Variant report

Variant	nsv897901
Chromosome Location	chr11:71316093-71441301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1410)
CpG islands
(count:2687)
Chromatin interactive
region (count:1)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1410 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
2	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
3	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
4	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
5	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
6	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
7	ATF1	chr11:71328834-71328851	K562	blood:	n/a	n/a
8	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
9	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
10	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
11	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
13	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
14	BATF	chr11:71364018-71364247	GM12878	blood:	n/a	chr11:71364110-71364121
15	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
16	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
17	BATF	chr11:71315927-71316371	GM12878	blood:	n/a	n/a
18	BATF	chr11:71325884-71326044	GM12878	blood:	n/a	n/a
19	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
20	BATF	chr11:71325819-71326075	GM12878	blood:	n/a	n/a
21	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
22	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
23	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
24	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
25	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
26	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
27	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
28	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
29	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
30	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:71422007-71422279	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:71398790-71398946	GM12878	blood:	n/a	chr11:71398860-71398869
33	BCL11A	chr11:71376209-71376453	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:71425402-71425946	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:71428574-71429024	GM12878	blood:	n/a	chr11:71428833-71428842
36	BCL11A	chr11:71426893-71427066	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:71398722-71399032	GM12878	blood:	n/a	chr11:71398860-71398869
38	BCL11A	chr11:71421911-71422277	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:71363953-71364282	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:71369783-71369963	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:71315909-71316399	GM12878	blood:	n/a	n/a
42	BCL11A	chr11:71425028-71425302	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:71421456-71421625	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:71428570-71428787	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:71316096-71316292	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:71406992-71407565	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:71376120-71376905	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:71407051-71407260	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:71425414-71425925	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:71364327-71364546	GM12878	blood:	n/a	n/a

(count:2687 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71350743-71350793	HNPCEpiC	eye:	n/a
2	chr11:71351271-71351321	GM06990	blood:	n/a
3	chr11:71327380-71327430	NHDF-neo	bronchial:	n/a
4	chr11:71350743-71350793	HNPCEpiC	eye:	n/a
5	chr11:71351271-71351321	GM06990	blood:	n/a
6	chr11:71327380-71327430	NHDF-neo	bronchial:	n/a
7	chr11:71420485-71420535	GM12891	blood:	n/a
8	chr11:71421279-71421329	Hela-S3	cervix:	n/a
9	chr11:71346528-71346578	HRCEpiC	kidney:	n/a
10	chr11:71320617-71320667	SK-N-MC	brain:	n/a
11	chr11:71322873-71322923	A549	lung:	n/a
12	chr11:71346528-71346578	GM12878	blood:	n/a
13	chr11:71322699-71322749	GM19239	blood:	n/a
14	chr11:71318870-71318920	LNCaP	prostate:	n/a
15	chr11:71420947-71420997	A549	lung:	n/a
16	chr11:71418204-71418254	PANC-1	pancreas:	n/a
17	chr11:71346528-71346578	HCT-116	colon:	n/a
18	chr11:71350346-71350396	AG10803	skin:	n/a
19	chr11:71320735-71320785	BJ	skin:	n/a
20	chr11:71324188-71324238	MCF10A-Er-Src	breast:	n/a
21	chr11:71319400-71319450	PrEC	prostate:	n/a
22	chr11:71327897-71327947	MCF-7	breast:	n/a
23	chr11:71327885-71327935	HRCEpiC	kidney:	n/a
24	chr11:71319400-71319450	RPTEC	kidney:	n/a
25	chr11:71340352-71340402	AG09319	gingival:	n/a
26	chr11:71319400-71319450	HCF	heart:	n/a
27	chr11:71350743-71350793	AoSMC	blood vessel:	n/a
28	chr11:71352122-71352172	ECC-1	luminal epithelium:	n/a
29	chr11:71322873-71322923	HepG2	liver:	n/a
30	chr11:71322873-71322923	AoSMC	blood vessel:	n/a
31	chr11:71324346-71324396	NB4	blood:	n/a
32	chr11:71320617-71320667	HIPEpiC	eye:	n/a
33	chr11:71327353-71327403	GM12878	blood:	n/a
34	chr11:71327885-71327935	Jurkat	blood:	n/a
35	chr11:71320766-71320816	BJ	skin:	n/a
36	chr11:71352122-71352172	HCT-116	colon:	n/a
37	chr11:71350743-71350793	SKMC	muscle:	n/a
38	chr11:71420467-71420517	RPTEC	kidney:	n/a
39	chr11:71318057-71318107	HCF	heart:	n/a
40	chr11:71420467-71420517	A549	lung:	n/a
41	chr11:71418204-71418254	AG04449	skin:	fetal
42	chr11:71417657-71417707	AG04449	skin:	fetal
43	chr11:71324188-71324238	AG10803	skin:	n/a
44	chr11:71350888-71350938	A549	lung:	n/a
45	chr11:71322128-71322178	MCF-7	breast:	n/a
46	chr11:71340182-71340232	BJ	skin:	n/a
47	chr11:71322699-71322749	AG10803	skin:	n/a
48	chr11:71350346-71350396	NHBE	bronchial:	n/a
49	chr11:71321132-71321182	AG04450	lung:	fetal
50	chr11:71350975-71351025	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
2	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
3	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
4	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
5	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
6	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
7	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
8	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
9	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
10	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
11	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
12	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
13	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701

