Variant report

Variant	nsv523683
Chromosome Location	chr11:113341391-113346955
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	ATF2	chr11:113345041-113345358	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:113345027-113345341	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:113345095-113345626	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:113345840-113345922	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr11:113345022-113345389	K562	blood:	n/a	n/a
6	CCNT2	chr11:113345045-113345294	K562	blood:	n/a	n/a
7	CHD1	chr11:113345096-113345379	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr11:113345213-113345255	K562	blood:	n/a	n/a
9	CHD2	chr11:113345124-113345430	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr11:113344917-113345704	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr11:113345460-113345610	SK-N-SH_RA	brain:	n/a	chr11:113345525-113345538
12	CTCF	chr11:113344194-113344248	GM20000	blood:	n/a	n/a
13	E2F4	chr11:113345070-113345423	MCF10A-Er-Src	breast:	n/a	chr11:113345248-113345260
14	E2F6	chr11:113345119-113345320	K562	blood:	n/a	chr11:113345248-113345260
15	GTF2F1	chr11:113345142-113345306	H1-hESC	embryonic stem cell:	n/a	n/a
16	HCFC1	chr11:113345106-113345333	K562	blood:	n/a	n/a
17	HDAC2	chr11:113345105-113345295	H1-hESC	embryonic stem cell:	n/a	chr11:113345222-113345241
18	HDAC2	chr11:113345035-113345432	H1-hESC	embryonic stem cell:	n/a	chr11:113345222-113345241
19	HMGN3	chr11:113345075-113345429	K562	blood:	n/a	n/a
20	JUND	chr11:113345026-113345343	H1-hESC	embryonic stem cell:	n/a	n/a
21	JUND	chr11:113345116-113345324	K562	blood:	n/a	n/a
22	KAP1	chr11:113344995-113345413	HEK293	kidney:	n/a	chr11:113345197-113345205 chr11:113345030-113345038
23	MAX	chr11:113345124-113345348	K562	blood:	n/a	n/a
24	MAX	chr11:113345066-113345373	MCF-7	breast:	n/a	n/a
25	MAX	chr11:113344985-113345420	ECC-1	luminal epithelium:	n/a	n/a
26	MAZ	chr11:113345075-113345404	K562	blood:	n/a	n/a
27	MAZ	chr11:113345189-113345377	HepG2	liver:	n/a	n/a
28	MAZ	chr11:113345102-113345490	IMR90	lung:	n/a	n/a
29	MXI1	chr11:113345031-113345489	H1-hESC	embryonic stem cell:	n/a	n/a
30	MXI1	chr11:113345245-113345294	K562	blood:	n/a	n/a
31	MYC	chr11:113345116-113345365	H1-hESC	embryonic stem cell:	n/a	n/a
32	MYC	chr11:113345206-113345277	MCF10A-Er-Src	breast:	n/a	n/a
33	MYC	chr11:113345174-113345291	K562	blood:	n/a	n/a
34	POLR2A	chr11:113344709-113345465	H1-neurons	neurons:	n/a	n/a
35	POLR2A	chr11:113345982-113346053	A549	lung:	n/a	n/a
36	RAD21	chr11:113345040-113345417	H1-hESC	embryonic stem cell:	n/a	n/a
37	RAD21	chr11:113345123-113345341	SK-N-SH_RA	brain:	n/a	n/a
38	RAD21	chr11:113344900-113345445	H1-hESC	embryonic stem cell:	n/a	n/a
39	RAD21	chr11:113345132-113345336	SK-N-SH_RA	brain:	n/a	n/a
40	RAD21	chr11:113345084-113345322	H1-hESC	embryonic stem cell:	n/a	n/a
41	RCOR1	chr11:113345119-113345393	HepG2	liver:	n/a	n/a
42	RCOR1	chr11:113344708-113345450	IMR90	lung:	n/a	n/a
43	RCOR1	chr11:113345200-113345282	K562	blood:	n/a	n/a
44	RCOR1	chr11:113345142-113345348	Hela-S3	cervix:	n/a	n/a
45	RCOR1	chr11:113345060-113345430	K562	blood:	n/a	n/a
46	REST	chr11:113345803-113345910	PANC-1	pancreas:	n/a	chr11:113345888-113345901 chr11:113345879-113345892 chr11:113345852-113345862
47	REST	chr11:113344137-113344369	PFSK-1	brain:	n/a	n/a
48	REST	chr11:113344076-113346611	PFSK-1	brain:	n/a	chr11:113345221-113345241 chr11:113344906-113344915 chr11:113345968-113345981 chr11:113345232-113345241 chr11:113345227-113345236 chr11:113345888-113345901 chr11:113345716-113345729 chr11:113345221-113345241 chr11:113346219-113346227 chr11:113345879-113345892 chr11:113345513-113345526 chr11:113345222-113345240 chr11:113345852-113345862 chr11:113344873-113344891 chr11:113345488-113345501 chr11:113345221-113345235 chr11:113345225-113345238 chr11:113345221-113345241 chr11:113344902-113344920 chr11:113346127-113346136
49	REST	chr11:113345068-113345459	GM12878	blood:	n/a	chr11:113345221-113345241 chr11:113345232-113345241 chr11:113345227-113345236 chr11:113345221-113345241 chr11:113345222-113345240 chr11:113345221-113345235 chr11:113345225-113345238 chr11:113345221-113345241
50	REST	chr11:113344680-113345999	PANC-1	pancreas:	n/a	chr11:113345221-113345241 chr11:113344906-113344915 chr11:113345968-113345981 chr11:113345232-113345241 chr11:113345227-113345236 chr11:113345888-113345901 chr11:113345716-113345729 chr11:113345221-113345241 chr11:113345879-113345892 chr11:113345513-113345526 chr11:113345222-113345240 chr11:113345852-113345862 chr11:113344873-113344891 chr11:113345488-113345501 chr11:113345221-113345235 chr11:113345225-113345238 chr11:113345221-113345241 chr11:113344902-113344920

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:113346388-113346438	RPTEC	kidney:	n/a
2	chr11:113345686-113345736	CMK	blood:	n/a
3	chr11:113346388-113346438	RPTEC	kidney:	n/a
4	chr11:113345686-113345736	CMK	blood:	n/a
5	chr11:113346299-113346349	Hepatocyte	liver:	n/a
6	chr11:113345686-113345736	AoSMC	blood vessel:	n/a
7	chr11:113346491-113346541	CMK	blood:	n/a
8	chr11:113346428-113346478	HEEpiC	esophagus:	n/a
9	chr11:113346491-113346541	HCT-116	colon:	n/a
10	chr11:113346299-113346349	Jurkat	blood:	n/a
11	chr11:113346327-113346377	HIPEpiC	eye:	n/a
12	chr11:113342307-113342357	GM19239	blood:	n/a
13	chr11:113346388-113346438	HUVEC	blood vessel:	n/a
14	chr11:113346388-113346438	GM12891	blood:	n/a
15	chr11:113346327-113346377	HRE	kidney:	n/a
