Variant report

Variant	esv3369271
Chromosome Location	chr11:71307946-71334603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:290)
CpG islands
(count:1831)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:71328834-71328851	K562	blood:	n/a	n/a
2	BATF	chr11:71325819-71326075	GM12878	blood:	n/a	n/a
3	BATF	chr11:71315927-71316371	GM12878	blood:	n/a	n/a
4	BATF	chr11:71325884-71326044	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:71316096-71316292	GM12878	blood:	n/a	n/a
6	BCL11A	chr11:71315909-71316399	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:71325637-71325647	HepG2	liver:	n/a	n/a
8	CTCF	chr11:71316240-71316390	HEK293	kidney:	n/a	n/a
9	CTCF	chr11:71316300-71316450	HCM	heart:	n/a	n/a
10	CTCF	chr11:71316260-71316410	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr11:71316260-71316410	GM12872	blood:	n/a	n/a
12	CTCF	chr11:71315780-71315930	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr11:71316360-71316510	HCM	heart:	n/a	n/a
14	CTCF	chr11:71316260-71316410	AG09319	gingival:	n/a	n/a
15	CTCF	chr11:71316180-71316330	GM12872	blood:	n/a	n/a
16	CTCF	chr11:71312016-71312119	Lung_OC	lung:	n/a	n/a
17	CTCF	chr11:71315920-71316070	GM12867	blood:	n/a	n/a
18	CTCF	chr11:71316220-71316370	GM12870	blood:	n/a	n/a
19	CTCF	chr11:71316220-71316370	GM12869	blood:	n/a	n/a
20	CTCF	chr11:71315940-71316090	HCFaa	heart:	n/a	n/a
21	CTCF	chr11:71316240-71316390	GM12878	blood:	n/a	n/a
22	CTCF	chr11:71315846-71315972	GM19239	blood:	n/a	n/a
23	CTCF	chr11:71315800-71315950	GM12864	blood:	n/a	n/a
24	CTCF	chr11:71316340-71316490	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr11:71316127-71316334	MCF-7	breast:	n/a	n/a
26	CTCF	chr11:71316100-71316365	LNCaP	prostate:	n/a	n/a
27	CTCF	chr11:71316520-71316670	GM12872	blood:	n/a	n/a
28	CTCF	chr11:71316280-71316430	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr11:71315854-71315973	GM19238	blood:	n/a	n/a
30	CTCF	chr11:71316220-71316370	HVMF	connective:	n/a	n/a
31	CTCF	chr11:71310809-71310861	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr11:71316340-71316490	AG09309	skin:	n/a	n/a
33	CTCF	chr11:71315869-71315969	GM12891	blood:	n/a	n/a
34	CTCF	chr11:71316240-71316390	BE2_C	brain:	n/a	n/a
35	CTCF	chr11:71316260-71316410	BJ	skin:	n/a	n/a
36	CTCF	chr11:71316090-71316382	GM13977	blood:	n/a	n/a
37	CTCF	chr11:71316112-71316346	GM19238	blood:	n/a	n/a
38	CTCF	chr11:71316113-71316366	GM20000	blood:	n/a	n/a
39	CTCF	chr11:71316120-71316346	GM12878	blood:	n/a	n/a
40	CTCF	chr11:71316121-71316336	A549	lung:	n/a	n/a
41	CTCF	chr11:71316104-71316345	Gliobla	brain:	n/a	n/a
42	CTCF	chr11:71315890-71315945	ProgFib	skin:	n/a	n/a
43	CTCF	chr11:71316200-71316350	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr11:71316260-71316410	HPF	lung:	n/a	n/a
45	CTCF	chr11:71315280-71315430	GM12864	blood:	n/a	n/a
46	CTCF	chr11:71316240-71316390	GM12865	blood:	n/a	n/a
47	CTCF	chr11:71316240-71316390	GM12864	blood:	n/a	n/a
48	CTCF	chr11:71316087-71316374	GM10248	blood:	n/a	n/a
49	CTCF	chr11:71315920-71316070	GM12874	blood:	n/a	n/a
50	CTCF	chr11:71315886-71315947	HUVEC	blood vessel:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71324525-71324575	HRPEpiC	eye:	n/a
2	chr11:71324525-71324575	HRPEpiC	eye:	n/a
3	chr11:71321226-71321276	Hela-S3	cervix:	n/a
4	chr11:71320735-71320785	ECC-1	luminal epithelium:	n/a
5	chr11:71322873-71322923	PFSK-1	brain:	n/a
6	chr11:71326282-71326332	GM19239	blood:	n/a
7	chr11:71326486-71326536	NT2-D1	testis:	n/a
8	chr11:71322128-71322178	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:71321058-71321108	AG04449	skin:	fetal
10	chr11:71321058-71321108	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:71326486-71326536	NH-A	brain:	n/a
12	chr11:71327353-71327403	ProgFib	skin:	n/a
13	chr11:71313750-71313800	HUVEC	blood vessel:	n/a
14	chr11:71320513-71320563	AG04449	skin:	fetal
15	chr11:71327380-71327430	PANC-1	pancreas:	n/a
16	chr11:71326282-71326332	HRE	kidney:	n/a
17	chr11:71318057-71318107	HUVEC	blood vessel:	n/a
18	chr11:71326282-71326332	NHBE	bronchial:	n/a
19	chr11:71313750-71313800	PANC-1	pancreas:	n/a
20	chr11:71326282-71326332	Caco-2	colon:	n/a
21	chr11:71321132-71321182	RPTEC	kidney:	n/a
22	chr11:71321132-71321182	HCF	heart:	n/a
23	chr11:71322128-71322178	BJ	skin:	n/a
24	chr11:71313232-71313282	H1-hESC	embryonic stem cell:	embryo
25	chr11:71321132-71321182	PANC-1	pancreas:	n/a
26	chr11:71321226-71321276	HL-60	blood:	n/a
27	chr11:71327380-71327430	GM12878	blood:	n/a
28	chr11:71327885-71327935	SK-N-MC	brain:	n/a
29	chr11:71324346-71324396	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:71327380-71327430	SK-N-SH_RA	brain:	n/a
31	chr11:71322165-71322215	HepG2	liver:	n/a
32	chr11:71327897-71327947	GM19239	blood:	n/a
33	chr11:71313232-71313282	ovcar-3	ovarian:	n/a
