Variant report

Variant	nsv1019680
Chromosome Location	chr5:30292001-30431119
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	chr5:30334740-30334775	K562	blood:	n/a	n/a
2	BACH1	chr5:30405560-30405672	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr5:30337300-30337674	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:30337301-30337609	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:30392803-30392994	A549	lung:	n/a	n/a
6	CEBPB	chr5:30356493-30356736	HepG2	liver:	n/a	chr5:30356586-30356597
7	CEBPB	chr5:30356521-30356732	A549	lung:	n/a	chr5:30356586-30356597
8	CEBPB	chr5:30324366-30324430	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:30326920-30327209	MCF-7	breast:	n/a	n/a
10	CEBPB	chr5:30326792-30327081	MCF-7	breast:	n/a	n/a
11	CEBPB	chr5:30336225-30336401	HepG2	liver:	n/a	n/a
12	CTCF	chr5:30401720-30401870	GM12864	blood:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
13	CTCF	chr5:30413774-30413930	MCF-7	breast:	n/a	chr5:30413835-30413853 chr5:30413837-30413858
14	CTCF	chr5:30324340-30324490	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr5:30413760-30413910	AG09319	gingival:	n/a	chr5:30413835-30413853 chr5:30413837-30413858
16	CTCF	chr5:30401740-30401890	BE2_C	brain:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
17	CTCF	chr5:30401711-30401860	Fibrobl	skin:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
18	CTCF	chr5:30401670-30401883	A549	lung:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
19	CTCF	chr5:30413740-30413890	AG04450	lung:	n/a	chr5:30413835-30413853 chr5:30413837-30413858
20	CTCF	chr5:30324400-30324550	HepG2	liver:	n/a	n/a
21	CTCF	chr5:30413720-30413870	HRPEpiC	eye:	n/a	chr5:30413835-30413853 chr5:30413837-30413858
22	CTCF	chr5:30413750-30413870	HepG2	liver:	n/a	chr5:30413835-30413853 chr5:30413837-30413858
23	CTCF	chr5:30401620-30401770	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr5:30401720-30401870	RPTEC	kidney:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
25	CTCF	chr5:30401668-30401898	MCF-7	breast:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
26	CTCF	chr5:30401680-30401830	AG09309	skin:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
27	CTCF	chr5:30401644-30401953	K562	blood:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
28	CTCF	chr5:30401740-30401890	Hela-S3	cervix:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
29	CTCF	chr5:30413740-30413890	AG09319	gingival:	n/a	chr5:30413835-30413853 chr5:30413837-30413858
30	CTCF	chr5:30401720-30401870	WERI-Rb-1	eye:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
31	CTCF	chr5:30321640-30321790	WI-38	lung:	n/a	n/a
32	CTCF	chr5:30324285-30324470	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr5:30401660-30401810	AG10803	skin:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
34	CTCF	chr5:30361072-30361110	Lung_OC	lung:	n/a	n/a
35	CTCF	chr5:30308330-30308455	GM10248	blood:	n/a	n/a
36	CTCF	chr5:30401800-30401950	BJ	skin:	n/a	n/a
37	CTCF	chr5:30401640-30401790	GM12870	blood:	n/a	n/a
38	CTCF	chr5:30386215-30386224	GM13976	blood:	n/a	n/a
39	CTCF	chr5:30401505-30401955	MCF-7	breast:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
40	CTCF	chr5:30401638-30401926	Hela-S3	cervix:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
41	CTCF	chr5:30401700-30401850	GM12874	blood:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
42	CTCF	chr5:30401740-30401890	NB4	blood:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
43	CTCF	chr5:30401660-30401810	GM12865	blood:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
44	CTCF	chr5:30324320-30324470	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr5:30401740-30401890	NHLF	lung:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
46	CTCF	chr5:30401800-30401950	HCM	heart:	n/a	n/a
47	CTCF	chr5:30413780-30413930	HRE	kidney:	n/a	chr5:30413835-30413853 chr5:30413837-30413858
48	CTCF	chr5:30401700-30401850	GM12868	blood:	n/a	chr5:30401778-30401796 chr5:30401781-30401794
49	CTCF	chr5:30360680-30360830	K562	blood:	n/a	n/a
50	CTCF	chr5:30401660-30401810	NHEK	skin:	n/a	chr5:30401778-30401796 chr5:30401781-30401794

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:30346809-30346859	HUVEC	blood vessel:	n/a
2	chr5:30346809-30346859	HUVEC	blood vessel:	n/a
3	chr5:30346020-30346070	H1-hESC	embryonic stem cell:	embryo
4	chr5:30346164-30346214	SK-N-SH_RA	brain:	n/a
5	chr5:30346020-30346070	GM19239	blood:	n/a
6	chr5:30390070-30390120	GM12892	blood:	n/a
7	chr5:30346809-30346859	GM06990	blood:	n/a
8	chr5:30346020-30346070	HCF	heart:	n/a
9	chr5:30390070-30390120	T-47D	breast:	n/a
10	chr5:30429329-30429379	Jurkat	blood:	n/a
11	chr5:30346164-30346214	AG04449	skin:	fetal
12	chr5:30429329-30429379	HEEpiC	esophagus:	n/a
13	chr5:30390070-30390120	GM12878	blood:	n/a
14	chr5:30346020-30346070	GM06990	blood:	n/a
15	chr5:30346020-30346070	SK-N-MC	brain:	n/a
16	chr5:30346020-30346070	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:30390070-30390120	NHBE	bronchial:	n/a
18	chr5:30429433-30429483	GM12892	blood:	n/a
19	chr5:30429433-30429483	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:30346164-30346214	GM06990	blood:	n/a
21	chr5:30390070-30390120	SK-N-SH_RA	brain:	n/a
22	chr5:30390070-30390120	Jurkat	blood:	n/a
23	chr5:30346020-30346070	HEK293	kidney:	embryo
