Variant report

Variant	nsv1030631
Chromosome Location	chr6:63111798-63225697
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	BHLHE40	chr6:63115576-63115579	GM12878	blood:	n/a	n/a
2	CEBPB	chr6:63184719-63185081	H1-hESC	embryonic stem cell:	n/a	chr6:63184880-63184891
3	CEBPB	chr6:63137661-63138000	HepG2	liver:	n/a	chr6:63137839-63137850
4	CEBPB	chr6:63184708-63185066	IMR90	lung:	n/a	chr6:63184880-63184891
5	CEBPB	chr6:63195691-63195891	A549	lung:	n/a	chr6:63195781-63195792
6	CEBPB	chr6:63184713-63185024	A549	lung:	n/a	chr6:63184880-63184891
7	CEBPB	chr6:63165587-63165869	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:63200359-63200638	HepG2	liver:	n/a	chr6:63200482-63200495 chr6:63200482-63200493 chr6:63200484-63200495 chr6:63200482-63200495 chr6:63200482-63200495 chr6:63200484-63200495
9	CEBPB	chr6:63184778-63185113	ECC-1	luminal epithelium:	n/a	chr6:63184880-63184891
10	CEBPB	chr6:63216022-63216260	HepG2	liver:	n/a	chr6:63216135-63216146 chr6:63216135-63216148 chr6:63216132-63216149
11	CEBPB	chr6:63184716-63185068	HepG2	liver:	n/a	chr6:63184880-63184891
12	CEBPB	chr6:63176620-63176650	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:63189520-63189747	A549	lung:	n/a	chr6:63189603-63189614 chr6:63189604-63189615 chr6:63189602-63189619 chr6:63189603-63189616
14	CEBPB	chr6:63195619-63195937	IMR90	lung:	n/a	chr6:63195781-63195792
15	CEBPB	chr6:63137819-63137947	A549	lung:	n/a	chr6:63137839-63137850
16	CEBPB	chr6:63195602-63195944	HepG2	liver:	n/a	chr6:63195781-63195792
17	CEBPB	chr6:63200426-63200489	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr6:63184706-63185048	ECC-1	luminal epithelium:	n/a	chr6:63184880-63184891
19	CEBPB	chr6:63184725-63185043	Hela-S3	cervix:	n/a	chr6:63184880-63184891
20	CEBPB	chr6:63186918-63187244	HepG2	liver:	n/a	chr6:63187071-63187082
21	CEBPB	chr6:63209671-63210000	HepG2	liver:	n/a	chr6:63209812-63209823
22	CEBPB	chr6:63135857-63136005	K562	blood:	n/a	chr6:63135923-63135932 chr6:63135921-63135934 chr6:63135923-63135932 chr6:63135923-63135932 chr6:63135923-63135932 chr6:63135923-63135934
23	CEBPB	chr6:63195679-63195883	H1-hESC	embryonic stem cell:	n/a	chr6:63195781-63195792
24	CEBPB	chr6:63139603-63139831	HepG2	liver:	n/a	chr6:63139771-63139782
25	CEBPB	chr6:63189473-63189777	HepG2	liver:	n/a	chr6:63189603-63189614 chr6:63189604-63189615 chr6:63189602-63189619 chr6:63189603-63189616
26	CTCF	chr6:63120770-63120842	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr6:63191682-63191733	GM12878	blood:	n/a	chr6:63191698-63191716
28	CTCF	chr6:63191629-63191763	LNCaP	prostate:	n/a	chr6:63191698-63191716
29	CTCF	chr6:63119223-63119236	GM10248	blood:	n/a	n/a
30	CTCF	chr6:63159000-63159152	LNCaP	prostate:	n/a	n/a
31	CTCF	chr6:63191531-63191813	MCF-7	breast:	n/a	chr6:63191698-63191716
32	CTCF	chr6:63159012-63159193	GM12878	blood:	n/a	n/a
33	CTCF	chr6:63159014-63159149	LNCaP	prostate:	n/a	n/a
34	CTCF	chr6:63123877-63123967	GM10248	blood:	n/a	n/a
35	CTCF	chr6:63191646-63191749	LNCaP	prostate:	n/a	chr6:63191698-63191716
36	CTCF	chr6:63217360-63217510	GM12872	blood:	n/a	chr6:63217373-63217394 chr6:63217378-63217396
37	E2F4	chr6:63196095-63196295	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr6:63223120-63223262	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr6:63224669-63224857	MCF10A-Er-Src	breast:	n/a	n/a
40	EP300	chr6:63189488-63190150	ECC-1	luminal epithelium:	n/a	chr6:63189601-63189615
41	ESR1	chr6:63222794-63223220	ECC-1	luminal epithelium:	n/a	chr6:63222958-63222975 chr6:63222959-63222976 chr6:63222959-63222974
42	ESR1	chr6:63222744-63223163	ECC-1	luminal epithelium:	n/a	chr6:63222958-63222975 chr6:63222959-63222976 chr6:63222959-63222974
43	ESR1	chr6:63222827-63223068	ECC-1	luminal epithelium:	n/a	chr6:63222958-63222975 chr6:63222959-63222976 chr6:63222959-63222974
44	ESR1	chr6:63222695-63223315	ECC-1	luminal epithelium:	n/a	chr6:63222958-63222975 chr6:63222959-63222976 chr6:63222959-63222974
45	ESR1	chr6:63189692-63190123	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr6:63222792-63223176	ECC-1	luminal epithelium:	n/a	chr6:63222958-63222975 chr6:63222959-63222976 chr6:63222959-63222974
47	FOS	chr6:63185088-63185270	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr6:63217176-63217293	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr6:63217129-63217255	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr6:63217180-63217335	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63157784-63157834	ovcar-3	ovarian:	n/a
2	chr6:63157784-63157834	Caco-2	colon:	n/a
3	chr6:63157784-63157834	IMR90	lung:	fetal
4	chr6:63157784-63157834	HCM	heart:	n/a
5	chr6:63157784-63157834	AG09309	skin:	n/a
6	chr6:63157784-63157834	HepG2	liver:	n/a
7	chr6:63157784-63157834	HEEpiC	esophagus:	n/a
8	chr6:63157784-63157834	HNPCEpiC	eye:	n/a
9	chr6:63157784-63157834	MCF-7	breast:	n/a
10	chr6:63157784-63157834	AG04449	skin:	fetal
11	chr6:63157784-63157834	HL-60	blood:	n/a
12	chr6:63157784-63157834	ProgFib	skin:	n/a
13	chr6:63157784-63157834	HRE	kidney:	n/a
14	chr6:63157784-63157834	HIPEpiC	eye:	n/a
