5243048-5250847..11:5425882-5426881	GM12878	blood:
29	chr11:5454190..5457946-chr11:5459430..5461152,3	K562	blood:
30	11:5488942-5494633..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
31	11:5460021-5463864..11:5469052-5469844	H1-hESC	embryonic stem cell:	embryo
32	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:
33	chr11:5487225..5489832-chr11:5524336..5528064,4	K562	blood:
34	11:5421776-5424121..11:5425882-5426881	GM12878	blood:
35	11:5482799-5488942..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
36	11:4778081-4789138..11:5482799-5488942	Hela-S3	cervix:
37	chr11:5330393..5334206-chr11:5464650..5469323,6	K562	blood:
38	11:5146608-5154908..11:5475173-5482799	GM12878	blood:
39	chr11:5452403..5455534-chr11:5455885..5459349,3	K562	blood:
40	11:5146608-5154908..11:5469052-5469844	H1-hESC	embryonic stem cell:	embryo
41	chr11:5454551..5456372-chr11:5525349..5527757,2	K562	blood:

No data

Variant related genes	Relation type
OR51I2	TF binding region
OR51I1	TF binding region
OR51K1P	TF binding region
OR51A10P	TF binding region
OR51J1	TF binding region
OR51Q1	TF binding region
OR51I2	CpG island
OR51I1	CpG island
OR51K1P	CpG island
OR51A10P	CpG island
OR51J1	CpG island
OR51Q1	CpG island
ENSG00000175520	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000181616	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000184698	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000167360	chromatin interactions
ENSG00000167359	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000184321	chromatin interactions
ENSG00000248424	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000167355	chromatin interactions

Extended variants
information (count: 4009 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:4009 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1532514	chr11:5416622-5416623	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1532515	chr11:5416688-5416689	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558397670	chr11:5416693-5416694	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530071010	chr11:5416696-5416697	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs137908558	chr11:5416712-5416713	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543503523	chr11:5416732-5416733	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563584365	chr11:5416837-5416838	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78650791	chr11:5416842-5416843	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533184252	chr11:5416844-5416845	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370163443	chr11:5416846-5416847	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115300062	chr11:5416861-5416862	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187634814	chr11:5416874-5416875	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150162127	chr11:5416897-5416898	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576856274	chr11:5416898-5416899	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs951746	chr11:5416911-5416912	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2723388	chr11:5416914-5416915	Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs192266678	chr11:5416923-5416924	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs5789396	chr11:5416927-5416928	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183993729	chr11:5416972-5416973	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138662972	chr11:5416978-5416979	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375094952	chr11:5416998-5416999	Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142789383	chr11:5417028-5417029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113043372	chr11:5417029-5417030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs951747	chr11:5417034-5417035	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs187459544	chr11:5417057-5417058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556033680	chr11:5417084-5417085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538072634	chr11:5417111-5417112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562879597	chr11:5417134-5417135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533147693	chr11:5417142-5417143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551409717	chr11:5417147-5417148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147409576	chr11:5417149-5417150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs951748	chr11:5417167-5417168	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs549228664	chr11:5417174-5417175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556690974	chr11:5417179-5417180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537675038	chr11:5417191-5417192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550037902	chr11:5417239-5417240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78363222	chr11:5417272-5417273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192010227	chr11:5417284-5417285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553762413	chr11:5417298-5417299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568051896	chr11:5417324-5417325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572086377	chr11:5417359-5417360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs137972570	chr11:5417365-5417366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367707195	chr11:5417386-5417387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143531721	chr11:5417409-5417410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544520963	chr11:5417424-5417425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371606944	chr11:5417431-5417432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577869111	chr11:5417444-5417445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570413129	chr11:5417446-5417447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560083252	chr11:5417447-5417448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2647558	chr11:5417448-5417449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5415000-5417000	Strong transcription	K562	blood
2	chr11:5415800-5417000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:5417000-5417400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:5417000-5420000	Weak transcription	K562	blood
5	chr11:5417400-5420800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:5420000-5423000	Strong transcription	K562	blood
7	chr11:5420800-5421000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:5422000-5422200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:5423000-5424200	Weak transcription	K562	blood
10	chr11:5424200-5425800	Strong transcription	K562	blood
11	chr11:5425800-5432400	Weak transcription	K562	blood
12	chr11:5429600-5430000	Enhancers	Fetal Kidney	kidney
13	chr11:5432400-5433400	Enhancers	K562	blood
14	chr11:5433000-5433400	Enhancers	Hela-S3	cervix
15	chr11:5433200-5433600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr11:5433200-5433800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:5433400-5433600	Flanking Active TSS	K562	blood
18	chr11:5433400-5433800	Active TSS	A549	lung
19	chr11:5433600-5433800	Active TSS	K562	blood
20	chr11:5433600-5434000	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr11:5433800-5434400	Enhancers	K562	blood
22	chr11:5434400-5440400	Weak transcription	K562	blood
23	chr11:5440400-5441200	Strong transcription	K562	blood
24	chr11:5441200-5442400	Weak transcription	K562	blood
25	chr11:5442400-5444400	Strong transcription	K562	blood
26	chr11:5444000-5445000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr11:5444400-5447000	Weak transcription	K562	blood
28	chr11:5445000-5445200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:5445200-5445600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr11:5445400-5446000	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr11:5445600-5448400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:5446800-5447200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:5447000-5448800	Strong transcription	K562	blood
34	chr11:5447200-5447800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:5447800-5448000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:5448000-5448200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:5448200-5448400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:5448400-5448600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr11:5448400-5448600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:5448600-5449000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:5448800-5450000	Weak transcription	K562	blood
42	chr11:5449000-5451400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:5450000-5450800	Genic enhancers	K562	blood
44	chr11:5450400-5450800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:5450800-5453400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:5450800-5458800	Strong transcription	K562	blood
47	chr11:5451400-5451800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:5451800-5459200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:5458800-5460800	Weak transcription	K562	blood
50	chr11:5459200-5460000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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