Variant report

Variant	nsv895459
Chromosome Location	chr10:56795078-57139743
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	ARID3A	chr10:57023730-57024067	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:56824881-56825361	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:56851552-56851852	HepG2	liver:	n/a	n/a
4	ATF1	chr10:56823985-56824004	K562	blood:	n/a	n/a
5	ATF1	chr10:56923483-56923663	K562	blood:	n/a	n/a
6	ATF3	chr10:57082402-57082655	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:56915619-56915866	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr10:56963172-56963378	GM12878	blood:	n/a	n/a
9	BATF	chr10:56963158-56963370	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:56824052-56824306	HepG2	liver:	n/a	chr10:56824192-56824201
11	BHLHE40	chr10:56825093-56825293	HepG2	liver:	n/a	n/a
12	BHLHE40	chr10:56824108-56824176	K562	blood:	n/a	n/a
13	BRCA1	chr10:56905896-56906096	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr10:56952521-56952565	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr10:57091511-57091621	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr10:57094577-57094601	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr10:57060510-57060769	A549	lung:	n/a	chr10:57060613-57060624
18	CEBPB	chr10:56980767-56981087	A549	lung:	n/a	chr10:56980929-56980940
19	CEBPB	chr10:56823617-56823850	HepG2	liver:	n/a	chr10:56823740-56823751
20	CEBPB	chr10:56848835-56849143	A549	lung:	n/a	chr10:56848975-56848988 chr10:56848975-56848986 chr10:56848956-56848967
21	CEBPB	chr10:57128479-57128741	A549	lung:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
22	CEBPB	chr10:57014381-57014683	IMR90	lung:	n/a	chr10:57014540-57014553
23	CEBPB	chr10:57000106-57000426	HepG2	liver:	n/a	chr10:57000251-57000262
24	CEBPB	chr10:56824968-56825269	HepG2	liver:	n/a	n/a
25	CEBPB	chr10:57000172-57000294	A549	lung:	n/a	chr10:57000251-57000262
26	CEBPB	chr10:56800037-56800274	H1-hESC	embryonic stem cell:	n/a	chr10:56800184-56800197
27	CEBPB	chr10:56877961-56878276	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr10:57060537-57060765	K562	blood:	n/a	chr10:57060613-57060624
29	CEBPB	chr10:57020877-57021146	HepG2	liver:	n/a	n/a
30	CEBPB	chr10:56904226-56904557	IMR90	lung:	n/a	chr10:56904375-56904386 chr10:56904377-56904386 chr10:56904376-56904387
31	CEBPB	chr10:57130666-57130959	HepG2	liver:	n/a	chr10:57130811-57130822
32	CEBPB	chr10:56975199-56975467	A549	lung:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
33	CEBPB	chr10:57070782-57071102	IMR90	lung:	n/a	chr10:57070961-57070978 chr10:57070962-57070973 chr10:57070830-57070841 chr10:57070932-57070945 chr10:57070932-57070943 chr10:57070963-57070975 chr10:57070828-57070841
34	CEBPB	chr10:57014403-57014700	HepG2	liver:	n/a	chr10:57014540-57014553
35	CEBPB	chr10:56980787-56981098	K562	blood:	n/a	chr10:56980929-56980940
36	CEBPB	chr10:57128461-57128779	HepG2	liver:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
37	CEBPB	chr10:57128470-57128745	IMR90	lung:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
38	CEBPB	chr10:56887559-56887835	HepG2	liver:	n/a	chr10:56887722-56887735 chr10:56887723-56887734 chr10:56887722-56887733
39	CEBPB	chr10:57000100-57000403	IMR90	lung:	n/a	chr10:57000251-57000262
40	CEBPB	chr10:56997265-56997554	Hela-S3	cervix:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
41	CEBPB	chr10:56934020-56934033	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr10:57060433-57060785	HepG2	liver:	n/a	chr10:57060613-57060624
43	CEBPB	chr10:57129864-57130320	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr10:56975295-56975404	H1-hESC	embryonic stem cell:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
45	CEBPB	chr10:56891925-56892145	HepG2	liver:	n/a	chr10:56892023-56892036 chr10:56891994-56892005 chr10:56892023-56892036 chr10:56892023-56892034
46	CEBPB	chr10:57082447-57082681	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr10:56987661-56987948	HepG2	liver:	n/a	chr10:56987791-56987802 chr10:56987855-56987868
48	CEBPB	chr10:56905802-56906206	Hela-S3	cervix:	n/a	chr10:56905996-56906007 chr10:56905996-56906007 chr10:56905997-56906008
49	CEBPB	chr10:57023727-57023998	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr10:56975198-56975541	HepG2	liver:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57026776-57026826	NT2-D1	testis:	n/a
2	chr10:57026776-57026826	AG04449	skin:	fetal
3	chr10:57026776-57026826	GM19239	blood:	n/a
4	chr10:57026776-57026826	Hepatocyte	liver:	n/a
5	chr10:57026776-57026826	AoSMC	blood vessel:	n/a
6	chr10:57026776-57026826	Caco-2	colon:	n/a
7	chr10:57026776-57026826	NHDF-neo	bronchial:	n/a
8	chr10:57026776-57026826	HCT-116	colon:	n/a
9	chr10:57026776-57026826	HEEpiC	esophagus:	n/a
10	chr10:57026776-57026826	HCF	heart:	n/a
11	chr10:57026776-57026826	AG04450	lung:	fetal
12	chr10:57026776-57026826	T-47D	breast:	n/a
13	chr10:57026776-57026826	HCM	heart:	n/a
14	chr10:57026776-57026826	AG10803	skin:	n/a
15	chr10:57026776-57026826	AG09319	gingival:	n/a
16	chr10:57026776-57026826	HPAEpiC	pulmonary alveolar:	n/a
17	chr10:57026776-57026826	HUVEC	blood vessel:	n/a
18	chr10:57026776-57026826	BJ	skin:	n/a
19	chr10:57026776-57026826	GM12891	blood:	n/a
20	chr10:57026776-57026826	U87	brain:	n/a
21	chr10:57026776-57026826	SK-N-SH_RA	brain:	n/a
22	chr10:57026776-57026826	LNCaP	prostate:	n/a
23	chr10:57026776-57026826	HIPEpiC	eye:	n/a
24	chr10:57026776-57026826	IMR90	lung:	fetal
25	chr10:57026776-57026826	PFSK-1	brain:	n/a
26	chr10:57026776-57026826	SK-N-SH	brain:	n/a
27	chr10:57026776-57026826	MCF10A-Er-Src	breast:	n/a