No data

Variant related genes	Relation type
OR7E4P	TF binding region
ENSG00000254805	TF binding region
ENPP7P8	TF binding region
ENSG00000221458	TF binding region
ENSG00000255415	TF binding region
ENSG00000223235	TF binding region
ENSG00000254972	TF binding region
ENSG00000187811	TF binding region
KRTAP5-11	TF binding region
RPS3AP41	TF binding region
OR7E4P	CpG island
ENSG00000254805	CpG island
ENPP7P8	CpG island
ENSG00000221458	CpG island
ENSG00000255415	CpG island
ENSG00000223235	CpG island
ENSG00000254972	CpG island
ENSG00000187811	CpG island
KRTAP5-11	CpG island
RPS3AP41	CpG island

Extended variants
information (count: 6820 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:6820 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79105830	chr11:71316093-71316094	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs542216989	chr11:71316131-71316132	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs35746259	chr11:71316160-71316161	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs1060714	chr11:71316164-71316165	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs531532026	chr11:71316178-71316179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs550030743	chr11:71316196-71316197	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs202076569	chr11:71316222-71316223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs182011604	chr11:71316229-71316230	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200629504	chr11:71316254-71316255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs202059297	chr11:71316255-71316256	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs200039174	chr11:71316258-71316259	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547051771	chr11:71316272-71316273	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs565670787	chr11:71316275-71316276	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs539118552	chr11:71316276-71316277	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200107223	chr11:71316278-71316279	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs575776041	chr11:71316287-71316288	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543657769	chr11:71316288-71316289	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs201038584	chr11:71316289-71316290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs373933261	chr11:71316314-71316315	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs200838898	chr11:71316334-71316335	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs186350589	chr11:71316335-71316336	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs542513027	chr11:71316337-71316338	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs560247317	chr11:71316362-71316363	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs377180958	chr11:71316385-71316386	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs11826569	chr11:71316406-71316407	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532182680	chr11:71316415-71316416	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs546268049	chr11:71316497-71316498	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs564551947	chr11:71316505-71316506	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531878382	chr11:71316514-71316515	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs111983756	chr11:71316537-71316538	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs200032416	chr11:71316544-71316545	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201003709	chr11:71316596-71316597	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs202239260	chr11:71316657-71316658	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529126703	chr11:71316673-71316674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547676004	chr11:71316702-71316703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs76972142	chr11:71316713-71316714	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs190848345	chr11:71316732-71316733	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs200145359	chr11:71316772-71316773	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs141932951	chr11:71316780-71316781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs149564428	chr11:71316784-71316785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs72966296	chr11:71316802-71316803	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs539414012	chr11:71316809-71316810	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs533842583	chr11:71316811-71316812	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs550990080	chr11:71316824-71316825	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs11824488	chr11:71316825-71316826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs182641263	chr11:71316835-71316836	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs558477986	chr11:71317812-71317813	Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs141790052	chr11:71317815-71317816	Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs546143133	chr11:71317826-71317827	Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs192340855	chr11:71317880-71317881	Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD

Chromatin state (count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71316400-71316600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
2	chr11:71316400-71316600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
3	chr11:71317800-71318000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:71317800-71319000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr11:71317800-71319000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:71317800-71319600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
7	chr11:71318000-71318200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
8	chr11:71318000-71318200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
9	chr11:71318000-71318200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:71318000-71318200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr11:71318000-71318400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:71318000-71318600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
13	chr11:71318000-71318600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
14	chr11:71318000-71318600	Bivalent Enhancer	Placenta	Placenta
15	chr11:71318000-71318600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
16	chr11:71318000-71318800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:71318000-71318800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
18	chr11:71318000-71319000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr11:71318000-71319000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
20	chr11:71318000-71319000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr11:71318000-71319000	Bivalent Enhancer	Stomach Mucosa	stomach
22	chr11:71318000-71319000	Bivalent Enhancer	HMEC	breast
23	chr11:71318000-71319600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
24	chr11:71318000-71319600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr11:71318200-71318400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:71318200-71318400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:71318200-71318400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr11:71318200-71318400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:71318200-71318400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:71318200-71318400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
31	chr11:71318200-71318400	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr11:71318200-71318400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
33	chr11:71318200-71318400	Bivalent Enhancer	Right Ventricle	heart
34	chr11:71318200-71318600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr11:71318200-71318600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:71318200-71318600	Bivalent Enhancer	Left Ventricle	heart
37	chr11:71318200-71318600	Enhancers	Right Atrium	heart
38	chr11:71318200-71318800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr11:71318200-71318800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
40	chr11:71318200-71318800	Bivalent Enhancer	Adipose Nuclei	Adipose
41	chr11:71318200-71318800	Enhancers	Esophagus	oesophagus
42	chr11:71318200-71318800	Bivalent/Poised TSS	Fetal Intestine Small	intestine
43	chr11:71318200-71318800	Bivalent Enhancer	Lung	lung
44	chr11:71318200-71319000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr11:71318200-71319000	Active TSS	H9 Cell Line	embryonic stem cell
46	chr11:71318200-71319000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr11:71318200-71319000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
48	chr11:71318200-71319000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
49	chr11:71318200-71319000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr11:71318200-71319200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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