15	chr6:63157784-63157834	HCPEpiC	choroid plexus:	n/a
16	chr6:63157784-63157834	NB4	blood:	n/a
17	chr6:63157784-63157834	NHBE	bronchial:	n/a
18	chr6:63157784-63157834	HMEC	breast:	n/a
19	chr6:63157784-63157834	K562	blood:	n/a
20	chr6:63157784-63157834	SK-N-MC	brain:	n/a
21	chr6:63157784-63157834	BE2_C	brain:	n/a
22	chr6:63157784-63157834	HUVEC	blood vessel:	n/a
23	chr6:63157784-63157834	Jurkat	blood:	n/a
24	chr6:63157784-63157834	LNCaP	prostate:	n/a
25	chr6:63157784-63157834	GM19239	blood:	n/a
26	chr6:63157784-63157834	U87	brain:	n/a
27	chr6:63157784-63157834	HRCEpiC	kidney:	n/a
28	chr6:63157784-63157834	MCF10A-Er-Src	breast:	n/a
29	chr6:63157784-63157834	HEK293	kidney:	embryo
30	chr6:63157784-63157834	GM06990	blood:	n/a
31	chr6:63157784-63157834	H1-hESC	embryonic stem cell:	embryo
32	chr6:63157784-63157834	Hepatocyte	liver:	n/a
33	chr6:63157784-63157834	AG04450	lung:	fetal
34	chr6:63157784-63157834	Hela-S3	cervix:	n/a
35	chr6:63157784-63157834	T-47D	breast:	n/a
36	chr6:63157784-63157834	HAEpiC	amniotic membrane:	n/a
37	chr6:63157784-63157834	SK-N-SH_RA	brain:	n/a
38	chr6:63157784-63157834	AoSMC	blood vessel:	n/a
39	chr6:63157784-63157834	SK-N-SH	brain:	n/a
40	chr6:63157784-63157834	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:63157784-63157834	NT2-D1	testis:	n/a
42	chr6:63157784-63157834	GM12891	blood:	n/a
43	chr6:63157784-63157834	AG10803	skin:	n/a
44	chr6:63157784-63157834	BJ	skin:	n/a
45	chr6:63157784-63157834	GM12878	blood:	n/a
46	chr6:63157784-63157834	HRPEpiC	eye:	n/a
47	chr6:63157784-63157834	SKMC	muscle:	n/a
48	chr6:63157784-63157834	ECC-1	luminal epithelium:	n/a
49	chr6:63157784-63157834	SAEC	small airway:	n/a
50	chr6:63157784-63157834	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:
2	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KHDRBS2-2	chr6:63170845-63171408	NONHSAT113333

Variant related genes	Relation type
ENSG00000216859	TF binding region
ENSG00000216859	CpG island

Extended variants
information (count: 1447 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1447 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2492803	chr6:63111798-63111799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540258386	chr6:63111846-63111847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561731042	chr6:63111888-63111889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529386220	chr6:63111911-63111912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564014923	chr6:63111915-63111916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148470499	chr6:63111919-63111920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533372088	chr6:63111940-63111941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551916441	chr6:63111971-63111972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141196655	chr6:63111997-63111998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541308487	chr6:63112001-63112002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567075786	chr6:63112020-63112021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534477128	chr6:63112106-63112107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549035640	chr6:63112110-63112111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567263627	chr6:63112145-63112146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370949803	chr6:63112223-63112224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141649784	chr6:63112240-63112241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371770841	chr6:63112249-63112250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs13218380	chr6:63112359-63112360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189723686	chr6:63112417-63112418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570003871	chr6:63112444-63112445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369318205	chr6:63112445-63112446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115249971	chr6:63112455-63112456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182374073	chr6:63112474-63112475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531637730	chr6:63112499-63112500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77713453	chr6:63112502-63112503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572043380	chr6:63112506-63112507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542502263	chr6:63112563-63112564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561792338	chr6:63112600-63112601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573702678	chr6:63112601-63112602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533105254	chr6:63112602-63112603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187809569	chr6:63112616-63112617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577871402	chr6:63112621-63112622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533437666	chr6:63112641-63112642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12189946	chr6:63112644-63112645	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs559175839	