16	chr11:113346299-113346349	GM06990	blood:	n/a
17	chr11:113346327-113346377	GM19239	blood:	n/a
18	chr11:113346388-113346438	NHDF-neo	bronchial:	n/a
19	chr11:113346183-113346233	NH-A	brain:	n/a
20	chr11:113345325-113345375	ovcar-3	ovarian:	n/a
21	chr11:113346207-113346257	CMK	blood:	n/a
22	chr11:113346183-113346233	H1-hESC	embryonic stem cell:	embryo
23	chr11:113346485-113346535	HEK293	kidney:	embryo
24	chr11:113342307-113342357	Hepatocyte	liver:	n/a
25	chr11:113346485-113346535	SK-N-SH_RA	brain:	n/a
26	chr11:113346327-113346377	U87	brain:	n/a
27	chr11:113345618-113345668	A549	lung:	n/a
28	chr11:113346388-113346438	NB4	blood:	n/a
29	chr11:113342307-113342357	HCPEpiC	choroid plexus:	n/a
30	chr11:113346207-113346257	LNCaP	prostate:	n/a
31	chr11:113346327-113346377	SAEC	small airway:	n/a
32	chr11:113346388-113346438	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:113342307-113342357	HL-60	blood:	n/a
34	chr11:113346299-113346349	NH-A	brain:	n/a
35	chr11:113346428-113346478	MCF-7	breast:	n/a
36	chr11:113346183-113346233	NT2-D1	testis:	n/a
37	chr11:113346327-113346377	AG04450	lung:	fetal
38	chr11:113344987-113345037	GM12878	blood:	n/a
39	chr11:113344987-113345037	Hela-S3	cervix:	n/a
40	chr11:113346176-113346226	GM12892	blood:	n/a
41	chr11:113346428-113346478	GM12892	blood:	n/a
42	chr11:113346299-113346349	Hela-S3	cervix:	n/a
43	chr11:113346299-113346349	NHDF-neo	bronchial:	n/a
44	chr11:113345618-113345668	NHBE	bronchial:	n/a
45	chr11:113344987-113345037	IMR90	lung:	fetal
46	chr11:113346176-113346226	SK-N-SH	brain:	n/a
47	chr11:113345686-113345736	HCF	heart:	n/a
48	chr11:113346183-113346233	MCF-7	breast:	n/a
49	chr11:113346207-113346257	IMR90	lung:	fetal
50	chr11:113346176-113346226	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:113334256..113337805-chr11:113341499..113343738,3	K562	blood:
2	chr11:113341089..113342617-chr11:113343236..113346107,2	K562	blood:
3	chr11:113346625..113349262-chr11:113351811..113353655,2	K562	blood:

Variant related genes	Relation type
DRD2	TF binding region
DRD2	CpG island
ENSG00000149295	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4938019	chr11:113341391-113341392	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371191259	chr11:113341397-113341398	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190132497	chr11:113341418-113341419	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs562437024	chr11:113341435-113341436	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs151067008	chr11:113341455-113341456	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs34164777	chr11:113341483-113341484	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs35659571	chr11:113341583-113341584	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527472745	chr11:113341656-113341657	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547623342	chr11:113341668-113341669	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs567727585	chr11:113341670-113341671	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs536281213	chr11:113341695-113341696	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556160552	chr11:113341728-113341729	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569667055	chr11:113341745-113341746	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140913852	chr11:113341772-113341773	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559192842	chr11:113341781-113341782	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374820434	chr11:113341796-113341797	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149772623	chr11:113341800-113341801	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs182608277	chr11:113341811-113341812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553616933	chr11:113341848-113341849	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186029787	chr11:113341909-113341910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs61902806	chr11:113341929-113341930	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs562473356	chr11:113341944-113341945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs531293784	chr11:113341971-113341972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs184018993	chr11:113342037-113342038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545017076	chr11:113342056-113342057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565183748	chr11:113342071-113342072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375556732	chr11:113342078-113342079	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12417718	chr11:113342083-113342084	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147640473	chr11:113342110-113342111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs111888432	chr11:113342128-113342129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs368563508	chr11:113342132-113342133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs142310975	chr11:113342166-113342167	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558038099	chr11:113342185-113342186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188658390	chr11:113342186-113342187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs145926374	chr11:113342193-113342194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs372524113	chr11:113342211-113342212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549821302	chr11:113342236-113342237	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577807362	