Variant report

Variant	nsv1044020
Chromosome Location	chr10:56038546-56224736
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	chr10:56148845-56148855	K562	blood:	n/a	n/a
2	BACH1	chr10:56123236-56123565	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr10:56123241-56123554	K562	blood:	n/a	n/a
4	CEBPB	chr10:56122448-56122536	HepG2	liver:	n/a	chr10:56122474-56122485
5	CEBPB	chr10:56079201-56079479	A549	lung:	n/a	chr10:56079355-56079366
6	CEBPB	chr10:56074308-56074560	K562	blood:	n/a	chr10:56074380-56074391
7	CEBPB	chr10:56074216-56074562	A549	lung:	n/a	chr10:56074380-56074391
8	CEBPB	chr10:56200706-56200999	A549	lung:	n/a	chr10:56200831-56200842 chr10:56200829-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200829-56200842 chr10:56200831-56200840 chr10:56200829-56200842
9	CEBPB	chr10:56074202-56074568	HepG2	liver:	n/a	chr10:56074380-56074391
10	CEBPB	chr10:56200782-56200984	Hela-S3	cervix:	n/a	chr10:56200831-56200842 chr10:56200829-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200829-56200842 chr10:56200831-56200840 chr10:56200829-56200842
11	CEBPB	chr10:56074242-56074533	H1-hESC	embryonic stem cell:	n/a	chr10:56074380-56074391
12	CEBPB	chr10:56070828-56071132	HepG2	liver:	n/a	chr10:56070964-56070975 chr10:56070986-56070997
13	CEBPB	chr10:56204103-56204212	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:56079183-56079542	HepG2	liver:	n/a	chr10:56079355-56079366
15	CEBPB	chr10:56106935-56106999	H1-hESC	embryonic stem cell:	n/a	chr10:56106957-56106970
16	CEBPB	chr10:56070861-56071086	A549	lung:	n/a	chr10:56070964-56070975 chr10:56070986-56070997
17	CEBPB	chr10:56200440-56201020	IMR90	lung:	n/a	chr10:56200831-56200842 chr10:56200630-56200641 chr10:56200494-56200505 chr10:56200628-56200641 chr10:56200630-56200641 chr10:56200829-56200840 chr10:56200831-56200840 chr10:56200494-56200503 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200829-56200842 chr10:56200831-56200840 chr10:56200829-56200842
18	CEBPB	chr10:56173535-56173641	A549	lung:	n/a	n/a
19	CEBPB	chr10:56079189-56079516	IMR90	lung:	n/a	chr10:56079355-56079366
20	CEBPB	chr10:56080492-56080769	HepG2	liver:	n/a	chr10:56080656-56080667
21	CEBPB	chr10:56074230-56074549	IMR90	lung:	n/a	chr10:56074380-56074391
22	CEBPB	chr10:56079320-56079376	K562	blood:	n/a	chr10:56079355-56079366
23	CEBPB	chr10:56200675-56201003	HepG2	liver:	n/a	chr10:56200831-56200842 chr10:56200829-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200829-56200842 chr10:56200831-56200840 chr10:56200829-56200842
24	CEBPB	chr10:56079250-56079494	H1-hESC	embryonic stem cell:	n/a	chr10:56079355-56079366
25	CEBPB	chr10:56200707-56200930	H1-hESC	embryonic stem cell:	n/a	chr10:56200831-56200842 chr10:56200829-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200831-56200840 chr10:56200829-56200842 chr10:56200831-56200840 chr10:56200829-56200842
26	CTCF	chr10:56162460-56162610	GM12871	blood:	n/a	n/a
27	CTCF	chr10:56162500-56162650	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr10:56162400-56162550	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr10:56162360-56162510	HFF	foreskin:	n/a	n/a
30	CTCF	chr10:56162420-56162570	GM06990	blood:	n/a	n/a
31	CTCF	chr10:56162434-56162437	HepG2	liver:	n/a	n/a
32	CTCF	chr10:56162460-56162610	HMEC	breast:	n/a	n/a
33	CTCF	chr10:56128880-56129030	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:56175940-56176090	GM12872	blood:	n/a	n/a
35	CTCF	chr10:56162447-56162678	LNCaP	prostate:	n/a	n/a
36	CTCF	chr10:56162460-56162610	GM12867	blood:	n/a	n/a
37	CTCF	chr10:56162440-56162590	HPF	lung:	n/a	n/a
38	CTCF	chr10:56162480-56162623	K562	blood:	n/a	n/a
39	CTCF	chr10:56108080-56108230	Caco-2	colon:	n/a	n/a
40	CTCF	chr10:56162520-56162670	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr10:56162441-56162669	Medullo	brain:	n/a	n/a
42	CTCF	chr10:56175423-56175505	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr10:56162460-56162610	RPTEC	kidney:	n/a	n/a
44	CTCF	chr10:56175428-56175524	LNCaP	prostate:	n/a	n/a
45	CTCF	chr10:56162469-56162663	LNCaP	prostate:	n/a	n/a
46	CTCF	chr10:56162486-56162614	GM10248	blood:	n/a	n/a
47	CTCF	chr10:56201483-56201598	A549	lung:	n/a	n/a
48	CTCF	chr10:56154530-56154590	HepG2	liver:	n/a	n/a
49	CTCF	chr10:56162500-56162650	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr10:56162480-56162630	HA-sp	spinal cord:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:56057923-56057973	HPAEpiC	pulmonary alveolar:	n/a
2	chr10:56057923-56057973	SK-N-SH_RA	brain:	n/a
3	chr10:56057923-56057973	ovcar-3	ovarian:	n/a
4	chr10:56057923-56057973	HL-60	blood:	n/a
5	chr10:56057923-56057973	GM12878	blood:	n/a
6	chr10:56057923-56057973	GM12892	blood:	n/a
7	chr10:56057923-56057973	AG04450	lung:	fetal
8	chr10:56057923-56057973	PrEC	prostate:	n/a
9	chr10:56057923-56057973	NB4	blood:	n/a
10	chr10:56057923-56057973	HAEpiC	amniotic membrane:	n/a
11	chr10:56057923-56057973	AG09319	gingival:	n/a
12	chr10:56057923-56057973	AoSMC	blood vessel:	n/a
13	chr10:56057923-56057973	HEEpiC	esophagus:	n/a
14	chr10:56057923-56057973	SK-N-SH	brain:	n/a
15	chr10:56057923-56057973	HRPEpiC	eye:	n/a
