Variant report

Variant	nsv983478
Chromosome Location	chr12:123062133-123080307
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:84)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:84 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:123069052-123069353	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr12:123068900-123069475	MCF-7	breast:	n/a	n/a
3	CEBPB	chr12:123075604-123075881	HepG2	liver:	n/a	n/a
4	CEBPB	chr12:123075612-123075793	K562	blood:	n/a	n/a
5	CEBPB	chr12:123075581-123075895	A549	lung:	n/a	n/a
6	CEBPB	chr12:123075580-123075896	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:123075618-123075852	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:123068986-123069358	MCF-7	breast:	n/a	n/a
9	CHD1	chr12:123066666-123066740	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:123071193-123071298	Lung_OC	lung:	n/a	n/a
11	CTCF	chr12:123072600-123072750	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr12:123071549-123071659	GM10248	blood:	n/a	n/a
13	E2F4	chr12:123072640-123072840	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr12:123067999-123068173	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr12:123069072-123069238	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr12:123067997-123068145	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr12:123068035-123068235	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr12:123069059-123069348	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:123069107-123069341	MCF10A-Er-Src	breast:	n/a	n/a
20	FOXA2	chr12:123066867-123067057	HepG2	liver:	n/a	n/a
21	GATA3	chr12:123068998-123069382	MCF-7	breast:	n/a	n/a
22	GATA3	chr12:123068799-123069560	MCF-7	breast:	n/a	n/a
23	GATA3	chr12:123068793-123069530	MCF-7	breast:	n/a	n/a
24	GATA3	chr12:123068813-123069413	MCF-7	breast:	n/a	n/a
25	HEY1	chr12:123077273-123077536	K562	blood:	n/a	n/a
26	HEY1	chr12:123077261-123077511	HepG2	liver:	n/a	n/a
27	JUN	chr12:123072454-123072516	H1-hESC	embryonic stem cell:	n/a	n/a
28	MAFF	chr12:123068813-123068925	K562	blood:	n/a	n/a
29	MAFK	chr12:123072884-123073027	HepG2	liver:	n/a	chr12:123072950-123072961 chr12:123072951-123072962 chr12:123072950-123072961 chr12:123072949-123072963 chr12:123072951-123072962
30	MAFK	chr12:123064546-123064792	HepG2	liver:	n/a	chr12:123064685-123064701
31	MAZ	chr12:123072393-123072444	HepG2	liver:	n/a	n/a
32	NFYB	chr12:123077223-123077434	GM12878	blood:	n/a	n/a
33	NFYB	chr12:123077055-123077467	K562	blood:	n/a	n/a
34	POLR2A	chr12:123072477-123072570	ProgFib	skin:	n/a	n/a
35	POLR2A	chr12:123067739-123068126	K562	blood:	n/a	n/a
36	POLR2A	chr12:123076887-123077068	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr12:123071481-123071551	Gliobla	brain:	n/a	n/a
38	POLR2A	chr12:123078651-123078659	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:123078310-123078419	MCF-7	breast:	n/a	n/a
40	POLR2A	chr12:123078128-123078261	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr12:123067303-123067625	K562	blood:	n/a	n/a
42	POLR2A	chr12:123078262-123078279	MCF-7	breast:	n/a	n/a
43	POLR2A	chr12:123078334-123078361	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr12:123068738-123069129	H1-neurons	neurons:	n/a	n/a
45	POLR2A	chr12:123068507-123068696	HL-60	blood:	n/a	n/a
46	POLR2A	chr12:123079174-123079211	K562	blood:	n/a	n/a
47	POLR2A	chr12:123062217-123062335	GM12878	blood:	n/a	n/a
