Variant report

Variant	nsv832245
Chromosome Location	chr11:100138648-100276829
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	BACH1	chr11:100199919-100199946	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr11:100199819-100200012	GM12878	blood:	n/a	chr11:100199912-100199923
3	BRCA1	chr11:100274239-100274950	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr11:100274001-100274004	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:100216255-100216543	HepG2	liver:	n/a	chr11:100216405-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416
6	CEBPB	chr11:100216281-100216538	Hela-S3	cervix:	n/a	chr11:100216405-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416
7	CEBPB	chr11:100216346-100216498	K562	blood:	n/a	chr11:100216405-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416
8	CEBPB	chr11:100181375-100181675	A549	lung:	n/a	n/a
9	CEBPB	chr11:100216315-100216448	H1-hESC	embryonic stem cell:	n/a	chr11:100216405-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416
10	CEBPB	chr11:100211875-100212029	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:100216258-100216563	IMR90	lung:	n/a	chr11:100216405-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416 chr11:100216407-100216416
12	CEBPB	chr11:100222431-100222809	A549	lung:	n/a	chr11:100222512-100222523
13	CEBPB	chr11:100207294-100207608	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:100181392-100181558	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr11:100181334-100181674	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:100274429-100274979	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:100275216-100275645	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:100181344-100181656	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:100211693-100211808	H1-hESC	embryonic stem cell:	n/a	chr11:100211767-100211780
20	CEBPB	chr11:100222377-100222630	HepG2	liver:	n/a	chr11:100222411-100222422 chr11:100222512-100222523 chr11:100222411-100222422
21	CTCF	chr11:100199400-100199550	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr11:100275930-100275954	HepG2	liver:	n/a	n/a
23	CTCF	chr11:100199460-100199610	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr11:100199510-100199619	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:100199440-100199590	SAEC	small airway:	n/a	n/a
26	CTCF	chr11:100199503-100199638	NHEK	skin:	n/a	n/a
27	CTCF	chr11:100268260-100268410	GM12869	blood:	n/a	n/a
28	CTCF	chr11:100199460-100199610	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr11:100275901-100276001	GM12878	blood:	n/a	n/a
30	CTCF	chr11:100199440-100199590	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr11:100199480-100199630	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr11:100158466-100158502	GM13976	blood:	n/a	n/a
33	CTCF	chr11:100199492-100199649	MCF-7	breast:	n/a	n/a
34	CTCF	chr11:100145517-100145558	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr11:100199500-100199650	NHEK	skin:	n/a	n/a
36	CTCF	chr11:100237078-100237102	Lung_OC	lung:	n/a	n/a
37	CTCF	chr11:100143840-100143990	GM12866	blood:	n/a	n/a
38	CTCF	chr11:100275939-100275990	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:100263680-100263830	GM12869	blood:	n/a	n/a
40	CTCF	chr11:100199480-100199630	AG04450	lung:	n/a	n/a
41	CTCF	chr11:100275680-100275830	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr11:100199500-100199650	HMEC	breast:	n/a	n/a
43	CTCF	chr11:100199600-100199750	WI-38	lung:	n/a	n/a
44	CTCF	chr11:100199420-100199570	RPTEC	kidney:	n/a	n/a
45	CTCF	chr11:100275931-100275992	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr11:100199480-100199630	HEK293	kidney:	n/a	n/a
47	CTCF	chr11:100209460-100209610	WI-38	lung:	n/a	n/a
48	CTCF	chr11:100181680-100181830	GM12872	blood:	n/a	n/a
49	CTCF	chr11:100199384-100199689	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:100199510-100199617	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:100156776-100156826	SK-N-MC	brain:	n/a
2	chr11:100227279-100227329	HL-60	blood:	n/a
3	chr11:100267892-100267942	HepG2	liver:	n/a
4	chr11:100168001-100168051	HMEC	breast:	n/a
5	chr11:100211450-100211500	MCF10A-Er-Src	breast:	n/a
6	chr11:100267892-100267942	HRCEpiC	kidney:	n/a
7	chr11:100275402-100275452	BE2_C	brain:	n/a
8	chr11:100211450-100211500	NHBE	bronchial:	n/a
9	chr11:100227279-100227329	SK-N-MC	brain:	n/a
10	chr11:100156776-100156826	SKMC	muscle:	n/a
11	chr11:100227279-100227329	HEEpiC	esophagus:	n/a
12	chr11:100168001-100168051	HAEpiC	amniotic membrane:	n/a
13	chr11:100227279-100227329	LNCaP	prostate:	n/a
14	chr11:100267892-100267942	GM19239	blood:	n/a
15	chr11:100211450-100211500	HAEpiC	amniotic membrane:	n/a
16	chr11:100211450-100211500	HRE	kidney:	n/a
17	chr11:100227279-100227329	GM12891	blood:	n/a
18	chr11:100227279-100227329	BE2_C	brain:	n/a
19	chr11:100156776-100156826	Caco-2	colon:	n/a
20	chr11:100275402-100275452	BJ	skin:	n/a
21	chr11:100227279-100227329	CMK	blood:	n/a
