Variant report

Variant	nsv887820
Chromosome Location	chr7:19378959-19448729
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	ATF3	chr7:19444572-19445053	A549	lung:	n/a	n/a
2	ATF3	chr7:19401699-19402094	HCT-116	colon:	n/a	n/a
3	ATF3	chr7:19444493-19444867	A549	lung:	n/a	n/a
4	BCL3	chr7:19444394-19444990	A549	lung:	n/a	chr7:19444641-19444650
5	BHLHE40	chr7:19422585-19422633	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:19437440-19437816	GM12878	blood:	n/a	n/a
7	CBX3	chr7:19444505-19444941	HCT-116	colon:	n/a	n/a
8	CEBPB	chr7:19406922-19407130	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:19444511-19445576	Hela-S3	cervix:	n/a	chr7:19445336-19445347
10	CEBPB	chr7:19401780-19402111	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:19379888-19380200	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:19446082-19446303	A549	lung:	n/a	n/a
13	CEBPB	chr7:19444404-19445628	A549	lung:	n/a	chr7:19445336-19445347
14	CEBPB	chr7:19379927-19380128	A549	lung:	n/a	n/a
15	CEBPB	chr7:19379880-19380108	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:19444478-19444920	A549	lung:	n/a	n/a
17	CEBPB	chr7:19445197-19445390	K562	blood:	n/a	chr7:19445336-19445347
18	CEBPB	chr7:19444429-19445027	HCT-116	colon:	n/a	n/a
19	CEBPB	chr7:19445196-19445500	A549	lung:	n/a	chr7:19445336-19445347
20	CEBPB	chr7:19444492-19445539	IMR90	lung:	n/a	chr7:19445336-19445347
21	CEBPB	chr7:19431952-19432321	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:19401785-19402098	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:19445213-19445455	HepG2	liver:	n/a	chr7:19445336-19445347
24	CHD2	chr7:19444604-19444999	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr7:19417480-19417630	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr7:19420200-19420350	GM12871	blood:	n/a	n/a
27	CTCF	chr7:19424104-19424180	Gliobla	brain:	n/a	n/a
28	CTCF	chr7:19414707-19414785	ProgFib	skin:	n/a	n/a
29	CTCF	chr7:19438560-19438710	SK-N-SH_RA	brain:	n/a	n/a
30	CUX1	chr7:19437572-19437772	GM12878	blood:	n/a	n/a
31	E2F4	chr7:19444475-19444985	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr7:19426135-19426335	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr7:19400767-19401001	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr7:19401473-19402035	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr7:19437513-19437833	GM12878	blood:	n/a	n/a
36	EGR1	chr7:19444335-19444860	HCT-116	colon:	n/a	chr7:19444572-19444583 chr7:19444570-19444585
37	EGR1	chr7:19444360-19444973	HCT-116	colon:	n/a	chr7:19444572-19444583 chr7:19444570-19444585
38	ELK1	chr7:19447125-19447233	GM12878	blood:	n/a	n/a
39	EP300	chr7:19444537-19444987	Hela-S3	cervix:	n/a	chr7:19444641-19444650
40	EP300	chr7:19444357-19445176	A549	lung:	n/a	chr7:19444641-19444650
41	EP300	chr7:19447044-19447155	GM12878	blood:	n/a	n/a
42	EP300	chr7:19444509-19444813	SK-N-SH_RA	brain:	n/a	chr7:19444641-19444650
43	EP300	chr7:19445189-19445513	Hela-S3	cervix:	n/a	n/a
44	EP300	chr7:19444530-19444846	SK-N-SH_RA	brain:	n/a	chr7:19444641-19444650
45	EP300	chr7:19444376-19445548	SK-N-SH	brain:	n/a	chr7:19444641-19444650
46	EP300	chr7:19444309-19445094	A549	lung:	n/a	chr7:19444641-19444650
47	EP300	chr7:19406047-19406052	GM12878	blood:	n/a	n/a
48	FOS	chr7:19444453-19444891	MCF10A-Er-Src	breast:	n/a	chr7:19444676-19444686 chr7:19444639-19444650 chr7:19444639-19444651 chr7:19444640-19444649
49	FOS	chr7:19401746-19402123	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:19417254-19417376	MCF10A-Er-Src	breast:	n/a	chr7:19417310-19417319 chr7:19417327-19417335 chr7:19417326-19417336 chr7:19417328-19417335 chr7:19417327-19417335 chr7:19417326-19417336 chr7:19417311-19417320 chr7:19417326-19417336 chr7:19417326-19417336 chr7:19417312-19417321 chr7:19417325-19417337

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19408343-19408393	HCM	heart:	n/a
2	chr7:19408343-19408393	HCM	heart:	n/a
3	chr7:19417585-19417635	Hepatocyte	liver:	n/a
4	chr7:19417585-19417635	MCF-7	breast:	n/a
5	chr7:19443825-19443875	U87	brain:	n/a
6	chr7:19443825-19443875	HAEpiC	amniotic membrane:	n/a
7	chr7:19408343-19408393	SK-N-SH_RA	brain:	n/a
8	chr7:19417585-19417635	T-47D	breast:	n/a
9	chr7:19408343-19408393	AoSMC	blood vessel:	n/a
10	chr7:19408343-19408393	PFSK-1	brain:	n/a
11	chr7:19408343-19408393	PANC-1	pancreas:	n/a
12	chr7:19443825-19443875	HCF	heart:	n/a
13	chr7:19443825-19443875	GM12892	blood:	n/a
14	chr7:19417585-19417635	PFSK-1	brain:	n/a
15	chr7:19417585-19417635	HL-60	blood:	n/a
16	chr7:19443825-19443875	PFSK-1	brain:	n/a
17	chr7:19408343-19408393	HEEpiC	esophagus:	n/a
18	chr7:19417585-19417635	MCF10A-Er-Src	breast:	n/a
19	chr7:19417585-19417635	IMR90	lung:	fetal
20	chr7:19408343-19408393	CMK	blood:	n/a
21	chr7:19443825-19443875	HEK293	kidney:	embryo
22	chr7:19443825-19443875	BE2_C	brain:	n/a
23	chr7:19408343-19408393	NH-A	brain:	n/a
