Variant report

Variant	nsv1037493
Chromosome Location	chr10:56603003-56800009
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	BACH1	chr10:56657200-56657414	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:56666691-56667053	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr10:56660366-56660650	GM12878	blood:	n/a	n/a
4	BATF	chr10:56660332-56660649	GM12878	blood:	n/a	n/a
5	CEBPB	chr10:56749441-56749588	HepG2	liver:	n/a	n/a
6	CEBPB	chr10:56702919-56703193	HepG2	liver:	n/a	chr10:56703062-56703073
7	CEBPB	chr10:56656738-56657181	HepG2	liver:	n/a	chr10:56657061-56657072 chr10:56656774-56656786
8	CEBPB	chr10:56650557-56650899	IMR90	lung:	n/a	chr10:56650711-56650728 chr10:56650714-56650725 chr10:56650714-56650727
9	CEBPB	chr10:56627703-56627915	HepG2	liver:	n/a	chr10:56627789-56627800
10	CEBPB	chr10:56650589-56650899	A549	lung:	n/a	chr10:56650711-56650728 chr10:56650714-56650725 chr10:56650714-56650727
11	CEBPB	chr10:56706744-56706860	K562	blood:	n/a	n/a
12	CEBPB	chr10:56702944-56703116	H1-hESC	embryonic stem cell:	n/a	chr10:56703062-56703073
13	CEBPB	chr10:56776288-56776585	HepG2	liver:	n/a	chr10:56776454-56776465
14	CEBPB	chr10:56650580-56650902	HepG2	liver:	n/a	chr10:56650711-56650728 chr10:56650714-56650725 chr10:56650714-56650727
15	CEBPB	chr10:56650630-56650734	K562	blood:	n/a	chr10:56650711-56650728 chr10:56650714-56650725 chr10:56650714-56650727
16	CEBPB	chr10:56657095-56657292	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr10:56735780-56735945	A549	lung:	n/a	chr10:56735825-56735838 chr10:56735825-56735836 chr10:56735825-56735838 chr10:56735825-56735838
18	CEBPB	chr10:56785578-56785802	HepG2	liver:	n/a	chr10:56785697-56785708 chr10:56785697-56785710
19	CEBPB	chr10:56702954-56703181	A549	lung:	n/a	chr10:56703062-56703073
20	CHD1	chr10:56799840-56799854	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr10:56700344-56700435	HepG2	liver:	n/a	n/a
22	CTCF	chr10:56745700-56745850	GM12869	blood:	n/a	n/a
23	CTCF	chr10:56745620-56745770	WERI-Rb-1	eye:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
24	CTCF	chr10:56745584-56745763	LNCaP	prostate:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
25	CTCF	chr10:56745600-56745750	GM12865	blood:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
26	CTCF	chr10:56745280-56745430	AG10803	skin:	n/a	n/a
27	CTCF	chr10:56745333-56745441	GM13977	blood:	n/a	n/a
28	CTCF	chr10:56745582-56745773	GM10248	blood:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
29	CTCF	chr10:56614238-56614316	HepG2	liver:	n/a	n/a
30	CTCF	chr10:56745440-56745590	BJ	skin:	n/a	n/a
31	CTCF	chr10:56745370-56745448	GM10266	blood:	n/a	n/a
32	CTCF	chr10:56745340-56745436	GM12878	blood:	n/a	n/a
33	CTCF	chr10:56745880-56746030	GM12878	blood:	n/a	n/a
34	CTCF	chr10:56745635-56745753	Gliobla	brain:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
35	CTCF	chr10:56700340-56700490	GM12865	blood:	n/a	n/a
36	CTCF	chr10:56745860-56746010	AG10803	skin:	n/a	n/a
37	CTCF	chr10:56745580-56745730	GM12801	blood:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
38	CTCF	chr10:56745080-56745230	RPTEC	kidney:	n/a	n/a
39	CTCF	chr10:56745603-56745762	K562	blood:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
40	CTCF	chr10:56745624-56745751	GM13976	blood:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
41	CTCF	chr10:56745607-56745757	Kidney_OC	kidney:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
42	CTCF	chr10:56745620-56745770	AG04450	lung:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
43	CTCF	chr10:56745560-56745710	HEK293	kidney:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
44	CTCF	chr10:56745627-56745768	MCF-7	breast:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
45	CTCF	chr10:56745240-56745390	GM12873	blood:	n/a	n/a
46	CTCF	chr10:56700360-56700510	HAc	cerebellar:	n/a	n/a
47	CTCF	chr10:56745600-56745750	HMEC	breast:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
48	CTCF	chr10:56745645-56745741	MCF-7	breast:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
49	CTCF	chr10:56745603-56745766	Pancreas_OC	pancreas:	n/a	chr10:56745680-56745696 chr10:56745679-56745697 chr10:56745683-56745690 chr10:56745681-56745702
50	CTCF	chr10:56745351-56745438	Medullo	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:56666396-56666446	HEEpiC	esophagus:	n/a
2	chr10:56666396-56666446	U87	brain:	n/a
3	chr10:56666396-56666446	K562	blood:	n/a
4	chr10:56666396-56666446	MCF-7	breast:	n/a
5	chr10:56666396-56666446	HAEpiC	amniotic membrane:	n/a
6	chr10:56666396-56666446	AG10803	skin:	n/a
7	chr10:56666396-56666446	SK-N-SH_RA	brain:	n/a
8	chr10:56666396-56666446	GM12892	blood:	n/a
9	chr10:56666396-56666446	SKMC	muscle:	n/a
10	chr10:56666396-56666446	NH-A	brain:	n/a
11	chr10:56666396-56666446	HMEC	breast:	n/a
12	chr10:56666396-56666446	SK-N-SH	brain:	n/a
13	chr10:56666396-56666446	HPAEpiC	pulmonary alveolar:	n/a
14	chr10:56666396-56666446	HEK293	kidney:	embryo
15	chr10:56666396-56666446	AG09309	skin:	n/a
16	chr10:56666396-56666446	HRE	kidney:	n/a
17	chr10:56666396-56666446	GM12891	blood:	n/a
18	chr10:56666396-56666446	HNPCEpiC	eye:	n/a
19	chr10:56666396-56666446	HCPEpiC	choroid plexus:	n/a
20	chr10:56666396-56666446	HepG2	liver:	n/a
21	chr10:56666396-56666446	BJ	skin:	n/a
22	chr10:56666396-56666446	AG04449	skin:	fetal
23	chr10:56666396-56666446	NHDF-neo	bronchial:	n/a
24	chr10:56666396-56666446	HRCEpiC	kidney:	n/a
