Variant report

Variant	nsv1052378
Chromosome Location	chr10:4286880-4307024
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	chr10:4304785-4304985	K562	blood:	n/a	n/a
2	ATF1	chr10:4296957-4297180	K562	blood:	n/a	n/a
3	BCL3	chr10:4304705-4304906	GM12878	blood:	n/a	n/a
4	BCL3	chr10:4304633-4304899	GM12878	blood:	n/a	n/a
5	CBX3	chr10:4302647-4303081	HCT-116	colon:	n/a	n/a
6	CEBPB	chr10:4305612-4305739	IMR90	lung:	n/a	n/a
7	CEBPB	chr10:4296810-4297453	IMR90	lung:	n/a	n/a
8	CEBPB	chr10:4292740-4292819	HepG2	liver:	n/a	chr10:4292773-4292784
9	CEBPB	chr10:4296845-4297267	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr10:4305189-4305928	Hela-S3	cervix:	n/a	chr10:4305239-4305250
11	CEBPB	chr10:4288948-4289680	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:4296947-4297179	A549	lung:	n/a	n/a
13	CTCF	chr10:4288900-4289050	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr10:4288940-4289090	AG10803	skin:	n/a	n/a
15	CTCF	chr10:4300325-4300371	A549	lung:	n/a	n/a
16	CTCF	chr10:4288940-4289090	BJ	skin:	n/a	n/a
17	CTCF	chr10:4288960-4289110	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr10:4290801-4290982	GM19239	blood:	n/a	chr10:4290882-4290903
19	CTCF	chr10:4290848-4290968	NHEK	skin:	n/a	chr10:4290882-4290903
20	CTCF	chr10:4288960-4289110	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr10:4290826-4290944	GM19238	blood:	n/a	chr10:4290882-4290903
22	CTCF	chr10:4288980-4289130	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr10:4288940-4289090	HMF	breast:	n/a	n/a
24	CTCF	chr10:4290809-4290943	Spleen_OC	spleen:	n/a	chr10:4290882-4290903
25	CTCF	chr10:4288960-4289110	AG04449	skin:	n/a	n/a
26	CTCF	chr10:4290829-4290961	GM19240	blood:	n/a	chr10:4290882-4290903
27	CTCF	chr10:4288940-4289090	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr10:4288900-4289050	HCFaa	heart:	n/a	n/a
29	CTCF	chr10:4300340-4300490	HepG2	liver:	n/a	n/a
30	E2F4	chr10:4289182-4289539	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr10:4302505-4303001	MCF10A-Er-Src	breast:	n/a	n/a
32	EP300	chr10:4288679-4289994	SK-N-SH	brain:	n/a	chr10:4289856-4289864 chr10:4288827-4288841 chr10:4289446-4289460
33	EP300	chr10:4289620-4289919	SK-N-SH_RA	brain:	n/a	chr10:4289856-4289864
34	EP300	chr10:4296249-4297489	SK-N-SH	brain:	n/a	chr10:4296873-4296887 chr10:4297021-4297028
35	EP300	chr10:4288839-4289798	SK-N-SH	brain:	n/a	chr10:4289446-4289460
36	EP300	chr10:4302723-4303153	SK-N-SH_RA	brain:	n/a	chr10:4302890-4302899 chr10:4302889-4302898
37	EP300	chr10:4288973-4289853	SK-N-SH_RA	brain:	n/a	chr10:4289446-4289460
38	EP300	chr10:4296854-4297218	Hela-S3	cervix:	n/a	chr10:4296873-4296887 chr10:4297021-4297028
39	EP300	chr10:4287203-4287528	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr10:4296923-4297217	SK-N-SH_RA	brain:	n/a	chr10:4297021-4297028
41	EP300	chr10:4288964-4289611	SK-N-SH_RA	brain:	n/a	chr10:4289446-4289460
42	EP300	chr10:4302522-4303279	SK-N-SH	brain:	n/a	chr10:4302890-4302899 chr10:4302889-4302898 chr10:4303205-4303219
43	FOS	chr10:4302686-4303078	MCF10A-Er-Src	breast:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302888-4302899 chr10:4302890-4302899 chr10:4302889-4302898
44	FOS	chr10:4302638-4303268	HUVEC	blood vessel:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302888-4302899 chr10:4302890-4302899 chr10:4302889-4302898
45	FOS	chr10:4298120-4298248	MCF10A-Er-Src	breast:	n/a	chr10:4298181-4298188 chr10:4298181-4298189 chr10:4298180-4298190 chr10:4298181-4298189
46	FOS	chr10:4291998-4292950	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr10:4289128-4289491	MCF10A-Er-Src	breast:	n/a	chr10:4289311-4289322 chr10:4289289-4289300
48	FOS	chr10:4288919-4289875	HUVEC	blood vessel:	n/a	chr10:4289311-4289322 chr10:4289289-4289300
49	FOS	chr10:4292007-4292946	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr10:4289066-4289549	MCF10A-Er-Src	breast:	n/a	chr10:4289311-4289322 chr10:4289289-4289300

