Variant report

Variant	nsv945327
Chromosome Location	chr1:225991086-225998770
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	ATF3	chr1:225997531-225998039	A549	lung:	n/a	n/a
2	BACH1	chr1:225997933-225998327	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:225997618-225997643	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr1:225997604-225998098	GM12878	blood:	n/a	chr1:225997839-225997852 chr1:225997838-225997851
5	BHLHE40	chr1:225997592-225998277	K562	blood:	n/a	chr1:225998034-225998050 chr1:225997982-225997998 chr1:225997841-225997857
6	BRCA1	chr1:225998094-225998235	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr1:225997619-225997829	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr1:225997944-225998284	K562	blood:	n/a	n/a
9	CCNT2	chr1:225997585-225998296	K562	blood:	n/a	chr1:225997975-225997984
10	CEBPB	chr1:225993168-225993456	A549	lung:	n/a	chr1:225993309-225993320
11	CEBPB	chr1:225993208-225993408	HepG2	liver:	n/a	chr1:225993309-225993320
12	CEBPB	chr1:225998489-225998618	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr1:225997587-225998007	HepG2	liver:	n/a	n/a
14	CHD1	chr1:225997535-225998121	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr1:225998728-225998992	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr1:225997622-225997831	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr1:225997645-225997713	K562	blood:	n/a	n/a
18	CHD2	chr1:225998698-225999080	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr1:225997565-225998236	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr1:225997993-225998189	K562	blood:	n/a	n/a
21	CHD2	chr1:225997998-225998185	HepG2	liver:	n/a	n/a
22	CREB1	chr1:225997585-225998280	A549	lung:	n/a	n/a
23	CTCF	chr1:225997960-225998110	GM12875	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
24	CTCF	chr1:225997980-225998130	GM12871	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
25	CTCF	chr1:225998020-225998170	GM12878	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
26	CTCF	chr1:225997887-225998258	GM12878	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
27	CTCF	chr1:225998000-225998150	HMEC	breast:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
28	CTCF	chr1:225998014-225998132	GM20000	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
29	CTCF	chr1:225997980-225998130	HVMF	connective:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
30	CTCF	chr1:225997960-225998110	Caco-2	colon:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
31	CTCF	chr1:225997980-225998130	GM06990	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
32	CTCF	chr1:225998000-225998150	HCPEpiC	choroid plexus:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
33	CTCF	chr1:225996780-225996930	GM12878	blood:	n/a	n/a
34	CTCF	chr1:225997995-225998168	LNCaP	prostate:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
35	CTCF	chr1:225998020-225998170	HUVEC	blood vessel:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
36	CTCF	chr1:225997997-225998185	GM12878	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
37	CTCF	chr1:225998000-225998150	AG09309	skin:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
38	CTCF	chr1:225998020-225998170	K562	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
39	CTCF	chr1:225998000-225998150	HUVEC	blood vessel:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
40	CTCF	chr1:225997991-225998196	GM10266	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
41	CTCF	chr1:225998005-225998127	GM13977	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
42	CTCF	chr1:225997980-225998130	BJ	skin:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
43	CTCF	chr1:225997993-225998130	SK-N-SH_RA	brain:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
44	CTCF	chr1:225998000-225998150	HBMEC	blood vessel:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
45	CTCF	chr1:225998000-225998150	GM12869	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
46	CTCF	chr1:225996760-225996910	GM12866	blood:	n/a	n/a
47	CTCF	chr1:225998039-225998148	Kidney_OC	kidney:	n/a	chr1:225998063-225998076
48	CTCF	chr1:225996800-225996950	GM12873	blood:	n/a	n/a
49	CTCF	chr1:225997923-225998149	HepG2	liver:	n/a	chr1:225998063-225998076 chr1:225998027-225998040
50	CTCF	chr1:225997960-225998110	GM12873	blood:	n/a	chr1:225998063-225998076 chr1:225998027-225998040

