Variant report

Variant	esv2758222
Chromosome Location	chr10:56833543-57111393
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	chr10:56851552-56851852	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:57023730-57024067	HepG2	liver:	n/a	n/a
3	ATF1	chr10:56923483-56923663	K562	blood:	n/a	n/a
4	ATF3	chr10:57082402-57082655	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:56915619-56915866	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:56963158-56963370	GM12878	blood:	n/a	n/a
7	BATF	chr10:56963172-56963378	GM12878	blood:	n/a	n/a
8	BRCA1	chr10:56905896-56906096	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr10:57094577-57094601	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr10:56952521-56952565	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr10:57091511-57091621	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr10:57060510-57060769	A549	lung:	n/a	chr10:57060613-57060624
13	CEBPB	chr10:57023727-57023998	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:57014429-57014701	Hela-S3	cervix:	n/a	chr10:57014540-57014553
15	CEBPB	chr10:56987661-56987948	HepG2	liver:	n/a	chr10:56987791-56987802 chr10:56987855-56987868
16	CEBPB	chr10:57022653-57022930	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr10:57000172-57000294	A549	lung:	n/a	chr10:57000251-57000262
18	CEBPB	chr10:56980767-56981087	A549	lung:	n/a	chr10:56980929-56980940
19	CEBPB	chr10:56848796-56849144	HepG2	liver:	n/a	chr10:56848975-56848988 chr10:56848975-56848986 chr10:56848956-56848967
20	CEBPB	chr10:57000080-57000434	Hela-S3	cervix:	n/a	chr10:57000251-57000262
21	CEBPB	chr10:56868542-56868727	HepG2	liver:	n/a	n/a
22	CEBPB	chr10:56975295-56975404	H1-hESC	embryonic stem cell:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
23	CEBPB	chr10:57000100-57000403	IMR90	lung:	n/a	chr10:57000251-57000262
24	CEBPB	chr10:56980747-56981119	IMR90	lung:	n/a	chr10:56980929-56980940
25	CEBPB	chr10:56877961-56878276	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:56997265-56997554	Hela-S3	cervix:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
27	CEBPB	chr10:56887559-56887835	HepG2	liver:	n/a	chr10:56887722-56887735 chr10:56887723-56887734 chr10:56887722-56887733
28	CEBPB	chr10:56980832-56981047	H1-hESC	embryonic stem cell:	n/a	chr10:56980929-56980940
29	CEBPB	chr10:56905802-56906206	Hela-S3	cervix:	n/a	chr10:56905996-56906007 chr10:56905996-56906007 chr10:56905997-56906008
30	CEBPB	chr10:56975199-56975467	A549	lung:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
31	CEBPB	chr10:56989960-56990287	HepG2	liver:	n/a	chr10:56990029-56990042 chr10:56990029-56990042 chr10:56990031-56990042 chr10:56990031-56990042
32	CEBPB	chr10:56934020-56934033	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr10:56975198-56975541	HepG2	liver:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
34	CEBPB	chr10:57014403-57014700	HepG2	liver:	n/a	chr10:57014540-57014553
35	CEBPB	chr10:56848835-56849143	A549	lung:	n/a	chr10:56848975-56848988 chr10:56848975-56848986 chr10:56848956-56848967
36	CEBPB	chr10:56980759-56981124	HepG2	liver:	n/a	chr10:56980929-56980940
37	CEBPB	chr10:56904226-56904557	IMR90	lung:	n/a	chr10:56904375-56904386 chr10:56904377-56904386 chr10:56904376-56904387
38	CEBPB	chr10:56997254-56997579	IMR90	lung:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
39	CEBPB	chr10:57038695-57038853	H1-hESC	embryonic stem cell:	n/a	chr10:57038777-57038788 chr10:57038777-57038788