22	chr11:100211450-100211500	HRCEpiC	kidney:	n/a
23	chr11:100227279-100227329	T-47D	breast:	n/a
24	chr11:100275402-100275452	CMK	blood:	n/a
25	chr11:100156776-100156826	LNCaP	prostate:	n/a
26	chr11:100211450-100211500	HMEC	breast:	n/a
27	chr11:100211450-100211500	IMR90	lung:	fetal
28	chr11:100156776-100156826	GM06990	blood:	n/a
29	chr11:100168001-100168051	BE2_C	brain:	n/a
30	chr11:100227279-100227329	Jurkat	blood:	n/a
31	chr11:100168001-100168051	K562	blood:	n/a
32	chr11:100211450-100211500	AG10803	skin:	n/a
33	chr11:100211450-100211500	K562	blood:	n/a
34	chr11:100267892-100267942	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:100211450-100211500	PFSK-1	brain:	n/a
36	chr11:100267892-100267942	AG04449	skin:	fetal
37	chr11:100168001-100168051	MCF-7	breast:	n/a
38	chr11:100211450-100211500	NB4	blood:	n/a
39	chr11:100211450-100211500	Hepatocyte	liver:	n/a
40	chr11:100211450-100211500	NHDF-neo	bronchial:	n/a
41	chr11:100156776-100156826	AG10803	skin:	n/a
42	chr11:100168001-100168051	SK-N-SH	brain:	n/a
43	chr11:100275402-100275452	GM12892	blood:	n/a
44	chr11:100267892-100267942	HUVEC	blood vessel:	n/a
45	chr11:100275402-100275452	HepG2	liver:	n/a
46	chr11:100275402-100275452	HAEpiC	amniotic membrane:	n/a
47	chr11:100227279-100227329	PFSK-1	brain:	n/a
48	chr11:100275402-100275452	NB4	blood:	n/a
49	chr11:100168001-100168051	T-47D	breast:	n/a
50	chr11:100227279-100227329	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:100179230..100181320-chr11:100182968..100185690,2	K562	blood:
2	chr11:100179230..100181320-chr11:100182968..100185690,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP42-1	chr11:100208358-100208622	NONHSAT023836

Variant related genes	Relation type
RPA2P3	TF binding region
RPA2P3	CpG island

Extended variants
information (count: 2285 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577474056	chr11:100140807-100140808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536862732	chr11:100140817-100140818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556849343	chr11:100140846-100140847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540136079	chr11:100140872-100140873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552146180	chr11:100140873-100140874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184818305	chr11:100140938-100140939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190104618	chr11:100140981-100140982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115698216	chr11:100140993-100140994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545380686	chr11:100141049-100141050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565595863	chr11:100141058-100141059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192085903	chr11:100141061-100141062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551186352	chr11:100141117-100141118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561309944	chr11:100141144-100141145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77445354	chr11:100141154-100141155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570674	chr11:100143801-100143802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556523005	chr11:100143846-100143847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146968080	chr11:100143847-100143848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187852790	chr11:100143862-100143863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150960190	chr11:100143874-100143875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546788170	chr11:100143879-100143880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371356570	chr11:100143880-100143881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111450559	chr11:100143886-100143887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116276130	chr11:100143918-100143919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111797049	chr11:100143963-100143964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547165164	chr11:100143965-100143966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192367358	chr11:100144017-100144018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369433824	chr11:100144077-100144078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61909781	chr11:100144083-100144084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185632686	chr11:100144085-100144086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189354420	chr11:100144087-100144088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562233314	chr11:100144120-100144121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527758895	chr11:100144132-100144133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535911445	chr11:100144161-100144162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180847751	chr11:100144162-100144163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570505033	chr11:100144206-100144207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184796127	