Variant report

Variant	nsv1037480
Chromosome Location	chr10:55102814-55289571
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	chr10:55236413-55237624	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:55238974-55239521	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	chr10:55190762-55191068	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:55191987-55192023	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	chr10:55250331-55250691	HepG2	liver:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
13	CEBPB	chr10:55250360-55250591	A549	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
14	CEBPB	chr10:55250388-55250668	H1-hESC	embryonic stem cell:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
15	CEBPB	chr10:55250346-55250673	IMR90	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
16	CEBPB	chr10:55121736-55122030	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:55233744-55234036	HepG2	liver:	n/a	chr10:55233869-55233880
18	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
19	CEBPB	chr10:55121071-55121398	HepG2	liver:	n/a	chr10:55121222-55121233
20	CEBPB	chr10:55250334-55250666	K562	blood:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
21	CEBPB	chr10:55121105-55121362	HepG2	liver:	n/a	chr10:55121222-55121233
22	CEBPB	chr10:55121112-55121293	HepG2	liver:	n/a	chr10:55121222-55121233
23	CEBPB	chr10:55239054-55239539	H1-hESC	embryonic stem cell:	n/a	chr10:55239464-55239475 chr10:55239371-55239383
24	CEBPB	chr10:55163410-55163758	MCF-7	breast:	n/a	n/a
25	CEBPB	chr10:55250389-55250679	Hela-S3	cervix:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
26	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
27	CEBPB	chr10:55121041-55121415	HepG2	liver:	n/a	chr10:55121222-55121233
28	CEBPB	chr10:55188572-55188772	HepG2	liver:	n/a	n/a
29	CEBPD	chr10:55121085-55121349	HepG2	liver:	n/a	n/a
30	CHD1	chr10:55269600-55269603	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr10:55239006-55239395	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr10:55236611-55237504	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr10:55238997-55239826	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr10:55212980-55213130	HAc	cerebellar:	n/a	chr10:55213102-55213110
35	CTCF	chr10:55213100-55213250	GM12870	blood:	n/a	chr10:55213102-55213110
36	CTCF	chr10:55213064-55213243	HepG2	liver:	n/a	chr10:55213102-55213110
37	CTCF	chr10:55213063-55213254	HUVEC	blood vessel:	n/a	chr10:55213102-55213110
38	CTCF	chr10:55213080-55213230	GM12869	blood:	n/a	chr10:55213102-55213110
39	CTCF	chr10:55213040-55213190	HPF	lung:	n/a	chr10:55213102-55213110
40	CTCF	chr10:55213060-55213210	GM12870	blood:	n/a	chr10:55213102-55213110
41	CTCF	chr10:55213093-55213166	Medullo	brain:	n/a	chr10:55213102-55213110
42	CTCF	chr10:55174899-55174937	GM13976	blood:	n/a	n/a
43	CTCF	chr10:55213120-55213270	NHEK	skin:	n/a	n/a
44	CTCF	chr10:55213100-55213250	BE2_C	brain:	n/a	chr10:55213102-55213110
45	CTCF	chr10:55213060-55213210	HPF	lung:	n/a	chr10:55213102-55213110
46	CTCF	chr10:55213060-55213210	HA-sp	spinal cord:	n/a	chr10:55213102-55213110
47	CTCF	chr10:55213142-55213163	K562	blood:	n/a	n/a
48	CTCF	chr10:55213097-55213196	GM10266	blood:	n/a	chr10:55213102-55213110
49	CTCF	chr10:55213093-55213177	SK-N-SH_RA	brain:	n/a	chr10:55213102-55213110
50	CTCF	chr10:55213120-55213270	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55259527-55259577	LNCaP	prostate:	n/a
2	chr10:55118360-55118410	BJ	skin:	n/a
3	chr10:55259527-55259577	HIPEpiC	eye:	n/a
4	chr10:55259527-55259577	AG09309	skin:	n/a
5	chr10:55118360-55118410	HNPCEpiC	eye:	n/a
6	chr10:55118360-55118410	T-47D	breast:	n/a
7	chr10:55118360-55118410	BE2_C	brain:	n/a
8	chr10:55259527-55259577	Hepatocyte	liver:	n/a
9	chr10:55118360-55118410	CMK	blood:	n/a
10	chr10:55259527-55259577	BJ	skin:	n/a
11	chr10:55118360-55118410	HCT-116	colon:	n/a
12	chr10:55148775-55148825	GM12891	blood:	n/a
13	chr10:55148775-55148825	GM12878	blood:	n/a
14	chr10:55259527-55259577	GM12892	blood:	n/a
15	chr10:55148775-55148825	Hepatocyte	liver:	n/a
16	chr10:55259527-55259577	HNPCEpiC	eye:	n/a
17	chr10:55118360-55118410	AoSMC	blood vessel:	n/a
18	chr10:55148775-55148825	ProgFib	skin:	n/a
19	chr10:55148775-55148825	T-47D	breast:	n/a
20	chr10:55118360-55118410	HEEpiC	esophagus:	n/a
21	chr10:55118360-55118410	HMEC	breast:	n/a
22	chr10:55259527-55259577	ProgFib	skin:	n/a
23	chr10:55118360-55118410	GM12891	blood:	n/a
24	chr10:55118360-55118410	SKMC	muscle:	n/a
25	chr10:55148775-55148825	NB4	blood:	n/a
26	chr10:55259527-55259577	HEK293	kidney:	embryo
27	chr10:55259527-55259577	HUVEC	blood vessel:	n/a
28	chr10:55259527-55259577	MCF-7	breast:	n/a
29	chr10:55118360-55118410	SK-N-MC	brain:	n/a
30	chr10:55118360-55118410	SK-N-SH_RA	brain:	n/a
31	chr10:55259527-55259577	PFSK-1	brain:	n/a
32	chr10:55118360-55118410	HPAEpiC	pulmonary alveolar:	n/a
33	chr10:55259527-55259577	HRE	kidney:	n/a
34	chr10:55259527-55259577	HL-60	blood:	n/a
35	chr10:55259527-55259577	Jurkat	blood:	n/a
36	chr10:55148775-55148825	K562	blood:	n/a
37	chr10:55148775-55148825	HL-60	blood:	n/a
38	chr10:55148775-55148825	PANC-1	pancreas:	n/a
39	chr10:55118360-55118410	HEK293	kidney:	embryo
40	chr10:55259527-55259577	HAEpiC	amniotic membrane:	n/a
41	chr10:55118360-55118410	HepG2	liver:	n/a
42	chr10:55118360-55118410	AG10803	skin:	n/a
43	chr10:55148775-55148825	HCM	heart:	n/a
44	chr10:55259527-55259577	NH-A	brain:	n/a
45	chr10:55148775-55148825	CMK	blood:	n/a
46	chr10:55148775-55148825	SK-N-MC	brain:	n/a
47	chr10:55259527-55259577	HCT-116	colon:	n/a
48	chr10:55148775-55148825	ovcar-3	ovarian:	n/a
49	chr10:55148775-55148825	U87	brain:	n/a
50	chr10:55259527-55259577	IMR90	lung:	fetal

