Variant report

Variant	nsv559102
Chromosome Location	chr12:60164408-60221898
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	BATF	chr12:60174486-60174690	GM12878	blood:	n/a	n/a
2	CEBPB	chr12:60218649-60218854	HepG2	liver:	n/a	chr12:60218812-60218823
3	CEBPB	chr12:60190709-60190882	A549	lung:	n/a	chr12:60190769-60190780
4	CEBPB	chr12:60190587-60190853	MCF-7	breast:	n/a	chr12:60190769-60190780
5	CEBPB	chr12:60167068-60167230	HepG2	liver:	n/a	chr12:60167176-60167187
6	CEBPB	chr12:60193571-60193636	A549	lung:	n/a	n/a
7	CEBPB	chr12:60214552-60214941	IMR90	lung:	n/a	chr12:60214730-60214741
8	CEBPB	chr12:60214628-60214847	Hela-S3	cervix:	n/a	chr12:60214730-60214741
9	CEBPB	chr12:60190635-60190912	HepG2	liver:	n/a	chr12:60190769-60190780
10	CEBPB	chr12:60202229-60202494	MCF-7	breast:	n/a	n/a
11	CEBPB	chr12:60190660-60190908	IMR90	lung:	n/a	chr12:60190769-60190780
12	CEBPB	chr12:60214615-60214860	HepG2	liver:	n/a	chr12:60214730-60214741
13	CEBPB	chr12:60214574-60214865	A549	lung:	n/a	chr12:60214730-60214741
14	CHD2	chr12:60190427-60190459	GM12878	blood:	n/a	n/a
15	CTCF	chr12:60174656-60174753	GM12892	blood:	n/a	n/a
16	CTCF	chr12:60202840-60203110	HA-sp	spinal cord:	n/a	n/a
17	CTCF	chr12:60174660-60174810	HRE	kidney:	n/a	n/a
18	CTCF	chr12:60202280-60202430	SAEC	small airway:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
19	CTCF	chr12:60202220-60202370	GM12878	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
20	CTCF	chr12:60202220-60202370	HCFaa	heart:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
21	CTCF	chr12:60174663-60174775	LNCaP	prostate:	n/a	n/a
22	CTCF	chr12:60202240-60202390	GM12801	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
23	CTCF	chr12:60174654-60174744	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:60174673-60174779	GM10248	blood:	n/a	n/a
25	CTCF	chr12:60202056-60202473	MCF-7	breast:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
26	CTCF	chr12:60174640-60174790	Caco-2	colon:	n/a	n/a
27	CTCF	chr12:60174529-60174834	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:60202169-60202414	Lung_OC	lung:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
29	CTCF	chr12:60174800-60174950	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr12:60202220-60202370	GM12865	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
31	CTCF	chr12:60202200-60202350	GM12878	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
32	CTCF	chr12:60174680-60174830	AG09309	skin:	n/a	n/a
33	CTCF	chr12:60202220-60202370	BE2_C	brain:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
34	CTCF	chr12:60174620-60174770	GM12864	blood:	n/a	n/a
35	CTCF	chr12:60174640-60174790	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr12:60202155-60202444	K562	blood:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
37	CTCF	chr12:60174580-60174730	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr12:60174660-60174810	AG04449	skin:	n/a	n/a
39	CTCF	chr12:60174436-60174990	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:60174630-60174803	HepG2	liver:	n/a	n/a
41	CTCF	chr12:60202236-60202401	A549	lung:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
42	CTCF	chr12:60206119-60206133	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:60174637-60174824	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr12:60202220-60202370	AoAF	blood vessel:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
45	CTCF	chr12:60174620-60174770	GM12873	blood:	n/a	n/a
46	CTCF	chr12:60174680-60174830	NHEK	skin:	n/a	n/a
47	CTCF	chr12:60174547-60174907	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:60174642-60174757	GM19240	blood:	n/a	n/a
49	CTCF	chr12:60202199-60202373	T-47D	breast:	n/a	chr12:60202281-60202302 chr12:60202286-60202304 chr12:60202291-60202299
50	CTCF	chr12:60174569-60174858	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60174815-60174865	NH-A	brain:	n/a
2	chr12:60174815-60174865	K562	blood:	n/a
3	chr12:60174815-60174865	GM06990	blood:	n/a
4	chr12:60174815-60174865	HRPEpiC	eye:	n/a
5	chr12:60174815-60174865	IMR90	lung:	fetal
6	chr12:60174815-60174865	HCM	heart:	n/a
7	chr12:60174815-60174865	PFSK-1	brain:	n/a
8	chr12:60174815-60174865	AG10803	skin:	n/a
9	chr12:60174815-60174865	SKMC	muscle:	n/a
10	chr12:60174815-60174865	HCPEpiC	choroid plexus:	n/a
11	chr12:60174815-60174865	RPTEC	kidney:	n/a
12	chr12:60174815-60174865	HNPCEpiC	eye:	n/a
13	chr12:60174815-60174865	Hepatocyte	liver:	n/a
14	chr12:60174815-60174865	T-47D	breast:	n/a
15	chr12:60174815-60174865	HEK293	kidney:	embryo
16	chr12:60174815-60174865	MCF10A-Er-Src	breast:	n/a
17	chr12:60174815-60174865	BE2_C	brain:	n/a
18	chr12:60174815-60174865	HMEC	breast:	n/a
19	chr12:60174815-60174865	SK-N-SH_RA	brain:	n/a
20	chr12:60174815-60174865	SK-N-MC	brain:	n/a
21	chr12:60174815-60174865	HCF	heart:	n/a
22	chr12:60174815-60174865	Hela-S3	cervix:	n/a
23	chr12:60174815-60174865	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:60174815-60174865	NHBE	bronchial:	n/a
25	chr12:60174815-60174865	PANC-1	pancreas:	n/a
