Variant report

Variant	nsv1035530
Chromosome Location	chr11:93114111-93148948
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	chr11:93140996-93141323	K562	blood:	n/a	n/a
2	ATF3	chr11:93141005-93141334	K562	blood:	n/a	n/a
3	CEBPB	chr11:93146378-93146499	K562	blood:	n/a	n/a
4	CEBPB	chr11:93140897-93141476	HCT-116	colon:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
5	CEBPB	chr11:93140958-93141353	Hela-S3	cervix:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
6	CEBPB	chr11:93140969-93141354	HepG2	liver:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
7	CEBPB	chr11:93140924-93141389	A549	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
8	CEBPB	chr11:93141014-93141258	HepG2	liver:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
9	CEBPB	chr11:93140980-93141347	IMR90	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
10	CEBPB	chr11:93126167-93126441	K562	blood:	n/a	n/a
11	CEBPB	chr11:93140968-93141291	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
12	CEBPB	chr11:93145425-93145556	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr11:93126186-93126397	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:93140988-93141325	H1-hESC	embryonic stem cell:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
15	CEBPB	chr11:93146382-93146537	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr11:93141045-93141317	ECC-1	luminal epithelium:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
17	CEBPB	chr11:93140894-93141393	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
18	CEBPB	chr11:93140940-93141345	HCT-116	colon:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
19	CEBPB	chr11:93140968-93141348	K562	blood:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
20	CEBPB	chr11:93140982-93141344	A549	lung:	n/a	chr11:93141160-93141177 chr11:93141162-93141173 chr11:93141136-93141153 chr11:93141139-93141150
21	CTCF	chr11:93133720-93133870	GM06990	blood:	n/a	n/a
22	E2F4	chr11:93137300-93137492	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr11:93121708-93121751	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr11:93141003-93141303	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr11:93134550-93134655	MCF10A-Er-Src	breast:	n/a	n/a
26	EGR1	chr11:93141099-93141328	K562	blood:	n/a	chr11:93141235-93141248 chr11:93141234-93141249
27	EGR1	chr11:93141132-93141341	K562	blood:	n/a	chr11:93141235-93141248 chr11:93141234-93141249
28	EP300	chr11:93140926-93141303	K562	blood:	n/a	chr11:93141159-93141173 chr11:93141140-93141154
29	EP300	chr11:93141013-93141299	Hela-S3	cervix:	n/a	chr11:93141159-93141173 chr11:93141140-93141154
30	FOS	chr11:93140989-93141337	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr11:93140976-93141342	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr11:93140982-93141346	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr11:93140976-93141333	MCF10A-Er-Src	breast:	n/a	n/a
34	FOXA1	chr11:93122857-93123144	T-47D	breast:	n/a	n/a
35	FOXA1	chr11:93120072-93120274	T-47D	breast:	n/a	n/a
36	GATA3	chr11:93133863-93133977	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr11:93116255-93116358	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr11:93122744-93123123	T-47D	breast:	n/a	n/a
39	JUN	chr11:93141080-93141306	HepG2	liver:	n/a	chr11:93141159-93141172
40	JUND	chr11:93141002-93141332	HepG2	liver:	n/a	n/a
41	JUND	chr11:93140982-93141348	K562	blood:	n/a	n/a
42	JUND	chr11:93137233-93137302	H1-hESC	embryonic stem cell:	n/a	n/a
43	JUND	chr11:93129535-93129558	H1-hESC	embryonic stem cell:	n/a	n/a
44	KAP1	chr11:93121444-93121704	K562	blood:	n/a	n/a
45	KAP1	chr11:93114483-93114865	K562	blood:	n/a	n/a
46	KAP1	chr11:93145828-93146215	K562	blood:	n/a	n/a
47	MAFF	chr11:93139363-93139622	K562	blood:	n/a	n/a
48	MAFF	chr11:93144904-93145236	HepG2	liver:	n/a	chr11:93145052-93145070
49	MAFF	chr11:93126149-93126340	K562	blood:	n/a	n/a
50	MAFF	chr11:93129390-93129590	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93143810-93143860	GM06990	blood:	n/a
2	chr11:93143810-93143860	BE2_C	brain:	n/a
3	chr11:93143810-93143860	PrEC	prostate:	n/a
4	chr11:93143810-93143860	AoSMC	blood vessel:	n/a
5	chr11:93143810-93143860	NT2-D1	testis:	n/a
6	chr11:93143810-93143860	PFSK-1	brain:	n/a
7	chr11:93143810-93143860	T-47D	breast:	n/a
8	chr11:93143810-93143860	CMK	blood:	n/a
9	chr11:93143810-93143860	HNPCEpiC	eye:	n/a
10	chr11:93143810-93143860	HCF	heart:	n/a
11	chr11:93143810-93143860	SK-N-MC	brain:	n/a
12	chr11:93143810-93143860	HEEpiC	esophagus:	n/a
13	chr11:93143810-93143860	HMEC	breast:	n/a
14	chr11:93143810-93143860	LNCaP	prostate:	n/a
15	chr11:93143810-93143860	Hela-S3	cervix:	n/a
16	chr11:93143810-93143860	GM12891	blood:	n/a
17	chr11:93143810-93143860	AG04450	lung:	fetal
18	chr11:93143810-93143860	AG09319	gingival:	n/a
19	chr11:93143810-93143860	H1-hESC	embryonic stem cell:	embryo
20	chr11:93143810-93143860	ProgFib	skin:	n/a
21	chr11:93143810-93143860	SK-N-SH	brain:	n/a
22	chr11:93143810-93143860	GM19239	blood:	n/a