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

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

Extended variants
information (count: 7113 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7113 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568859190	chr10:55102818-55102819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375789680	chr10:55102823-55102824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192166027	chr10:55102828-55102829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568192387	chr10:55102829-55102830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533973184	chr10:55102837-55102838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74134532	chr10:55102842-55102843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570614740	chr10:55102845-55102846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184752718	chr10:55102853-55102854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542578306	chr10:55102916-55102917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558650443	chr10:55102942-55102943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575252534	chr10:55103040-55103041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189518091	chr10:55103046-55103047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554621271	chr10:55103071-55103072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75588978	chr10:55103145-55103146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369210931	chr10:55103169-55103170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574637632	chr10:55103171-55103172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557981889	chr10:55103200-55103201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192205746	chr10:55103207-55103208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184358949	chr10:55103230-55103231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577414721	chr10:55103240-55103241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76115739	chr10:55103242-55103243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7084385	chr10:55103258-55103259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189345355	chr10:55103284-55103285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531312748	chr10:55103285-55103286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548255812	chr10:55103292-55103293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561758290	chr10:55103293-55103294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139599730	chr10:55103302-55103303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs80071355	chr10:55103329-55103330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576450581	chr10:55103382-55103383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570647054	chr10:55103414-55103415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147617310	chr10:55103418-55103419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79745784	chr10:55103427-55103428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564894654	chr10:55103428-55103429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149743510	chr10:55103434-55103435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569641809	chr10:55103445-55103446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145485720	chr10:55103448-55103449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554582630	chr10:55103461-55103462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574549752	chr10:55103471-55103472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572049431	chr10:55103489-55103490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534301887	chr10:55103518-55103519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148397788	chr10:55103572-55103573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540922151	chr10:55103575-55103576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181363634	chr10:55103616-55103617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185491730	chr10:55103665-55103666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74134533	chr10:55103673-55103674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181592097	chr10:55103725-55103726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541807153	chr10:55103766-55103767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115676810	chr10:55103775-55103776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186146655	chr10:55103781-55103782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190811094	chr10:55103786-55103787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55096600-55104000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:55098400-55103600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr10:55098600-55103600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr10:55098800-55103600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr10:55098800-55103600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr10:55099400-55103800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr10:55103000-55104600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr10:55103600-55103800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr10:55103600-55104400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr10:55103600-55104400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr10:55103600-55104400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr10:55103600-55104400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr10:55103600-55104600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr10:55103600-55104600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr10:55103600-55104600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr10:55103800-55104400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr10:55103800-55104800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr10:55104000-55104400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr10:55104400-55105800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr10:55104400-55105800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr10:55104400-55108000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr10:55104400-55109400	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr10:55104400-55117400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr10:55105800-55106000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr10:55106000-55106200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr10:55108000-55108200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr10:55109400-55109600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr10:55115800-55116000	Enhancers	H9 Cell Line	embryonic stem cell
29	chr10:55116000-55116200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr10:55116000-55116400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:55116000-55117400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr10:55116000-55118400	Enhancers	HMEC	breast
33	chr10:55116200-55117200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr10:55116400-55116800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr10:55116400-55116800	Enhancers	Fetal Heart	heart
36	chr10:55116400-55118000	Enhancers	NHEK	skin
37	chr10:55116400-55118600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr10:55116600-55117000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr10:55116800-55117200	Weak transcription	Fetal Heart	heart
40	chr10:55116800-55117800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr10:55116800-55117800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr10:55116800-55118000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr10:55116800-55118200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr10:55117000-55117400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr10:55117000-55119400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr10:55117200-55117800	Enhancers	Fetal Heart	heart
47	chr10:55117200-55118400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr10:55117200-55119400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr10:55117200-55119400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr10:55117200-55119600	Enhancers	HUES64 Cell Line	embryonic stem cell

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