26	chr12:60174815-60174865	PrEC	prostate:	n/a
27	chr12:60174815-60174865	LNCaP	prostate:	n/a
28	chr12:60174815-60174865	SAEC	small airway:	n/a
29	chr12:60174815-60174865	NT2-D1	testis:	n/a
30	chr12:60174815-60174865	HEEpiC	esophagus:	n/a
31	chr12:60174815-60174865	ProgFib	skin:	n/a
32	chr12:60174815-60174865	GM12891	blood:	n/a
33	chr12:60174815-60174865	AoSMC	blood vessel:	n/a
34	chr12:60174815-60174865	GM12892	blood:	n/a
35	chr12:60174815-60174865	SK-N-SH	brain:	n/a
36	chr12:60174815-60174865	Caco-2	colon:	n/a
37	chr12:60174815-60174865	BJ	skin:	n/a
38	chr12:60174815-60174865	HUVEC	blood vessel:	n/a
39	chr12:60174815-60174865	ovcar-3	ovarian:	n/a
40	chr12:60174815-60174865	HAEpiC	amniotic membrane:	n/a
41	chr12:60174815-60174865	HRE	kidney:	n/a
42	chr12:60174815-60174865	NHDF-neo	bronchial:	n/a
43	chr12:60174815-60174865	U87	brain:	n/a
44	chr12:60174815-60174865	GM19239	blood:	n/a
45	chr12:60174815-60174865	MCF-7	breast:	n/a
46	chr12:60174815-60174865	HepG2	liver:	n/a
47	chr12:60174815-60174865	ECC-1	luminal epithelium:	n/a
48	chr12:60174815-60174865	HCT-116	colon:	n/a
49	chr12:60174815-60174865	HIPEpiC	eye:	n/a
50	chr12:60174815-60174865	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:59838603..59839620-chr12:60174016..60175145,3	MCF-7	breast:
2	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:
3	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
4	chr12:59825209..59825865-chr12:60201866..60202550,2	MCF-7	breast:
5	chr12:60163187..60165402-chr12:60167180..60169412,2	K562	blood:
6	chr12:60175752..60177961-chr12:60179247..60181650,2	K562	blood:
7	chr12:59824786..59825486-chr12:60174654..60175192,2	MCF-7	breast:
8	chr12:60201872..60202711-chr12:60228771..60229623,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000237176	TF binding region
ENSG00000237176	CpG island

Extended variants
information (count: 2062 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2062 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11173138	chr12:60164408-60164409	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151100131	chr12:60164438-60164439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552109651	chr12:60164439-60164440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373375559	chr12:60164486-60164487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543406045	chr12:60164510-60164511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557015834	chr12:60164524-60164525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74096452	chr12:60164585-60164586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs545563694	chr12:60164594-60164595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559438691	chr12:60164620-60164621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528268921	chr12:60164624-60164625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74096453	chr12:60164673-60164674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs112677207	chr12:60164696-60164697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530735433	chr12:60164729-60164730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142427938	chr12:60164781-60164782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569422952	chr12:60164786-60164787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146606336	chr12:60164828-60164829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139125274	chr12:60164864-60164865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533406001	chr12:60164870-60164871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184144128	chr12:60164899-60164900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566957189	chr12:60164924-60164925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535630826	chr12:60164953-60164954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111381750	chr12:60164955-60164956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189441918	chr12:60164978-60164979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368475464	chr12:60164988-60164989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538517319	chr12:60164998-60164999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144716529	chr12:60165031-60165032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558522051	chr12:60165038-60165039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148114133	chr12:60165039-60165040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141923225	chr12:60165042-60165043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150664550	chr12:60165043-60165044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs80245181	chr12:60165048-60165049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370225843	chr12:60165064-60165065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374313420	chr12:60165096-60165097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200049323	chr12:60165116-60165117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140968673	chr12:60165118-60165119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368211618	