Variant report

Variant	nsv949349
Chromosome Location	chr11:56371633-56593610
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	chr11:56392054-56392405	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:56392115-56392370	K562	blood:	n/a	n/a
3	ATF1	chr11:56439580-56439612	K562	blood:	n/a	n/a
4	ATF1	chr11:56416106-56416186	K562	blood:	n/a	n/a
5	ATF2	chr11:56392130-56392439	GM12878	blood:	n/a	n/a
6	ATF2	chr11:56427149-56427629	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:56427208-56427626	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr11:56483721-56484112	GM12878	blood:	n/a	n/a
9	ATF3	chr11:56517803-56518031	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr11:56392162-56392399	K562	blood:	n/a	n/a
11	BATF	chr11:56390864-56391136	GM12878	blood:	n/a	chr11:56390998-56391009
12	BATF	chr11:56392134-56392479	GM12878	blood:	n/a	chr11:56392263-56392274 chr11:56392281-56392292
13	BATF	chr11:56392069-56392469	GM12878	blood:	n/a	chr11:56392263-56392274 chr11:56392281-56392292
14	BATF	chr11:56483821-56484012	GM12878	blood:	n/a	chr11:56483931-56483942
15	BATF	chr11:56483790-56484093	GM12878	blood:	n/a	chr11:56483931-56483942
16	BCL11A	chr11:56392083-56392500	GM12878	blood:	n/a	n/a
17	BCL11A	chr11:56392145-56392429	GM12878	blood:	n/a	n/a
18	BCL11A	chr11:56427166-56427558	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr11:56427204-56427533	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:56464859-56465477	HepG2	liver:	n/a	chr11:56465014-56465025
21	CEBPB	chr11:56446979-56447090	H1-hESC	embryonic stem cell:	n/a	chr11:56447028-56447039
22	CEBPB	chr11:56399444-56399543	K562	blood:	n/a	chr11:56399532-56399543
23	CEBPB	chr11:56568845-56568849	A549	lung:	n/a	n/a
24	CEBPB	chr11:56446972-56447172	HepG2	liver:	n/a	chr11:56447028-56447039
25	CEBPB	chr11:56484043-56484454	MCF-7	breast:	n/a	chr11:56484335-56484346
26	CEBPB	chr11:56588032-56588235	HepG2	liver:	n/a	chr11:56588126-56588137
27	CEBPB	chr11:56446950-56447140	A549	lung:	n/a	chr11:56447028-56447039
28	CEBPB	chr11:56517644-56518052	HepG2	liver:	n/a	chr11:56517867-56517884
29	CEBPB	chr11:56434199-56434512	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:56568286-56568976	HepG2	liver:	n/a	chr11:56568406-56568417 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568405-56568416 chr11:56568832-56568845 chr11:56568405-56568418
31	CEBPB	chr11:56565598-56565920	A549	lung:	n/a	n/a
32	CEBPB	chr11:56434211-56434516	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:56517620-56518023	HepG2	liver:	n/a	chr11:56517867-56517884
34	CEBPB	chr11:56517722-56518003	MCF-7	breast:	n/a	chr11:56517867-56517884
35	CEBPB	chr11:56517651-56518070	H1-hESC	embryonic stem cell:	n/a	chr11:56517867-56517884
36	CEBPB	chr11:56464932-56465171	A549	lung:	n/a	chr11:56465014-56465025
37	CEBPB	chr11:56517634-56517959	IMR90	lung:	n/a	chr11:56517867-56517884
38	CEBPB	chr11:56434205-56434531	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:56399397-56399674	IMR90	lung:	n/a	chr11:56399532-56399543
40	CEBPB	chr11:56517717-56517991	A549	lung:	n/a	chr11:56517867-56517884
41	CEBPB	chr11:56517810-56517951	K562	blood:	n/a	chr11:56517867-56517884
42	CEBPB	chr11:56434237-56434514	A549	lung:	n/a	n/a
43	CEBPB	chr11:56568721-56568994	IMR90	lung:	n/a	chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568832-56568845
44	CEBPB	chr11:56437710-56437976	A549	lung:	n/a	chr11:56437842-56437853
45	CEBPB	chr11:56399354-56399655	HepG2	liver:	n/a	chr11:56399532-56399543
46	CEBPB	chr11:56484117-56484430	A549	lung:	n/a	chr11:56484335-56484346
47	CEBPB	chr11:56488019-56488253	HepG2	liver:	n/a	chr11:56488133-56488144
48	CEBPB	chr11:56437737-56437962	HepG2	liver:	n/a	chr11:56437842-56437853
49	CEBPB	chr11:56545897-56545901	A549	lung:	n/a	n/a
50	CEBPB	chr11:56517761-56517904	HepG2	liver:	n/a	chr11:56517867-56517884