24	chr7:19417585-19417635	SAEC	small airway:	n/a
25	chr7:19408343-19408393	H1-hESC	embryonic stem cell:	embryo
26	chr7:19417585-19417635	HCF	heart:	n/a
27	chr7:19417585-19417635	AG09319	gingival:	n/a
28	chr7:19408343-19408393	ECC-1	luminal epithelium:	n/a
29	chr7:19443825-19443875	HEEpiC	esophagus:	n/a
30	chr7:19443825-19443875	RPTEC	kidney:	n/a
31	chr7:19417585-19417635	HRCEpiC	kidney:	n/a
32	chr7:19443825-19443875	PANC-1	pancreas:	n/a
33	chr7:19417585-19417635	HEEpiC	esophagus:	n/a
34	chr7:19443825-19443875	SAEC	small airway:	n/a
35	chr7:19408343-19408393	NHBE	bronchial:	n/a
36	chr7:19443825-19443875	HepG2	liver:	n/a
37	chr7:19443825-19443875	HIPEpiC	eye:	n/a
38	chr7:19443825-19443875	HCM	heart:	n/a
39	chr7:19443825-19443875	ProgFib	skin:	n/a
40	chr7:19408343-19408393	HRE	kidney:	n/a
41	chr7:19417585-19417635	HCT-116	colon:	n/a
42	chr7:19417585-19417635	GM12878	blood:	n/a
43	chr7:19443825-19443875	HNPCEpiC	eye:	n/a
44	chr7:19408343-19408393	HCPEpiC	choroid plexus:	n/a
45	chr7:19408343-19408393	GM19239	blood:	n/a
46	chr7:19408343-19408393	MCF-7	breast:	n/a
47	chr7:19417585-19417635	HEK293	kidney:	embryo
48	chr7:19408343-19408393	AG10803	skin:	n/a
49	chr7:19408343-19408393	HRCEpiC	kidney:	n/a
50	chr7:19417585-19417635	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
2	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:
3	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
4	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC9-12	chr7:19411480-19411518	NONHSAT119386
2	lnc-HDAC9-5	chr7:19394363-19394508	ENSG00000223838
3	lnc-HDAC9-5	chr7:19393157-19393264	ENSG00000223838
4	lnc-HDAC9-5	chr7:19443324-19443386	ENSG00000223838
5	lnc-HDAC9-5	chr7:19444955-19444993	ENSG00000223838
6	lnc-HDAC9-12	chr7:19409849-19409911	NONHSAT119386

Variant related genes	Relation type
ENSG00000223838	TF binding region
ENSG00000223838	CpG island

Extended variants
information (count: 1833 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10155945	chr7:19378959-19378960	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115497916	chr7:19378987-19378988	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373932880	chr7:19379010-19379011	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13227250	chr7:19379014-19379015	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13227251	chr7:19379015-19379016	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13239930	chr7:19379028-19379029	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs56270326	chr7:19379048-19379049	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs576095448	chr7:19379075-19379076	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4721758	chr7:19379081-19379082	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs535555159	chr7:19379083-19379084	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575683474	chr7:19379092-19379093	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577135322	chr7:19379099-19379100	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541188752	chr7:19379134-19379135	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559267153	chr7:19379139-19379140	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555436023	chr7:19379151-19379152	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572530623	chr7:19379196-19379197	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542753040	chr7:19379199-19379200	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573439192	chr7:19379246-19379247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144774557	chr7:19379281-19379282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79996149	chr7:19379306-19379307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550082213	chr7:19379319-19379320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147935286	chr7:19379335-19379336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140362502	chr7:19379354-19379355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547994945	chr7:19379383-19379384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190627392	chr7:19379411-19379412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2390087	chr7:19379422-19379423	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372378187	chr7:19379488-19379489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs151138199	chr7:19379491-19379492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565325028	chr7:19379505-19379506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369927016	chr7:19379522-19379523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531034032	chr7:19379536-19379537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537018642	chr7:19379588-19379589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558910138	chr7:19379644-19379645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3948645	chr7:19379686-19379687	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs561287271	