25	chr10:56666396-56666446	HRPEpiC	eye:	n/a
26	chr10:56666396-56666446	AG04450	lung:	fetal
27	chr10:56666396-56666446	HCT-116	colon:	n/a
28	chr10:56666396-56666446	HIPEpiC	eye:	n/a
29	chr10:56666396-56666446	BE2_C	brain:	n/a
30	chr10:56666396-56666446	HL-60	blood:	n/a
31	chr10:56666396-56666446	HCF	heart:	n/a
32	chr10:56666396-56666446	NHBE	bronchial:	n/a
33	chr10:56666396-56666446	AG09319	gingival:	n/a
34	chr10:56666396-56666446	PrEC	prostate:	n/a
35	chr10:56666396-56666446	NT2-D1	testis:	n/a
36	chr10:56666396-56666446	NB4	blood:	n/a
37	chr10:56666396-56666446	ovcar-3	ovarian:	n/a
38	chr10:56666396-56666446	SK-N-MC	brain:	n/a
39	chr10:56666396-56666446	PANC-1	pancreas:	n/a
40	chr10:56666396-56666446	AoSMC	blood vessel:	n/a
41	chr10:56666396-56666446	HUVEC	blood vessel:	n/a
42	chr10:56666396-56666446	Caco-2	colon:	n/a
43	chr10:56666396-56666446	RPTEC	kidney:	n/a
44	chr10:56666396-56666446	T-47D	breast:	n/a
45	chr10:56666396-56666446	ProgFib	skin:	n/a
46	chr10:56666396-56666446	HCM	heart:	n/a
47	chr10:56666396-56666446	Hepatocyte	liver:	n/a
48	chr10:56666396-56666446	Jurkat	blood:	n/a
49	chr10:56666396-56666446	ECC-1	luminal epithelium:	n/a
50	chr10:56666396-56666446	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:56741188..56742845-chr10:56743617..56746520,3	K562	blood:
2	chr10:56637516..56639044-chr10:56640862..56643411,2	K562	blood:
3	chr10:56765862..56768226-chr10:56771478..56774525,3	K562	blood:
4	chr10:56741188..56742845-chr10:56743617..56746520,3	K562	blood:
5	chr10:56765862..56768226-chr10:56771478..56774525,3	K562	blood:
6	chr10:56700000..56702785-chr10:56708737..56710411,2	K562	blood:
7	chr10:56732642..56733602-chr10:56755180..56756034,2	MCF-7	breast:
8	chr10:56732642..56733602-chr10:56755180..56756034,2	MCF-7	breast:
9	chr10:56621759..56622362-chr4:187295967..187296841,2	MCF-7	breast:
10	chr10:56713690..56716657-chr10:56717278..56720130,2	K562	blood:
11	chr10:56716657..56719103-chr10:56719705..56721791,2	MCF-7	breast:
12	chr10:56637516..56639044-chr10:56640862..56643411,2	K562	blood:
13	chr10:56713690..56716657-chr10:56717278..56720130,2	K562	blood:
14	chr10:56598785..56601451-chr10:56605100..56606903,2	K562	blood:
15	chr10:56716657..56719103-chr10:56719705..56721791,2	MCF-7	breast:
16	chr10:56700000..56702785-chr10:56708737..56710411,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZWINT-5	chr10:56628799-56628882	ENSG00000236958.1
2	lnc-ZWINT-5	chr10:56624434-56624556	ENSG00000236958.1
3	lnc-ZWINT-5	chr10:56624309-56624556	NONHSAT013459
4	lnc-ZWINT-5	chr10:56628799-56628906	NONHSAT013459

Variant related genes	Relation type
ENSG00000236958	TF binding region
ENSG00000236958	CpG island

Extended variants
information (count: 1949 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1949 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565679660	chr10:56603007-56603008	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs144791736	chr10:56603009-56603010	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs565619106	chr10:56603060-56603061	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs148548074	chr10:56603088-56603089	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs2061046	chr10:56603117-56603118	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs184585129	chr10:56603121-56603122	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs559096211	chr10:56603132-56603133	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs377270646	chr10:56603263-56603264	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs569397796	chr10:56603284-56603285	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs538129849	chr10:56603287-56603288	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs554879145	chr10:56603317-56603318	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs574458053	chr10:56603324-56603325	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs188489164	chr10:56603354-56603355	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs11004593	chr10:56603382-56603383	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs533125312	chr10:56603408-56603409	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs371994392	chr10:56603415-56603416	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs9633549	chr10:56603443-56603444	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142986081	chr10:56603557-56603558	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs546027225	chr10:56603565-56603566	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs562680007	chr10:56603574-56603575	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs78506165	chr10:56603575-56603576	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs111612410	chr10:56603582-56603583	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs537471866	chr10:56603631-56603632	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs561982307	chr10:56603672-56603673	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs527236887	chr10:56603674-56603675	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs547377384	chr10:56603696-56603697	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570391149	chr10:56603719-56603720	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs555861232	chr10:56603727-56603728	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs146625336	chr10:56603738-56603739	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs141251975	