Variant report

Variant	nsv832249
Chromosome Location	chr11:101571819-101749073
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	chr11:101731532-101731870	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:101737106-101738062	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	chr11:101737263-101737875	A549	lung:	n/a	n/a
7	ATF3	chr11:101737281-101737875	A549	lung:	n/a	n/a
8	ATF3	chr11:101741116-101741650	A549	lung:	n/a	n/a
9	BCL3	chr11:101589021-101589450	GM12878	blood:	n/a	chr11:101589371-101589380 chr11:101589370-101589379
10	BCL3	chr11:101737142-101737973	A549	lung:	n/a	n/a
11	BCL3	chr11:101589220-101589514	GM12878	blood:	n/a	chr11:101589371-101589380 chr11:101589370-101589379
12	BCL3	chr11:101737262-101737759	A549	lung:	n/a	n/a
13	BCL3	chr11:101741121-101741689	A549	lung:	n/a	chr11:101741365-101741374
14	BCL3	chr11:101740952-101741643	A549	lung:	n/a	chr11:101741365-101741374
15	BHLHE40	chr11:101741337-101741613	A549	lung:	n/a	n/a
16	BRCA1	chr11:101737238-101737813	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr11:101732986-101733673	HCT-116	colon:	n/a	n/a
18	CBX3	chr11:101741041-101741830	HCT-116	colon:	n/a	n/a
19	CBX3	chr11:101741194-101741727	HCT-116	colon:	n/a	n/a
20	CCNT2	chr11:101630610-101630773	K562	blood:	n/a	n/a
21	CEBPB	chr11:101577268-101577577	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:101732879-101733604	Hela-S3	cervix:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
23	CEBPB	chr11:101737274-101738089	Hela-S3	cervix:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
24	CEBPB	chr11:101733070-101733515	ECC-1	luminal epithelium:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
25	CEBPB	chr11:101696354-101696596	HepG2	liver:	n/a	chr11:101696432-101696443
26	CEBPB	chr11:101741058-101742090	A549	lung:	n/a	n/a
27	CEBPB	chr11:101645728-101646049	MCF-7	breast:	n/a	n/a
28	CEBPB	chr11:101732981-101733618	HCT-116	colon:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
29	CEBPB	chr11:101732987-101733472	HepG2	liver:	n/a	chr11:101733268-101733279
30	CEBPB	chr11:101741001-101741638	A549	lung:	n/a	n/a
31	CEBPB	chr11:101630741-101631129	Hela-S3	cervix:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938
32	CEBPB	chr11:101733024-101733440	MCF-7	breast:	n/a	chr11:101733268-101733279
33	CEBPB	chr11:101733064-101733569	MCF-7	breast:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
34	CEBPB	chr11:101740996-101741629	IMR90	lung:	n/a	n/a
35	CEBPB	chr11:101630705-101631172	A549	lung:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938
36	CEBPB	chr11:101733013-101733836	IMR90	lung:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
37	CEBPB	chr11:101733008-101733479	H1-hESC	embryonic stem cell:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
38	CEBPB	chr11:101737120-101737886	HCT-116	colon:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
39	CEBPB	chr11:101733015-101733475	A549	lung:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
40	CEBPB	chr11:101737249-101737836	HCT-116	colon:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
41	CEBPB	chr11:101599848-101600179	Hela-S3	cervix:	n/a	chr11:101600005-101600016
42	CEBPB	chr11:101737065-101738223	A549	lung:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
43	CEBPB	chr11:101577289-101577622	A549	lung:	n/a	n/a
44	CEBPB	chr11:101589177-101589542	A549	lung:	n/a	n/a
45	CEBPB	chr11:101740927-101741725	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:101645826-101646056	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:101599859-101600186	IMR90	lung:	n/a	chr11:101600005-101600016
48	CEBPB	chr11:101737286-101738027	A549	lung:	n/a	chr11:101737368-101737380 chr11:101737475-101737486 chr11:101737475-101737488 chr11:101737476-101737487 chr11:101737475-101737488
49	CEBPB	chr11:101732866-101733657	A549	lung:	n/a	chr11:101733461-101733474 chr11:101733268-101733279
50	CEBPB	chr11:101630788-101631036	A549	lung:	n/a	chr11:101630927-101630938 chr11:101630925-101630938 chr11:101630925-101630936 chr11:101630925-101630938

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:101664126-101664176	GM12891	blood:	n/a
2	chr11:101588566-101588616	HUVEC	blood vessel:	n/a
3	chr11:101588566-101588616	ProgFib	skin:	n/a
4	chr11:101664126-101664176	ProgFib	skin:	n/a
5	chr11:101588566-101588616	GM06990	blood:	n/a
6	chr11:101664126-101664176	ECC-1	luminal epithelium:	n/a
7	chr11:101664126-101664176	MCF10A-Er-Src	breast:	n/a
8	chr11:101664126-101664176	Caco-2	colon:	n/a
9	chr11:101646253-101646303	Hela-S3	cervix:	n/a
10	chr11:101646253-101646303	Hepatocyte	liver:	n/a
11	chr11:101646253-101646303	HRPEpiC	eye:	n/a
12	chr11:101681939-101681989	AG04449	skin:	fetal
13	chr11:101619453-101619503	GM12878	blood:	n/a
14	chr11:101588566-101588616	HCPEpiC	choroid plexus:	n/a
15	chr11:101587210-101587260	HAEpiC	amniotic membrane:	n/a
16	chr11:101668461-101668511	AG04449	skin:	fetal
17	chr11:101668461-101668511	SAEC	small airway:	n/a
18	chr11:101587210-101587260	HCT-116	colon:	n/a
19	chr11:101668461-101668511	GM12878	blood:	n/a
20	chr11:101619453-101619503	PANC-1	pancreas:	n/a
21	chr11:101681939-101681989	U87	brain:	n/a
22	chr11:101711789-101711839	PFSK-1	brain:	n/a
23	chr11:101668461-101668511	ovcar-3	ovarian:	n/a
24	chr11:101619453-101619503	HEK293	kidney:	embryo
25	chr11:101711789-101711839	BJ	skin:	n/a
26	chr11:101619453-101619503	HEEpiC	esophagus:	n/a
27	chr11:101587210-101587260	AG09309	skin:	n/a
28	chr11:101576844-101576894	HCPEpiC	choroid plexus:	n/a
29	chr11:101576844-101576894	Jurkat	blood:	n/a
30	chr11:101587210-101587260	HNPCEpiC	eye:	n/a
31	chr11:101619453-101619503	HCF	heart:	n/a
32	chr11:101664126-101664176	BJ	skin:	n/a
33	chr11:101711789-101711839	Caco-2	colon:	n/a
34	chr11:101646253-101646303	HRE	kidney:	n/a
35	chr11:101681939-101681989	CMK	blood:	n/a
36	chr11:101588566-101588616	K562	blood:	n/a
37	chr11:101576844-101576894	HRE	kidney:	n/a