chr7:19379688-19379689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553180192	chr7:19379704-19379705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182920806	chr7:19379755-19379756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368888130	chr7:19379772-19379773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543110122	chr7:19379804-19379805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186148818	chr7:19379901-19379902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576044424	chr7:19379902-19379903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190811071	chr7:19379903-19379904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564912158	chr7:19379908-19379909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532884470	chr7:19379917-19379918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541350126	chr7:19379923-19379924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548809946	chr7:19379938-19379939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369465718	chr7:19379942-19379943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543130287	chr7:19379955-19379956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530190348	chr7:19379984-19379985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56046612	chr7:19380010-19380011	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19378800-19379200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:19378800-19380400	Enhancers	Placenta	Placenta
3	chr7:19380000-19380400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:19391000-19393400	Enhancers	NHDF-Ad	bronchial
5	chr7:19391200-19391800	Enhancers	Dnd41	blood
6	chr7:19391400-19392200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:19391600-19392000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:19391600-19392800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:19391600-19393200	Enhancers	HSMM	muscle
10	chr7:19391600-19393600	Enhancers	Osteobl	bone
11	chr7:19391800-19393200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:19391800-19393400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr7:19392000-19393000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:19392200-19393400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:19393000-19393800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr7:19393400-19394800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:19394000-19394400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr7:19394000-19394800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:19401000-19403200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:19401600-19402200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr7:19401600-19402400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:19401600-19402400	Enhancers	NHDF-Ad	bronchial
23	chr7:19401800-19402200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr7:19401800-19402400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:19401800-19402400	Enhancers	Brain Hippocampus Middle	brain
26	chr7:19402000-19402400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr7:19402000-19402600	Enhancers	Brain Cingulate Gyrus	brain
28	chr7:19402000-19402600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:19402400-19402800	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr7:19402400-19407600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:19402400-19407600	Weak transcription	NHDF-Ad	bronchial
32	chr7:19402600-19406000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr7:19404000-19406000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:19404200-19404400	Enhancers	H9 Cell Line	embryonic stem cell
35	chr7:19404200-19404800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:19404200-19404800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr7:19404200-19405200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:19404200-19406000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:19404200-19406200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:19404400-19404800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:19404400-19405000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:19404400-19405000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr7:19404400-19408200	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr7:19404800-19405200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr7:19404800-19407800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr7:19404800-19408400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:19405000-19405200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr7:19405000-19408000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:19405200-19406400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:19405200-19408000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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