chr10:56603770-56603771	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs193097099	chr10:56603827-56603828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567792571	chr10:56603847-56603848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200544726	chr10:56603894-56603895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554813780	chr10:56603909-56603910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73256016	chr10:56603920-56603921	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533893585	chr10:56603953-56603954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185884283	chr10:56604051-56604052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190357526	chr10:56604056-56604057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539905971	chr10:56604080-56604081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116422869	chr10:56604093-56604094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146830297	chr10:56604112-56604113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556191233	chr10:56604123-56604124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113042388	chr10:56604145-56604146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534593555	chr10:56604163-56604164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375778260	chr10:56604189-56604190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572358864	chr10:56604219-56604220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541011683	chr10:56604243-56604244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs180975154	chr10:56604331-56604332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532825729	chr10:56604334-56604335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549816053	chr10:56604344-56604345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56601400-56606200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr10:56602200-56603200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr10:56602600-56603200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr10:56602600-56603400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr10:56602600-56603800	Enhancers	Fetal Brain Female	brain
6	chr10:56602600-56604400	Enhancers	Fetal Heart	heart
7	chr10:56602800-56603200	Active TSS	Left Ventricle	heart
8	chr10:56602800-56603800	Active TSS	Right Ventricle	heart
9	chr10:56603200-56606400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr10:56603400-56606800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr10:56606200-56606600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr10:56606400-56606800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr10:56606800-56607800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr10:56611400-56611600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr10:56611600-56615000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:56613600-56614000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr10:56615000-56615200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:56626800-56629000	Active TSS	Right Ventricle	heart
19	chr10:56628000-56628800	Active TSS	Left Ventricle	heart
20	chr10:56628400-56631200	Enhancers	Fetal Heart	heart
21	chr10:56629600-56629800	Enhancers	Left Ventricle	heart
22	chr10:56654200-56654800	Enhancers	Fetal Heart	heart
23	chr10:56662000-56663000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr10:56662200-56662600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr10:56662200-56663000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr10:56662200-56663000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr10:56662400-56662800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr10:56662400-56663000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr10:56662800-56666600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr10:56663000-56666600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr10:56663000-56674000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr10:56663600-56663800	Enhancers	Brain Germinal Matrix	brain
33	chr10:56664400-56667000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr10:56665200-56666000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:56665400-56665800	Enhancers	Brain Germinal Matrix	brain
36	chr10:56666600-56667000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr10:56666600-56667000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr10:56666600-56667000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr10:56669000-56669400	Enhancers	Fetal Muscle Trunk	muscle
40	chr10:56673800-56674200	Enhancers	HUVEC	blood vessel
41	chr10:56693200-56693600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr10:56720800-56722600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr10:56721400-56722600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr10:56722000-56722400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr10:56722000-56723000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr10:56748600-56749400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr10:56760400-56761600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr10:56760800-56761600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
49	chr10:56761000-56761600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr10:56761400-56762200	Enhancers	Skeletal Muscle Male	skeletal muscle

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