34	chr11:71322873-71322923	MCF10A-Er-Src	breast:	n/a
35	chr11:71322699-71322749	Hela-S3	cervix:	n/a
36	chr11:71313838-71313888	ProgFib	skin:	n/a
37	chr11:71326486-71326536	AoSMC	blood vessel:	n/a
38	chr11:71326486-71326536	CMK	blood:	n/a
39	chr11:71327885-71327935	HCM	heart:	n/a
40	chr11:71313838-71313888	LNCaP	prostate:	n/a
41	chr11:71318870-71318920	HCT-116	colon:	n/a
42	chr11:71324028-71324078	AoSMC	blood vessel:	n/a
43	chr11:71327380-71327430	LNCaP	prostate:	n/a
44	chr11:71324028-71324078	NH-A	brain:	n/a
45	chr11:71326282-71326332	IMR90	lung:	fetal
46	chr11:71327380-71327430	Jurkat	blood:	n/a
47	chr11:71322699-71322749	K562	blood:	n/a
48	chr11:71321132-71321182	U87	brain:	n/a
49	chr11:71320617-71320667	GM12892	blood:	n/a
50	chr11:71319400-71319450	HUVEC	blood vessel:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-3	chr11:71314349-71314399	NONHSAT022693
2	lnc-AP000867.1-3	chr11:71310043-71310371	NONHSAT022693

No data

Variant related genes	Relation type
OR7E4P	TF binding region
ENSG00000187811	TF binding region
KRTAP5-11	TF binding region
UNC93B6	TF binding region
OR7E4P	CpG island
ENSG00000187811	CpG island
KRTAP5-11	CpG island
UNC93B6	CpG island

Extended variants
information (count: 895 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:895 , 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	rs372632867	chr11:71310057-71310058	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs199938980	chr11:71310059-71310060	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs201107966	chr11:71310076-71310077	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs202241585	chr11:71310105-71310106	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs552667723	chr11:71310118-71310119	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs200303945	chr11:71310122-71310123	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs537388093	chr11:71310123-71310124	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs555030850	chr11:71310127-71310128	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs182724496	chr11:71310144-71310145	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs566947969	chr11:71310166-71310167	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs534370746	chr11:71310178-71310179	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs552661092	chr11:71310180-71310181	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs187357383	chr11:71310184-71310185	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs113432097	chr11:71310189-71310190	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs377259478	chr11:71310191-71310192	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs546079150	chr11:71310243-71310244	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs76464829	chr11:71310248-71310249	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs558360300	chr11:71310266-71310267	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs568359700	chr11:71310271-71310272	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs576645621	chr11:71310289-71310290	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs74668610	chr11:71310300-71310301	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs544110059	chr11:71310313-71310314	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs369640234	chr11:71310321-71310322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs562033749	chr11:71310323-71310324	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs7114998	chr11:71310326-71310327	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs141926396	chr11:71310814-71310815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs528141398	chr11:71310834-71310835	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs77999877	chr11:71310836-71310837	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs548806711	chr11:71310837-71310838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147307957	chr11:71310847-71310848	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs528399858	chr11:71310848-71310849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs373745653	chr11:71310854-71310855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs111279062	chr11:71310860-71310861	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs138318717	chr11:71311452-71311453	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs144124964	chr11:71311454-71311455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141387485	chr11:71311456-71311457	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs79923403	chr11:71311461-71311462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs148794134	chr11:71311488-71311489	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs74436641	chr11:71311493-71311494	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs576983992	