Variant report

Variant	nsv540629
Chromosome Location	chr10:55003164-55283251
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	chr10:55025742-55025775	K562	blood:	n/a	n/a
6	BACH1	chr10:55217223-55217233	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr10:55239200-55239377	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
8	BCL11A	chr10:55239117-55239415	H1-hESC	embryonic stem cell:	n/a	chr10:55239353-55239362
9	BHLHE40	chr10:55191987-55192023	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:55190762-55191068	GM12878	blood:	n/a	n/a
11	BRCA1	chr10:55040336-55040499	GM12878	blood:	n/a	n/a
12	BRCA1	chr10:55236620-55237424	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr10:55239096-55239406	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:55250360-55250591	A549	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
15	CEBPB	chr10:55063709-55063996	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr10:55074637-55075013	IMR90	lung:	n/a	n/a
17	CEBPB	chr10:55121071-55121398	HepG2	liver:	n/a	chr10:55121222-55121233
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	chr10:55188572-55188772	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:55163410-55163758	MCF-7	breast:	n/a	n/a
21	CEBPB	chr10:55030423-55030723	A549	lung:	n/a	chr10:55030581-55030592
22	CEBPB	chr10:55077103-55077366	H1-hESC	embryonic stem cell:	n/a	chr10:55077105-55077118 chr10:55077104-55077121
23	CEBPB	chr10:55250388-55250668	H1-hESC	embryonic stem cell:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
24	CEBPB	chr10:55030433-55030717	Hela-S3	cervix:	n/a	chr10:55030581-55030592
25	CEBPB	chr10:55030463-55030602	H1-hESC	embryonic stem cell:	n/a	chr10:55030581-55030592
26	CEBPB	chr10:55233744-55234036	HepG2	liver:	n/a	chr10:55233869-55233880
27	CEBPB	chr10:55070800-55070915	H1-hESC	embryonic stem cell:	n/a	chr10:55070859-55070872 chr10:55070861-55070870 chr10:55070861-55070870 chr10:55070861-55070870
28	CEBPB	chr10:55239054-55239539	H1-hESC	embryonic stem cell:	n/a	chr10:55239464-55239475 chr10:55239371-55239383
29	CEBPB	chr10:55250389-55250679	Hela-S3	cervix:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
30	CEBPB	chr10:55063815-55064038	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr10:55063756-55064049	A549	lung:	n/a	n/a
32	CEBPB	chr10:55016346-55017038	Hela-S3	cervix:	n/a	chr10:55016409-55016420
33	CEBPB	chr10:55063725-55064069	HepG2	liver:	n/a	n/a
34	CEBPB	chr10:55121736-55122030	HepG2	liver:	n/a	n/a
35	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
36	CEBPB	chr10:55016353-55016995	H1-hESC	embryonic stem cell:	n/a	chr10:55016409-55016420
37	CEBPB	chr10:55070715-55071009	IMR90	lung:	n/a	chr10:55070859-55070872 chr10:55070861-55070870 chr10:55070861-55070870 chr10:55070861-55070870
38	CEBPB	chr10:55054100-55054129	K562	blood:	n/a	n/a
39	CEBPB	chr10:55250331-55250691	HepG2	liver:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
40	CEBPB	chr10:55016818-55017080	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:55121041-55121415	HepG2	liver:	n/a	chr10:55121222-55121233
42	CEBPB	chr10:55030411-55030719	IMR90	lung:	n/a	chr10:55030581-55030592
43	CEBPB	chr10:55250334-55250666	K562	blood:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
44	CEBPB	chr10:55250346-55250673	IMR90	lung:	n/a	chr10:55250515-55250526 chr10:55250495-55250506
45	CEBPB	chr10:55063721-55064073	IMR90	lung:	n/a	n/a
46	CEBPB	chr10:55121105-55121362	HepG2	liver:	n/a	chr10:55121222-55121233
47	CEBPB	chr10:55030432-55030743	HepG2	liver:	n/a	chr10:55030581-55030592
48	CEBPB	chr10:55121112-55121293	HepG2	liver:	n/a	chr10:55121222-55121233
49	CEBPD	chr10:55121085-55121349	HepG2	liver:	n/a	n/a
50	CHD1	chr10:55236611-55237504	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55118360-55118410	HepG2	liver:	n/a
2	chr10:55118360-55118410	Jurkat	blood:	n/a
3	chr10:55118360-55118410	ovcar-3	ovarian:	n/a
4	chr10:55118360-55118410	HepG2	liver:	n/a
5	chr10:55118360-55118410	Jurkat	blood:	n/a
6	chr10:55118360-55118410	ovcar-3	ovarian:	n/a
7	chr10:55016939-55016989	HNPCEpiC	eye:	n/a
8	chr10:55259527-55259577	IMR90	lung:	fetal
9	chr10:55016939-55016989	SAEC	small airway:	n/a
10	chr10:55148775-55148825	HUVEC	blood vessel:	n/a
11	chr10:55148775-55148825	AG09319	gingival:	n/a
12	chr10:55016939-55016989	HMEC	breast:	n/a
13	chr10:55259527-55259577	T-47D	breast:	n/a
14	chr10:55118360-55118410	IMR90	lung:	fetal
15	chr10:55118360-55118410	A549	lung:	n/a
16	chr10:55148775-55148825	U87	brain:	n/a
17	chr10:55118360-55118410	AG04449	skin:	fetal
18	chr10:55148775-55148825	HEEpiC	esophagus:	n/a
19	chr10:55118360-55118410	MCF-7	breast:	n/a
20	chr10:55016939-55016989	ProgFib	skin:	n/a
21	chr10:55148775-55148825	T-47D	breast:	n/a
22	chr10:55259527-55259577	HRE	kidney:	n/a
23	chr10:55016939-55016989	Caco-2	colon:	n/a
24	chr10:55148775-55148825	GM06990	blood:	n/a
25	chr10:55259527-55259577	AoSMC	blood vessel:	n/a
26	chr10:55016939-55016989	AG09319	gingival:	n/a
27	chr10:55148775-55148825	PFSK-1	brain:	n/a
28	chr10:55259527-55259577	GM19239	blood:	n/a
29	chr10:55016939-55016989	ECC-1	luminal epithelium:	n/a
30	chr10:55148775-55148825	NT2-D1	testis:	n/a
31	chr10:55016939-55016989	HCT-116	colon:	n/a
32	chr10:55259527-55259577	HEK293	kidney:	embryo