23	chr11:93143810-93143860	HAEpiC	amniotic membrane:	n/a
24	chr11:93143810-93143860	HL-60	blood:	n/a
25	chr11:93143810-93143860	Jurkat	blood:	n/a
26	chr11:93143810-93143860	HIPEpiC	eye:	n/a
27	chr11:93143810-93143860	PANC-1	pancreas:	n/a
28	chr11:93143810-93143860	A549	lung:	n/a
29	chr11:93143810-93143860	HRCEpiC	kidney:	n/a
30	chr11:93143810-93143860	HepG2	liver:	n/a
31	chr11:93143810-93143860	HUVEC	blood vessel:	n/a
32	chr11:93143810-93143860	HCPEpiC	choroid plexus:	n/a
33	chr11:93143810-93143860	HRE	kidney:	n/a
34	chr11:93143810-93143860	NB4	blood:	n/a
35	chr11:93143810-93143860	IMR90	lung:	fetal
36	chr11:93143810-93143860	K562	blood:	n/a
37	chr11:93143810-93143860	RPTEC	kidney:	n/a
38	chr11:93143810-93143860	NHBE	bronchial:	n/a
39	chr11:93143810-93143860	AG04449	skin:	fetal
40	chr11:93143810-93143860	ECC-1	luminal epithelium:	n/a
41	chr11:93143810-93143860	AG10803	skin:	n/a
42	chr11:93143810-93143860	GM12878	blood:	n/a
43	chr11:93143810-93143860	NHDF-neo	bronchial:	n/a
44	chr11:93143810-93143860	Hepatocyte	liver:	n/a
45	chr11:93143810-93143860	NH-A	brain:	n/a
46	chr11:93143810-93143860	SK-N-SH_RA	brain:	n/a
47	chr11:93143810-93143860	BJ	skin:	n/a
48	chr11:93143810-93143860	Caco-2	colon:	n/a
49	chr11:93143810-93143860	U87	brain:	n/a
50	chr11:93143810-93143860	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:93135720..93137774-chr11:93142733..93145703,2	K562	blood:
2	chr11:93139427..93141896-chr11:93145102..93147867,3	K562	blood:
3	chr11:93139427..93141388-chr11:93145450..93147867,2	K562	blood:

Variant related genes	Relation type
ENSG00000221565	TF binding region
CCDC67	TF binding region
ENSG00000221565	CpG island
CCDC67	CpG island
ENSG00000221565	chromatin interactions
ENSG00000165325	chromatin interactions

Extended variants
information (count: 1164 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1164 , 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	rs12292127	chr11:93114111-93114112	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555781129	chr11:93114131-93114132	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs11820713	chr11:93114156-93114157	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs367624238	chr11:93114204-93114205	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556279213	chr11:93114217-93114218	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs181031182	chr11:93114250-93114251	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs535280603	chr11:93114277-93114278	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs555108559	chr11:93114397-93114398	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs111645830	chr11:93114400-93114401	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs12805883	chr11:93114439-93114440	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs577609984	chr11:93114471-93114472	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539884198	chr11:93114477-93114478	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2925363	chr11:93114521-93114522	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557754217	chr11:93114544-93114545	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs576648137	chr11:93114553-93114554	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs148014847	chr11:93114565-93114566	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562091186	chr11:93114585-93114586	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs574245361	chr11:93114639-93114640	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554010537	chr11:93114645-93114646	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs377227015	chr11:93114679-93114680	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs541374914	chr11:93114875-93114876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12275682	chr11:93114933-93114934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533364042	chr11:93114958-93114959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572923986	chr11:93114976-93114977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563829683	chr11:93114988-93114989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561517441	chr11:93115006-93115007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531340287	chr11:93115088-93115089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549345042	chr11:93115159-93115160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11020294	chr11:93115163-93115164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs535709185	chr11:93115191-93115192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185469741	chr11:93115242-93115243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547386873	chr11:93115302-93115303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565823321	chr11:93115305-93115306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190828061	chr11:93115306-93115307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558015254	chr11:93115311-93115312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543261659	chr11:93115349-93115350	