24	chr5:30429433-30429483	Hepatocyte	liver:	n/a
25	chr5:30346164-30346214	T-47D	breast:	n/a
26	chr5:30429433-30429483	HepG2	liver:	n/a
27	chr5:30429433-30429483	BJ	skin:	n/a
28	chr5:30429433-30429483	HRPEpiC	eye:	n/a
29	chr5:30390070-30390120	Hela-S3	cervix:	n/a
30	chr5:30390070-30390120	HRCEpiC	kidney:	n/a
31	chr5:30429329-30429379	NB4	blood:	n/a
32	chr5:30346164-30346214	GM12891	blood:	n/a
33	chr5:30429433-30429483	AG04449	skin:	fetal
34	chr5:30390070-30390120	HCF	heart:	n/a
35	chr5:30346164-30346214	HCM	heart:	n/a
36	chr5:30346164-30346214	HUVEC	blood vessel:	n/a
37	chr5:30346809-30346859	HEEpiC	esophagus:	n/a
38	chr5:30346809-30346859	BJ	skin:	n/a
39	chr5:30346164-30346214	Hela-S3	cervix:	n/a
40	chr5:30346020-30346070	AG10803	skin:	n/a
41	chr5:30346164-30346214	U87	brain:	n/a
42	chr5:30346164-30346214	HEEpiC	esophagus:	n/a
43	chr5:30346809-30346859	GM12892	blood:	n/a
44	chr5:30346164-30346214	HIPEpiC	eye:	n/a
45	chr5:30346809-30346859	NB4	blood:	n/a
46	chr5:30429433-30429483	Jurkat	blood:	n/a
47	chr5:30346020-30346070	NHDF-neo	bronchial:	n/a
48	chr5:30346809-30346859	Hela-S3	cervix:	n/a
49	chr5:30429329-30429379	ProgFib	skin:	n/a
50	chr5:30429433-30429483	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:30329682..30331741-chr5:30336346..30338195,2	MCF-7	breast:
2	chr5:30304961..30306799-chr5:30312361..30314543,2	K562	blood:
3	chr5:30352726..30354416-chr5:30354463..30356083,2	MCF-7	breast:
4	chr5:30411663..30414613-chr5:30418173..30421082,2	MCF-7	breast:
5	chr5:30411663..30414613-chr5:30418173..30421082,2	MCF-7	breast:
6	chr5:30401282..30402426-chr5:31231996..31233048,6	MCF-7	breast:
7	chr5:30335608..30338399-chr5:30338549..30341547,3	MCF-7	breast:
8	chr5:30040588..30041199-chr5:30401364..30401866,2	MCF-7	breast:
9	chr5:30385785..30388014-chr5:30430823..30433281,2	K562	blood:
10	chr5:30401497..30402171-chr5:31186491..31187231,2	MCF-7	breast:
11	chr5:30348749..30351521-chr5:30376148..30377890,2	K562	blood:
12	chr5:30385785..30388014-chr5:30430823..30433281,2	K562	blood:
13	chr5:30352726..30354416-chr5:30354463..30356083,2	MCF-7	breast:
14	chr5:30348749..30351521-chr5:30376148..30377890,2	K562	blood:
15	chr5:30329682..30331741-chr5:30336346..30338195,2	MCF-7	breast:
16	chr5:30306752..30308851-chr5:30323163..30325456,2	MCF-7	breast:
17	chr5:30306752..30308851-chr5:30323163..30325456,2	MCF-7	breast:
18	chr5:30304961..30306799-chr5:30312361..30314543,2	K562	blood:
19	chr5:30335608..30338399-chr5:30338549..30341547,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000250118	TF binding region
ENSG00000250118	CpG island

Extended variants
information (count: 1309 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1309 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112713582	chr5:30299045-30299046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6883071	chr5:30299046-30299047	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs4492127	chr5:30299100-30299101	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535569264	chr5:30299145-30299146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547864795	chr5:30301807-30301808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114701866	chr5:30301823-30301824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531685851	chr5:30301828-30301829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372932343	chr5:30301832-30301833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551858770	chr5:30301861-30301862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530101955	chr5:30301882-30301883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527933591	chr5:30301972-30301973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548086681	chr5:30302028-30302029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10071127	chr5:30302035-30302036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs536958817	chr5:30302058-30302059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113745078	chr5:30302077-30302078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184807377	chr5:30302104-30302105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568838443	chr5:30302121-30302122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537501970	chr5:30302122-30302123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557874377	chr5:30302160-30302161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577760441	chr5:30302169-30302170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189661288	chr5:30302201-30302202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11743556	chr5:30302202-30302203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs553634854	chr5:30302217-30302218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573565279	chr5:30302221-30302222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139938870	chr5:30302259-30302260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576226014	chr5:30302284-30302285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562695008	chr5:30302311-30302312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116413102	chr5:30302369-30302370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545164080	chr5:30302382-30302383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545299270	chr5:30302385-30302386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565404926	