33	chr10:55016939-55016989	U87	brain:	n/a
34	chr10:55259527-55259577	GM12891	blood:	n/a
35	chr10:55118360-55118410	Caco-2	colon:	n/a
36	chr10:55148775-55148825	HepG2	liver:	n/a
37	chr10:55148775-55148825	HIPEpiC	eye:	n/a
38	chr10:55148775-55148825	HCPEpiC	choroid plexus:	n/a
39	chr10:55118360-55118410	CMK	blood:	n/a
40	chr10:55118360-55118410	AoSMC	blood vessel:	n/a
41	chr10:55148775-55148825	RPTEC	kidney:	n/a
42	chr10:55118360-55118410	GM12892	blood:	n/a
43	chr10:55118360-55118410	AG09309	skin:	n/a
44	chr10:55016939-55016989	SK-N-MC	brain:	n/a
45	chr10:55118360-55118410	GM06990	blood:	n/a
46	chr10:55148775-55148825	HRCEpiC	kidney:	n/a
47	chr10:55016939-55016989	HRPEpiC	eye:	n/a
48	chr10:55118360-55118410	Hela-S3	cervix:	n/a
49	chr10:55148775-55148825	AG09309	skin:	n/a
50	chr10:55259527-55259577	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
2	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
3	chr10:55271750..55273969-chr10:55282270..55285131,2	MCF-7	breast:
4	chr10:55015124..55017354-chr10:55018929..55021209,2	K562	blood:
5	chr10:55028156..55030475-chr10:55032367..55034713,2	K562	blood:
6	chr10:55028397..55030475-chr10:55031728..55034713,2	K562	blood:
7	chr10:55171490..55173538-chr10:55175367..55178317,2	K562	blood:
8	chr10:55107674..55109690-chr10:55123080..55124587,2	K562	blood:
9	chr10:55107674..55109690-chr10:55123080..55124587,2	K562	blood:
10	chr10:55105553..55107958-chr10:55109358..55111015,2	K562	blood:
11	chr10:55228435..55230987-chr10:55235490..55236993,2	K562	blood:
12	chr10:55057963..55058535-chr10:55568196..55569129,2	MCF-7	breast:
13	chr10:55015124..55017354-chr10:55018929..55021209,2	K562	blood:
14	chr10:55028156..55030475-chr10:55032367..55034713,2	K562	blood:
15	chr10:55028397..55030475-chr10:55031728..55034713,2	K562	blood:
16	chr10:55105553..55107958-chr10:55109358..55111015,2	K562	blood:
17	chr10:55278002..55279503-chr7:30548599..30550148,2	MCF-7	breast:
18	chr10:55010159..55011051-chr10:101190203..101191138,2	Hela-S3	cervix:
19	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
ENSG00000120053	chromatin interactions
ENSG00000224934	chromatin interactions

Extended variants
information (count: 9631 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:9631 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568706601	chr10:55003181-55003182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372003643	chr10:55003197-55003198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374031607	chr10:55003228-55003229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531485299	chr10:55003246-55003247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547988303	chr10:55003257-55003258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191980477	chr10:55003299-55003300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533575286	chr10:55003309-55003310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182139320	chr10:55003315-55003316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537845832	chr10:55003325-55003326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2891448	chr10:55003338-55003339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs540128022	chr10:55003351-55003352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556844685	chr10:55003375-55003376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12261573	chr10:55003381-55003382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576564570	chr10:55003402-55003403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186725636	chr10:55003461-55003462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555597096	chr10:55003482-55003483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542398755	chr10:55003525-55003526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10824957	chr10:55003631-55003632	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs150644456	chr10:55003717-55003718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189950569	chr10:55003742-55003743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539712249	chr10:55003763-55003764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564127141	chr10:55003779-55003780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140060168	chr10:55003872-55003873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78735942	chr10:55003955-55003956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562401030	chr10:55004000-55004001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114806930	chr10:55004050-55004051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188140594	chr10:55004059-55004060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193028820	chr10:55004098-55004099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148653415	chr10:55004108-55004109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185179861	chr10:55004132-55004133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547457549	chr10:55004137-55004138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188937995	chr10:55004171-55004172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539393317	chr10:55004176-55004177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550506898	