Variant report

Variant	nsv430425
Chromosome Location	chr11:101626575-101741691
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	ARID3A	chr11:101737106-101738062	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:101731532-101731870	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:101733165-101733894	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:101718978-101719316	HepG2	liver:	n/a	n/a
5	ATF3	chr11:101741166-101741680	A549	lung:	n/a	n/a
6	ATF3	chr11:101741116-101741650	A549	lung:	n/a	n/a
7	ATF3	chr11:101737263-101737875	A549	lung:	n/a	n/a
8	ATF3	chr11:101737281-101737875	A549	lung:	n/a	n/a
9	BCL3	chr11:101741121-101741689	A549	lung:	n/a	chr11:101741365-101741374
10	BCL3	chr11:101737262-101737759	A549	lung:	n/a	n/a
11	BCL3	chr11:101740952-101741643	A549	lung:	n/a	chr11:101741365-101741374
12	BCL3	chr11:101737142-101737973	A549	lung:	n/a	n/a
13	BHLHE40	chr11:101741337-101741613	A549	lung:	n/a	n/a
14	BRCA1	chr11:101737238-101737813	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr11:101732986-101733673	HCT-116	colon:	n/a	n/a
16	CBX3	chr11:101741041-101741830	HCT-116	colon:	n/a	n/a
17	CBX3	chr11:101741194-101741727	HCT-116	colon:	n/a	n/a
18	CCNT2	chr11:101630610-101630773	K562	blood:	n/a	n/a
19	CEBPB	chr11:101733005-101733530	HepG2	liver:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
20	CEBPB	chr11:101733015-101733475	A549	lung:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
21	CEBPB	chr11:101696354-101696596	HepG2	liver:	n/a	chr11:101696432-101696443
22	CEBPB	chr11:101732879-101733604	Hela-S3	cervix:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
23	CEBPB	chr11:101733064-101733569	MCF-7	breast:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
24	CEBPB	chr11:101733013-101733836	IMR90	lung:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
25	CEBPB	chr11:101735183-101735408	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:101737395-101737660	MCF-7	breast:	n/a	chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
27	CEBPB	chr11:101740919-101741843	A549	lung:	n/a	n/a
28	CEBPB	chr11:101733070-101733515	ECC-1	luminal epithelium:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
29	CEBPB	chr11:101630783-101631123	A549	lung:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938
30	CEBPB	chr11:101733008-101733479	H1-hESC	embryonic stem cell:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
31	CEBPB	chr11:101630739-101631160	MCF-7	breast:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938
32	CEBPB	chr11:101733092-101733474	HepG2	liver:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
33	CEBPB	chr11:101741001-101741638	A549	lung:	n/a	n/a
34	CEBPB	chr11:101737248-101737673	HepG2	liver:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
35	CEBPB	chr11:101732987-101733472	HepG2	liver:	n/a	chr11:101733268-101733279
36	CEBPB	chr11:101737065-101738223	A549	lung:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
37	CEBPB	chr11:101733047-101733525	A549	lung:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
38	CEBPB	chr11:101729488-101729775	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:101645742-101646099	IMR90	lung:	n/a	n/a
40	CEBPB	chr11:101740950-101741938	HCT-116	colon:	n/a	n/a
41	CEBPB	chr11:101731521-101731893	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:101733024-101733440	MCF-7	breast:	n/a	chr11:101733268-101733279
43	CEBPB	chr11:101741058-101742090	A549	lung:	n/a	n/a
44	CEBPB	chr11:101630699-101631222	MCF-7	breast:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938
45	CEBPB	chr11:101733071-101733463	ECC-1	luminal epithelium:	n/a	chr11:101733268-101733279
46	CEBPB	chr11:101630741-101631129	Hela-S3	cervix:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938
47	CEBPB	chr11:101737318-101737689	HepG2	liver:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
48	CEBPB	chr11:101630788-101631036	A549	lung:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938
49	CEBPB	chr11:101737341-101737627	HepG2	liver:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
50	CEBPB	chr11:101732937-101733673	HCT-116	colon:	n/a	chr11:101733461-101733474 chr11:101733268-101733279

