Variant report

Variant	nsv438
Chromosome Location	chr11:93034411-93080513
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	chr11:93059982-93060208	K562	blood:	n/a	n/a
2	ATF1	chr11:93063176-93063364	K562	blood:	n/a	n/a
3	ATF1	chr11:93056980-93057280	K562	blood:	n/a	n/a
4	ATF1	chr11:93073459-93073734	K562	blood:	n/a	n/a
5	ATF1	chr11:93078004-93078238	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	chr11:93043035-93043161	HepG2	liver:	n/a	n/a
10	BHLHE40	chr11:93059971-93060083	K562	blood:	n/a	n/a
11	BHLHE40	chr11:93063542-93064049	K562	blood:	n/a	chr11:93063671-93063687 chr11:93063669-93063685 chr11:93063674-93063690 chr11:93063677-93063693 chr11:93063680-93063696
12	BRCA1	chr11:93039483-93039653	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr11:93052412-93052741	K562	blood:	n/a	n/a
14	CBX3	chr11:93063074-93063896	K562	blood:	n/a	n/a
15	CCNT2	chr11:93063473-93064104	K562	blood:	n/a	n/a
16	CEBPB	chr11:93076511-93076704	HepG2	liver:	n/a	chr11:93076588-93076599
17	CEBPB	chr11:93076498-93076676	IMR90	lung:	n/a	chr11:93076588-93076599
18	CEBPB	chr11:93043012-93043183	HepG2	liver:	n/a	chr11:93043058-93043069
19	CEBPB	chr11:93078005-93078205	HepG2	liver:	n/a	chr11:93078108-93078119
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	CEBPB	chr11:93076477-93076696	Hela-S3	cervix:	n/a	chr11:93076588-93076599
23	CEBPB	chr11:93077953-93078190	K562	blood:	n/a	chr11:93078108-93078119
24	CEBPB	chr11:93059937-93060137	K562	blood:	n/a	n/a
25	CHD2	chr11:93063635-93063765	GM12878	blood:	n/a	n/a
26	CHD2	chr11:93063536-93064041	H1-hESC	embryonic stem cell:	n/a	chr11:93063965-93063975
27	CHD2	chr11:93063467-93063877	K562	blood:	n/a	n/a
28	CTCF	chr11:93052200-93052450	GM06990	blood:	n/a	n/a
29	CTCF	chr11:93047891-93047937	Medullo	brain:	n/a	n/a
30	CTCF	chr11:93078273-93078315	GM13977	blood:	n/a	n/a
31	CTCF	chr11:93069563-93069591	GM20000	blood:	n/a	n/a
32	CTCF	chr11:93072940-93073090	GM12870	blood:	n/a	n/a
33	CUX1	chr11:93078105-93078115	K562	blood:	n/a	n/a
34	CUX1	chr11:93063168-93063627	K562	blood:	n/a	n/a
35	E2F4	chr11:93063454-93064272	K562	blood:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 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	chr11:93063177-93064200	K562	blood:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
38	E2F6	chr11:93063510-93064021	K562	blood:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
39	E2F6	chr11:93063447-93064273	H1-hESC	embryonic stem cell:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
40	E2F6	chr11:93063176-93064262	H1-hESC	embryonic stem cell:	n/a	chr11:93063682-93063692 chr11:93063676-93063686 chr11:93063767-93063778 chr11:93063679-93063689
41	EBF1	chr11:93063574-93063590	GM12878	blood:	n/a	n/a
42	EP300	chr11:93056984-93057167	K562	blood:	n/a	n/a
43	EP300	chr11:93063209-93063953	K562	blood:	n/a	chr11:93063682-93063691 chr11:93063679-93063688
44	EP300	chr11:93077764-93078351	K562	blood:	n/a	chr11:93077852-93077862
45	FOXA1	chr11:93046103-93046264	ECC-1	luminal epithelium:	n/a	n/a
46	FOXA1	chr11:93050148-93050815	T-47D	breast:	n/a	n/a
47	FOXA1	chr11:93077895-93078204	HepG2	liver:	n/a	n/a
48	FOXA2	chr11:93077964-93078198	HepG2	liver:	n/a	n/a
49	GATA3	chr11:93050490-93050713	SH-SY5Y	brain:	n/a	chr11:93050513-93050521
50	GATA3	chr11:93050230-93050745	MCF-7	breast:	n/a	chr11:93050513-93050521