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56587256-56587306	BE2_C	brain:	n/a
2	chr11:56410673-56410723	HRPEpiC	eye:	n/a
3	chr11:56466731-56466781	HRPEpiC	eye:	n/a
4	chr11:56587256-56587306	BE2_C	brain:	n/a
5	chr11:56410673-56410723	HRPEpiC	eye:	n/a
6	chr11:56466731-56466781	HRPEpiC	eye:	n/a
7	chr11:56545039-56545089	ovcar-3	ovarian:	n/a
8	chr11:56430801-56430851	HNPCEpiC	eye:	n/a
9	chr11:56439354-56439404	SK-N-SH_RA	brain:	n/a
10	chr11:56457571-56457621	HMEC	breast:	n/a
11	chr11:56381677-56381727	MCF-7	breast:	n/a
12	chr11:56457812-56457862	HCT-116	colon:	n/a
13	chr11:56430801-56430851	NT2-D1	testis:	n/a
14	chr11:56428702-56428752	HEK293	kidney:	embryo
15	chr11:56468348-56468398	HEEpiC	esophagus:	n/a
16	chr11:56411376-56411426	T-47D	breast:	n/a
17	chr11:56439354-56439404	NT2-D1	testis:	n/a
18	chr11:56411376-56411426	HRPEpiC	eye:	n/a
19	chr11:56431525-56431575	HepG2	liver:	n/a
20	chr11:56587595-56587645	LNCaP	prostate:	n/a
21	chr11:56381067-56381117	NT2-D1	testis:	n/a
22	chr11:56381677-56381727	Caco-2	colon:	n/a
23	chr11:56430801-56430851	PFSK-1	brain:	n/a
24	chr11:56457571-56457621	NHDF-neo	bronchial:	n/a
25	chr11:56545039-56545089	HCT-116	colon:	n/a
26	chr11:56392848-56392898	HIPEpiC	eye:	n/a
27	chr11:56457777-56457827	PANC-1	pancreas:	n/a
28	chr11:56587595-56587645	NHBE	bronchial:	n/a
29	chr11:56439354-56439404	SK-N-SH	brain:	n/a
30	chr11:56467944-56467994	GM19239	blood:	n/a
31	chr11:56468348-56468398	HCF	heart:	n/a
32	chr11:56587256-56587306	GM12878	blood:	n/a
33	chr11:56545039-56545089	BJ	skin:	n/a
34	chr11:56511248-56511298	PrEC	prostate:	n/a
35	chr11:56439354-56439404	BJ	skin:	n/a
36	chr11:56380614-56380664	AG04449	skin:	fetal
37	chr11:56457571-56457621	HEEpiC	esophagus:	n/a
38	chr11:56381124-56381174	A549	lung:	n/a
39	chr11:56545039-56545089	SK-N-SH_RA	brain:	n/a
40	chr11:56409533-56409583	HUVEC	blood vessel:	n/a
41	chr11:56381124-56381174	BE2_C	brain:	n/a
42	chr11:56511248-56511298	AG04449	skin:	fetal
43	chr11:56457812-56457862	AG04449	skin:	fetal
44	chr11:56457812-56457862	PANC-1	pancreas:	n/a
45	chr11:56457812-56457862	HMEC	breast:	n/a
46	chr11:56466578-56466628	HRCEpiC	kidney:	n/a
47	chr11:56457571-56457621	A549	lung:	n/a
48	chr11:56411376-56411426	Hela-S3	cervix:	n/a
49	chr11:56457571-56457621	ProgFib	skin:	n/a
50	chr11:56587256-56587306	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:56402833..56405618-chr11:56410277..56412823,2	K562	blood:
2	chr11:56288968..56289520-chr11:56550857..56551450,2	MCF-7	breast:
3	chr11:56391852..56392531-chr11:56550628..56551135,2	MCF-7	breast:
4	chr11:56562414..56565346-chr11:56565920..56568664,2	K562	blood:
5	chr11:56489679..56491375-chr11:56501753..56504134,2	K562	blood:
6	chr11:56415487..56417805-chr11:56427719..56429875,2	K562	blood:
7	chr11:56562414..56565346-chr11:56565920..56568664,2	K562	blood:
8	chr11:56415487..56417805-chr11:56427719..56429875,2	K562	blood:
9	chr11:56391852..56392531-chr11:56550628..56551135,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR9G4-1	chr11:56570001-56570030	NONHSAT021395
2	lnc-OR9G1-1	chr11:56457941-56458199	NONHSAT021391
3	lnc-OR5AR1-1	chr11:56395143-56395303	ucscGeneNc_uc001njj_1
4	lnc-OR9G4-1	chr11:56570184-56570284	NONHSAT021395
5	lnc-OR5AR1-1	chr11:56399649-56402130	ucscGeneNc_uc001njj_1
6	lnc-OR9G4-1	chr11:56587057-56587123	NONHSAT021395
7	lnc-OR5AR1-1	chr11:56372530-56372667	ucscGeneNc_uc001njj_1
8	lnc-OR9G4-1	chr11:56569552-56569670	NONHSAT021395

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6128	chr11:56511419-56511437	MIMAT0024611