38	chr11:101711789-101711839	Hela-S3	cervix:	n/a
39	chr11:101619453-101619503	AG04449	skin:	fetal
40	chr11:101588566-101588616	HAEpiC	amniotic membrane:	n/a
41	chr11:101576844-101576894	T-47D	breast:	n/a
42	chr11:101619453-101619503	AG09309	skin:	n/a
43	chr11:101576844-101576894	BE2_C	brain:	n/a
44	chr11:101588566-101588616	HNPCEpiC	eye:	n/a
45	chr11:101576844-101576894	GM19239	blood:	n/a
46	chr11:101576844-101576894	PFSK-1	brain:	n/a
47	chr11:101681939-101681989	HCPEpiC	choroid plexus:	n/a
48	chr11:101664126-101664176	SK-N-SH_RA	brain:	n/a
49	chr11:101576844-101576894	HCT-116	colon:	n/a
50	chr11:101664126-101664176	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:101624030..101625631-chr11:101628031..101630002,2	MCF-7	breast:
2	chr11:101585641..101587293-chr11:101587607..101589983,2	K562	blood:
3	chr11:101611797..101613703-chr11:101613756..101615793,2	MCF-7	breast:
4	chr11:101686463..101689388-chr11:101690529..101692168,2	K562	blood:
5	chr11:101722724..101723429-chr11:101878801..101879552,2	MCF-7	breast:
6	chr11:101722861..101723655-chr11:101731427..101731999,2	MCF-7	breast:
7	chr11:101585641..101587293-chr11:101587607..101589983,2	K562	blood:
8	chr11:101722861..101723655-chr11:101731427..101731999,2	MCF-7	breast:
9	chr11:101630508..101631518-chr11:101718726..101719557,3	MCF-7	breast:
10	chr11:101627581..101630112-chr11:101632671..101635019,2	K562	blood:
11	chr11:101731243..101732246-chr11:101878260..101879259,5	MCF-7	breast:
12	chr11:101686463..101689388-chr11:101690529..101692168,2	K562	blood:
13	chr11:101626223..101628218-chr11:101649338..101651189,2	MCF-7	breast:
14	chr11:101621795..101624545-chr11:101625193..101627217,2	MCF-7	breast:
15	chr11:101626223..101628218-chr11:101649338..101651189,2	MCF-7	breast:
16	chr11:101722375..101723959-chr11:101880701..101883311,2	MCF-7	breast:
17	chr11:101732949..101733736-chr11:101878285..101879187,3	MCF-7	breast:
18	chr11:101635429..101638102-chr11:101641064..101643321,2	MCF-7	breast:
19	chr11:101621795..101624545-chr11:101625193..101627217,2	MCF-7	breast:
20	chr11:101635429..101638102-chr11:101641064..101643321,2	MCF-7	breast:
21	chr11:101601852..101603833-chr11:101605803..101608471,2	MCF-7	breast:
22	chr11:101631523..101632519-chr11:101671488..101672112,2	MCF-7	breast:
23	chr11:101611797..101613703-chr11:101613756..101615793,2	MCF-7	breast:
24	chr11:101601852..101603833-chr11:101605803..101608471,2	MCF-7	breast:
25	chr11:101627581..101630112-chr11:101632671..101635019,2	K562	blood:
26	chr11:101710531..101712863-chr11:101715498..101717187,2	K562	blood:
27	chr11:101624030..101625631-chr11:101628031..101630002,2	MCF-7	breast:
28	chr11:101732867..101733850-chr11:101750344..101751609,3	MCF-7	breast:
29	chr11:101731437..101732505-chr11:101878341..101879203,3	MCF-7	breast:
30	chr11:101710531..101712863-chr11:101715498..101717187,2	K562	blood:
31	chr11:101327259..101328354-chr11:101718588..101719686,4	MCF-7	breast:
32	chr11:101732957..101733938-chr11:101844765..101845588,3	MCF-7	breast:
33	chr11:101630508..101631518-chr11:101718726..101719557,3	MCF-7	breast:
34	chr11:101631523..101632519-chr11:101671488..101672112,2	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
TRPC6	TF binding region
ENSG00000254534	CpG island
TRPC6	CpG island

Extended variants
information (count: 5444 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:5444 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202243200	chr11:101571906-101571907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200879179	chr11:101572143-101572144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543896342	chr11:101572377-101572378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368326721	chr11:101572381-101572382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111564172	chr11:101572633-101572634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186570378	chr11:101572636-101572637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560759383	chr11:101572704-101572705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529672047	chr11:101572720-101572721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546252337	chr11:101572783-101572784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560857122	chr11:101572813-101572814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532814958	chr11:101572823-101572824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113987562	chr11:101572851-101572852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201707807	chr11:101572913-101572914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113099014	chr11:101572948-101572949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200541745	chr11:101572989-101572990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111630018	chr11:101572994-101572995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113693713	chr11:101573024-101573025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372207115	chr11:101573038-101573039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113490702	chr11:101573113-101573114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374014536	chr11:101573219-101573220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111921481	chr11:101573325-101573326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367832007	chr11:101573366-101573367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371194567	chr11:101573380-101573381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201576263	chr11:101573559-101573560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141493952	chr11:101573562-101573563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113160054	chr11:101573607-101573608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113351854	chr11:101573644-101573645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370011144	