16	chr10:56057923-56057973	GM06990	blood:	n/a
17	chr10:56057923-56057973	LNCaP	prostate:	n/a
18	chr10:56057923-56057973	ECC-1	luminal epithelium:	n/a
19	chr10:56057923-56057973	HRE	kidney:	n/a
20	chr10:56057923-56057973	AG04449	skin:	fetal
21	chr10:56057923-56057973	HCPEpiC	choroid plexus:	n/a
22	chr10:56057923-56057973	HEK293	kidney:	embryo
23	chr10:56057923-56057973	HepG2	liver:	n/a
24	chr10:56057923-56057973	GM12891	blood:	n/a
25	chr10:56057923-56057973	AG09309	skin:	n/a
26	chr10:56057923-56057973	NH-A	brain:	n/a
27	chr10:56057923-56057973	HRCEpiC	kidney:	n/a
28	chr10:56057923-56057973	HIPEpiC	eye:	n/a
29	chr10:56057923-56057973	HUVEC	blood vessel:	n/a
30	chr10:56057923-56057973	RPTEC	kidney:	n/a
31	chr10:56057923-56057973	GM19239	blood:	n/a
32	chr10:56057923-56057973	HCM	heart:	n/a
33	chr10:56057923-56057973	IMR90	lung:	fetal
34	chr10:56057923-56057973	A549	lung:	n/a
35	chr10:56057923-56057973	HNPCEpiC	eye:	n/a
36	chr10:56057923-56057973	MCF-7	breast:	n/a
37	chr10:56057923-56057973	SK-N-MC	brain:	n/a
38	chr10:56057923-56057973	PANC-1	pancreas:	n/a
39	chr10:56057923-56057973	AG10803	skin:	n/a
40	chr10:56057923-56057973	Hela-S3	cervix:	n/a
41	chr10:56057923-56057973	PFSK-1	brain:	n/a
42	chr10:56057923-56057973	MCF10A-Er-Src	breast:	n/a
43	chr10:56057923-56057973	HMEC	breast:	n/a
44	chr10:56057923-56057973	K562	blood:	n/a
45	chr10:56057923-56057973	NT2-D1	testis:	n/a
46	chr10:56057923-56057973	BJ	skin:	n/a
47	chr10:56057923-56057973	NHBE	bronchial:	n/a
48	chr10:56057923-56057973	Hepatocyte	liver:	n/a
49	chr10:56057923-56057973	HCT-116	colon:	n/a
50	chr10:56057923-56057973	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:55757420..55758328-chr10:56162156..56162806,2	MCF-7	breast:
2	chr10:56063971..56064546-chr4:85391561..85392244,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263921	TF binding region
RNU6-687P	TF binding region
ENSG00000263921	CpG island
RNU6-687P	CpG island

Extended variants
information (count: 1952 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1952 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547735360	chr10:56041605-56041606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148888732	chr10:56041608-56041609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531999647	chr10:56041616-56041617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146980825	chr10:56041618-56041619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7918002	chr10:56041626-56041627	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs549887867	chr10:56041646-56041647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138225533	chr10:56041684-56041685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569907589	chr10:56041685-56041686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535643832	chr10:56041737-56041738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555046804	chr10:56041782-56041783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181959555	chr10:56041798-56041799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565924387	chr10:56041836-56041837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562434286	chr10:56041862-56041863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112933364	chr10:56041881-56041882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115174705	chr10:56041896-56041897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs61853312	chr10:56041906-56041907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372190470	chr10:56041939-56041940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577897529	chr10:56041951-56041952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543627375	chr10:56041982-56041983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529642451	chr10:56041986-56041987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547822717	chr10:56042026-56042027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185823469	chr10:56042051-56042052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7907468	chr10:56042069-56042070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76576828	chr10:56042111-56042112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189602075	chr10:56042128-56042129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12262364	chr10:56042135-56042136	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs527679465	chr10:56042202-56042203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547795507	chr10:56042205-56042206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35804115	chr10:56042236-56042237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574462397	chr10:56042247-56042248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181203449	chr10:56042278-56042279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564606939	chr10:56042325-56042326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527393504	chr10:56042367-56042368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186758460	chr10:56042388-56042389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188090431	