Variant report

Variant	esv3424840
Chromosome Location	chr12:123334149-123336322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:306)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:123335460-123335610	HUVEC	blood vessel:	n/a	n/a
2	EGR1	chr12:123335630-123335824	K562	blood:	n/a	chr12:123335706-123335721
3	FOS	chr12:123335407-123335601	MCF10A-Er-Src	breast:	n/a	n/a
4	FOSL2	chr12:123336271-123336957	SK-N-SH	brain:	n/a	chr12:123336657-123336667 chr12:123336657-123336667 chr12:123336657-123336667 chr12:123336531-123336542 chr12:123336657-123336667 chr12:123336535-123336543 chr12:123336658-123336666
5	MXI1	chr12:123335330-123335745	IMR90	lung:	n/a	n/a
6	MYC	chr12:123335514-123335538	HUVEC	blood vessel:	n/a	n/a
7	MYC	chr12:123335590-123335597	HUVEC	blood vessel:	n/a	n/a
8	MYC	chr12:123335399-123335487	HUVEC	blood vessel:	n/a	n/a
9	MYC	chr12:123335542-123335577	HUVEC	blood vessel:	n/a	n/a
10	MYC	chr12:123335607-123335612	HUVEC	blood vessel:	n/a	n/a
11	PBX3	chr12:123336313-123336794	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr12:123336258-123336840	U87	brain:	n/a	n/a
13	POLR2A	chr12:123335459-123335631	K562	blood:	n/a	n/a
14	POLR2A	chr12:123336251-123336907	HUVEC	blood vessel:	n/a	n/a
15	POLR2A	chr12:123336169-123336228	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr12:123336235-123336795	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr12:123335557-123335652	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr12:123336317-123336517	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr12:123336306-123336944	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr12:123336246-123337135	HUVEC	blood vessel:	n/a	n/a
21	POLR2A	chr12:123336179-123337383	HUVEC	blood vessel:	n/a	n/a
22	YY1	chr12:123336321-123336751	SK-N-SH	brain:	n/a	chr12:123336508-123336518

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123335687-123335737	ECC-1	luminal epithelium:	n/a
2	chr12:123335687-123335737	ECC-1	luminal epithelium:	n/a
3	chr12:123335687-123335737	ovcar-3	ovarian:	n/a
4	chr12:123335687-123335737	HEK293	kidney:	embryo
5	chr12:123335687-123335737	H1-hESC	embryonic stem cell:	embryo
6	chr12:123335444-123335494	LNCaP	prostate:	n/a
7	chr12:123335357-123335407	HEEpiC	esophagus:	n/a
8	chr12:123335444-123335494	HCM	heart:	n/a
9	chr12:123335687-123335737	AG09319	gingival:	n/a
10	chr12:123334513-123334563	HRCEpiC	kidney:	n/a
11	chr12:123335687-123335737	Hela-S3	cervix:	n/a
12	chr12:123335444-123335494	HMEC	breast:	n/a
13	chr12:123334709-123334759	HEK293	kidney:	embryo
14	chr12:123335444-123335494	GM12891	blood:	n/a
15	chr12:123334709-123334759	A549	lung:	n/a
16	chr12:123335687-123335737	Caco-2	colon:	n/a
17	chr12:123335357-123335407	HRE	kidney:	n/a
18	chr12:123334513-123334563	HEK293	kidney:	embryo
19	chr12:123334709-123334759	HRE	kidney:	n/a
20	chr12:123335687-123335737	AG04449	skin:	fetal
21	chr12:123335357-123335407	NT2-D1	testis:	n/a
22	chr12:123334513-123334563	NT2-D1	testis:	n/a
23	chr12:123335357-123335407	Hepatocyte	liver:	n/a
24	chr12:123334709-123334759	AG09309	skin:	n/a
25	chr12:123335687-123335737	HRPEpiC	eye:	n/a
26	chr12:123335444-123335494	AG04450	lung:	fetal
27	chr12:123334709-123334759	NH-A	brain:	n/a
28	chr12:123335357-123335407	HCF	heart:	n/a
29	chr12:123334513-123334563	AG09319	gingival:	n/a
30	chr12:123335687-123335737	HEEpiC	esophagus:	n/a
31	chr12:123334513-123334563	HUVEC	blood vessel:	n/a
32	chr12:123334709-123334759	Hepatocyte	liver:	n/a
33	chr12:123335444-123335494	HRCEpiC	kidney:	n/a
34	chr12:123334513-123334563	NHBE	bronchial:	n/a
35	chr12:123335444-123335494	HIPEpiC	eye:	n/a
36	chr12:123335444-123335494	AoSMC	blood vessel:	n/a
37	chr12:123334709-123334759	HCPEpiC	choroid plexus:	n/a
38	chr12:123335357-123335407	PFSK-1	brain:	n/a
39	chr12:123334513-123334563	RPTEC	kidney:	n/a
40	chr12:123335357-123335407	GM12878	blood:	n/a
41	chr12:123334709-123334759	H1-hESC	embryonic stem cell:	embryo
42	chr12:123335357-123335407	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:123335357-123335407	HCPEpiC	choroid plexus:	n/a
44	chr12:123335357-123335407	PANC-1	pancreas:	n/a
45	chr12:123334709-123334759	LNCaP	prostate:	n/a
46	chr12:123334709-123334759	ECC-1	luminal epithelium:	n/a
47	chr12:123334513-123334563	HCM	heart:	n/a
48	chr12:123334709-123334759	K562	blood:	n/a
49	chr12:123335444-123335494	GM12878	blood:	n/a
50	chr12:123335687-123335737	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:123329734..123338030-chr12:123339120..123345153,11	MCF-7	breast:
2	chr12:123319497..123321053-chr12:123333768..123335476,2	K562	blood:

No data

Variant related genes	Relation type
HIP1R	TF binding region
HIP1R	CpG island
ENSG00000130787	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575500056	chr12:123334169-123334170	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs543064202	chr12:123334195-123334196	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs561330156	chr12:123334199-123334200	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528578039	chr12:123334212-123334213	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145393918	chr12:123334327-123334328	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559279413	chr12:123334333-123334334	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372319692	chr12:123334349-123334350	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533193550	chr12:123334372-123334373	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs35904336	chr12:123334420-123334421	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373368900	chr12:123334433-123334434	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145255391	chr12:123334436-123334437	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375128048	chr12:123334438-123334439	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs35465127	chr12:123334442-123334443	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200665144	chr12:123334518-123334519	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs59065210	chr12:123334539-123334540	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs373090169	chr12:123334544-123334545	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548584172	chr12:123334557-123334558	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370283420	chr12:123334561-123334562	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs556979438	chr12:123334571-123334572	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375497752	chr12:123334603-123334604	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534393785	chr12:123334643-123334644	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552700131	chr12:123334660-123334661	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375845202	chr12:123334684-123334685	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147270360	chr12:123334710-123334711	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs539232427	chr12:123334717-123334718	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs557340185	chr12:123334718-123334719	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs199779424	chr12:123334726-123334727	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs200886571	chr12:123334744-123334745	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201536073	chr12:123334747-123334748	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs148746514	chr12:123334748-123334749	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200503518	chr12:123334750-123334751	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs543373503	chr12:123334767-123334768	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542727986	chr12:123334866-123334867	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554977320	chr12:123334867-123334868	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573320572	chr12:123334880-123334881	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7489275	chr12:123334929-123334930	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540720375	chr12:123334932-123334933	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs56342419	chr12:123334946-123334947	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7487892	chr12:123334960-123334961	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs56133920	chr12:123334967-123334968	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs59315869	chr12:123334971-123334972	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs55723415	chr12:123334984-123334985	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs55841420	chr12:123334992-123334993	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs58115474	chr12:123335001-123335002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371694011	chr12:123335008-123335009	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532936569	chr12:123335015-123335016	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187894122	chr12:123335022-123335023	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs59259782	chr12:123335029-123335030	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192674205	chr12:123335069-123335070	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184248909	chr12:123335084-123335085	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	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
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123321800-123336800	Weak transcription	Aorta	Aorta
2	chr12:123322800-123334400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:123322800-123339600	Weak transcription	Dnd41	blood
4	chr12:123322800-123353000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr12:123323200-123340800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr12:123323200-123352000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr12:123323400-123335200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:123323600-123340800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr12:123324600-123344800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr12:123324600-123352800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr12:123324800-123351600	Weak transcription	Small Intestine	intestine
12	chr12:123325000-123338400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:123325200-123335400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr12:123326600-123335600	Weak transcription	NHLF	lung
15	chr12:123326600-123336800	Weak transcription	Psoas Muscle	Psoas
16	chr12:123326600-123345000	Weak transcription	A549	lung
17	chr12:123326800-123335400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr12:123327200-123337000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr12:123327200-123340000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr12:123327200-123344200	Weak transcription	Hela-S3	cervix
21	chr12:123327400-123336400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr12:123327400-123352600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr12:123327600-123334200	Weak transcription	Adipose Nuclei	Adipose
24	chr12:123327600-123335400	Weak transcription	HUVEC	blood vessel
25	chr12:123327600-123337000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:123327600-123353400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr12:123328200-123336800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:123328400-123336200	Weak transcription	Placenta	Placenta
29	chr12:123329200-123335600	Weak transcription	Primary T cells from cord blood	blood
30	chr12:123329200-123337600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr12:123329200-123355000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr12:123329400-123341800	Weak transcription	HepG2	liver
33	chr12:123329600-123336600	Strong transcription	Fetal Stomach	stomach
34	chr12:123329600-123344600	Strong transcription	Fetal Intestine Small	intestine
35	chr12:123330000-123335400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr12:123330000-123340400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr12:123330400-123335400	Weak transcription	Right Atrium	heart
38	chr12:123330400-123344400	Strong transcription	Primary B cells from peripheral blood	blood
39	chr12:123330400-123349200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:123330800-123334200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr12:123330800-123335400	Weak transcription	Fetal Brain Male	brain
42	chr12:123330800-123335600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr12:123330800-123336800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:123331000-123335400	Weak transcription	Stomach Mucosa	stomach
45	chr12:123331000-123335400	Weak transcription	HMEC	breast
46	chr12:123331000-123337000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:123331000-123340800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr12:123331200-123336800	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr12:123331400-123336800	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr12:123331600-123335400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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