Variant report

Variant	esv2752952
Chromosome Location	chr10:54900994-55497594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1548)
CpG islands
(count:611)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1548 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:55379164-55379197	K562	blood:	n/a	n/a
2	ARID3A	chr10:55361088-55361391	HepG2	liver:	n/a	n/a
3	ATF1	chr10:55149336-55149397	K562	blood:	n/a	n/a
4	ATF1	chr10:55128678-55128839	K562	blood:	n/a	n/a
5	ATF2	chr10:55357030-55358165	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr10:55236413-55237624	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr10:55238974-55239521	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr10:55357496-55358125	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr10:55358549-55359145	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:55410674-55410823	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:55025742-55025775	K562	blood:	n/a	n/a
12	BACH1	chr10:55217223-55217233	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:54999946-54999953	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr10:55357742-55358035	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr10:55239117-55239415	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
16	BCL11A	chr10:55358747-55359028	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr10:54926130-54926399	GM12878	blood:	n/a	n/a
18	BCL11A	chr10:55239200-55239377	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
19	BCL11A	chr10:55358639-55359002	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr10:55190762-55191068	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:55191987-55192023	GM12878	blood:	n/a	n/a
22	BHLHE40	chr10:54974049-54974075	GM12878	blood:	n/a	n/a
23	BRCA1	chr10:55040336-55040499	GM12878	blood:	n/a	n/a
24	BRCA1	chr10:55239096-55239406	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr10:55436651-55436653	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr10:55236620-55237424	H1-hESC	embryonic stem cell:	n/a	n/a
27	CCNT2	chr10:54935491-54935665	K562	blood:	n/a	n/a
28	CCNT2	chr10:55407553-55407753	K562	blood:	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	chr10:55233744-55234036	HepG2	liver:	n/a	chr10:55233869-55233880
31	CEBPB	chr10:55250346-55250673	IMR90	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
32	CEBPB	chr10:55121105-55121362	HepG2	liver:	n/a	chr10:55121222-55121233
33	CEBPB	chr10:55495107-55495314	A549	lung:	n/a	n/a
34	CEBPB	chr10:54923353-54923602	H1-hESC	embryonic stem cell:	n/a	chr10:54923452-54923463 chr10:54923453-54923464 chr10:54923452-54923465 chr10:54923540-54923553 chr10:54923452-54923465
35	CEBPB	chr10:55361129-55361360	A549	lung:	n/a	n/a
36	CEBPB	chr10:55063815-55064038	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr10:55070800-55070915	H1-hESC	embryonic stem cell:	n/a	chr10:55070859-55070872 chr10:55070861-55070870 chr10:55070861-55070870 chr10:55070861-55070870
38	CEBPB	chr10:55016346-55017038	Hela-S3	cervix:	n/a	chr10:55016409-55016420
39	CEBPB	chr10:55250389-55250679	Hela-S3	cervix:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
40	CEBPB	chr10:55030433-55030717	Hela-S3	cervix:	n/a	chr10:55030581-55030592
41	CEBPB	chr10:55316193-55316425	HepG2	liver:	n/a	chr10:55316279-55316290
42	CEBPB	chr10:55440217-55440437	IMR90	lung:	n/a	chr10:55440348-55440359
43	CEBPB	chr10:55250360-55250591	A549	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
44	CEBPB	chr10:55063721-55064073	IMR90	lung:	n/a	n/a
45	CEBPB	chr10:55030463-55030602	H1-hESC	embryonic stem cell:	n/a	chr10:55030581-55030592
46	CEBPB	chr10:55494993-55495303	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:55440562-55440588	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr10:54980854-54980893	K562	blood:	n/a	chr10:54980869-54980880 chr10:54980870-54980879
49	CEBPB	chr10:55311076-55311349	HepG2	liver:	n/a	chr10:55311194-55311205
50	CEBPB	chr10:54923324-54923567	A549	lung:	n/a	chr10:54923452-54923463 chr10:54923453-54923464 chr10:54923452-54923465 chr10:54923540-54923553 chr10:54923452-54923465

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55118360-55118410	AoSMC	blood vessel:	n/a
2	chr10:55118360-55118410	AoSMC	blood vessel:	n/a
3	chr10:55419714-55419764	Hepatocyte	liver:	n/a
4	chr10:55118360-55118410	U87	brain:	n/a
5	chr10:55419927-55419977	SK-N-MC	brain:	n/a
6	chr10:55016939-55016989	HNPCEpiC	eye:	n/a
7	chr10:55419714-55419764	NT2-D1	testis:	n/a
8	chr10:54969710-54969760	Caco-2	colon:	n/a
9	chr10:55148775-55148825	NHDF-neo	bronchial:	n/a
10	chr10:55357618-55357668	GM12892	blood:	n/a
11	chr10:55393450-55393500	GM06990	blood:	n/a
12	chr10:55419714-55419764	NH-A	brain:	n/a
13	chr10:55148775-55148825	AG09309	skin:	n/a
14	chr10:55118360-55118410	SKMC	muscle:	n/a
15	chr10:55393450-55393500	HL-60	blood:	n/a
16	chr10:55118360-55118410	NH-A	brain:	n/a
17	chr10:54969710-54969760	SK-N-SH	brain:	n/a
18	chr10:54984564-54984614	AG09309	skin:	n/a
19	chr10:55419714-55419764	AG09309	skin:	n/a
20	chr10:55419714-55419764	MCF-7	breast:	n/a
21	chr10:55419714-55419764	PrEC	prostate:	n/a
22	chr10:55419714-55419764	BJ	skin:	n/a
23	chr10:55148775-55148825	HIPEpiC	eye:	n/a
24	chr10:55118360-55118410	HRCEpiC	kidney:	n/a
25	chr10:55393450-55393500	GM19239	blood:	n/a
26	chr10:55016939-55016989	HEK293	kidney:	embryo
27	chr10:55393450-55393500	Hela-S3	cervix:	n/a
28	chr10:55419927-55419977	Hepatocyte	liver:	n/a
29	chr10:55118360-55118410	HepG2	liver:	n/a
30	chr10:55016939-55016989	Caco-2	colon:	n/a
31	chr10:55419927-55419977	T-47D	breast:	n/a
32	chr10:55357618-55357668	NHBE	bronchial:	n/a
33	chr10:55148775-55148825	SK-N-SH_RA	brain:	n/a
34	chr10:55016939-55016989	HMEC	breast:	n/a
35	chr10:55357618-55357668	U87	brain:	n/a
36	chr10:55357618-55357668	T-47D	breast:	n/a
37	chr10:55259527-55259577	BE2_C	brain:	n/a