chr6:63112658-63112659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372217064	chr6:63112694-63112695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549557196	chr6:63112717-63112718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549697149	chr6:63112718-63112719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567914840	chr6:63112719-63112720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114495692	chr6:63112733-63112734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150507890	chr6:63112745-63112746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571279664	chr6:63112776-63112777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563154205	chr6:63112779-63112780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376920708	chr6:63112791-63112792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143042958	chr6:63112793-63112794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76068567	chr6:63112797-63112798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553724222	chr6:63112834-63112835	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs565533547	chr6:63112836-63112837	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs376497188	chr6:63112850-63112851	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs115682116	chr6:63112867-63112868	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Lung cancer	19547694	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63111000-63113200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:63111400-63111800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:63111800-63112800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:63112800-63113000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:63113000-63113200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:63113200-63113600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:63113200-63113600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:63113600-63115600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:63146400-63149000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:63149000-63149200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:63149200-63149800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:63149800-63151000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:63151200-63151400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:63151400-63155400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:63155400-63155800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:63155400-63155800	ZNF genes & repeats	Pancreas	Pancrea
17	chr6:63156400-63157000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:63156600-63157200	Enhancers	Primary B cells from peripheral blood	blood
19	chr6:63156600-63157800	Enhancers	Primary B cells from cord blood	blood
20	chr6:63157000-63158000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:63157200-63158000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr6:63157600-63158000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr6:63157600-63158000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:63157600-63158000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:63157600-63158200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr6:63166200-63166600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:63174400-63175800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:63174800-63175600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:63187800-63188400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr6:63188200-63188400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr6:63188400-63188600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr6:63188400-63189400	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr6:63188400-63189400	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr6:63188600-63189600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:63189400-63190200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr6:63189400-63190400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:63189600-63190000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:63189600-63190000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:63189600-63190200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:63189800-63190200	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:63190000-63190400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr6:63190200-63190400	Enhancers	Fetal Intestine Small	intestine
43	chr6:63190400-63191800	Weak transcription	Fetal Intestine Small	intestine
44	chr6:63191800-63193000	Enhancers	Fetal Intestine Small	intestine
45	chr6:63201200-63201400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr6:63202200-63202600	Active TSS	HepG2	liver
47	chr6:63210600-63217400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:63217400-63217600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:63220200-63220400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:63220600-63225000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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