28	chr10:57026776-57026826	HRE	kidney:	n/a
29	chr10:57026776-57026826	Jurkat	blood:	n/a
30	chr10:57026776-57026826	SKMC	muscle:	n/a
31	chr10:57026776-57026826	HCPEpiC	choroid plexus:	n/a
32	chr10:57026776-57026826	NH-A	brain:	n/a
33	chr10:57026776-57026826	HMEC	breast:	n/a
34	chr10:57026776-57026826	Hela-S3	cervix:	n/a
35	chr10:57026776-57026826	K562	blood:	n/a
36	chr10:57026776-57026826	AG09309	skin:	n/a
37	chr10:57026776-57026826	MCF-7	breast:	n/a
38	chr10:57026776-57026826	NB4	blood:	n/a
39	chr10:57026776-57026826	GM06990	blood:	n/a
40	chr10:57026776-57026826	ProgFib	skin:	n/a
41	chr10:57026776-57026826	ovcar-3	ovarian:	n/a
42	chr10:57026776-57026826	GM12878	blood:	n/a
43	chr10:57026776-57026826	SK-N-MC	brain:	n/a
44	chr10:57026776-57026826	HNPCEpiC	eye:	n/a
45	chr10:57026776-57026826	HRCEpiC	kidney:	n/a
46	chr10:57026776-57026826	H1-hESC	embryonic stem cell:	embryo
47	chr10:57026776-57026826	CMK	blood:	n/a
48	chr10:57026776-57026826	GM12892	blood:	n/a
49	chr10:57026776-57026826	A549	lung:	n/a
50	chr10:57026776-57026826	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:57045296..57046208-chr13:38876652..38877471,2	MCF-7	breast:
2	chr10:56848923..56849830-chr22:31212899..31213539,2	MCF-7	breast:
3	chr10:57046815..57047629-chr10:57390561..57391169,3	MCF-7	breast:
4	chr10:56851202..56852127-chr10:57023430..57024403,6	MCF-7	breast:
5	chr10:57077687..57079914-chr10:57092227..57093981,2	K562	blood:
6	chr10:55757466..55757977-chr10:57022925..57023910,2	MCF-7	breast:
7	chr10:57128438..57131267-chr10:57136615..57139314,2	K562	blood:
8	chr10:56860242..56861881-chr10:56864566..56866178,2	K562	blood:
9	chr10:56851202..56852127-chr10:57023430..57024403,6	MCF-7	breast:
10	chr10:56926801..56928606-chr10:56934525..56937343,2	K562	blood:
11	chr10:56856112..56857067-chr10:57023573..57024305,2	MCF-7	breast:
12	chr10:56926801..56928606-chr10:56934525..56937343,2	K562	blood:
13	chr10:57046804..57047423-chr10:57260630..57261301,2	MCF-7	breast:
14	chr10:57063877..57064377-chr19:2475827..2476338,2	HCT-116	colon:
15	chr10:57128438..57131267-chr10:57136615..57139314,2	K562	blood:
16	chr10:57012609..57015608-chr6:34209555..34212466,2	K562	blood:
17	chr10:57070275..57072956-chr10:57073924..57076698,2	K562	blood:
18	chr10:56802881..56805062-chr10:56805603..56807529,2	K562	blood:
19	chr10:57070275..57072956-chr10:57073924..57076698,2	K562	blood:
20	chr10:56860242..56861881-chr10:56864566..56866178,2	K562	blood:
21	chr10:56930146..56932824-chr10:56934216..56936608,2	K562	blood:
22	chr10:56802881..56805062-chr10:56805603..56807529,2	K562	blood:
23	chr10:56930146..56932824-chr10:56934216..56936608,2	K562	blood:
24	chr10:56856112..56857067-chr10:57023573..57024305,2	MCF-7	breast:
25	chr10:57047149..57047763-chr10:57389634..57390254,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZWINT-4	chr10:57125852-57125973	ENSG00000236744.1
2	lnc-ZWINT-4	chr10:57007515-57007648	ENSG00000236744.2
3	lnc-ZWINT-4	chr10:57007508-57007648	ENSG00000236744.1
4	lnc-ZWINT-4	chr10:57125852-57125973	ENSG00000236744.2

Variant related genes	Relation type
PCDH15	TF binding region
PCDH15	CpG island
ENSG00000150275	chromatin interactions
ENSG00000099860	chromatin interactions

Extended variants
information (count: 3752 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3752 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534474913	chr10:56799021-56799022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181853726	chr10:56799029-56799030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530280695	chr10:56799171-56799172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11004696	chr10:56799192-56799193	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs74136333	chr10:56799193-56799194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532847202	chr10:56799225-56799226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552281818	chr10:56799232-56799233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190703873	chr10:56799235-56799236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146936540	chr10:56799317-56799318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2178646	chr10:56799334-56799335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114486722	chr10:56799345-56799346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533721003	chr10:56799365-56799366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553936526	chr10:56799374-56799375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541223067	chr10:56807802-56807803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186903454	chr10:56807846-56807847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192109813	chr10:56807855-56807856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550063360	chr10:56807907-56807908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569987053	chr10:56807986-56807987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201354665	chr10:56808027-56808028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72801621	chr10:56808057-56808058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548713873	chr10:56808134-56808135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs202134629	chr10:56808145-56808146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565759947	chr10:56808215-56808216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534468290	chr10:56808228-56808229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185014993	chr10:56808235-56808236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190209947	chr10:56808248-56808249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193147814	