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:101711789-101711839	CMK	blood:	n/a
2	chr11:101711789-101711839	CMK	blood:	n/a
3	chr11:101668461-101668511	NT2-D1	testis:	n/a
4	chr11:101646253-101646303	Hela-S3	cervix:	n/a
5	chr11:101711789-101711839	H1-hESC	embryonic stem cell:	embryo
6	chr11:101711789-101711839	NB4	blood:	n/a
7	chr11:101646253-101646303	GM06990	blood:	n/a
8	chr11:101681939-101681989	U87	brain:	n/a
9	chr11:101681939-101681989	NT2-D1	testis:	n/a
10	chr11:101668461-101668511	Caco-2	colon:	n/a
11	chr11:101646253-101646303	SKMC	muscle:	n/a
12	chr11:101668461-101668511	SK-N-SH_RA	brain:	n/a
13	chr11:101681939-101681989	HRCEpiC	kidney:	n/a
14	chr11:101681939-101681989	BE2_C	brain:	n/a
15	chr11:101646253-101646303	HCM	heart:	n/a
16	chr11:101668461-101668511	GM12891	blood:	n/a
17	chr11:101681939-101681989	AG04450	lung:	fetal
18	chr11:101681939-101681989	AG09319	gingival:	n/a
19	chr11:101711789-101711839	IMR90	lung:	fetal
20	chr11:101681939-101681989	GM19239	blood:	n/a
21	chr11:101668461-101668511	ECC-1	luminal epithelium:	n/a
22	chr11:101711789-101711839	SKMC	muscle:	n/a
23	chr11:101664126-101664176	NHBE	bronchial:	n/a
24	chr11:101681939-101681989	SK-N-MC	brain:	n/a
25	chr11:101664126-101664176	LNCaP	prostate:	n/a
26	chr11:101711789-101711839	Hepatocyte	liver:	n/a
27	chr11:101668461-101668511	HCF	heart:	n/a
28	chr11:101664126-101664176	ProgFib	skin:	n/a
29	chr11:101668461-101668511	AoSMC	blood vessel:	n/a
30	chr11:101664126-101664176	SK-N-SH_RA	brain:	n/a
31	chr11:101664126-101664176	GM12878	blood:	n/a
32	chr11:101711789-101711839	U87	brain:	n/a
33	chr11:101646253-101646303	GM12878	blood:	n/a
34	chr11:101668461-101668511	AG10803	skin:	n/a
35	chr11:101664126-101664176	AG04449	skin:	fetal
36	chr11:101646253-101646303	PrEC	prostate:	n/a
37	chr11:101668461-101668511	MCF-7	breast:	n/a
38	chr11:101681939-101681989	NB4	blood:	n/a
39	chr11:101668461-101668511	HCPEpiC	choroid plexus:	n/a
40	chr11:101664126-101664176	NH-A	brain:	n/a
41	chr11:101664126-101664176	HRPEpiC	eye:	n/a
42	chr11:101664126-101664176	PrEC	prostate:	n/a
43	chr11:101664126-101664176	BJ	skin:	n/a
44	chr11:101664126-101664176	HRCEpiC	kidney:	n/a
45	chr11:101681939-101681989	HRE	kidney:	n/a
46	chr11:101646253-101646303	Hepatocyte	liver:	n/a
47	chr11:101664126-101664176	NB4	blood:	n/a
48	chr11:101681939-101681989	NHBE	bronchial:	n/a
49	chr11:101711789-101711839	Caco-2	colon:	n/a
50	chr11:101646253-101646303	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr11:101327259..101328354-chr11:101718588..101719686,4	MCF-7	breast:
2	chr11:101722861..101723655-chr11:101731427..101731999,2	MCF-7	breast:
3	chr11:101731243..101732246-chr11:101878260..101879259,5	MCF-7	breast:
4	chr11:101626223..101628218-chr11:101649338..101651189,2	MCF-7	breast:
5	chr11:101731437..101732505-chr11:101878341..101879203,3	MCF-7	breast:
6	chr11:101686463..101689388-chr11:101690529..101692168,2	K562	blood:
7	chr11:101630508..101631518-chr11:101718726..101719557,3	MCF-7	breast:
8	chr11:101635429..101638102-chr11:101641064..101643321,2	MCF-7	breast:
9	chr11:101732949..101733736-chr11:101878285..101879187,3	MCF-7	breast:
10	chr11:101722724..101723429-chr11:101878801..101879552,2	MCF-7	breast:
11	chr11:101624030..101625631-chr11:101628031..101630002,2	MCF-7	breast:
12	chr11:101626223..101628218-chr11:101649338..101651189,2	MCF-7	breast:
13	chr11:101710531..101712863-chr11:101715498..101717187,2	K562	blood:
14	chr11:101631523..101632519-chr11:101671488..101672112,2	MCF-7	breast:
15	chr11:101722861..101723655-chr11:101731427..101731999,2	MCF-7	breast:
16	chr11:101627581..101630112-chr11:101632671..101635019,2	K562	blood:
17	chr11:101710531..101712863-chr11:101715498..101717187,2	K562	blood:
18	chr11:101631523..101632519-chr11:101671488..101672112,2	MCF-7	breast:
19	chr11:101686463..101689388-chr11:101690529..101692168,2	K562	blood:
20	chr11:101722375..101723959-chr11:101880701..101883311,2	MCF-7	breast:
21	chr11:101621795..101624545-chr11:101625193..101627217,2	MCF-7	breast:
22	chr11:101627581..101630112-chr11:101632671..101635019,2	K562	blood:
23	chr11:101630508..101631518-chr11:101718726..101719557,3	MCF-7	breast:
24	chr11:101732867..101733850-chr11:101750344..101751609,3	MCF-7	breast:
25	chr11:101732957..101733938-chr11:101844765..101845588,3	MCF-7	breast:
26	chr11:101635429..101638102-chr11:101641064..101643321,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPTL5-1	chr11:101636666-101637899	NONHSAT023862
2	lnc-ANGPTL5-1	chr11:101640264-101640692	NONHSAT023862

