Variant report

Variant	nsv898180
Chromosome Location	chr11:93045561-93082053
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	ATF1	chr11:93063176-93063364	K562	blood:	n/a	n/a
2	ATF1	chr11:93073459-93073734	K562	blood:	n/a	n/a
3	ATF1	chr11:93056980-93057280	K562	blood:	n/a	n/a
4	ATF1	chr11:93078004-93078238	K562	blood:	n/a	n/a
5	ATF1	chr11:93059982-93060208	K562	blood:	n/a	n/a
6	ATF3	chr11:93077944-93078278	K562	blood:	n/a	n/a
7	BACH1	chr11:93063382-93063797	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr11:93075237-93075532	GM12878	blood:	n/a	chr11:93075411-93075422
9	BHLHE40	chr11:93063542-93064049	K562	blood:	n/a	chr11:93063671-93063687 chr11:93063669-93063685 chr11:93063674-93063690 chr11:93063677-93063693 chr11:93063680-93063696
10	BHLHE40	chr11:93059971-93060083	K562	blood:	n/a	n/a
11	CBX3	chr11:93052412-93052741	K562	blood:	n/a	n/a
12	CBX3	chr11:93063074-93063896	K562	blood:	n/a	n/a
13	CCNT2	chr11:93063473-93064104	K562	blood:	n/a	n/a
14	CEBPB	chr11:93077953-93078190	K562	blood:	n/a	chr11:93078108-93078119
15	CEBPB	chr11:93078005-93078205	HepG2	liver:	n/a	chr11:93078108-93078119
16	CEBPB	chr11:93076511-93076704	HepG2	liver:	n/a	chr11:93076588-93076599
17	CEBPB	chr11:93059937-93060137	K562	blood:	n/a	n/a
18	CEBPB	chr11:93076477-93076696	Hela-S3	cervix:	n/a	chr11:93076588-93076599
19	CEBPB	chr11:93076498-93076676	IMR90	lung:	n/a	chr11:93076588-93076599
20	CEBPB	chr11:93077901-93078294	K562	blood:	n/a	chr11:93078108-93078119
21	CEBPB	chr11:93077941-93078250	K562	blood:	n/a	chr11:93078108-93078119
22	CHD2	chr11:93063536-93064041	H1-hESC	embryonic stem cell:	n/a	chr11:93063965-93063975
23	CHD2	chr11:93063467-93063877	K562	blood:	n/a	n/a
24	CHD2	chr11:93063635-93063765	GM12878	blood:	n/a	n/a
25	CTCF	chr11:93047891-93047937	Medullo	brain:	n/a	n/a
26	CTCF	chr11:93069563-93069591	GM20000	blood:	n/a	n/a
27	CTCF	chr11:93078273-93078315	GM13977	blood:	n/a	n/a
28	CTCF	chr11:93052200-93052450	GM06990	blood:	n/a	n/a
29	CTCF	chr11:93072940-93073090	GM12870	blood:	n/a	n/a
30	CUX1	chr11:93063168-93063627	K562	blood:	n/a	n/a
31	CUX1	chr11:93078105-93078115	K562	blood:	n/a	n/a
32	E2F4	chr11:93063454-93064272	K562	blood:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063679-93063689
33	E2F6	chr11:93063447-93064273	H1-hESC	embryonic stem cell:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
34	E2F6	chr11:93063176-93064262	H1-hESC	embryonic stem cell:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
35	E2F6	chr11:93063177-93064200	K562	blood:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
36	E2F6	chr11:93063492-93064190	K562	blood:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
37	E2F6	chr11:93063510-93064021	K562	blood:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
38	EBF1	chr11:93063574-93063590	GM12878	blood:	n/a	n/a
39	EP300	chr11:93056984-93057167	K562	blood:	n/a	n/a
40	EP300	chr11:93082043-93082186	K562	blood:	n/a	n/a
41	EP300	chr11:93063209-93063953	K562	blood:	n/a	chr11:93063682-93063691 chr11:93063679-93063688
42	EP300	chr11:93077764-93078351	K562	blood:	n/a	chr11:93077852-93077862
43	FOXA1	chr11:93050148-93050815	T-47D	breast:	n/a	n/a
44	FOXA1	chr11:93077895-93078204	HepG2	liver:	n/a	n/a
45	FOXA1	chr11:93046103-93046264	ECC-1	luminal epithelium:	n/a	n/a
46	FOXA2	chr11:93077964-93078198	HepG2	liver:	n/a	n/a
47	GABPA	chr11:93081069-93081212	GM12878	blood:	n/a	n/a
48	GATA3	chr11:93050298-93050752	T-47D	breast:	n/a	chr11:93050513-93050521
49	GATA3	chr11:93050170-93050700	T-47D	breast:	n/a	chr11:93050513-93050521
50	GATA3	chr11:93054719-93054858	SH-SY5Y	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93063516-93063566	HL-60	blood:	n/a
2	chr11:93063662-93063712	NT2-D1	testis:	n/a
3	chr11:93062752-93062802	AG10803	skin:	n/a
4	chr11:93064234-93064284	GM06990	blood:	n/a
5	chr11:93063684-93063734	GM06990	blood:	n/a
6	chr11:93063684-93063734	NB4	blood:	n/a
7	chr11:93059814-93059864	NHBE	bronchial:	n/a
8	chr11:93062752-93062802	HCT-116	colon:	n/a
9	chr11:93064092-93064142	PrEC	prostate:	n/a
10	chr11:93064092-93064142	Jurkat	blood:	n/a
11	chr11:93063692-93063742	GM12878	blood:	n/a
12	chr11:93064092-93064142	MCF-7	breast:	n/a
13	chr11:93059814-93059864	SK-N-MC	brain:	n/a
14	chr11:93063888-93063938	GM19239	blood:	n/a
15	chr11:93062935-93062985	ProgFib	skin:	n/a
16	chr11:93063208-93063258	GM12892	blood:	n/a
17	chr11:93062935-93062985	NT2-D1	testis:	n/a
18	chr11:93063888-93063938	HAEpiC	amniotic membrane:	n/a
19	chr11:93067324-93067374	Hela-S3	cervix:	n/a
20	chr11:93062752-93062802	AG04449	skin:	fetal
21	chr11:93063888-93063938	SK-N-SH_RA	brain:	n/a
22	chr11:93063934-93063984	T-47D	breast:	n/a
23	chr11:93064092-93064142	K562	blood:	n/a
24	chr11:93059814-93059864	NHDF-neo	bronchial:	n/a
25	chr11:93063662-93063712	GM06990	blood:	n/a
26	chr11:93063662-93063712	ECC-1	luminal epithelium:	n/a
27	chr11:93062752-93062802	AG09319	gingival:	n/a
28	chr11:93063888-93063938	ovcar-3	ovarian:	n/a
29	chr11:93063684-93063734	BE2_C	brain:	n/a
30	chr11:93063886-93063936	AG04450	lung:	fetal
31	chr11:93067324-93067374	K562	blood:	n/a
32	chr11:93062752-93062802	GM12891	blood:	n/a
33	chr11:93062752-93062802	U87	brain:	n/a
34	chr11:93063934-93063984	HNPCEpiC	eye:	n/a
35	chr11:93063662-93063712	Hela-S3	cervix:	n/a