chr10:56808255-56808256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185596723	chr10:56808263-56808264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573788310	chr10:56808264-56808265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576667772	chr10:56808322-56808323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542196781	chr10:56808342-56808343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188416946	chr10:56808365-56808366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572480045	chr10:56808480-56808481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180734434	chr10:56808484-56808485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs55742901	chr10:56808501-56808502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564584349	chr10:56808562-56808563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577882030	chr10:56808563-56808564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185776014	chr10:56808617-56808618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563557088	chr10:56808623-56808624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529215210	chr10:56808695-56808696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548963025	chr10:56808804-56808805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10763176	chr10:56808806-56808807	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs528161665	chr10:56808832-56808833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562245115	chr10:56808848-56808849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368189109	chr10:56808858-56808859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10825449	chr10:56808870-56808871	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs571031435	chr10:56808895-56808896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539598952	chr10:56808961-56808962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117723843	chr10:56808967-56808968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570324844	chr10:56808980-56808981	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
small cell lung cancer	17426248	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56799000-56799400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr10:56807800-56809400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr10:56808200-56809200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:56808400-56809200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr10:56808400-56809400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr10:56808600-56809200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr10:56808800-56809200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr10:56808800-56809200	Enhancers	Brain Germinal Matrix	brain
9	chr10:56809000-56809200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr10:56824000-56825800	Enhancers	HepG2	liver
11	chr10:56840400-56841000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr10:56840800-56841200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr10:56841000-56841200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:56841200-56849000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr10:56847200-56847600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr10:56849000-56849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr10:56849000-56849200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:56849200-56849400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr10:56859800-56860200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:56868400-56868800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr10:56868600-56869000	Enhancers	HMEC	breast
22	chr10:56901200-56901800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr10:56903200-56903800	Enhancers	HMEC	breast
24	chr10:56903400-56904400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr10:56903400-56906400	Enhancers	HUVEC	blood vessel
26	chr10:56903800-56904200	Flanking Active TSS	HMEC	breast
27	chr10:56904000-56904400	Enhancers	Hela-S3	cervix
28	chr10:56904200-56905000	Enhancers	HMEC	breast
29	chr10:56905000-56905600	Weak transcription	HMEC	breast
30	chr10:56905600-56906400	Enhancers	HMEC	breast
31	chr10:56905600-56906400	Enhancers	NH-A	brain
32	chr10:56905800-56906600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:56914400-56915000	Enhancers	Fetal Heart	heart
34	chr10:56915000-56918200	Weak transcription	Fetal Heart	heart
35	chr10:56918200-56919000	Enhancers	Fetal Heart	heart
36	chr10:56918400-56918800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr10:56918400-56918800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr10:56918800-56920600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr10:56920000-56920600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr10:56920000-56920800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr10:56920000-56921800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr10:56920200-56920800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr10:56920200-56921400	Enhancers	HMEC	breast
44	chr10:56920400-56921200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr10:56920400-56921600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr10:56920600-56920800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr10:56920600-56921800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr10:56920800-56922400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr10:56921200-56921600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr10:56921600-56922800	Enhancers	HUES48 Cell Line	embryonic stem cell

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