chr12:60165128-60165129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372034754	chr12:60165140-60165141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181430482	chr12:60165196-60165197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552753886	chr12:60165251-60165252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2711659	chr12:60165271-60165272	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs541631589	chr12:60165274-60165275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561524472	chr12:60165288-60165289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575133189	chr12:60165308-60165309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544093956	chr12:60165329-60165330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564088375	chr12:60165359-60165360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116468909	chr12:60165416-60165417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17122972	chr12:60165423-60165424	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs560348175	chr12:60165486-60165487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529407449	chr12:60165649-60165650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549525027	chr12:60165696-60165697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60100000-60175200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr12:60124000-60168800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr12:60130800-60172200	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr12:60131000-60186000	Weak transcription	Pancreas	Pancrea
5	chr12:60132400-60165600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr12:60138600-60168400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:60138800-60173200	Weak transcription	Aorta	Aorta
8	chr12:60152000-60182200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr12:60159000-60168400	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr12:60159000-60172000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr12:60159800-60186400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:60160400-60186000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:60161200-60168800	Weak transcription	Adipose Nuclei	Adipose
14	chr12:60161200-60181600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr12:60161200-60186800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr12:60161400-60167800	Weak transcription	Primary T cells from cord blood	blood
17	chr12:60161400-60168400	Weak transcription	Left Ventricle	heart
18	chr12:60161400-60168600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:60161400-60176400	Weak transcription	GM12878-XiMat	blood
20	chr12:60161600-60168600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr12:60161600-60169000	Weak transcription	Dnd41	blood
22	chr12:60161600-60176400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr12:60161800-60186000	Weak transcription	Lung	lung
24	chr12:60162200-60164800	Weak transcription	Primary B cells from cord blood	blood
25	chr12:60162400-60169200	Weak transcription	Right Ventricle	heart
26	chr12:60162600-60175000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:60162600-60186000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr12:60162800-60184000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:60162800-60186000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr12:60163200-60168600	Weak transcription	Primary B cells from peripheral blood	blood
31	chr12:60163800-60174400	Weak transcription	NHDF-Ad	bronchial
32	chr12:60164400-60174600	Weak transcription	Fetal Thymus	thymus
33	chr12:60164800-60167200	Strong transcription	Primary B cells from cord blood	blood
34	chr12:60165600-60167000	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr12:60166600-60177000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr12:60167000-60167400	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr12:60167000-60177400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr12:60167200-60168800	Weak transcription	Primary B cells from cord blood	blood
39	chr12:60167200-60168800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr12:60167400-60169200	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr12:60167400-60170400	Weak transcription	Gastric	stomach
42	chr12:60167800-60170200	Strong transcription	Primary T cells from cord blood	blood
43	chr12:60167800-60177400	Weak transcription	Ovary	ovary
44	chr12:60168400-60169200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr12:60168400-60169200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr12:60168400-60169400	Strong transcription	Left Ventricle	heart
47	chr12:60168600-60169200	Strong transcription	Primary B cells from peripheral blood	blood
48	chr12:60168600-60169200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr12:60168600-60169400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:60168800-60169200	Strong transcription	Primary B cells from cord blood	blood

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