38	chr10:55419714-55419764	Jurkat	blood:	n/a
39	chr10:55357618-55357668	NHDF-neo	bronchial:	n/a
40	chr10:55118360-55118410	GM12878	blood:	n/a
41	chr10:55419927-55419977	HCPEpiC	choroid plexus:	n/a
42	chr10:55357618-55357668	ECC-1	luminal epithelium:	n/a
43	chr10:54984564-54984614	PFSK-1	brain:	n/a
44	chr10:55357618-55357668	Jurkat	blood:	n/a
45	chr10:55357618-55357668	IMR90	lung:	fetal
46	chr10:55016939-55016989	SKMC	muscle:	n/a
47	chr10:55393450-55393500	NHDF-neo	bronchial:	n/a
48	chr10:55419714-55419764	HCF	heart:	n/a
49	chr10:55148775-55148825	GM12892	blood:	n/a
50	chr10:55419714-55419764	HRCEpiC	kidney:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:55303514..55305516-chr10:55305569..55307810,2	K562	blood:
2	chr10:55107674..55109690-chr10:55123080..55124587,2	K562	blood:
3	chr10:55010159..55011051-chr10:101190203..101191138,2	Hela-S3	cervix:
4	chr10:55298474..55301304-chr10:55304357..55306392,2	MCF-7	breast:
5	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
6	chr10:55028397..55030475-chr10:55031728..55034713,2	K562	blood:
7	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
8	chr10:55028156..55030475-chr10:55032367..55034713,2	K562	blood:
9	chr10:55105553..55107958-chr10:55109358..55111015,2	K562	blood:
10	chr10:55015124..55017354-chr10:55018929..55021209,2	K562	blood:
11	chr10:55466040..55468835-chr10:55471879..55474110,2	K562	blood:
12	chr10:54974391..54976394-chr10:54976441..54978497,2	MCF-7	breast:
13	chr10:55028397..55030475-chr10:55031728..55034713,2	K562	blood:
14	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
15	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:
16	chr10:54912408..54915011-chr10:54917539..54919981,2	MCF-7	breast:
17	chr10:54961525..54963201-chr10:54972554..54974128,2	K562	blood:
18	chr1:121484537..121485403-chr10:54967003..54967520,2	MCF-7	breast:
19	chr10:55360709..55361787-chr10:55606233..55607054,5	MCF-7	breast:
20	chr10:55360883..55361625-chr10:55568215..55569121,2	MCF-7	breast:
21	chr10:55028156..55030475-chr10:55032367..55034713,2	K562	blood:
22	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
23	chr10:55405153..55407581-chr5:63345532..63348450,2	MCF-7	breast:
24	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
25	chr10:55105553..55107958-chr10:55109358..55111015,2	K562	blood:
26	chr10:55107674..55109690-chr10:55123080..55124587,2	K562	blood:
27	chr10:55481740..55482260-chr20:52673713..52674214,2	MCF-7	breast:
28	chr10:55015124..55017354-chr10:55018929..55021209,2	K562	blood:
29	chr10:55313361..55315052-chr10:55318156..55320737,2	K562	blood:
30	chr10:55057963..55058535-chr10:55568196..55569129,2	MCF-7	breast:
31	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:
32	chr10:55313361..55315052-chr10:55318156..55320737,2	K562	blood:
33	chr10:54961525..54963201-chr10:54972554..54974128,2	K562	blood:
34	chr10:55303514..55305516-chr10:55305569..55307810,2	K562	blood:
35	chr10:55298474..55301304-chr10:55304357..55306392,2	MCF-7	breast:
36	chr10:54974391..54976394-chr10:54976441..54978497,2	MCF-7	breast:
37	chr10:54912408..54915011-chr10:54917539..54919981,2	MCF-7	breast:
38	chr10:55278002..55279503-chr7:30548599..30550148,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
RNA5SP318	TF binding region
ENSG00000226296	TF binding region
RNA5SP318	CpG island
ENSG00000226296	CpG island
ENSG00000224934	chromatin interactions
ENSG00000120053	chromatin interactions

Extended variants
information (count: 18260 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:18260 , 50 per page) page: 1 2 3 4 5 6 7 ... 366

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372827678	chr10:54900996-54900997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1871072	chr10:54901002-54901003	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs560381955	chr10:54901009-54901010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537035495	chr10:54901011-54901012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530711715	chr10:54901062-54901063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145916789	chr10:54901096-54901097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189953879	chr10:54901097-54901098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1871073	chr10:54901106-54901107	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs181710311	chr10:54901118-54901119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573377429	chr10:54901169-54901170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545198443	chr10:54901242-54901243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371302983	chr10:54901271-54901272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185449692	chr10:54901277-54901278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544636490	chr10:54901278-54901279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561219946	chr10:54901284-54901285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138324921	chr10:54901432-54901433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12357122	chr10:54901434-54901435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559329827	chr10:54901437-54901438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560157415	chr10:54901476-54901477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528888918	chr10:54901478-54901479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149145395	chr10:54901483-54901484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551222826	chr10:54901494-54901495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564577727	chr10:54901495-54901496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571336539	chr10:54901586-54901587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143228280	chr10:54901597-54901598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550166291	chr10:54901600-54901601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75956436	