chr5:30302397-30302398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141329056	chr5:30302412-30302413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150803895	chr5:30302419-30302420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539319855	chr5:30302440-30302441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374255417	chr5:30302466-30302467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530370294	chr5:30302509-30302510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181054385	chr5:30302571-30302572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568749196	chr5:30302687-30302688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10063737	chr5:30302789-30302790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186025218	chr5:30302791-30302792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371487871	chr5:30302828-30302829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571045899	chr5:30302835-30302836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376296927	chr5:30302838-30302839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13186324	chr5:30302839-30302840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548408035	chr5:30302943-30302944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553525784	chr5:30302959-30302960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76999436	chr5:30303006-30303007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536118565	chr5:30303093-30303094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535682410	chr5:30303109-30303110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556464195	chr5:30303125-30303126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:30299000-30299200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:30301800-30310200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:30310400-30310800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr5:30314600-30315600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr5:30315400-30315600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:30337400-30337600	Enhancers	Pancreas	Pancrea
7	chr5:30345600-30345800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:30346000-30346400	Active TSS	H1 Cell Line	embryonic stem cell
9	chr5:30346000-30346400	Active TSS	Cortex derived primary cultured neurospheres	brain
10	chr5:30346000-30346400	Active TSS	HSMM	muscle
11	chr5:30346000-30346400	Active TSS	NHEK	skin
12	chr5:30366400-30378800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:30373200-30373600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:30373600-30376400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:30376400-30376800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:30380400-30380800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr5:30383800-30384400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:30384000-30384600	Enhancers	Brain Germinal Matrix	brain
19	chr5:30387400-30387600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr5:30387600-30387800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr5:30387600-30388000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr5:30387600-30388200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:30387600-30388600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr5:30387800-30388200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr5:30387800-30389200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:30387800-30390200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr5:30388000-30388200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr5:30388000-30388600	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr5:30388200-30388600	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr5:30388200-30388600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:30388200-30388800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr5:30388600-30388800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr5:30388600-30389000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr5:30388600-30389000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:30388600-30389400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr5:30388600-30391200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr5:30388800-30390000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr5:30388800-30390200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr5:30389000-30389200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr5:30389000-30390000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr5:30389200-30390200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr5:30389200-30390600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:30389200-30391200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr5:30389600-30389800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr5:30390000-30390400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr5:30390000-30390600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr5:30390000-30390600	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr5:30390200-30390400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:30390200-30390600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr5:30390200-30390600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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