Variant report

Variant	nsv972040
Chromosome Location	chr11:71315526-71330518
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:1528)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 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	chr11:71325884-71326044	GM12878	blood:	n/a	n/a
4	BATF	chr11:71315927-71316371	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	chr11:71316260-71316410	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr11:71315941-71316517	K562	blood:	n/a	n/a
10	CTCF	chr11:71316260-71316410	HRE	kidney:	n/a	n/a
11	CTCF	chr11:71315760-71315910	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr11:71316177-71316304	HepG2	liver:	n/a	n/a
13	CTCF	chr11:71317981-71318004	GM20000	blood:	n/a	n/a
14	CTCF	chr11:71316126-71316334	GM19239	blood:	n/a	n/a
15	CTCF	chr11:71315854-71315973	GM19238	blood:	n/a	n/a
16	CTCF	chr11:71316220-71316370	HVMF	connective:	n/a	n/a
17	CTCF	chr11:71316109-71316362	GM13976	blood:	n/a	n/a
18	CTCF	chr11:71316400-71316550	AG09319	gingival:	n/a	n/a
19	CTCF	chr11:71316260-71316550	HepG2	liver:	n/a	n/a
20	CTCF	chr11:71316240-71316390	GM12865	blood:	n/a	n/a
21	CTCF	chr11:71315515-71315532	GM10248	blood:	n/a	n/a
22	CTCF	chr11:71316136-71316323	Fibrobl	skin:	n/a	n/a
23	CTCF	chr11:71316137-71316323	MCF-7	breast:	n/a	n/a
24	CTCF	chr11:71316260-71316410	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr11:71316340-71316490	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr11:71316126-71316329	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr11:71316019-71316416	A549	lung:	n/a	n/a
28	CTCF	chr11:71316200-71316350	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr11:71315877-71315959	GM19240	blood:	n/a	n/a
30	CTCF	chr11:71316113-71316366	GM20000	blood:	n/a	n/a
31	CTCF	chr11:71315780-71315930	HCM	heart:	n/a	n/a
32	CTCF	chr11:71318347-71318401	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr11:71316420-71316570	BE2_C	brain:	n/a	n/a
34	CTCF	chr11:71316260-71316410	HCT-116	colon:	n/a	n/a
35	CTCF	chr11:71315780-71315930	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr11:71315850-71315971	GM12892	blood:	n/a	n/a
37	CTCF	chr11:71315780-71315930	GM12872	blood:	n/a	n/a
38	CTCF	chr11:71316200-71316350	GM12870	blood:	n/a	n/a
39	CTCF	chr11:71315920-71316070	HFF	foreskin:	n/a	n/a
40	CTCF	chr11:71315960-71316110	GM12872	blood:	n/a	n/a
41	CTCF	chr11:71316137-71316309	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr11:71315939-71315950	GM10266	blood:	n/a	n/a
43	CTCF	chr11:71316280-71316430	GM12866	blood:	n/a	n/a
44	CTCF	chr11:71316120-71316346	GM12878	blood:	n/a	n/a
45	CTCF	chr11:71316260-71316410	GM12875	blood:	n/a	n/a
46	CTCF	chr11:71316180-71316330	GM12872	blood:	n/a	n/a
47	CTCF	chr11:71316041-71316444	K562	blood:	n/a	n/a
48	CTCF	chr11:71316200-71316350	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr11:71316260-71316410	GM06990	blood:	n/a	n/a
50	CTCF	chr11:71316280-71316430	HRPEpiC	eye:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71327897-71327947	GM19239	blood:	n/a
2	chr11:71322128-71322178	GM06990	blood:	n/a
3	chr11:71318057-71318107	HRCEpiC	kidney:	n/a
4	chr11:71327897-71327947	GM19239	blood:	n/a
5	chr11:71322128-71322178	GM06990	blood:	n/a
6	chr11:71318057-71318107	HRCEpiC	kidney:	n/a
7	chr11:71326282-71326332	BJ	skin:	n/a
8	chr11:71319400-71319450	ovcar-3	ovarian:	n/a
9	chr11:71318870-71318920	GM12891	blood:	n/a
10	chr11:71322873-71322923	NHBE	bronchial:	n/a
11	chr11:71321226-71321276	A549	lung:	n/a
12	chr11:71327353-71327403	CMK	blood:	n/a
13	chr11:71327380-71327430	K562	blood:	n/a
14	chr11:71327380-71327430	Caco-2	colon:	n/a
15	chr11:71320766-71320816	Hepatocyte	liver:	n/a
16	chr11:71327353-71327403	HAEpiC	amniotic membrane:	n/a
17	chr11:71320735-71320785	PrEC	prostate:	n/a
18	chr11:71321226-71321276	K562	blood:	n/a
19	chr11:71320617-71320667	NH-A	brain:	n/a
20	chr11:71321058-71321108	HIPEpiC	eye:	n/a
21	chr11:71321132-71321182	ProgFib	skin:	n/a
22	chr11:71321226-71321276	HNPCEpiC	eye:	n/a
23	chr11:71324028-71324078	GM12891	blood:	n/a
24	chr11:71320735-71320785	HAEpiC	amniotic membrane:	n/a
25	chr11:71324346-71324396	Caco-2	colon:	n/a
26	chr11:71324188-71324238	IMR90	lung:	fetal
27	chr11:71326486-71326536	LNCaP	prostate:	n/a
28	chr11:71324346-71324396	U87	brain:	n/a
29	chr11:71318870-71318920	SK-N-SH_RA	brain:	n/a
30	chr11:71324188-71324238	AG04449	skin:	fetal
31	chr11:71324028-71324078	AG10803	skin:	n/a
32	chr11:71322873-71322923	LNCaP	prostate:	n/a
33	chr11:71320735-71320785	SAEC	small airway:	n/a
34	chr11:71326486-71326536	HAEpiC	amniotic membrane:	n/a
35	chr11:71327380-71327430	H1-hESC	embryonic stem cell:	embryo
36	chr11:71315863-71315913	Hela-S3	cervix:	n/a
37	chr11:71321132-71321182	PFSK-1	brain:	n/a
38	chr11:71327380-71327430	U87	brain:	n/a
39	chr11:71324525-71324575	Caco-2	colon:	n/a
40	chr11:71324346-71324396	HEK293	kidney:	embryo
41	chr11:71322873-71322923	ProgFib	skin:	n/a
42	chr11:71324188-71324238	HIPEpiC	eye:	n/a
43	chr11:71318870-71318920	HEEpiC	esophagus:	n/a
44	chr11:71320617-71320667	NHDF-neo	bronchial:	n/a
45	chr11:71319400-71319450	RPTEC	kidney:	n/a
46	chr11:71320513-71320563	SKMC	muscle:	n/a
47	chr11:71324188-71324238	Caco-2	colon:	n/a
48	chr11:71321058-71321108	AG09309	skin:	n/a
49	chr11:71322128-71322178	LNCaP	prostate:	n/a
50	chr11:71326486-71326536	AG09309	skin:	n/a

