Variant report

Variant	nsv433411
Chromosome Location	chr10:42858154-42953581
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	CBX3	chr10:42863291-42863724	K562	blood:	n/a	n/a
2	CCNT2	chr10:42863141-42863422	K562	blood:	n/a	n/a
3	CCNT2	chr10:42876568-42876697	K562	blood:	n/a	n/a
4	CEBPB	chr10:42862252-42862433	K562	blood:	n/a	n/a
5	CEBPB	chr10:42926578-42926926	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
6	CEBPB	chr10:42926636-42926923	MCF-7	breast:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
7	CEBPB	chr10:42926561-42926923	ECC-1	luminal epithelium:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
8	CEBPB	chr10:42940399-42940458	K562	blood:	n/a	chr10:42940438-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940432-42940441 chr10:42940440-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940440-42940451 chr10:42940430-42940441 chr10:42940432-42940443 chr10:42940432-42940441
9	CEBPB	chr10:42926607-42926907	Hela-S3	cervix:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
10	CEBPB	chr10:42926554-42927004	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
11	CEBPB	chr10:42940311-42940534	HepG2	liver:	n/a	chr10:42940438-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940432-42940441 chr10:42940440-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940440-42940451 chr10:42940430-42940441 chr10:42940432-42940443 chr10:42940432-42940441
12	CEBPB	chr10:42926569-42926928	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
13	CEBPB	chr10:42903832-42903893	IMR90	lung:	n/a	chr10:42903853-42903864
14	CEBPB	chr10:42940373-42940490	IMR90	lung:	n/a	chr10:42940438-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940432-42940441 chr10:42940440-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940440-42940451 chr10:42940430-42940441 chr10:42940432-42940443 chr10:42940432-42940441
15	CEBPB	chr10:42926558-42926930	K562	blood:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
16	CEBPB	chr10:42926541-42926950	ECC-1	luminal epithelium:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
17	CEBPB	chr10:42861983-42862018	K562	blood:	n/a	n/a
18	CEBPB	chr10:42926615-42926811	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
19	CEBPB	chr10:42926634-42926893	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
20	CEBPB	chr10:42926584-42926914	K562	blood:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
21	CEBPB	chr10:42926600-42926883	H1-hESC	embryonic stem cell:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
22	CEBPB	chr10:42926575-42926908	IMR90	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
23	CEBPB	chr10:42926578-42926940	MCF-7	breast:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
24	CEBPB	chr10:42903805-42903926	HepG2	liver:	n/a	chr10:42903853-42903864
25	CEBPB	chr10:42926626-42926861	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
26	CEBPB	chr10:42886922-42886990	HepG2	liver:	n/a	chr10:42886933-42886944
27	CEBPD	chr10:42876429-42876788	K562	blood:	n/a	n/a
28	CHD2	chr10:42863371-42863685	K562	blood:	n/a	n/a
29	CHD2	chr10:42863523-42863535	GM12878	blood:	n/a	n/a
30	CTCF	chr10:42924120-42924270	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr10:42923963-42924370	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:42924140-42924290	MCF-7	breast:	n/a	n/a
33	CTCF	chr10:42924121-42924264	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr10:42924099-42924285	GM12878	blood:	n/a	n/a
35	CTCF	chr10:42924080-42924230	GM12870	blood:	n/a	n/a
36	CTCF	chr10:42924060-42924210	HepG2	liver:	n/a	n/a
37	CTCF	chr10:42924113-42924283	ProgFib	skin:	n/a	n/a
38	CTCF	chr10:42924136-42924242	GM10266	blood:	n/a	n/a
39	CTCF	chr10:42924020-42924170	HMEC	breast:	n/a	n/a
40	CTCF	chr10:42924080-42924230	SAEC	small airway:	n/a	n/a
41	CTCF	chr10:42924080-42924230	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr10:42924120-42924270	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr10:42923830-42924420	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr10:42924120-42924270	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr10:42924100-42924250	SAEC	small airway:	n/a	n/a
46	CTCF	chr10:42924120-42924270	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:42924080-42924230	GM12865	blood:	n/a	n/a
48	CTCF	chr10:42924127-42924274	GM13977	blood:	n/a	n/a
49	CTCF	chr10:42924000-42924150	GM12864	blood:	n/a	n/a
50	CTCF	chr10:42924137-42924248	GM10248	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42862876-42862926	Caco-2	colon:	n/a
2	chr10:42862876-42862926	Caco-2	colon:	n/a
3	chr10:42863594-42863644	Hela-S3	cervix:	n/a
4	chr10:42863539-42863589	SKMC	muscle:	n/a
5	chr10:42862876-42862926	ProgFib	skin:	n/a
6	chr10:42863550-42863600	GM12892	blood:	n/a
7	chr10:42859004-42859054	HCM	heart:	n/a
8	chr10:42863068-42863118	HMEC	breast:	n/a
9	chr10:42864912-42864962	Hela-S3	cervix:	n/a
10	chr10:42864912-42864962	LNCaP	prostate:	n/a
11	chr10:42863594-42863644	SK-N-MC	brain:	n/a
12	chr10:42863508-42863558	HAEpiC	amniotic membrane:	n/a
13	chr10:42862876-42862926	HCM	heart:	n/a
14	chr10:42863173-42863223	SK-N-SH	brain:	n/a
15	chr10:42863550-42863600	GM12891	blood:	n/a
16	chr10:42864633-42864683	ECC-1	luminal epithelium:	n/a
17	chr10:42931123-42931173	AG04450	lung:	fetal
18	chr10:42862876-42862926	HEEpiC	esophagus:	n/a
19	chr10:42863068-42863118	BE2_C	brain:	n/a
