Variant report

Variant	nsv540633
Chromosome Location	chr10:55925471-56196447
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:494)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:55932524-55932527	K562	blood:	n/a	n/a
2	ARID3A	chr10:56001192-56001197	K562	blood:	n/a	n/a
3	ATF1	chr10:56148845-56148855	K562	blood:	n/a	n/a
4	ATF2	chr10:55954527-55954836	GM12878	blood:	n/a	n/a
5	BACH1	chr10:56123241-56123554	K562	blood:	n/a	n/a
6	BACH1	chr10:56123236-56123565	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr10:55954594-55954781	GM12878	blood:	n/a	n/a
8	BCL3	chr10:55954589-55954815	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:55959548-55959726	GM12878	blood:	n/a	n/a
10	CEBPB	chr10:55926116-55926304	HepG2	liver:	n/a	chr10:55926240-55926251 chr10:55926279-55926290
11	CEBPB	chr10:56070828-56071132	HepG2	liver:	n/a	chr10:56070964-56070975 chr10:56070986-56070997
12	CEBPB	chr10:56079189-56079516	IMR90	lung:	n/a	chr10:56079355-56079366
13	CEBPB	chr10:56074230-56074549	IMR90	lung:	n/a	chr10:56074380-56074391
14	CEBPB	chr10:56074308-56074560	K562	blood:	n/a	chr10:56074380-56074391
15	CEBPB	chr10:56034370-56034600	HepG2	liver:	n/a	chr10:56034471-56034482 chr10:56034470-56034483 chr10:56034470-56034483 chr10:56034470-56034481
16	CEBPB	chr10:56122448-56122536	HepG2	liver:	n/a	chr10:56122474-56122485
17	CEBPB	chr10:56079183-56079542	HepG2	liver:	n/a	chr10:56079355-56079366
18	CEBPB	chr10:56010051-56010175	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr10:56080492-56080769	HepG2	liver:	n/a	chr10:56080656-56080667
20	CEBPB	chr10:56070861-56071086	A549	lung:	n/a	chr10:56070964-56070975 chr10:56070986-56070997
21	CEBPB	chr10:56079201-56079479	A549	lung:	n/a	chr10:56079355-56079366
22	CEBPB	chr10:56173535-56173641	A549	lung:	n/a	n/a
23	CEBPB	chr10:56074242-56074533	H1-hESC	embryonic stem cell:	n/a	chr10:56074380-56074391
24	CEBPB	chr10:56074216-56074562	A549	lung:	n/a	chr10:56074380-56074391
25	CEBPB	chr10:56079250-56079494	H1-hESC	embryonic stem cell:	n/a	chr10:56079355-56079366
26	CEBPB	chr10:56074202-56074568	HepG2	liver:	n/a	chr10:56074380-56074391
27	CEBPB	chr10:56106935-56106999	H1-hESC	embryonic stem cell:	n/a	chr10:56106957-56106970
28	CEBPB	chr10:56079320-56079376	K562	blood:	n/a	chr10:56079355-56079366
29	CHD2	chr10:55954630-55954951	GM12878	blood:	n/a	n/a
30	CTCF	chr10:56128900-56129050	GM12873	blood:	n/a	n/a
31	CTCF	chr10:56162350-56162725	T-47D	breast:	n/a	n/a
32	CTCF	chr10:56128880-56129030	MCF-7	breast:	n/a	n/a
33	CTCF	chr10:56162469-56162663	LNCaP	prostate:	n/a	n/a
34	CTCF	chr10:56154530-56154590	HepG2	liver:	n/a	n/a
35	CTCF	chr10:56162405-56162645	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr10:55957880-55958030	GM12865	blood:	n/a	n/a
37	CTCF	chr10:56162440-56162590	HPF	lung:	n/a	n/a
38	CTCF	chr10:56162460-56162610	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr10:56162460-56162610	GM12873	blood:	n/a	n/a
40	CTCF	chr10:56162480-56162630	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr10:56162500-56162650	SAEC	small airway:	n/a	n/a
42	CTCF	chr10:56162427-56162702	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr10:56164199-56164232	Medullo	brain:	n/a	n/a
44	CTCF	chr10:56162440-56162590	NB4	blood:	n/a	n/a
45	CTCF	chr10:56154086-56154145	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr10:56154442-56154631	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr10:56162460-56162610	MCF-7	breast:	n/a	n/a
48	CTCF	chr10:56162460-56162610	HepG2	liver:	n/a	n/a
49	CTCF	chr10:56162298-56162771	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:56162520-56162670	GM12866	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:56057923-56057973	HUVEC	blood vessel:	n/a
2	chr10:56057923-56057973	U87	brain:	n/a
3	chr10:56057923-56057973	ProgFib	skin:	n/a
4	chr10:56057923-56057973	ECC-1	luminal epithelium:	n/a
5	chr10:56057923-56057973	NB4	blood:	n/a
6	chr10:56057923-56057973	NHBE	bronchial:	n/a
7	chr10:56057923-56057973	HL-60	blood:	n/a
8	chr10:56057923-56057973	HRCEpiC	kidney:	n/a
9	chr10:56057923-56057973	SK-N-SH_RA	brain:	n/a
10	chr10:56057923-56057973	PrEC	prostate:	n/a
11	chr10:56057923-56057973	HRPEpiC	eye:	n/a
12	chr10:56057923-56057973	IMR90	lung:	fetal
13	chr10:56057923-56057973	SAEC	small airway:	n/a
14	chr10:56057923-56057973	HCF	heart:	n/a
15	chr10:56057923-56057973	SKMC	muscle:	n/a
16	chr10:56057923-56057973	Hepatocyte	liver:	n/a
17	chr10:56057923-56057973	GM06990	blood:	n/a
18	chr10:56057923-56057973	HNPCEpiC	eye:	n/a
19	chr10:56057923-56057973	HIPEpiC	eye:	n/a
20	chr10:56057923-56057973	HMEC	breast:	n/a
21	chr10:56057923-56057973	SK-N-SH	brain:	n/a
22	chr10:56057923-56057973	GM19239	blood:	n/a
23	chr10:56057923-56057973	SK-N-MC	brain:	n/a
24	chr10:56057923-56057973	AG04450	lung:	fetal
25	chr10:56057923-56057973	ovcar-3	ovarian:	n/a
26	chr10:56057923-56057973	AoSMC	blood vessel:	n/a
27	chr10:56057923-56057973	BJ	skin:	n/a
28	chr10:56057923-56057973	NT2-D1	testis:	n/a
29	chr10:56057923-56057973	CMK	blood:	n/a