chr10:55004178-55004179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570297400	chr10:55004180-55004181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192571811	chr10:55004187-55004188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11003483	chr10:55004195-55004196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555909192	chr10:55004261-55004262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184825222	chr10:55004326-55004327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534786746	chr10:55004342-55004343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10824958	chr10:55004345-55004346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs562200613	chr10:55004375-55004376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577622102	chr10:55004490-55004491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78994729	chr10:55004503-55004504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11003484	chr10:55004514-55004515	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562660636	chr10:55004576-55004577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576265154	chr10:55004602-55004603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541692942	chr10:55004604-55004605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561911084	chr10:55004635-55004636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527430156	chr10:55004690-55004691	Weak transcription	n/a	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:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54985200-55005200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:55003200-55004000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr10:55005200-55006200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:55005600-55007000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr10:55005800-55006000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr10:55006000-55006800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr10:55006200-55011000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:55006800-55007200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr10:55006800-55007200	Enhancers	Placenta Amnion	Placenta Amnion
10	chr10:55011000-55011200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr10:55011200-55011600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr10:55011200-55012000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:55012000-55013800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:55012000-55014400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr10:55012200-55013600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:55012200-55014400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
17	chr10:55012600-55014600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr10:55012600-55016200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr10:55013200-55014400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
20	chr10:55013400-55014400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr10:55013400-55014600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
22	chr10:55013600-55013800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:55013800-55014600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:55013800-55016200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr10:55014200-55018400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr10:55014400-55016000	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr10:55014400-55016000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr10:55014400-55016200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr10:55014400-55016200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr10:55014600-55015800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr10:55014600-55016200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr10:55015200-55015600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr10:55015400-55017400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr10:55015800-55016800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr10:55015800-55017000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr10:55016000-55017000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr10:55016000-55017000	Enhancers	NHEK	skin
38	chr10:55016000-55017200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr10:55016000-55018000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr10:55016200-55016600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr10:55016200-55016800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr10:55016200-55016800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:55016200-55016800	Enhancers	H9 Cell Line	embryonic stem cell
44	chr10:55016200-55016800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr10:55016200-55016800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr10:55016200-55017000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr10:55016200-55017000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:55016200-55017000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr10:55016200-55017000	Enhancers	HMEC	breast
50	chr10:55016200-55017800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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