chr10:54901635-54901636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536591737	chr10:54901652-54901653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553250017	chr10:54901667-54901668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566985730	chr10:54901671-54901672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190222142	chr10:54901691-54901692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558853315	chr10:54901714-54901715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4408237	chr10:54901719-54901720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs544677257	chr10:54901734-54901735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555042619	chr10:54901735-54901736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574881803	chr10:54901741-54901742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2891434	chr10:54901813-54901814	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs559584670	chr10:54901837-54901838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111852187	chr10:54901912-54901913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148328386	chr10:54901917-54901918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373558043	chr10:54901921-54901922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143063301	chr10:54901940-54901941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564884038	chr10:54901941-54901942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530532354	chr10:54902002-54902003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147408126	chr10:54902032-54902033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10762930	chr10:54902038-54902039	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs529623132	chr10:54902084-54902085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181953426	chr10:54902100-54902101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539997020	chr10:54902102-54902103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567172324	chr10:54902112-54902113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1118 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54900000-54901200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:54900800-54902600	Weak transcription	Fetal Intestine Small	intestine
3	chr10:54902200-54902600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:54902600-54903200	Enhancers	Fetal Intestine Small	intestine
5	chr10:54908800-54909000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:54909400-54909600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr10:54910200-54910400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr10:54910200-54910400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr10:54910200-54910400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chr10:54910200-54910400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr10:54910800-54911000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
12	chr10:54918000-54918400	Enhancers	Stomach Mucosa	stomach
13	chr10:54922000-54922600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr10:54922600-54923200	Enhancers	Liver	Liver
15	chr10:54934000-54934400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr10:54934000-54934400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr10:54935000-54935200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr10:54936800-54938000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr10:54951400-54951600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:54951600-54960800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr10:54960800-54961200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr10:54961200-54965000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr10:54964200-54966000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr10:54965000-54965400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:54965400-54966400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:54966000-54969600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr10:54966400-54981600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr10:54968600-54968800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr10:54968600-54970800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr10:54968800-54970000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr10:54968800-54970200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr10:54968800-54970600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr10:54969400-54970400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr10:54969600-54970400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr10:54969600-54970400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr10:54969600-54970800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr10:54969800-54970200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr10:54969800-54970400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr10:54970000-54970400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr10:54970000-54970400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr10:54970000-54970400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr10:54970000-54970400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr10:54970400-54974600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr10:54970800-54971400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr10:54971400-54971600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr10:54972600-54972800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr10:54979600-54980000	Enhancers	Fetal Heart	heart
48	chr10:54981600-54983200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr10:54981600-54983200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:54982000-54984000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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