Variant related genes	Relation type
ENSG00000254534	TF binding region
ENSG00000254534	CpG island

Extended variants
information (count: 3242 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3242 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1006330	chr11:101626601-101626602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368304080	chr11:101626603-101626604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533610869	chr11:101626702-101626703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188206719	chr11:101626757-101626758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35813310	chr11:101626798-101626799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs947993	chr11:101626818-101626819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143011405	chr11:101626832-101626833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373307205	chr11:101626839-101626840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116035601	chr11:101626844-101626845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192358025	chr11:101626880-101626881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555894642	chr11:101626907-101626908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375337433	chr11:101626912-101626913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs80156831	chr11:101626920-101626921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141162360	chr11:101626925-101626926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372514352	chr11:101626949-101626950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538446677	chr11:101626956-101626957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533352260	chr11:101626981-101626982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183733367	chr11:101627003-101627004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs947994	chr11:101627017-101627018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs531565781	chr11:101627054-101627055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578097453	chr11:101627138-101627139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187982023	chr11:101627157-101627158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568221592	chr11:101627158-101627159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191220718	chr11:101627177-101627178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547050724	chr11:101627208-101627209	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs570154055	chr11:101627222-101627223	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs147007506	chr11:101627239-101627240	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs534327502	chr11:101627241-101627242	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs556844407	chr11:101627282-101627283	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs570238622	chr11:101627286-101627287	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs138238170	chr11:101627311-101627312	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs141709033	chr11:101627349-101627350	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs572629728	chr11:101627350-101627351	ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs540879267	chr11:101629034-101629035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538571341	chr11:101629081-101629082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563946881	chr11:101629188-101629189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577759349	chr11:101629197-101629198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551762949	chr11:101629231-101629232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563371942	chr11:101629233-101629234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528913125	chr11:101629275-101629276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115117399	chr11:101629281-101629282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374967823	chr11:101629300-101629301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78951197	chr11:101629354-101629355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555230180	chr11:101629365-101629366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs36016692	chr11:101629393-101629394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180863320	chr11:101629441-101629442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138768290	chr11:101629442-101629443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376184878	chr11:101629471-101629472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571791552	chr11:101629478-101629479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576374045	chr11:101629505-101629506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
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
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164920	CNVD
Breast cancer	17142309	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101626600-101627200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:101627200-101627400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:101627200-101627400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:101629000-101631200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr11:101629400-101630000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr11:101631200-101632000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr11:101631400-101632800	Enhancers	Hela-S3	cervix
8	chr11:101631800-101632200	Enhancers	A549	lung
9	chr11:101632000-101632600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr11:101632600-101632800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr11:101632800-101634800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr11:101634800-101635000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:101635000-101639600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr11:101639600-101640000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr11:101645000-101646600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:101645200-101646200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:101646200-101646400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:101646400-101646600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:101646600-101648200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr11:101648200-101648800	Enhancers	Fetal Lung	lung
21	chr11:101648400-101648800	Enhancers	Aorta	Aorta
22	chr11:101648600-101648800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:101655000-101655200	ZNF genes & repeats	Psoas Muscle	Psoas
24	chr11:101655200-101657200	Weak transcription	Psoas Muscle	Psoas
25	chr11:101656000-101656800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:101656600-101658200	Enhancers	Fetal Lung	lung
27	chr11:101656800-101657200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:101657000-101658200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:101657200-101657400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:101657200-101658200	Enhancers	NHDF-Ad	bronchial
31	chr11:101657400-101657600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:101657400-101658000	Enhancers	Osteobl	bone
33	chr11:101657400-101658400	Enhancers	Muscle Satellite Cultured Cells	--
34	chr11:101658200-101668000	Weak transcription	Fetal Lung	lung
35	chr11:101658400-101667600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr11:101663000-101663400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
37	chr11:101663200-101663600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
38	chr11:101663200-101664400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr11:101663400-101663800	Enhancers	Ovary	ovary
40	chr11:101663400-101664400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr11:101663400-101665000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr11:101663400-101665000	Enhancers	NHDF-Ad	bronchial
43	chr11:101663600-101663800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr11:101663600-101664000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr11:101663600-101664400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr11:101663600-101664600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr11:101663800-101664000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr11:101663800-101664600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr11:101663800-101665000	Enhancers	Osteobl	bone
50	chr11:101663800-101668400	Weak transcription	Ovary	ovary

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