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93063516-93063566	HIPEpiC	eye:	n/a
2	chr11:93063516-93063566	HIPEpiC	eye:	n/a
3	chr11:93063208-93063258	ovcar-3	ovarian:	n/a
4	chr11:93063692-93063742	T-47D	breast:	n/a
5	chr11:93063662-93063712	AG10803	skin:	n/a
6	chr11:93063888-93063938	SK-N-SH	brain:	n/a
7	chr11:93063208-93063258	Hela-S3	cervix:	n/a
8	chr11:93059814-93059864	HL-60	blood:	n/a
9	chr11:93064092-93064142	MCF-7	breast:	n/a
10	chr11:93062752-93062802	HEEpiC	esophagus:	n/a
11	chr11:93063208-93063258	AG04450	lung:	fetal
12	chr11:93063888-93063938	HPAEpiC	pulmonary alveolar:	n/a
13	chr11:93063302-93063352	BJ	skin:	n/a
14	chr11:93063662-93063712	SKMC	muscle:	n/a
15	chr11:93063684-93063734	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:93059814-93059864	NT2-D1	testis:	n/a
17	chr11:93063888-93063938	HUVEC	blood vessel:	n/a
18	chr11:93063888-93063938	SK-N-SH_RA	brain:	n/a
19	chr11:93062752-93062802	H1-hESC	embryonic stem cell:	embryo
20	chr11:93063662-93063712	HIPEpiC	eye:	n/a
21	chr11:93059814-93059864	ovcar-3	ovarian:	n/a
22	chr11:93059814-93059864	Hela-S3	cervix:	n/a
23	chr11:93067324-93067374	HepG2	liver:	n/a
24	chr11:93062935-93062985	GM12892	blood:	n/a
25	chr11:93064092-93064142	T-47D	breast:	n/a
26	chr11:93063208-93063258	PANC-1	pancreas:	n/a
27	chr11:93064092-93064142	SK-N-SH	brain:	n/a
28	chr11:93067324-93067374	AG10803	skin:	n/a
29	chr11:93063886-93063936	HCM	heart:	n/a
30	chr11:93063888-93063938	HMEC	breast:	n/a
31	chr11:93063888-93063938	HEK293	kidney:	embryo
32	chr11:93063886-93063936	HEK293	kidney:	embryo
33	chr11:93059814-93059864	HRPEpiC	eye:	n/a
34	chr11:93063934-93063984	GM12878	blood:	n/a
35	chr11:93059814-93059864	NHBE	bronchial:	n/a
36	chr11:93062752-93062802	GM12878	blood:	n/a
37	chr11:93064092-93064142	SKMC	muscle:	n/a
38	chr11:93064092-93064142	LNCaP	prostate:	n/a
39	chr11:93059814-93059864	HepG2	liver:	n/a
40	chr11:93063302-93063352	HL-60	blood:	n/a
41	chr11:93063692-93063742	HNPCEpiC	eye:	n/a
42	chr11:93064234-93064284	PrEC	prostate:	n/a
43	chr11:93063684-93063734	HIPEpiC	eye:	n/a
44	chr11:93059814-93059864	GM19239	blood:	n/a
45	chr11:93063888-93063938	MCF10A-Er-Src	breast:	n/a
46	chr11:93063662-93063712	NB4	blood:	n/a
47	chr11:93059814-93059864	MCF-7	breast:	n/a
48	chr11:93062752-93062802	HAEpiC	amniotic membrane:	n/a
49	chr11:93067324-93067374	Caco-2	colon:	n/a
50	chr11:93063888-93063938	Hepatocyte	liver:	n/a