30	chr10:56057923-56057973	HEK293	kidney:	embryo
31	chr10:56057923-56057973	RPTEC	kidney:	n/a
32	chr10:56057923-56057973	T-47D	breast:	n/a
33	chr10:56057923-56057973	HCPEpiC	choroid plexus:	n/a
34	chr10:56057923-56057973	AG04449	skin:	fetal
35	chr10:56057923-56057973	Caco-2	colon:	n/a
36	chr10:56057923-56057973	PFSK-1	brain:	n/a
37	chr10:56057923-56057973	AG09319	gingival:	n/a
38	chr10:56057923-56057973	NHDF-neo	bronchial:	n/a
39	chr10:56057923-56057973	PANC-1	pancreas:	n/a
40	chr10:56057923-56057973	GM12878	blood:	n/a
41	chr10:56057923-56057973	BE2_C	brain:	n/a
42	chr10:56057923-56057973	MCF10A-Er-Src	breast:	n/a
43	chr10:56057923-56057973	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:56057923-56057973	HRE	kidney:	n/a
45	chr10:56057923-56057973	A549	lung:	n/a
46	chr10:56057923-56057973	AG09309	skin:	n/a
47	chr10:56057923-56057973	NH-A	brain:	n/a
48	chr10:56057923-56057973	H1-hESC	embryonic stem cell:	embryo
49	chr10:56057923-56057973	GM12892	blood:	n/a
50	chr10:56057923-56057973	AG10803	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	10:55527193-55535408..10:55949104-55956834	K562	blood:
2	chr10:55757420..55758328-chr10:56162156..56162806,2	MCF-7	breast:
3	chr10:55968347..55970600-chr10:55971292..55973381,2	K562	blood:
4	chr10:55961337..55963211-chr10:57586910..57589588,2	K562	blood:
5	chr10:55968347..55970600-chr10:55971292..55973381,2	K562	blood:
6	chr10:56063971..56064546-chr4:85391561..85392244,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000263921	TF binding region
ENSG00000263921	CpG island

Extended variants
information (count: 2172 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2172 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534338694	chr10:55926018-55926019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12251774	chr10:55926028-55926029	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs149657146	chr10:55926040-55926041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74593212	chr10:55926043-55926044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148837553	chr10:55926044-55926045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573790796	chr10:55926078-55926079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142428078	chr10:55926093-55926094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188257723	chr10:55926094-55926095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs118065200	chr10:55926131-55926132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75598143	chr10:55926133-55926134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541418492	chr10:55926161-55926162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572550232	chr10:55926162-55926163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564510031	chr10:55926174-55926175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563383306	chr10:55926182-55926183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369213807	chr10:55926261-55926262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113629778	chr10:55926294-55926295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550449921	chr10:55926310-55926311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570108904	chr10:55926342-55926343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534327899	chr10:55926363-55926364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368299625	chr10:55926391-55926392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372956037	chr10:55926435-55926436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529504309	chr10:55926451-55926452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146843507	chr10:55926466-55926467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140734661	chr10:55926480-55926481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59762003	chr10:55926492-55926493	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs113525524	chr10:55926524-55926525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs60459565	chr10:55926610-55926611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538763216	chr10:55926641-55926642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556855806	chr10:55926642-55926643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140941701	chr10:55926682-55926683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565725545	chr10:55926703-55926704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557239900	chr10:55926714-55926715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7900941	chr10:55926744-55926745	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs542825043	chr10:55926746-55926747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553240823	chr10:55926752-55926753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572558793	chr10:55926759-55926760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541581963	chr10:55926760-55926761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564424103	chr10:55926764-55926765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201688324	