20	chr10:42863444-42863494	T-47D	breast:	n/a
21	chr10:42863539-42863589	SK-N-SH_RA	brain:	n/a
22	chr10:42862876-42862926	NHBE	bronchial:	n/a
23	chr10:42863068-42863118	BJ	skin:	n/a
24	chr10:42862978-42863028	SK-N-SH_RA	brain:	n/a
25	chr10:42863594-42863644	HPAEpiC	pulmonary alveolar:	n/a
26	chr10:42863550-42863600	AoSMC	blood vessel:	n/a
27	chr10:42864912-42864962	BE2_C	brain:	n/a
28	chr10:42862978-42863028	AG09319	gingival:	n/a
29	chr10:42863444-42863494	PFSK-1	brain:	n/a
30	chr10:42863550-42863600	U87	brain:	n/a
31	chr10:42862978-42863028	SKMC	muscle:	n/a
32	chr10:42863508-42863558	LNCaP	prostate:	n/a
33	chr10:42864912-42864962	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:42862876-42862926	LNCaP	prostate:	n/a
35	chr10:42864912-42864962	A549	lung:	n/a
36	chr10:42864633-42864683	SKMC	muscle:	n/a
37	chr10:42859004-42859054	Hepatocyte	liver:	n/a
38	chr10:42862876-42862926	BE2_C	brain:	n/a
39	chr10:42863550-42863600	ProgFib	skin:	n/a
40	chr10:42863444-42863494	AoSMC	blood vessel:	n/a
41	chr10:42863594-42863644	BJ	skin:	n/a
42	chr10:42931123-42931173	SKMC	muscle:	n/a
43	chr10:42863550-42863600	GM19239	blood:	n/a
44	chr10:42863539-42863589	SK-N-MC	brain:	n/a
45	chr10:42864633-42864683	AG04450	lung:	fetal
46	chr10:42931123-42931173	H1-hESC	embryonic stem cell:	embryo
47	chr10:42863444-42863494	AG09309	skin:	n/a
48	chr10:42862876-42862926	SK-N-SH	brain:	n/a
49	chr10:42863444-42863494	SKMC	muscle:	n/a
50	chr10:42863173-42863223	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:
2	chr10:42860335..42863039-chr10:43132551..43135299,2	K562	blood:
3	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
4	chr10:42861377..42864864-chr10:42876467..42879026,3	K562	blood:
5	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
6	chr10:42846704..42848638-chr10:42856458..42859194,2	K562	blood:
7	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:
8	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:

Variant related genes	Relation type
CCNYL2	TF binding region
ENSG00000215146	TF binding region
CCNYL2	CpG island
ENSG00000215146	CpG island
ENSG00000196693	chromatin interactions
ENSG00000215146	chromatin interactions
ENSG00000272373	chromatin interactions

Extended variants
information (count: 523 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2466478	chr10:42858154-42858155	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117017732	chr10:42858180-42858181	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77635830	chr10:42858234-42858235	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35519056	chr10:42858240-42858241	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562087955	chr10:42858336-42858337	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2466479	chr10:42858342-42858343	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs3886725	chr10:42858385-42858386	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs191546885	chr10:42858440-42858441	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs199810178	chr10:42858451-42858452	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184079741	chr10:42858464-42858465	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141790433	chr10:42858467-42858468	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150575981	chr10:42858501-42858502	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539979829	chr10:42858517-42858518	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575406486	chr10:42858522-42858523	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544252512	chr10:42858525-42858526	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371313559	chr10:42858570-42858571	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560176047	chr10:42858584-42858585	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs71505606	chr10:42858614-42858615	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549195183	chr10:42858651-42858652	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188386479	chr10:42858698-42858699	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552598965	chr10:42858709-42858710	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192867512	chr10:42858721-42858722	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528721105	chr10:42858776-42858777	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185438704	chr10:42858802-42858803	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113759405	chr10:42858803-42858804	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78256989	chr10:42858841-42858842	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190365251	chr10:42858852-42858853	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139893065	chr10:42858857-42858858	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145330778	chr10:42858867-42858868	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs375560751	chr10:42858890-42858891	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147241045	chr10:42858915-42858916	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553003268	chr10:42858918-42858919	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566751953	chr10:42858948-42858949	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535337862	chr10:42858959-42858960	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555579711	chr10:42858990-42858991	