Variant report

Variant	nsv540630
Chromosome Location	chr10:55040577-55279797
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	chr10:55128678-55128839	K562	blood:	n/a	n/a
2	ATF1	chr10:55149336-55149397	K562	blood:	n/a	n/a
3	ATF2	chr10:55238974-55239521	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:55236413-55237624	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:55217223-55217233	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr10:55239117-55239415	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
7	BCL11A	chr10:55239200-55239377	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
8	BHLHE40	chr10:55191987-55192023	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:55190762-55191068	GM12878	blood:	n/a	n/a
10	BRCA1	chr10:55236620-55237424	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr10:55239096-55239406	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr10:55233744-55234036	HepG2	liver:	n/a	chr10:55233869-55233880
13	CEBPB	chr10:55188572-55188772	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:55250346-55250673	IMR90	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
15	CEBPB	chr10:55239054-55239539	H1-hESC	embryonic stem cell:	n/a	chr10:55239464-55239475 chr10:55239371-55239383
16	CEBPB	chr10:55163410-55163758	MCF-7	breast:	n/a	n/a
17	CEBPB	chr10:55063709-55063996	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr10:55054100-55054129	K562	blood:	n/a	n/a
19	CEBPB	chr10:55063721-55064073	IMR90	lung:	n/a	n/a
20	CEBPB	chr10:55250389-55250679	Hela-S3	cervix:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
21	CEBPB	chr10:55121041-55121415	HepG2	liver:	n/a	chr10:55121222-55121233
22	CEBPB	chr10:55070800-55070915	H1-hESC	embryonic stem cell:	n/a	chr10:55070859-55070872 chr10:55070861-55070870 chr10:55070861-55070870 chr10:55070861-55070870
23	CEBPB	chr10:55250334-55250666	K562	blood:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
24	CEBPB	chr10:55250388-55250668	H1-hESC	embryonic stem cell:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
25	CEBPB	chr10:55063725-55064069	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:55250331-55250691	HepG2	liver:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
27	CEBPB	chr10:55250360-55250591	A549	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
28	CEBPB	chr10:55074637-55075013	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:55152197-55152412	IMR90	lung:	n/a	chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152225-55152236 chr10:55152362-55152373 chr10:55152225-55152238 chr10:55152225-55152238 chr10:55152225-55152236 chr10:55152322-55152331 chr10:55152320-55152331
30	CEBPB	chr10:55152219-55152475	HepG2	liver:	n/a	chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152322-55152331 chr10:55152225-55152236 chr10:55152362-55152373 chr10:55152225-55152238 chr10:55152225-55152238 chr10:55152225-55152236 chr10:55152322-55152331 chr10:55152320-55152331
31	CEBPB	chr10:55063815-55064038	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr10:55077103-55077366	H1-hESC	embryonic stem cell:	n/a	chr10:55077105-55077118 chr10:55077104-55077121
33	CEBPB	chr10:55121736-55122030	HepG2	liver:	n/a	n/a
34	CEBPB	chr10:55121071-55121398	HepG2	liver:	n/a	chr10:55121222-55121233
35	CEBPB	chr10:55070715-55071009	IMR90	lung:	n/a	chr10:55070859-55070872 chr10:55070861-55070870 chr10:55070861-55070870 chr10:55070861-55070870
36	CEBPB	chr10:55121112-55121293	HepG2	liver:	n/a	chr10:55121222-55121233
37	CEBPB	chr10:55063756-55064049	A549	lung:	n/a	n/a
38	CEBPB	chr10:55121105-55121362	HepG2	liver:	n/a	chr10:55121222-55121233
39	CEBPD	chr10:55121085-55121349	HepG2	liver:	n/a	n/a
40	CHD1	chr10:55239006-55239395	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr10:55236611-55237504	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr10:55269600-55269603	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr10:55238997-55239826	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr10:55213100-55213250	HPAF	blood vessel:	n/a	chr10:55213102-55213110
45	CTCF	chr10:55058240-55058390	GM12874	blood:	n/a	n/a
46	CTCF	chr10:55058352-55058401	LNCaP	prostate:	n/a	n/a
47	CTCF	chr10:55212920-55213070	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr10:55213060-55213210	HA-sp	spinal cord:	n/a	chr10:55213102-55213110
49	CTCF	chr10:55213000-55213150	HEEpiC	esophagus:	n/a	chr10:55213102-55213110
50	CTCF	chr10:55213060-55213210	HRPEpiC	eye:	n/a	chr10:55213102-55213110