chr10:55926771-55926772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533370335	chr10:55926776-55926777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372865453	chr10:55926781-55926782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542935286	chr10:55926782-55926783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113315379	chr10:55926805-55926806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561177249	chr10:55926808-55926809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113928254	chr10:55926817-55926818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559566459	chr10:55926818-55926819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528130510	chr10:55926844-55926845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551072047	chr10:55926860-55926861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377412942	chr10:55926863-55926864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7903275	chr10:55926898-55926899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

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
Colorectal cancer	16774939	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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55926000-55926200	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr10:55926200-55926800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr10:55926200-55932400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr10:55926800-55929000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr10:55929000-55929400	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr10:55929000-55930600	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr10:55930600-55932200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr10:55932200-55932600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr10:55932400-55932600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr10:55962800-55963600	Enhancers	HUVEC	blood vessel
11	chr10:55966600-55967000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr10:55987000-55987400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:55987400-55990800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr10:55988600-55990800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr10:55990800-55991400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:55990800-55991600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr10:56000800-56001800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:56000800-56002600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr10:56019000-56019200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr10:56041600-56042200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr10:56041600-56042200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr10:56041600-56042200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr10:56041800-56042200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr10:56041800-56042400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:56043600-56044000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr10:56048600-56048800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:56058800-56066400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr10:56063400-56063800	Enhancers	Fetal Lung	lung
29	chr10:56066400-56066600	Enhancers	H9 Cell Line	embryonic stem cell
30	chr10:56067200-56067800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr10:56096000-56097800	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr10:56097600-56098200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr10:56097800-56098400	Active TSS	Primary hematopoietic stem cells	blood
34	chr10:56097800-56099000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr10:56097800-56099000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:56098200-56098600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr10:56098200-56098600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr10:56098200-56098800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr10:56098200-56099000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr10:56098400-56098600	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr10:56098400-56099000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr10:56098600-56099000	Enhancers	Primary hematopoietic stem cells	blood
43	chr10:56098600-56099000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr10:56098600-56101000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr10:56101000-56102800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
46	chr10:56101400-56102000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr10:56101400-56102800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr10:56102000-56102200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr10:56102000-56102600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr10:56102000-56102600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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