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs11020295	chr11:93115353-93115354	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs542682399	chr11:93115377-93115378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79900783	chr11:93115378-93115379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs72643375	chr11:93115447-93115448	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573960033	chr11:93115504-93115505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541662658	chr11:93115537-93115538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74592346	chr11:93115582-93115583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs578225877	chr11:93115623-93115624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545174987	chr11:93115715-93115716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545722485	chr11:93115756-93115757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563572839	chr11:93115767-93115768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565438695	chr11:93115832-93115833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532770162	chr11:93115834-93115835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80276632	chr11:93115877-93115878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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	22037309	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93106200-93117200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:93106400-93116600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:93111200-93128200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:93111400-93116400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:93116400-93116600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:93116400-93116600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr11:93116600-93116800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:93116600-93117400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr11:93116600-93122400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr11:93116800-93126000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr11:93117200-93117600	Enhancers	NHEK	skin
12	chr11:93117200-93117800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:93117400-93117600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr11:93117400-93117800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr11:93117400-93117800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr11:93118600-93124600	Weak transcription	Aorta	Aorta
17	chr11:93121000-93130200	Weak transcription	K562	blood
18	chr11:93122400-93123200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr11:93122800-93123200	Enhancers	Fetal Heart	heart
20	chr11:93122800-93123400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:93123200-93127800	Weak transcription	Fetal Heart	heart
22	chr11:93125000-93128600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr11:93125200-93128600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr11:93125400-93126200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr11:93125400-93127400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:93125400-93128000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:93125400-93128400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr11:93125600-93128600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr11:93125800-93126200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr11:93126000-93126200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr11:93126000-93126800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:93126000-93126800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr11:93126000-93127400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:93126000-93128000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:93126000-93128600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:93126200-93126800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr11:93126200-93126800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr11:93126200-93127200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr11:93126200-93127800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr11:93126400-93127600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr11:93126400-93127800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr11:93126400-93130000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:93126600-93127000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr11:93126600-93128400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr11:93126800-93129800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr11:93126800-93145200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:93127200-93128400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr11:93127400-93129600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:93127400-93129800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr11:93127600-93127800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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