chr10:56043604-56043605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374228100	chr10:56043611-56043612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376739976	chr10:56043615-56043616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370895250	chr10:56043619-56043620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10825296	chr10:56043660-56043661	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541378075	chr10:56043685-56043686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143837572	chr10:56043700-56043701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528682277	chr10:56043733-56043734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551417447	chr10:56043745-56043746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532372519	chr10:56043759-56043760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571408891	chr10:56043762-56043763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530519941	chr10:56043769-56043770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11593951	chr10:56043784-56043785	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs567283906	chr10:56043810-56043811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536521121	chr10:56043826-56043827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546579290	chr10:56043840-56043841	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56041600-56042200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr10:56041600-56042200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr10:56041600-56042200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr10:56041800-56042200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr10:56041800-56042400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr10:56043600-56044000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr10:56048600-56048800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:56058800-56066400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr10:56063400-56063800	Enhancers	Fetal Lung	lung
10	chr10:56066400-56066600	Enhancers	H9 Cell Line	embryonic stem cell
11	chr10:56067200-56067800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr10:56096000-56097800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr10:56097600-56098200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:56097800-56098400	Active TSS	Primary hematopoietic stem cells	blood
15	chr10:56097800-56099000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr10:56097800-56099000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr10:56098200-56098600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr10:56098200-56098600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr10:56098200-56098800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr10:56098200-56099000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr10:56098400-56098600	Flanking Active TSS	Primary hematopoietic stem cells	blood
22	chr10:56098400-56099000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr10:56098600-56099000	Enhancers	Primary hematopoietic stem cells	blood
24	chr10:56098600-56099000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr10:56098600-56101000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr10:56101000-56102800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
27	chr10:56101400-56102000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr10:56101400-56102800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr10:56102000-56102200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr10:56102000-56102600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:56102000-56102600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:56102000-56102800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
33	chr10:56102000-56103200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr10:56131400-56132200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr10:56137000-56138200	Enhancers	Fetal Kidney	kidney
36	chr10:56141000-56141200	Enhancers	Fetal Kidney	kidney
37	chr10:56153000-56153600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr10:56153000-56153800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr10:56153000-56154200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr10:56153600-56155200	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr10:56153800-56155200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr10:56154200-56155200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr10:56155200-56156800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr10:56155200-56157000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr10:56155200-56157200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr10:56155200-56157200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr10:56155200-56157800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr10:56155400-56156200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr10:56155800-56156200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr10:56155800-56157200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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