No data

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

Extended variants
information (count: 742 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:742 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570664472	chr11:71315554-71315555	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs11823761	chr11:71315598-71315599	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs556489437	chr11:71315611-71315612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201697256	chr11:71315628-71315629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189673888	chr11:71315670-71315671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144949370	chr11:71315678-71315679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553766095	chr11:71315690-71315691	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs545117539	chr11:71315702-71315703	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs181275861	chr11:71315769-71315770	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs545904067	chr11:71315864-71315865	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs370543289	chr11:71315932-71315933	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs558677710	chr11:71315966-71315967	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs577029345	chr11:71315983-71315984	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs544440970	chr11:71315986-71315987	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs562839175	chr11:71315990-71315991	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs554485802	chr11:71316015-71316016	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs530353126	chr11:71316025-71316026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186263145	chr11:71316050-71316051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs560550491	chr11:71316078-71316079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs527738255	chr11:71316083-71316084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572048178	chr11:71316085-71316086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs79105830	chr11:71316093-71316094	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs542216989	chr11:71316131-71316132	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs35746259	chr11:71316160-71316161	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs1060714	chr11:71316164-71316165	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs531532026	chr11:71316178-71316179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs550030743	chr11:71316196-71316197	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs202076569	chr11:71316222-71316223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs182011604	chr11:71316229-71316230	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs200629504	chr11:71316254-71316255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs202059297	chr11:71316255-71316256	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs200039174	chr11:71316258-71316259	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs547051771	chr11:71316272-71316273	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs565670787	chr11:71316275-71316276	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs539118552	chr11:71316276-71316277	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs200107223	chr11:71316278-71316279	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs575776041	chr11:71316287-71316288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs543657769	chr11:71316288-71316289	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs201038584	chr11:71316289-71316290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs373933261	chr11:71316314-71316315	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs200838898	chr11:71316334-71316335	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186350589	chr11:71316335-71316336	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs542513027	chr11:71316337-71316338	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs560247317	chr11:71316362-71316363	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs377180958	chr11:71316385-71316386	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs11826569	chr11:71316406-71316407	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs532182680	chr11:71316415-71316416	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546268049	chr11:71316497-71316498	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs564551947	chr11:71316505-71316506	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs531878382	chr11:71316514-71316515	Bivalent Enhancer	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:168 , 50 per page) page: 1 2 3 4

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

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