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4296406-4296456	HL-60	blood:	n/a
2	chr10:4296406-4296456	NHDF-neo	bronchial:	n/a
3	chr10:4296406-4296456	HRPEpiC	eye:	n/a
4	chr10:4296406-4296456	HNPCEpiC	eye:	n/a
5	chr10:4296406-4296456	HIPEpiC	eye:	n/a
6	chr10:4296406-4296456	HCM	heart:	n/a
7	chr10:4296406-4296456	GM12891	blood:	n/a
8	chr10:4296406-4296456	AG09309	skin:	n/a
9	chr10:4296406-4296456	NB4	blood:	n/a
10	chr10:4296406-4296456	MCF-7	breast:	n/a
11	chr10:4296406-4296456	LNCaP	prostate:	n/a
12	chr10:4296406-4296456	GM12892	blood:	n/a
13	chr10:4296406-4296456	PrEC	prostate:	n/a
14	chr10:4296406-4296456	GM06990	blood:	n/a
15	chr10:4296406-4296456	HRCEpiC	kidney:	n/a
16	chr10:4296406-4296456	Jurkat	blood:	n/a
17	chr10:4296406-4296456	HRE	kidney:	n/a
18	chr10:4296406-4296456	GM19239	blood:	n/a
19	chr10:4296406-4296456	PANC-1	pancreas:	n/a
20	chr10:4296406-4296456	SK-N-MC	brain:	n/a
21	chr10:4296406-4296456	AoSMC	blood vessel:	n/a
22	chr10:4296406-4296456	AG04449	skin:	fetal
23	chr10:4296406-4296456	BJ	skin:	n/a
24	chr10:4296406-4296456	Caco-2	colon:	n/a
25	chr10:4296406-4296456	NT2-D1	testis:	n/a
26	chr10:4296406-4296456	A549	lung:	n/a
27	chr10:4296406-4296456	NHBE	bronchial:	n/a
28	chr10:4296406-4296456	SKMC	muscle:	n/a
29	chr10:4296406-4296456	SAEC	small airway:	n/a
30	chr10:4296406-4296456	PFSK-1	brain:	n/a
31	chr10:4296406-4296456	Hela-S3	cervix:	n/a
32	chr10:4296406-4296456	HEEpiC	esophagus:	n/a
33	chr10:4296406-4296456	IMR90	lung:	fetal
34	chr10:4296406-4296456	Hepatocyte	liver:	n/a
35	chr10:4296406-4296456	GM12878	blood:	n/a
36	chr10:4296406-4296456	HCPEpiC	choroid plexus:	n/a
37	chr10:4296406-4296456	ECC-1	luminal epithelium:	n/a
38	chr10:4296406-4296456	K562	blood:	n/a
39	chr10:4296406-4296456	HMEC	breast:	n/a
40	chr10:4296406-4296456	CMK	blood:	n/a
41	chr10:4296406-4296456	ProgFib	skin:	n/a
42	chr10:4296406-4296456	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:4296406-4296456	HepG2	liver:	n/a
44	chr10:4296406-4296456	HAEpiC	amniotic membrane:	n/a
45	chr10:4296406-4296456	HCF	heart:	n/a
46	chr10:4296406-4296456	MCF10A-Er-Src	breast:	n/a
47	chr10:4296406-4296456	AG09319	gingival:	n/a
48	chr10:4296406-4296456	AG10803	skin:	n/a
49	chr10:4296406-4296456	HEK293	kidney:	embryo
50	chr10:4296406-4296456	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:3823986..3829739-chr10:4306109..4310504,8	MCF-7	breast:
2	chr10:3824875..3826995-chr10:4293449..4295482,2	MCF-7	breast:
3	chr10:4243895..4246337-chr10:4299306..4301962,2	MCF-7	breast:
4	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:
5	chr10:4304386..4306768-chr10:4318241..4320361,3	MCF-7	breast:
6	chr10:3826008..3828712-chr10:4299777..4301639,2	MCF-7	breast:
7	chr10:3825342..3830573-chr10:4304925..4310190,7	MCF-7	breast:
8	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:

Variant related genes	Relation type
LINC00702	TF binding region
LINC00702	CpG island
ENSG00000067082	chromatin interactions