chr11:113342245-113342246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534167117	chr11:113342250-113342251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569754732	chr11:113342308-113342309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538642157	chr11:113342408-113342409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs377032417	chr11:113342416-113342417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559013819	chr11:113342426-113342427	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192321211	chr11:113342463-113342464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs534969542	chr11:113342474-113342475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555170555	chr11:113342603-113342604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs74640347	chr11:113342716-113342717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138857345	chr11:113342769-113342770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58113363	chr11:113342889-113342890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs574110983	chr11:113342930-113342931	Weak transcription	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
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Cancer	21129771	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Neuroblastoma	20406844	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Mantle cell lymphoma	19029149	CNVD
Squamous cell cancer	19047905	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	21385341	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:113328800-113344400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:113337200-113344400	Weak transcription	HMEC	breast
3	chr11:113339000-113341800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:113339800-113344200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:113340800-113341600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:113341200-113341400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr11:113341400-113343200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:113343200-113343600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr11:113343200-113343600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr11:113343200-113343600	Active TSS	Brain Anterior Caudate	brain
11	chr11:113343200-113343800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr11:113343200-113345200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:113343400-113343600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr11:113343400-113343600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
15	chr11:113343600-113344400	Weak transcription	Brain Anterior Caudate	brain
16	chr11:113344200-113344400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
17	chr11:113344400-113344600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
18	chr11:113344400-113344600	Bivalent Enhancer	Brain Germinal Matrix	brain
19	chr11:113344400-113344800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
20	chr11:113344400-113344800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr11:113344400-113344800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr11:113344400-113344800	Active TSS	Brain Anterior Caudate	brain
23	chr11:113344400-113344800	Active TSS	HMEC	breast
24	chr11:113344400-113345000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr11:113344600-113344800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr11:113344600-113344800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr11:113344600-113344800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
28	chr11:113344600-113344800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
29	chr11:113344600-113344800	Bivalent Enhancer	Brain Hippocampus Middle	brain
30	chr11:113344600-113344800	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
31	chr11:113344600-113344800	Bivalent Enhancer	Brain Substantia Nigra	brain
32	chr11:113344600-113345200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr11:113344600-113345800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
34	chr11:113344800-113345000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
35	chr11:113344800-113345000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr11:113344800-113345000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:113344800-113345000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
38	chr11:113344800-113345000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
39	chr11:113344800-113345000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:113344800-113345000	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr11:113344800-113345000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
42	chr11:113344800-113345000	Bivalent Enhancer	Brain Angular Gyrus	brain
43	chr11:113344800-113345000	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
44	chr11:113344800-113345000	Bivalent Enhancer	Fetal Intestine Small	intestine
45	chr11:113344800-113345000	Bivalent Enhancer	HSMM	muscle
46	chr11:113344800-113345200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr11:113344800-113345200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
48	chr11:113344800-113345200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr11:113344800-113345200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
50	chr11:113344800-113345200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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