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55118360-55118410	T-47D	breast:	n/a
2	chr10:55118360-55118410	T-47D	breast:	n/a
3	chr10:55259527-55259577	MCF10A-Er-Src	breast:	n/a
4	chr10:55148775-55148825	LNCaP	prostate:	n/a
5	chr10:55118360-55118410	HAEpiC	amniotic membrane:	n/a
6	chr10:55148775-55148825	AoSMC	blood vessel:	n/a
7	chr10:55118360-55118410	PrEC	prostate:	n/a
8	chr10:55259527-55259577	SK-N-SH	brain:	n/a
9	chr10:55259527-55259577	AG04449	skin:	fetal
10	chr10:55148775-55148825	IMR90	lung:	fetal
11	chr10:55148775-55148825	GM19239	blood:	n/a
12	chr10:55118360-55118410	MCF-7	breast:	n/a
13	chr10:55259527-55259577	Caco-2	colon:	n/a
14	chr10:55148775-55148825	GM12892	blood:	n/a
15	chr10:55148775-55148825	Hepatocyte	liver:	n/a
16	chr10:55259527-55259577	Hela-S3	cervix:	n/a
17	chr10:55118360-55118410	HepG2	liver:	n/a
18	chr10:55118360-55118410	U87	brain:	n/a
19	chr10:55259527-55259577	HRE	kidney:	n/a
20	chr10:55118360-55118410	HCT-116	colon:	n/a
21	chr10:55148775-55148825	HPAEpiC	pulmonary alveolar:	n/a
22	chr10:55259527-55259577	AG10803	skin:	n/a
23	chr10:55259527-55259577	K562	blood:	n/a
24	chr10:55259527-55259577	BE2_C	brain:	n/a
25	chr10:55118360-55118410	AG09319	gingival:	n/a
26	chr10:55259527-55259577	ovcar-3	ovarian:	n/a
27	chr10:55148775-55148825	GM06990	blood:	n/a
28	chr10:55148775-55148825	HIPEpiC	eye:	n/a
29	chr10:55259527-55259577	PANC-1	pancreas:	n/a
30	chr10:55148775-55148825	NB4	blood:	n/a
31	chr10:55118360-55118410	HL-60	blood:	n/a
32	chr10:55148775-55148825	AG04450	lung:	fetal
33	chr10:55259527-55259577	Hepatocyte	liver:	n/a
34	chr10:55148775-55148825	Jurkat	blood:	n/a
35	chr10:55148775-55148825	GM12878	blood:	n/a
36	chr10:55118360-55118410	Jurkat	blood:	n/a
37	chr10:55118360-55118410	BJ	skin:	n/a
38	chr10:55148775-55148825	NH-A	brain:	n/a
39	chr10:55259527-55259577	HRCEpiC	kidney:	n/a
40	chr10:55118360-55118410	NHBE	bronchial:	n/a
41	chr10:55148775-55148825	SK-N-SH_RA	brain:	n/a
42	chr10:55148775-55148825	HCT-116	colon:	n/a
43	chr10:55259527-55259577	U87	brain:	n/a
44	chr10:55259527-55259577	SAEC	small airway:	n/a
45	chr10:55148775-55148825	RPTEC	kidney:	n/a
46	chr10:55259527-55259577	BJ	skin:	n/a
47	chr10:55118360-55118410	AoSMC	blood vessel:	n/a
48	chr10:55148775-55148825	NHDF-neo	bronchial:	n/a
49	chr10:55148775-55148825	HCPEpiC	choroid plexus:	n/a
50	chr10:55259527-55259577	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:55107674..55109690-chr10:55123080..55124587,2	K562	blood:
2	chr10:55105553..55107958-chr10:55109358..55111015,2	K562	blood:
3	chr10:55057963..55058535-chr10:55568196..55569129,2	MCF-7	breast:
4	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
5	chr10:55278002..55279503-chr7:30548599..30550148,2	MCF-7	breast:
6	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
7	chr10:55105553..55107958-chr10:55109358..55111015,2	K562	blood:
8	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
9	chr10:55107674..55109690-chr10:55123080..55124587,2	K562	blood:
10	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
11	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH15-1	chr10:55050832-55051354	XLOC_008827
2	lnc-PCDH15-1	chr10:55070752-55070825	XLOC_008827