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs140845126	chr10:42859005-42859006	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544345820	chr10:42859020-42859021	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2466480	chr10:42859060-42859061	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs577574538	chr10:42859084-42859085	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs182400479	chr10:42859126-42859127	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559840726	chr10:42859291-42859292	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528758765	chr10:42859311-42859312	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542049581	chr10:42859319-42859320	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550968954	chr10:42859330-42859331	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561957973	chr10:42859340-42859341	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112139216	chr10:42859364-42859365	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183631704	chr10:42859378-42859379	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570886910	chr10:42859386-42859387	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188341551	chr10:42859390-42859391	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565288723	chr10:42859391-42859392	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Lung cancer	18438408	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
Breast cancer	21509527	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	20622171	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Lung cancer	21569311	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Hirschsprung''s Disease	19925665	CNVD
Hirschsprung''s Disease	20456320	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42847000-42860600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:42848000-42862600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr10:42848800-42862000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr10:42850600-42862200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr10:42850600-42862200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:42850800-42859200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr10:42852200-42862600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr10:42854000-42861600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr10:42854200-42862600	Weak transcription	Colon Smooth Muscle	Colon
10	chr10:42854800-42858800	Strong transcription	K562	blood
11	chr10:42854800-42862600	Weak transcription	Adipose Nuclei	Adipose
12	chr10:42855200-42858200	Strong transcription	Ovary	ovary
13	chr10:42855400-42862600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr10:42855600-42862600	Weak transcription	Brain Angular Gyrus	brain
15	chr10:42856000-42858800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr10:42856400-42858800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr10:42856400-42859200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr10:42857000-42858200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr10:42857000-42861000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
20	chr10:42857400-42858200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
21	chr10:42857400-42858800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr10:42857400-42859000	Strong transcription	Left Ventricle	heart
23	chr10:42857600-42858200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr10:42857800-42858200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:42857800-42858200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr10:42857800-42858200	ZNF genes & repeats	NHEK	skin
27	chr10:42857800-42862800	Weak transcription	Aorta	Aorta
28	chr10:42858000-42860200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:42858000-42862000	Weak transcription	Pancreas	Pancrea
30	chr10:42858000-42862600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr10:42858000-42862800	Weak transcription	Gastric	stomach
32	chr10:42858200-42858800	Weak transcription	Ovary	ovary
33	chr10:42858200-42862400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:42858400-42858600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:42858800-42859000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr10:42858800-42859200	ZNF genes & repeats	Ovary	ovary
37	chr10:42858800-42859400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:42858800-42859800	Weak transcription	K562	blood
39	chr10:42858800-42860400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:42859000-42859200	ZNF genes & repeats	Left Ventricle	heart
41	chr10:42859000-42859800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr10:42859000-42863600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr10:42859200-42860200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr10:42859200-42860200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:42859200-42862400	Weak transcription	Ovary	ovary
46	chr10:42859200-42862600	Weak transcription	Left Ventricle	heart
47	chr10:42859400-42860400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr10:42859800-42860800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr10:42859800-42860800	ZNF genes & repeats	K562	blood
50	chr10:42860200-42860800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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