36	chr11:93059814-93059864	PrEC	prostate:	n/a
37	chr11:93062935-93062985	NHBE	bronchial:	n/a
38	chr11:93063888-93063938	Hela-S3	cervix:	n/a
39	chr11:93063302-93063352	U87	brain:	n/a
40	chr11:93063208-93063258	CMK	blood:	n/a
41	chr11:93063692-93063742	HAEpiC	amniotic membrane:	n/a
42	chr11:93064234-93064284	AoSMC	blood vessel:	n/a
43	chr11:93063302-93063352	NB4	blood:	n/a
44	chr11:93063662-93063712	GM19239	blood:	n/a
45	chr11:93062752-93062802	HL-60	blood:	n/a
46	chr11:93064092-93064142	H1-hESC	embryonic stem cell:	embryo
47	chr11:93063302-93063352	HCM	heart:	n/a
48	chr11:93063886-93063936	HAEpiC	amniotic membrane:	n/a
49	chr11:93063516-93063566	HCPEpiC	choroid plexus:	n/a
50	chr11:93062935-93062985	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:93055055..93056889-chr11:93058671..93061628,2	K562	blood:
2	chr11:93069580..93071990-chr11:93073052..93075008,3	K562	blood:
3	chr11:93061314..93067445-chr11:93068107..93073820,10	K562	blood:
4	chr11:93052299..93059527-chr11:93061747..93065843,7	K562	blood:
5	chr11:93069969..93071990-chr11:93073312..93075008,2	K562	blood:
6	chr11:93074787..93076635-chr11:93084115..93086331,2	K562	blood:
7	chr11:93073470..93075711-chr11:93076090..93078058,3	K562	blood:
8	chr11:93071693..93075420-chr11:93075820..93077590,4	K562	blood:
9	chr11:93058763..93061728-chr11:93061851..93065338,6	K562	blood:
10	chr11:93069969..93071990-chr11:93073312..93075008,2	K562	blood:
11	chr11:93048625..93050616-chr11:93051805..93054715,2	K562	blood:
12	chr11:93068449..93072526-chr11:93274941..93279025,3	K562	blood:
13	chr11:93055055..93056889-chr11:93058671..93061628,2	K562	blood:
14	chr11:93069580..93071990-chr11:93073052..93075008,3	K562	blood:
15	chr11:93048625..93050616-chr11:93051805..93054715,2	K562	blood:
16	chr11:93060266..93062077-chr11:93064556..93067228,3	K562	blood:
17	chr11:93073470..93075711-chr11:93076090..93078058,3	K562	blood:
18	chr11:93052299..93054935-chr11:93063280..93065843,2	K562	blood:
19	chr11:93071693..93075420-chr11:93075820..93077590,4	K562	blood:

Variant related genes	Relation type
CCDC67	TF binding region
CCDC67	CpG island
ENSG00000165325	chromatin interactions
ENSG00000166002	chromatin interactions

Extended variants
information (count: 1200 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1200 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11020261	chr11:93045561-93045562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11020262	chr11:93045786-93045787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563049783	chr11:93045809-93045810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190740140	chr11:93045826-93045827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374910342	chr11:93045827-93045828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117178607	chr11:93045833-93045834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555695537	chr11:93045837-93045838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560572119	chr11:93045892-93045893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201152914	chr11:93045894-93045895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528054248	chr11:93045910-93045911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546322726	chr11:93045911-93045912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564630826	chr11:93046016-93046017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532383896	chr11:93046018-93046019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200678710	chr11:93046047-93046048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550506238	chr11:93046080-93046081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568992949	chr11:93046114-93046115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183241290	chr11:93046141-93046142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548478692	chr11:93046168-93046169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566901846	chr11:93046228-93046229	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534174116	chr11:93046339-93046340	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537038012	chr11:93046369-93046370	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557076604	chr11:93046374-93046375	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369055050	chr11:93046386-93046387	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577267786	chr11:93046398-93046399	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113749778	chr11:93046399-93046400	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188546818	chr11:93046471-93046472	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs77647753	chr11:93046494-93046495	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs373231636	chr11:93046526-93046527	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs542144648	chr11:93046559-93046560	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs539645188	chr11:93046591-93046592	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs556098792	chr11:93046598-93046599	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs148655858	chr11:93046634-93046635	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs572546812	chr11:93046662-93046663	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs539839865	