Variant related genes	Relation type
RNA5SP318	TF binding region
ENSG00000226296	TF binding region
RNA5SP318	CpG island
ENSG00000226296	CpG island

Extended variants
information (count: 8545 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:8545 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550687057	chr10:55044211-55044212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567400214	chr10:55044217-55044218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79671135	chr10:55044258-55044259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17679181	chr10:55044288-55044289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566616828	chr10:55044332-55044333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2384180	chr10:55044349-55044350	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557685952	chr10:55044384-55044385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2384181	chr10:55044408-55044409	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs537087635	chr10:55044409-55044410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143838263	chr10:55044425-55044426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2384182	chr10:55044456-55044457	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs180712081	chr10:55044469-55044470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551974089	chr10:55044486-55044487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74827385	chr10:55044487-55044488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573410346	chr10:55044499-55044500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs35870500	chr10:55044503-55044504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112151688	chr10:55044505-55044506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565615980	chr10:55044514-55044515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530502888	chr10:55044526-55044527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544252500	chr10:55044579-55044580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147234680	chr10:55044587-55044588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529810811	chr10:55044628-55044629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115084106	chr10:55044673-55044674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572963606	chr10:55044696-55044697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532254790	chr10:55044719-55044720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74134517	chr10:55044724-55044725	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs182981829	chr10:55044741-55044742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74134518	chr10:55044759-55044760	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537028320	chr10:55044775-55044776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375507352	chr10:55044781-55044782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550585551	chr10:55044806-55044807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186722514	chr10:55044841-55044842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536751853	chr10:55044858-55044859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7095212	chr10:55044886-55044887	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs534428388	chr10:55044906-55044907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191418222	chr10:55044914-55044915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116641080	chr10:55044928-55044929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376256824	chr10:55044937-55044938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs386743814	chr10:55044965-55044966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12762352	chr10:55046206-55046207	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568690893	chr10:55046240-55046241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533756359	chr10:55046242-55046243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561853789	chr10:55046369-55046370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552012616	chr10:55046379-55046380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553506335	chr10:55046442-55046443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576491606	chr10:55046482-55046483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545488537	chr10:55046499-55046500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555878892	chr10:55046504-55046505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575815015	chr10:55046534-55046535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190472627	chr10:55050888-55050889	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Dysmorphic features	21948486	CNVD
Epilepsy	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	17363583	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

Chromatin state (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55044200-55045000	Enhancers	Stomach Mucosa	stomach
2	chr10:55046200-55046600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr10:55052800-55053800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr10:55053200-55053600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
5	chr10:55053400-55053800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr10:55053800-55054800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:55064400-55064600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr10:55064600-55073200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:55069000-55069200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:55069200-55074600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr10:55073200-55073400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:55073400-55084800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:55074000-55075400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:55074000-55076200	Enhancers	NH-A	brain
15	chr10:55074200-55074400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:55074200-55075400	Enhancers	HMEC	breast
17	chr10:55074200-55075400	Enhancers	HSMM	muscle
18	chr10:55074200-55075400	Enhancers	NHEK	skin
19	chr10:55074200-55077800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr10:55074400-55075200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr10:55074600-55074800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr10:55074600-55074800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr10:55074600-55075000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr10:55074600-55075000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:55074600-55075000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr10:55074600-55075200	Enhancers	Fetal Kidney	kidney
27	chr10:55074600-55076000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr10:55074800-55075000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr10:55074800-55075000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr10:55074800-55075200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr10:55074800-55075200	Enhancers	HUVEC	blood vessel
32	chr10:55074800-55075600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr10:55074800-55076000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr10:55074800-55077600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr10:55074800-55077600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr10:55075000-55075200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr10:55075000-55075800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr10:55075000-55076000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr10:55075000-55076200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr10:55075000-55076400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr10:55075600-55075800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr10:55075800-55076200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr10:55076000-55077000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr10:55076000-55077600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr10:55076200-55077000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr10:55076200-55077600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr10:55076400-55077000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr10:55076400-55077600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr10:55076400-55077800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:55077000-55077400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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