chr11:71311523-71311524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs182389875	chr11:71311535-71311536	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186116934	chr11:71311549-71311550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs190974938	chr11:71311554-71311555	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs370278653	chr11:71311559-71311560	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs541827616	chr11:71311560-71311561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201082858	chr11:71311565-71311566	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs4944096	chr11:71311566-71311567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78573013	chr11:71311569-71311570	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs368868802	chr11:71311577-71311578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs572137182	chr11:71311580-71311581	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Lung cancer	18438408	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
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71314200-71314600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:71314400-71314600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr11:71315200-71316000	Enhancers	Fetal Thymus	thymus
4	chr11:71316400-71316600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
5	chr11:71316400-71316600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr11:71317800-71318000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:71317800-71319000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
8	chr11:71317800-71319000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:71317800-71319600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr11:71318000-71318200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
11	chr11:71318000-71318200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
12	chr11:71318000-71318200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:71318000-71318200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr11:71318000-71318400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:71318000-71318600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
16	chr11:71318000-71318600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
17	chr11:71318000-71318600	Bivalent Enhancer	Placenta	Placenta
18	chr11:71318000-71318600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
19	chr11:71318000-71318800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:71318000-71318800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
21	chr11:71318000-71319000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr11:71318000-71319000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
23	chr11:71318000-71319000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr11:71318000-71319000	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr11:71318000-71319000	Bivalent Enhancer	HMEC	breast
26	chr11:71318000-71319600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
27	chr11:71318000-71319600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
28	chr11:71318200-71318400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:71318200-71318400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:71318200-71318400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:71318200-71318400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:71318200-71318400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr11:71318200-71318400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
34	chr11:71318200-71318400	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:71318200-71318400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
36	chr11:71318200-71318400	Bivalent Enhancer	Right Ventricle	heart
37	chr11:71318200-71318600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr11:71318200-71318600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr11:71318200-71318600	Bivalent Enhancer	Left Ventricle	heart
40	chr11:71318200-71318600	Enhancers	Right Atrium	heart
41	chr11:71318200-71318800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:71318200-71318800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:71318200-71318800	Bivalent Enhancer	Adipose Nuclei	Adipose
44	chr11:71318200-71318800	Enhancers	Esophagus	oesophagus
45	chr11:71318200-71318800	Bivalent/Poised TSS	Fetal Intestine Small	intestine
46	chr11:71318200-71318800	Bivalent Enhancer	Lung	lung
47	chr11:71318200-71319000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr11:71318200-71319000	Active TSS	H9 Cell Line	embryonic stem cell
49	chr11:71318200-71319000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr11:71318200-71319000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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