chr11:93046668-93046669	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs564493680	chr11:93046690-93046691	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs532117124	chr11:93046700-93046701	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs35837863	chr11:93046735-93046736	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs373056953	chr11:93046742-93046743	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs573214679	chr11:93046795-93046796	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs111458978	chr11:93048201-93048202	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs565058472	chr11:93048225-93048226	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs539633256	chr11:93048298-93048299	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs184898133	chr11:93048300-93048301	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs570327227	chr11:93048383-93048384	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs551178444	chr11:93048407-93048408	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs559562283	chr11:93048446-93048447	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs188234785	chr11:93048483-93048484	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs556136714	chr11:93048523-93048524	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs574455038	chr11:93048541-93048542	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs535572309	chr11:93048659-93048660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Prostate cancer	18632612	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
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93042800-93046400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:93046200-93046800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:93046400-93046800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:93048200-93048600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:93048200-93050400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr11:93048600-93049800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr11:93051000-93051200	Enhancers	Pancreas	Pancrea
8	chr11:93051200-93063000	Weak transcription	Pancreas	Pancrea
9	chr11:93057200-93057400	Enhancers	K562	blood
10	chr11:93057200-93058000	Enhancers	Fetal Intestine Large	intestine
11	chr11:93057400-93063000	Weak transcription	K562	blood
12	chr11:93057800-93058000	Enhancers	Fetal Intestine Small	intestine
13	chr11:93059600-93060200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:93060000-93060200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:93060800-93061000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:93062600-93063200	Bivalent Enhancer	Fetal Heart	heart
17	chr11:93062800-93064600	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr11:93063000-93063200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
19	chr11:93063000-93063200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
20	chr11:93063000-93063200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:93063000-93063200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:93063000-93063200	Enhancers	Adipose Nuclei	Adipose
23	chr11:93063000-93063200	Active TSS	Duodenum Mucosa	Duodenum
24	chr11:93063000-93063200	Enhancers	Pancreas	Pancrea
25	chr11:93063000-93063200	Bivalent/Poised TSS	NHEK	skin
26	chr11:93063000-93063400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
27	chr11:93063000-93063400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
28	chr11:93063000-93063400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr11:93063000-93063600	Flanking Active TSS	K562	blood
30	chr11:93063000-93063800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:93063000-93064000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:93063000-93064200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr11:93063000-93064200	Bivalent/Poised TSS	Fetal Brain Female	brain
34	chr11:93063000-93064200	Bivalent Enhancer	Placenta	Placenta
35	chr11:93063000-93064400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr11:93063000-93064600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
37	chr11:93063200-93063400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:93063200-93063400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:93063200-93063400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
40	chr11:93063200-93063400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:93063200-93063400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:93063200-93063400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:93063200-93063400	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:93063200-93063400	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr11:93063200-93063400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
46	chr11:93063200-93063400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
47	chr11:93063200-93063400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr11:93063200-93063400	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr11:93063200-93063400	Active TSS	Brain Germinal Matrix	brain
50	chr11:93063200-93063400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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