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

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

Extended variants
information (count: 1253 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551356789	chr11:93036497-93036498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144924587	chr11:93036503-93036504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149057555	chr11:93036508-93036509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549421442	chr11:93036533-93036534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567781877	chr11:93036574-93036575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535196617	chr11:93036595-93036596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11020253	chr11:93036658-93036659	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs571902917	chr11:93036663-93036664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111577631	chr11:93036688-93036689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557791927	chr11:93036710-93036711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184057372	chr11:93036774-93036775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370071080	chr11:93042810-93042811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551494076	chr11:93042816-93042817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563793930	chr11:93042836-93042837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34487174	chr11:93042886-93042887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531055309	chr11:93042962-93042963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549554519	chr11:93042982-93042983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567712636	chr11:93043013-93043014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373515557	chr11:93043036-93043037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547287728	chr11:93043076-93043077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543873136	chr11:93043141-93043142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143778776	chr11:93043196-93043197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187682347	chr11:93043203-93043204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79759856	chr11:93043222-93043223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199737098	chr11:93043233-93043234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375524943	chr11:93043234-93043235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201889085	chr11:93043237-93043238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549902773	chr11:93043243-93043244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201927163	chr11:93043245-93043246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567727806	chr11:93043246-93043247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75108886	chr11:93043247-93043248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7130661	chr11:93043258-93043259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199998248	chr11:93043264-93043265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7130668	chr11:93043265-93043266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191073994	chr11:93043273-93043274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148135812	chr11:93043288-93043289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113249281	chr11:93043318-93043319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554645607	chr11:93043343-93043344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112156440	chr11:93043364-93043365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377480639	chr11:93043397-93043398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182861949	chr11:93043413-93043414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141899345	chr11:93043415-93043416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559205645	chr11:93043463-93043464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78667291	chr11:93043547-93043548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188417897	chr11:93043548-93043549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563484878	chr11:93043569-93043570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192819393	chr11:93043582-93043583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549173469	chr11:93043592-93043593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79329815	chr11:93043667-93043668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528677360	chr11:93043669-93043670	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:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93036400-93036800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:93042800-93046400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:93046200-93046800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:93046400-93046800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:93048200-93048600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:93048200-93050400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr11:93048600-93049800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:93051000-93051200	Enhancers	Pancreas	Pancrea
9	chr11:93051200-93063000	Weak transcription	Pancreas	Pancrea
10	chr11:93057200-93057400	Enhancers	K562	blood
11	chr11:93057200-93058000	Enhancers	Fetal Intestine Large	intestine
12	chr11:93057400-93063000	Weak transcription	K562	blood
13	chr11:93057800-93058000	Enhancers	Fetal Intestine Small	intestine
14	chr11:93059600-93060200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:93060000-93060200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:93060800-93061000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:93062600-93063200	Bivalent Enhancer	Fetal Heart	heart
18	chr11:93062800-93064600	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr11:93063000-93063200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
20	chr11:93063000-93063200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
21	chr11:93063000-93063200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:93063000-93063200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:93063000-93063200	Enhancers	Adipose Nuclei	Adipose
24	chr11:93063000-93063200	Active TSS	Duodenum Mucosa	Duodenum
25	chr11:93063000-93063200	Enhancers	Pancreas	Pancrea
26	chr11:93063000-93063200	Bivalent/Poised TSS	NHEK	skin
27	chr11:93063000-93063400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
28	chr11:93063000-93063400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
29	chr11:93063000-93063400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:93063000-93063600	Flanking Active TSS	K562	blood
31	chr11:93063000-93063800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:93063000-93064000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:93063000-93064200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr11:93063000-93064200	Bivalent/Poised TSS	Fetal Brain Female	brain
35	chr11:93063000-93064200	Bivalent Enhancer	Placenta	Placenta
36	chr11:93063000-93064400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr11:93063000-93064600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
38	chr11:93063200-93063400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:93063200-93063400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:93063200-93063400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
41	chr11:93063200-93063400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:93063200-93063400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:93063200-93063400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:93063200-93063400	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:93063200-93063400	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:93063200-93063400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
47	chr11:93063200-93063400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
48	chr11:93063200-93063400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr11:93063200-93063400	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr11:93063200-93063400	Active TSS	Brain Germinal Matrix	brain

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