Variant related genes	Relation type
OR9G2P	TF binding region
OR5G3	TF binding region
ENSG00000254953	TF binding region
OR2AH1P	TF binding region
OR9G3P	TF binding region
OR5AM1P	TF binding region
ENSG00000263546	TF binding region
OR5G5P	TF binding region
OR5G4P	TF binding region
OR9G1	TF binding region
OR5G1P	TF binding region
OR5M12P	TF binding region
OR5M1	TF binding region
OR5AP1P	TF binding region
ENSG00000238041	TF binding region
OR5AR1	TF binding region
OR9G4	TF binding region
OR5AP2	TF binding region
OR9G2P	CpG island
OR5G3	CpG island
ENSG00000254953	CpG island
OR2AH1P	CpG island
OR9G3P	CpG island
OR5AM1P	CpG island
ENSG00000263546	CpG island
OR5G5P	CpG island
OR5G4P	CpG island
OR9G1	CpG island
OR5G1P	CpG island
OR5M12P	CpG island
OR5M1	CpG island
OR5AP1P	CpG island
ENSG00000238041	CpG island
OR5AR1	CpG island
OR9G4	CpG island
OR5AP2	CpG island
ENSG00000254953	chromatin interactions
ENSG00000263546	chromatin interactions

Extended variants
information (count: 4011 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4011 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574859891	chr11:56372609-56372610	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs546496205	chr11:56372636-56372637	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs564575262	chr11:56372638-56372639	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs61903268	chr11:56381067-56381068	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532664161	chr11:56381068-56381069	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs558738033	chr11:56381072-56381073	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs547611968	chr11:56381143-56381144	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs150454098	chr11:56381170-56381171	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs144076179	chr11:56381554-56381555	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs576076146	chr11:56381576-56381577	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183857443	chr11:56381611-56381612	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs188277270	chr11:56381643-56381644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs532700194	chr11:56381674-56381675	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs192975450	chr11:56381698-56381699	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs182820764	chr11:56381734-56381735	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs559525144	chr11:56381780-56381781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs530194689	chr11:56381783-56381784	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs12276247	chr11:56381809-56381810	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs186871218	chr11:56381818-56381819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs543678754	chr11:56387200-56387201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369778533	chr11:56387208-56387209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142606964	chr11:56387217-56387218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532527196	chr11:56387231-56387232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115009228	chr11:56387269-56387270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76114746	chr11:56387293-56387294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572139771	chr11:56387306-56387307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182552368	chr11:56387307-56387308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548308920	chr11:56387337-56387338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570007452	chr11:56387371-56387372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146000116	chr11:56387387-56387388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556458999	chr11:56387390-56387391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186879338	chr11:56387397-56387398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112408192	chr11:56387422-56387423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553912798	chr11:56387429-56387430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572076944	chr11:56387498-56387499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534288871	chr11:56387535-56387536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536308128	chr11:56387558-56387559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557757992	chr11:56387586-56387587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554287900	chr11:56387617-56387618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138775039	chr11:56387716-56387717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78876220	chr11:56387722-56387723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543321487	chr11:56387732-56387733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563283274	chr11:56387772-56387773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12418301	chr11:56387773-56387774	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs577118029	chr11:56387775-56387776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190601181	chr11:56387783-56387784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541291967	chr11:56387794-56387795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184095011	chr11:56387837-56387838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530158429	chr11:56387848-56387849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548619103	chr11:56387857-56387858	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56387200-56388000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr11:56388000-56392200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr11:56391800-56392800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr11:56392000-56392600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr11:56392000-56392600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:56392000-56392800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr11:56392000-56392800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:56392200-56392600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr11:56392200-56392600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:56392200-56392800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr11:56392400-56392600	Flanking Active TSS	A549	lung
12	chr11:56392600-56392800	Enhancers	A549	lung
13	chr11:56409200-56409800	Active TSS	Brain Substantia Nigra	brain
14	chr11:56417400-56419000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:56418600-56419200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr11:56419200-56427200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:56426200-56427000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:56426600-56426800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr11:56426600-56427000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr11:56426600-56427000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr11:56426600-56427000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr11:56426600-56427400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr11:56426600-56428000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:56426800-56427000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr11:56427000-56427200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr11:56427000-56427400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr11:56427000-56427600	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr11:56427000-56427600	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr11:56427000-56427800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:56427200-56427600	Active TSS	H1 Cell Line	embryonic stem cell
31	chr11:56427200-56427600	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr11:56427200-56427600	Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr11:56427200-56427600	Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr11:56427400-56427800	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr11:56427400-56427800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:56427400-56427800	Active TSS	H9 Cell Line	embryonic stem cell
37	chr11:56427400-56428000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr11:56427400-56428000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr11:56427600-56427800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
40	chr11:56427600-56427800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr11:56427600-56427800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr11:56427600-56428000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:56427600-56428000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr11:56427600-56428200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr11:56427600-56428200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr11:56427600-56428400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr11:56427600-56428800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:56427800-56428000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr11:56427800-56428000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr11:56427800-56428000	Active TSS	iPS-20b Cell Line	embryonic stem cell

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