40	CEBPB	chr10:56848844-56849153	IMR90	lung:	n/a	chr10:56848975-56848988 chr10:56848975-56848986 chr10:56848956-56848967
41	CEBPB	chr10:56975189-56975523	IMR90	lung:	n/a	chr10:56975355-56975368 chr10:56975193-56975206 chr10:56975355-56975368 chr10:56975355-56975366
42	CEBPB	chr10:56859321-56859594	HepG2	liver:	n/a	chr10:56859448-56859459
43	CEBPB	chr10:56989995-56990341	K562	blood:	n/a	chr10:56990029-56990042 chr10:56990029-56990042 chr10:56990031-56990042 chr10:56990031-56990042
44	CEBPB	chr10:57060537-57060765	K562	blood:	n/a	chr10:57060613-57060624
45	CEBPB	chr10:57014366-57014664	A549	lung:	n/a	chr10:57014540-57014553
46	CEBPB	chr10:57060444-57060785	Hela-S3	cervix:	n/a	chr10:57060613-57060624
47	CEBPB	chr10:57060454-57060783	IMR90	lung:	n/a	chr10:57060613-57060624
48	CEBPB	chr10:57000106-57000426	HepG2	liver:	n/a	chr10:57000251-57000262
49	CEBPB	chr10:56997308-56997584	H1-hESC	embryonic stem cell:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
50	CEBPB	chr10:57020877-57021146	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57026776-57026826	LNCaP	prostate:	n/a
2	chr10:57026776-57026826	ECC-1	luminal epithelium:	n/a
3	chr10:57026776-57026826	BJ	skin:	n/a
4	chr10:57026776-57026826	AG09319	gingival:	n/a
5	chr10:57026776-57026826	Hepatocyte	liver:	n/a
6	chr10:57026776-57026826	GM06990	blood:	n/a
7	chr10:57026776-57026826	SKMC	muscle:	n/a
8	chr10:57026776-57026826	HCM	heart:	n/a
9	chr10:57026776-57026826	Hela-S3	cervix:	n/a
10	chr10:57026776-57026826	HL-60	blood:	n/a
11	chr10:57026776-57026826	AG04449	skin:	fetal
12	chr10:57026776-57026826	NT2-D1	testis:	n/a
13	chr10:57026776-57026826	T-47D	breast:	n/a
14	chr10:57026776-57026826	MCF10A-Er-Src	breast:	n/a
15	chr10:57026776-57026826	Jurkat	blood:	n/a
16	chr10:57026776-57026826	SAEC	small airway:	n/a
17	chr10:57026776-57026826	BE2_C	brain:	n/a
18	chr10:57026776-57026826	HepG2	liver:	n/a
19	chr10:57026776-57026826	ovcar-3	ovarian:	n/a
20	chr10:57026776-57026826	AG04450	lung:	fetal
21	chr10:57026776-57026826	HRE	kidney:	n/a
22	chr10:57026776-57026826	HRPEpiC	eye:	n/a
23	chr10:57026776-57026826	Caco-2	colon:	n/a
24	chr10:57026776-57026826	NH-A	brain:	n/a
25	chr10:57026776-57026826	GM19239	blood:	n/a
26	chr10:57026776-57026826	MCF-7	breast:	n/a
27	chr10:57026776-57026826	GM12878	blood:	n/a
28	chr10:57026776-57026826	SK-N-SH	brain:	n/a
29	chr10:57026776-57026826	IMR90	lung:	fetal
30	chr10:57026776-57026826	AG09309	skin:	n/a
31	chr10:57026776-57026826	HCF	heart:	n/a
32	chr10:57026776-57026826	SK-N-SH_RA	brain:	n/a
33	chr10:57026776-57026826	HIPEpiC	eye:	n/a
34	chr10:57026776-57026826	PANC-1	pancreas:	n/a
35	chr10:57026776-57026826	HEEpiC	esophagus:	n/a
36	chr10:57026776-57026826	CMK	blood:	n/a
37	chr10:57026776-57026826	RPTEC	kidney:	n/a
38	chr10:57026776-57026826	HCT-116	colon:	n/a
39	chr10:57026776-57026826	HAEpiC	amniotic membrane:	n/a
40	chr10:57026776-57026826	H1-hESC	embryonic stem cell:	embryo
41	chr10:57026776-57026826	AoSMC	blood vessel:	n/a
42	chr10:57026776-57026826	PrEC	prostate:	n/a
43	chr10:57026776-57026826	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:57026776-57026826	A549	lung:	n/a
45	chr10:57026776-57026826	HUVEC	blood vessel:	n/a
46	chr10:57026776-57026826	HMEC	breast:	n/a
47	chr10:57026776-57026826	NHDF-neo	bronchial:	n/a
48	chr10:57026776-57026826	U87	brain:	n/a
49	chr10:57026776-57026826	PFSK-1	brain:	n/a
50	chr10:57026776-57026826	HCPEpiC	choroid plexus:	n/a