chr11:101573688-101573689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199697530	chr11:101573734-101573735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200340316	chr11:101573749-101573750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201402162	chr11:101573765-101573766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199759031	chr11:101573786-101573787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373937358	chr11:101573854-101573855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113367876	chr11:101573855-101573856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377487284	chr11:101573887-101573888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201616401	chr11:101573901-101573902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368799228	chr11:101573902-101573903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200833423	chr11:101573953-101573954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373093484	chr11:101573966-101573967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201835558	chr11:101573968-101573969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199649301	chr11:101574013-101574014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569464085	chr11:101574016-101574017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138517504	chr11:101574021-101574022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201885325	chr11:101574035-101574036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199744065	chr11:101574125-101574126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200658509	chr11:101574129-101574130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199606843	chr11:101574136-101574137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201397531	chr11:101574137-101574138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199781362	chr11:101574144-101574145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61918183	chr11:101574148-101574149	Weak transcription	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
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
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164920	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101564800-101578400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:101575200-101575600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr11:101575200-101575800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr11:101575200-101578800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr11:101575400-101575600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr11:101575400-101576200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr11:101575400-101576600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr11:101575600-101576600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:101575800-101576000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr11:101575800-101576400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:101575800-101577600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr11:101576000-101576200	Enhancers	Esophagus	oesophagus
13	chr11:101576000-101576800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr11:101576000-101577000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:101576000-101577000	Enhancers	Fetal Muscle Leg	muscle
16	chr11:101576000-101577000	Enhancers	Ovary	ovary
17	chr11:101576200-101576400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr11:101576200-101578400	Weak transcription	Esophagus	oesophagus
19	chr11:101576200-101578600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr11:101576400-101576800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr11:101576400-101576800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:101576600-101577000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr11:101576600-101577400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr11:101576600-101577400	Enhancers	A549	lung
25	chr11:101576600-101577600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr11:101576600-101577800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr11:101576800-101577000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:101576800-101577800	Enhancers	NHLF	lung
29	chr11:101576800-101578000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr11:101576800-101578000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:101576800-101578200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr11:101576800-101578200	Enhancers	NH-A	brain
33	chr11:101577000-101578200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr11:101577000-101578400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr11:101577000-101579600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr11:101577400-101577800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:101577400-101577800	Flanking Active TSS	A549	lung
38	chr11:101577400-101578400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr11:101577600-101577800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr11:101577600-101577800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr11:101577600-101577800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:101577800-101578200	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr11:101577800-101578200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr11:101577800-101578400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr11:101578000-101578200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr11:101578200-101578400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr11:101578200-101578600	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr11:101578200-101578600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:101578200-101578600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:101578200-101578800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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