48	POLR2A	chr12:123067317-123067654	K562	blood:	n/a	n/a
49	POLR2A	chr12:123078442-123078778	K562	blood:	n/a	n/a
50	POLR2A	chr12:123068392-123068525	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123076854-123076904	HNPCEpiC	eye:	n/a
2	chr12:123077350-123077400	ECC-1	luminal epithelium:	n/a
3	chr12:123076854-123076904	MCF-7	breast:	n/a
4	chr12:123077350-123077400	ProgFib	skin:	n/a
5	chr12:123077350-123077400	LNCaP	prostate:	n/a
6	chr12:123077521-123077571	SAEC	small airway:	n/a
7	chr12:123077350-123077400	SK-N-SH	brain:	n/a
8	chr12:123077521-123077571	GM19239	blood:	n/a
9	chr12:123077521-123077571	T-47D	breast:	n/a
10	chr12:123077521-123077571	GM12891	blood:	n/a
11	chr12:123076854-123076904	Hepatocyte	liver:	n/a
12	chr12:123077350-123077400	ovcar-3	ovarian:	n/a
13	chr12:123077350-123077400	HUVEC	blood vessel:	n/a
14	chr12:123077350-123077400	AoSMC	blood vessel:	n/a
15	chr12:123077521-123077571	SK-N-SH_RA	brain:	n/a
16	chr12:123077350-123077400	PrEC	prostate:	n/a
17	chr12:123076854-123076904	NHDF-neo	bronchial:	n/a
18	chr12:123077350-123077400	Jurkat	blood:	n/a
19	chr12:123077350-123077400	HL-60	blood:	n/a
20	chr12:123077521-123077571	HCM	heart:	n/a
21	chr12:123077350-123077400	NB4	blood:	n/a
22	chr12:123077521-123077571	HCPEpiC	choroid plexus:	n/a
23	chr12:123077350-123077400	GM12892	blood:	n/a
24	chr12:123076854-123076904	HCT-116	colon:	n/a
25	chr12:123077350-123077400	HAEpiC	amniotic membrane:	n/a
26	chr12:123077521-123077571	HEK293	kidney:	embryo
27	chr12:123076854-123076904	HUVEC	blood vessel:	n/a
28	chr12:123076854-123076904	HCF	heart:	n/a
29	chr12:123076854-123076904	ovcar-3	ovarian:	n/a
30	chr12:123076854-123076904	NT2-D1	testis:	n/a
31	chr12:123077521-123077571	MCF-7	breast:	n/a
32	chr12:123077350-123077400	HEK293	kidney:	embryo
33	chr12:123077521-123077571	AG04449	skin:	fetal
34	chr12:123077350-123077400	SK-N-SH_RA	brain:	n/a
35	chr12:123077521-123077571	HL-60	blood:	n/a
36	chr12:123077350-123077400	HMEC	breast:	n/a
37	chr12:123076854-123076904	GM12892	blood:	n/a
38	chr12:123076854-123076904	Caco-2	colon:	n/a
39	chr12:123077521-123077571	Caco-2	colon:	n/a
40	chr12:123077521-123077571	AoSMC	blood vessel:	n/a
41	chr12:123077521-123077571	HepG2	liver:	n/a
42	chr12:123076854-123076904	AG04449	skin:	fetal
43	chr12:123077521-123077571	CMK	blood:	n/a
44	chr12:123077350-123077400	HRE	kidney:	n/a
45	chr12:123077521-123077571	AG09319	gingival:	n/a
46	chr12:123077350-123077400	MCF-7	breast:	n/a
47	chr12:123076854-123076904	SK-N-SH	brain:	n/a
48	chr12:123076854-123076904	PANC-1	pancreas:	n/a
49	chr12:123077350-123077400	PANC-1	pancreas:	n/a
50	chr12:123077350-123077400	MCF10A-Er-Src	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123078659..123081368-chr12:123242413..123244541,2	K562	blood:
2	chr12:123067260..123069084-chr12:123070709..123072240,2	MCF-7	breast:
3	chr12:123004549..123007119-chr12:123070735..123073500,2	K562	blood:
4	chr12:123067260..123069084-chr12:123070709..123072240,2	MCF-7	breast:
5	chr12:123049783..123051932-chr12:123063399..123064990,2	K562	blood:
6	chr12:46122516..46123361-chr12:123078570..123079462,2	NB4	blood:
7	chr12:123075043..123077747-chr12:123078360..123080361,2	MCF-7	breast:
8	chr12:123057416..123060886-chr12:123062494..123065282,3	K562	blood:
9	chr12:123009714..123012123-chr12:123071284..123073590,2	MCF-7	breast:
10	chr12:123075043..123077747-chr12:123078360..123080361,2	MCF-7	breast:

No data

Variant related genes	Relation type
KNTC1	TF binding region
KNTC1	CpG island
ENSG00000184445	chromatin interactions
ENSG00000111011	chromatin interactions

Extended variants
information (count: 708 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554181476	chr12:123062151-123062152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372403130	chr12:123062168-123062169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201253327	chr12:123062219-123062220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186505286	chr12:123062233-123062234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201402164	chr12:123062253-123062254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527750148	chr12:123062291-123062292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371376144	chr12:123062300-123062301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374689028	chr12:123062308-123062309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552563596	chr12:123062321-123062322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565494072	chr12:123062339-123062340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570712898	chr12:123062375-123062376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538550958	chr12:123062384-123062385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550488505	chr12:123062391-123062392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568719782	chr12:123062395-123062396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368034541	chr12:123062412-123062413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536041280	chr12:123062423-123062424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146945040	chr12:123062481-123062482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11058796	chr12:123062489-123062490	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112809601	chr12:123062504-123062505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190079836	chr12:123062535-123062536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11058797	chr12:123062594-123062595	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs148010357	chr12:123062612-123062613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576420674	chr12:123062622-123062623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181607315	chr12:123062655-123062656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369072986	chr12:123062661-123062662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574328006	chr12:123062675-123062676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542023500	chr12:123062691-123062692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560061242	chr12:123062733-123062734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527788466	chr12:123062762-123062763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552351251	chr12:123062905-123062906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564548093	chr12:123062932-123062933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs137990747	chr12:123062933-123062934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373361759	chr12:123062938-123062939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531736026	chr12:123062960-123062961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186342938	chr12:123063006-123063007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141704799	chr12:123063030-123063031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536125458	chr12:123063121-123063122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547970286	chr12:123063140-123063141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566097921	chr12:123063169-123063170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191090206	chr12:123063188-123063189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558365599	chr12:123063195-123063196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150561159	chr12:123063202-123063203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183506563	chr12:123063210-123063211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115328082	chr12:123063259-123063260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574414556	chr12:123063268-123063269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186074909	chr12:123063300-123063301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541711719	chr12:123063316-123063317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190943541	chr12:123063380-123063381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12228803	chr12:123063419-123063420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572140253	chr12:123063435-123063436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123012400-123066000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:123012400-123114000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:123012400-123117000	Weak transcription	Pancreas	Pancrea
4	chr12:123012400-123121200	Weak transcription	Aorta	Aorta
5	chr12:123012600-123066200	Weak transcription	Psoas Muscle	Psoas
6	chr12:123012600-123095600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:123012800-123065800	Weak transcription	Brain Substantia Nigra	brain
8	chr12:123012800-123097400	Weak transcription	Brain Angular Gyrus	brain
9	chr12:123012800-123109200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr12:123013000-123076400	Weak transcription	Right Ventricle	heart
11	chr12:123013000-123109200	Weak transcription	Colon Smooth Muscle	Colon
12	chr12:123013200-123103000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:123013200-123112400	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:123013400-123080600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:123013400-123107400	Weak transcription	Fetal Heart	heart
16	chr12:123013400-123120600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:123014400-123084000	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr12:123014600-123085400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:123015400-123079800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:123015600-123115000	Strong transcription	Dnd41	blood
21	chr12:123022200-123084600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr12:123022600-123113800	Weak transcription	Colonic Mucosa	Colon
23	chr12:123026000-123076400	Weak transcription	Gastric	stomach
24	chr12:123026000-123081000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr12:123028600-123064400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr12:123029200-123085000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr12:123029200-123107600	Weak transcription	Brain Hippocampus Middle	brain
28	chr12:123032600-123095400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr12:123033400-123067000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr12:123036400-123074200	Weak transcription	Fetal Brain Male	brain
31	chr12:123037200-123113000	Weak transcription	Brain Anterior Caudate	brain
32	chr12:123037600-123095400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr12:123037800-123100600	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr12:123038400-123066200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr12:123038400-123120000	Weak transcription	Small Intestine	intestine
36	chr12:123042600-123107200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr12:123042800-123080000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr12:123043800-123066800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:123043800-123121800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr12:123046400-123073400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:123046400-123084800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr12:123046800-123064600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr12:123047200-123080600	Strong transcription	Fetal Thymus	thymus
44	chr12:123047800-123068600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr12:123047800-123078800	Strong transcription	Fetal Muscle Leg	muscle
46	chr12:123049000-123063200	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr12:123050600-123073000	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr12:123050800-123112600	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr12:123050800-123115200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr12:123051000-123072800	Strong transcription	H9 Cell Line	embryonic stem cell

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