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225997655-225997705	AoSMC	blood vessel:	n/a
2	chr1:225997655-225997705	AoSMC	blood vessel:	n/a
3	chr1:225997749-225997799	HL-60	blood:	n/a
4	chr1:225996810-225996860	Jurkat	blood:	n/a
5	chr1:225995381-225995431	PANC-1	pancreas:	n/a
6	chr1:225996933-225996983	ECC-1	luminal epithelium:	n/a
7	chr1:225998730-225998780	SK-N-SH_RA	brain:	n/a
8	chr1:225997836-225997886	HIPEpiC	eye:	n/a
9	chr1:225997678-225997728	SK-N-SH_RA	brain:	n/a
10	chr1:225996982-225997032	HNPCEpiC	eye:	n/a
11	chr1:225996377-225996427	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:225997749-225997799	Hepatocyte	liver:	n/a
13	chr1:225996377-225996427	ProgFib	skin:	n/a
14	chr1:225995381-225995431	CMK	blood:	n/a
15	chr1:225997655-225997705	PANC-1	pancreas:	n/a
16	chr1:225996377-225996427	NB4	blood:	n/a
17	chr1:225997655-225997705	Hela-S3	cervix:	n/a
18	chr1:225997749-225997799	AG10803	skin:	n/a
19	chr1:225997662-225997712	ProgFib	skin:	n/a
20	chr1:225997662-225997712	HMEC	breast:	n/a
21	chr1:225996982-225997032	H1-hESC	embryonic stem cell:	embryo
22	chr1:225997038-225997088	MCF10A-Er-Src	breast:	n/a
23	chr1:225998730-225998780	MCF-7	breast:	n/a
24	chr1:225997662-225997712	NB4	blood:	n/a
25	chr1:225998164-225998214	H1-hESC	embryonic stem cell:	embryo
26	chr1:225998232-225998282	Caco-2	colon:	n/a
27	chr1:225996933-225996983	GM06990	blood:	n/a
28	chr1:225998232-225998282	PrEC	prostate:	n/a
29	chr1:225997678-225997728	NT2-D1	testis:	n/a
30	chr1:225998232-225998282	CMK	blood:	n/a
31	chr1:225996982-225997032	GM12891	blood:	n/a
32	chr1:225998232-225998282	HCT-116	colon:	n/a
33	chr1:225996933-225996983	GM19239	blood:	n/a
34	chr1:225997649-225997699	BE2_C	brain:	n/a
35	chr1:225998232-225998282	AG10803	skin:	n/a
36	chr1:225997662-225997712	HEEpiC	esophagus:	n/a
37	chr1:225997678-225997728	HEK293	kidney:	embryo
38	chr1:225996982-225997032	NT2-D1	testis:	n/a
39	chr1:225995381-225995431	NB4	blood:	n/a
40	chr1:225997678-225997728	MCF10A-Er-Src	breast:	n/a
41	chr1:225996810-225996860	HL-60	blood:	n/a
42	chr1:225997662-225997712	HIPEpiC	eye:	n/a
43	chr1:225996933-225996983	ovcar-3	ovarian:	n/a
44	chr1:225997749-225997799	NB4	blood:	n/a
45	chr1:225997649-225997699	HEEpiC	esophagus:	n/a
46	chr1:225997836-225997886	BE2_C	brain:	n/a
47	chr1:225997749-225997799	HUVEC	blood vessel:	n/a
48	chr1:225996933-225996983	ProgFib	skin:	n/a
49	chr1:225997038-225997088	GM12892	blood:	n/a
50	chr1:225996810-225996860	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:225997801..225999336-chr5:38846074..38848337,2	MCF-7	breast:
2	chr1:225992081..225994588-chr1:225995896..225998047,2	MCF-7	breast:
3	chr1:225997762..225999546-chr1:226064729..226066981,2	MCF-7	breast:
4	chr1:225986362..225988061-chr1:225993922..225996421,2	MCF-7	breast:
5	chr1:225992085..225994324-chr1:226013953..226015752,2	K562	blood:
6	chr1:225992366..225996825-chr1:225996900..226001278,7	K562	blood:
7	chr1:225993855..225996522-chr1:225998184..225999868,2	MCF-7	breast:
8	chr1:225963904..225970275-chr1:225994893..226001084,15	K562	blood:
9	chr1:225989164..225991391-chr1:225995297..225997953,3	K562	blood:
10	chr1:225997868..225998526-chr3:143572696..143573196,2	K562	blood:
11	chr1:225997407..225998221-chr13:111367411..111367928,2	Hela-S3	cervix:
12	chr1:225993353..225995844-chr1:225998707..226001448,2	K562	blood:
13	chr1:225991700..225994994-chr1:226006068..226008999,3	K562	blood:
14	chr1:225975459..225978007-chr1:225998232..226000787,2	K562	blood:
15	chr1:225962862..225967352-chr1:225996084..226002774,11	MCF-7	breast:
16	chr1:225998339..226001333-chr1:226013491..226015022,2	K562	blood:
17	chr1:225989164..225991391-chr1:225995297..225997953,3	K562	blood:
18	chr1:225969259..225971858-chr1:225998628..226000469,2	K562	blood:
19	chr1:225963814..225970754-chr1:225996230..226002908,14	MCF-7	breast:
20	chr1:225995407..225997753-chr1:226172864..226175325,2	K562	blood:
21	chr1:225662607..225663273-chr1:225994915..225995627,2	K562	blood:
22	chr1:225993494..225995733-chr1:225996333..225998153,2	K562	blood:
23	chr1:225993353..225995844-chr1:225998707..226001448,2	K562	blood:
24	chr1:225993855..225996522-chr1:225998184..225999868,2	MCF-7	breast:
25	chr1:225962294..225967531-chr1:225994011..226002080,11	K562	blood:
26	chr1:225998663..226000298-chr1:226028489..226031143,2	MCF-7	breast:

Variant related genes	Relation type
EPHX1	TF binding region
EPHX1	CpG island
ENSG00000143819	chromatin interactions
ENSG00000234112	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000145623	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000196187	chromatin interactions

Extended variants
information (count: 336 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151159204	chr1:225991087-225991088	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs4653684	chr1:225991093-225991094	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs554021119	chr1:225991136-225991137	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs61746792	chr1:225991149-225991150	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11588766	chr1:225991165-225991166	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs58235164	chr1:225991169-225991170	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs4653685	chr1:225991176-225991177	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs544287212	chr1:225991190-225991191	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200159817	chr1:225991219-225991220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369282851	chr1:225991250-225991251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs55954107	chr1:225991297-225991298	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs577592896	chr1:225991303-225991304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530832028	chr1:225991304-225991305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140216763	chr1:225991317-225991318	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114676521	chr1:225991374-225991375	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs12737161	chr1:225991399-225991400	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs10706613	chr1:225991411-225991412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577347429	chr1:225991422-225991423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4653686	chr1:225991463-225991464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs369602052	chr1:225991492-225991493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs67362064	chr1:225991493-225991494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112302180	chr1:225991505-225991506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112798012	chr1:225991506-225991507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs67221143	chr1:225991510-225991511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377327878	chr1:225991551-225991552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56195257	chr1:225991581-225991582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549883844	chr1:225991600-225991601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571402832	chr1:225991621-225991622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576318763	chr1:225991631-225991632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532262733	chr1:225991651-225991652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547051636	chr1:225991676-225991677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7546108	chr1:225991717-225991718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs7553974	chr1:225991786-225991787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs572071469	chr1:225991818-225991819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11808973	chr1:225991836-225991837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs112028955	chr1:225991855-225991856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141095451	chr1:225991930-225991931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12727416	chr1:225991936-225991937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542177375	chr1:225991943-225991944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143001976	chr1:225991944-225991945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72416610	chr1:225991945-225991946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs57160926	chr1:225991953-225991954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577679959	chr1:225991959-225991960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191846852	chr1:225991963-225991964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553840898	chr1:225992048-225992049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12742123	chr1:225992061-225992062	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542949202	chr1:225992067-225992068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561595736	chr1:225992078-225992079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531929286	chr1:225992105-225992106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113484001	chr1:225992111-225992112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225975000-225997200	Weak transcription	Brain Substantia Nigra	brain
2	chr1:225975000-225997400	Weak transcription	Aorta	Aorta
3	chr1:225978800-225997200	Weak transcription	K562	blood
4	chr1:225979000-225993200	Weak transcription	HUVEC	blood vessel
5	chr1:225979200-225997200	Weak transcription	Right Ventricle	heart
6	chr1:225979600-225997200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:225979600-225997400	Weak transcription	Lung	lung
8	chr1:225979600-225997800	Weak transcription	Gastric	stomach
9	chr1:225979800-225997200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:225979800-225997200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr1:225979800-225997200	Weak transcription	A549	lung
12	chr1:225979800-225997400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:225979800-225997600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr1:225979800-225997600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr1:225980000-225997200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:225980000-225997200	Weak transcription	Fetal Stomach	stomach
17	chr1:225980000-225997200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr1:225980000-225997200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr1:225980000-225997400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:225980000-225997600	Weak transcription	Left Ventricle	heart
21	chr1:225981200-225997200	Weak transcription	Adipose Nuclei	Adipose
22	chr1:225982200-225997200	Weak transcription	Thymus	Thymus
23	chr1:225982200-225997400	Weak transcription	Fetal Muscle Leg	muscle
24	chr1:225982200-225997400	Weak transcription	Ovary	ovary
25	chr1:225982600-225997200	Weak transcription	Placenta	Placenta
26	chr1:225983000-225995000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:225983000-225997000	Weak transcription	Fetal Lung	lung
28	chr1:225983000-225997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr1:225983000-225997200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:225983000-225997200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:225983200-225996600	Weak transcription	Fetal Thymus	thymus
32	chr1:225983200-225997200	Weak transcription	HSMM	muscle
33	chr1:225983200-225997400	Weak transcription	Primary B cells from cord blood	blood
34	chr1:225983200-225997400	Weak transcription	Primary T cells from cord blood	blood
35	chr1:225983400-225993400	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr1:225983400-225997200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:225983600-225997200	Weak transcription	Fetal Brain Female	brain
38	chr1:225984200-225993600	Weak transcription	Fetal Intestine Small	intestine
39	chr1:225984200-225997200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:225984400-225997200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:225984600-225997400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:225984600-225997400	Weak transcription	Fetal Intestine Large	intestine
43	chr1:225984800-225992800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr1:225986000-225998000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:225986200-225997200	Weak transcription	Brain Germinal Matrix	brain
46	chr1:225988400-225996200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:225988600-225997400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:225988800-225997400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:225989200-225997400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr1:225989600-225997200	Weak transcription	Liver	Liver

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