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

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

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

Extended variants
information (count: 2918 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2918 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565323197	chr10:56840420-56840421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534344499	chr10:56840470-56840471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557428825	chr10:56840494-56840495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372529289	chr10:56840504-56840505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577707790	chr10:56840525-56840526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571004778	chr10:56840535-56840536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190585155	chr10:56840548-56840549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373922374	chr10:56840564-56840565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576599792	chr10:56840578-56840579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542503863	chr10:56840584-56840585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2250764	chr10:56840593-56840594	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572446386	chr10:56840600-56840601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140703759	chr10:56840627-56840628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183451502	chr10:56840628-56840629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374774594	chr10:56840632-56840633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74879474	chr10:56840646-56840647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377554803	chr10:56840653-56840654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533228566	chr10:56840654-56840655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1573227	chr10:56840690-56840691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370335599	chr10:56840717-56840718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75134975	chr10:56840733-56840734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10825457	chr10:56840738-56840739	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs10437360	chr10:56840745-56840746	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565684697	chr10:56840755-56840756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145647706	chr10:56840761-56840762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550924811	chr10:56840789-56840790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571226133	chr10:56840791-56840792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371956067	chr10:56840813-56840814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536721598	chr10:56840820-56840821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35517467	chr10:56840896-56840897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557032798	chr10:56840916-56840917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566708282	chr10:56840973-56840974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187774977	chr10:56840975-56840976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75675751	chr10:56841021-56841022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114570381	chr10:56841042-56841043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369550473	chr10:56841047-56841048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572815811	chr10:56841081-56841082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541755834	chr10:56841082-56841083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192716666	chr10:56841087-56841088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569836724	chr10:56841093-56841094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148083549	chr10:56841145-56841146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182373694	chr10:56841153-56841154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559136477	chr10:56841183-56841184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10825458	chr10:56841186-56841187	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548806747	chr10:56841209-56841210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559134221	chr10:56841238-56841239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551914548	chr10:56841242-56841243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538712963	chr10:56841265-56841266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551678069	chr10:56841274-56841275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115400294	chr10:56841324-56841325	Weak transcription	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:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56840400-56841000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr10:56840800-56841200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr10:56841000-56841200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:56841200-56849000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:56847200-56847600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr10:56849000-56849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr10:56849000-56849200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:56849200-56849400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr10:56859800-56860200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:56868400-56868800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr10:56868600-56869000	Enhancers	HMEC	breast
12	chr10:56901200-56901800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr10:56903200-56903800	Enhancers	HMEC	breast
14	chr10:56903400-56904400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:56903400-56906400	Enhancers	HUVEC	blood vessel
16	chr10:56903800-56904200	Flanking Active TSS	HMEC	breast
17	chr10:56904000-56904400	Enhancers	Hela-S3	cervix
18	chr10:56904200-56905000	Enhancers	HMEC	breast
19	chr10:56905000-56905600	Weak transcription	HMEC	breast
20	chr10:56905600-56906400	Enhancers	HMEC	breast
21	chr10:56905600-56906400	Enhancers	NH-A	brain
22	chr10:56905800-56906600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr10:56914400-56915000	Enhancers	Fetal Heart	heart
24	chr10:56915000-56918200	Weak transcription	Fetal Heart	heart
25	chr10:56918200-56919000	Enhancers	Fetal Heart	heart
26	chr10:56918400-56918800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr10:56918400-56918800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr10:56918800-56920600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr10:56920000-56920600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr10:56920000-56920800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr10:56920000-56921800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr10:56920200-56920800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr10:56920200-56921400	Enhancers	HMEC	breast
34	chr10:56920400-56921200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr10:56920400-56921600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr10:56920600-56920800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr10:56920600-56921800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr10:56920800-56922400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr10:56921200-56921600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr10:56921600-56922800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr10:56922200-56922400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr10:56922400-56922600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr10:56932200-56932600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr10:56932200-56932800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr10:56932200-56933000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr10:56932200-56933200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr10:56932600-56933000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr10:56932600-56933000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr10:56932800-56933000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr10:56932800-56934000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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