chr11:100144211-100144212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369473519	chr11:100144235-100144236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150144640	chr11:100144256-100144257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372579356	chr11:100144262-100144263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377089170	chr11:100144263-100144264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550455793	chr11:100144306-100144307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115265516	chr11:100144310-100144311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536060203	chr11:100144330-100144331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567073639	chr11:100144343-100144344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188480678	chr11:100144344-100144345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138579377	chr11:100144362-100144363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569363371	chr11:100144370-100144371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533854055	chr11:100144384-100144385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537850890	chr11:100144402-100144403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553842350	chr11:100144433-100144434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20685689	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:100140800-100141200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:100143800-100144200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:100144200-100144800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:100145800-100146600	Enhancers	Brain Germinal Matrix	brain
5	chr11:100146400-100146800	Enhancers	Fetal Brain Female	brain
6	chr11:100148000-100148400	Enhancers	Fetal Heart	heart
7	chr11:100156000-100156400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr11:100164400-100165200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr11:100165000-100166200	Enhancers	Brain Germinal Matrix	brain
10	chr11:100165200-100167400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr11:100165600-100165800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr11:100166200-100167200	Weak transcription	Brain Germinal Matrix	brain
13	chr11:100166400-100169600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:100166800-100168600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:100167000-100169000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr11:100167000-100169200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:100167200-100167400	Enhancers	Brain Germinal Matrix	brain
18	chr11:100167200-100168000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:100167400-100168800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr11:100167400-100169200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr11:100167600-100169200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr11:100168000-100168600	Enhancers	NH-A	brain
23	chr11:100171600-100175200	Enhancers	Fetal Heart	heart
24	chr11:100173200-100173600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:100177200-100177600	Enhancers	Brain Germinal Matrix	brain
26	chr11:100178800-100180000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:100179000-100179800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:100184400-100185200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:100184800-100185000	Enhancers	Fetal Brain Male	brain
30	chr11:100186600-100187000	Enhancers	Fetal Brain Male	brain
31	chr11:100187600-100188000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:100187600-100188200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:100187600-100188400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:100193800-100194200	Enhancers	Colon Smooth Muscle	Colon
35	chr11:100193800-100194200	Enhancers	Fetal Brain Male	brain
36	chr11:100193800-100194200	Enhancers	Fetal Brain Female	brain
37	chr11:100193800-100194200	Enhancers	Fetal Lung	lung
38	chr11:100194200-100194400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:100196600-100211400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:100198800-100200400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr11:100199200-100200400	Enhancers	Esophagus	oesophagus
42	chr11:100199200-100200600	Enhancers	HMEC	breast
43	chr11:100199400-100200400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:100199400-100200400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr11:100199400-100200600	Enhancers	NHEK	skin
46	chr11:100199600-100200200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr11:100199600-100200400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:100199600-100200400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:100199600-100200400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:100199600-100200600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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