Extended variants
information (count: 958 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10904206	chr10:4286880-4286881	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559507835	chr10:4286886-4286887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs540127371	chr10:4286896-4286897	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs10904207	chr10:4286897-4286898	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs139253246	chr10:4286917-4286918	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs12357030	chr10:4286918-4286919	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs143936120	chr10:4286928-4286929	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs192316302	chr10:4286951-4286952	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs548517406	chr10:4286989-4286990	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs147275691	chr10:4287006-4287007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10904208	chr10:4287070-4287071	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs117167812	chr10:4287134-4287135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549692926	chr10:4287148-4287149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114615922	chr10:4287154-4287155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184665013	chr10:4287168-4287169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189640779	chr10:4287204-4287205	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs115851040	chr10:4287222-4287223	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs539481990	chr10:4287223-4287224	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs560702489	chr10:4287308-4287309	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs76962151	chr10:4287313-4287314	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs372907041	chr10:4287318-4287319	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs34406036	chr10:4287328-4287329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs555227176	chr10:4287360-4287361	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs573565429	chr10:4287414-4287415	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs544219164	chr10:4287497-4287498	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs140770829	chr10:4287511-4287512	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs578040794	chr10:4287533-4287534	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545475374	chr10:4287537-4287538	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs144846021	chr10:4287584-4287585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527862937	chr10:4287587-4287588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549729393	chr10:4287694-4287695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561581424	chr10:4287695-4287696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531997829	chr10:4287697-4287698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145795743	chr10:4287710-4287711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148594968	chr10:4287713-4287714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539205609	chr10:4287717-4287718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553266553	chr10:4287725-4287726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551435768	chr10:4287726-4287727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142964627	chr10:4287727-4287728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542466122	chr10:4287747-4287748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533755211	chr10:4287773-4287774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543260427	chr10:4287787-4287788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573599674	chr10:4287799-4287800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140790258	chr10:4287805-4287806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574766709	chr10:4287817-4287818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372101552	chr10:4287826-4287827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556323487	chr10:4287850-4287851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577965384	chr10:4287863-4287864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180781451	chr10:4287876-4287877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545196686	chr10:4287878-4287879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21611746	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4276000-4292200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:4282800-4287200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr10:4283600-4287400	Enhancers	Hela-S3	cervix
4	chr10:4284200-4287800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr10:4284600-4287400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr10:4285000-4287000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:4285200-4288200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:4285200-4288600	Weak transcription	Fetal Thymus	thymus
9	chr10:4285200-4288800	Weak transcription	Ovary	ovary
10	chr10:4285200-4291800	Weak transcription	Psoas Muscle	Psoas
11	chr10:4285400-4288200	Weak transcription	Left Ventricle	heart
12	chr10:4285400-4288600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr10:4285600-4296200	Weak transcription	Fetal Muscle Leg	muscle
14	chr10:4285800-4287000	Enhancers	Colon Smooth Muscle	Colon
15	chr10:4285800-4288600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr10:4285800-4289400	Weak transcription	Adipose Nuclei	Adipose
17	chr10:4286000-4287000	Enhancers	NHEK	skin
18	chr10:4286000-4287400	Enhancers	NH-A	brain
19	chr10:4286000-4287600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr10:4286000-4288200	Weak transcription	Aorta	Aorta
21	chr10:4286000-4288600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr10:4286000-4288600	Enhancers	Osteobl	bone
23	chr10:4286000-4289000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr10:4286000-4289600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr10:4286000-4290200	Enhancers	HMEC	breast
26	chr10:4286000-4292400	Weak transcription	Right Ventricle	heart
27	chr10:4286000-4294800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr10:4286200-4289400	Enhancers	HSMM	muscle
29	chr10:4286400-4287200	Enhancers	Fetal Heart	heart
30	chr10:4286400-4287200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr10:4286400-4287200	Enhancers	NHLF	lung
32	chr10:4286400-4287600	Enhancers	HUVEC	blood vessel
33	chr10:4286400-4288000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr10:4286400-4288600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr10:4286400-4289000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr10:4286600-4287000	Enhancers	Placenta Amnion	Placenta Amnion
37	chr10:4286600-4287000	Flanking Active TSS	NHDF-Ad	bronchial
38	chr10:4286600-4287400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr10:4286800-4287000	Enhancers	HSMMtube	muscle
40	chr10:4286800-4287200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr10:4286800-4288200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr10:4286800-4288200	Weak transcription	Right Atrium	heart
43	chr10:4286800-4288600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:4286800-4288600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:4286800-4289000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr10:4286800-4296200	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr10:4287000-4288000	Weak transcription	HSMMtube	muscle
48	chr10:4287000-4288000	Weak transcription	NHEK	skin
49	chr10:4287000-4288600	Weak transcription	Colon Smooth Muscle	Colon
50	chr10:4287000-4288600	Weak transcription	Placenta Amnion	Placenta Amnion

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