Variant report

Variant	esv3488108
Chromosome Location	chr12:64178778-64195988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:0)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:64192427-64192579	HepG2	liver:	n/a	n/a
2	ATF3	chr12:64188809-64189099	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr12:64195903-64196069	K562	blood:	n/a	n/a
4	CEBPB	chr12:64178848-64178944	K562	blood:	n/a	chr12:64178867-64178878 chr12:64178866-64178879 chr12:64178866-64178877 chr12:64178868-64178877
5	CEBPB	chr12:64178705-64178967	HepG2	liver:	n/a	chr12:64178867-64178878 chr12:64178866-64178879 chr12:64178866-64178877 chr12:64178868-64178877
6	CTCF	chr12:64195779-64196137	HepG2	liver:	n/a	n/a
7	CTCF	chr12:64195878-64196072	LNCaP	prostate:	n/a	n/a
8	CTCF	chr12:64195722-64196157	A549	lung:	n/a	n/a
9	CTCF	chr12:64195790-64196180	K562	blood:	n/a	n/a
10	CTCF	chr12:64195920-64196070	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr12:64195894-64196080	GM13977	blood:	n/a	n/a
12	CTCF	chr12:64195940-64196090	GM06990	blood:	n/a	n/a
13	CTCF	chr12:64195896-64196060	MCF-7	breast:	n/a	n/a
14	CTCF	chr12:64195980-64196130	GM12868	blood:	n/a	n/a
15	CTCF	chr12:64195900-64196050	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:64195790-64196157	A549	lung:	n/a	n/a
17	CTCF	chr12:64195880-64196030	AG09319	gingival:	n/a	n/a
18	CTCF	chr12:64195900-64196050	BJ	skin:	n/a	n/a
19	CTCF	chr12:64195840-64195990	HVMF	connective:	n/a	n/a
20	CTCF	chr12:64195780-64195930	HCM	heart:	n/a	n/a
21	CTCF	chr12:64195909-64196072	GM10266	blood:	n/a	n/a
22	CTCF	chr12:64195880-64196030	AG09309	skin:	n/a	n/a
23	CTCF	chr12:64189103-64189158	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr12:64195920-64196070	GM12873	blood:	n/a	n/a
25	CTCF	chr12:64195980-64196130	A549	lung:	n/a	n/a
26	CTCF	chr12:64195900-64196050	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr12:64195860-64196010	SAEC	small airway:	n/a	n/a
28	CTCF	chr12:64195860-64196010	GM12870	blood:	n/a	n/a
29	CTCF	chr12:64195880-64196030	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr12:64195880-64196030	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr12:64195920-64196070	AG09309	skin:	n/a	n/a
32	CTCF	chr12:64195823-64196112	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr12:64195860-64196010	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr12:64195880-64196030	BJ	skin:	n/a	n/a
35	CTCF	chr12:64195900-64196050	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr12:64195940-64196090	GM12875	blood:	n/a	n/a
37	CTCF	chr12:64195776-64196136	K562	blood:	n/a	n/a
38	CTCF	chr12:64195900-64196050	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr12:64195940-64196090	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:64195880-64196030	GM12873	blood:	n/a	n/a
41	CTCF	chr12:64195900-64196050	AG10803	skin:	n/a	n/a
42	CTCF	chr12:64195940-64196090	SAEC	small airway:	n/a	n/a
43	CTCF	chr12:64195960-64196110	GM06990	blood:	n/a	n/a
44	CTCF	chr12:64195860-64196106	GM12878	blood:	n/a	n/a
45	CTCF	chr12:64195940-64196090	RPTEC	kidney:	n/a	n/a
46	CTCF	chr12:64195860-64196010	GM12872	blood:	n/a	n/a
47	CTCF	chr12:64195940-64196090	Caco-2	colon:	n/a	n/a
48	CTCF	chr12:64195940-64196090	GM12870	blood:	n/a	n/a
49	CTCF	chr12:64195880-64196030	GM12801	blood:	n/a	n/a
50	CTCF	chr12:64195900-64196050	HPAF	blood vessel:	n/a	n/a

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63813649..63814184-chr12:64195525..64196396,2	K562	blood:
2	chr12:64177549..64179477-chr12:64189531..64192221,2	K562	blood:
3	chr12:64180929..64182540-chr12:64189836..64191999,2	MCF-7	breast:
4	chr12:64172631..64179011-chr12:64187703..64190145,6	MCF-7	breast:
5	chr12:64188729..64190948-chr12:64197247..64198958,2	K562	blood:
6	chr12:64172395..64175865-chr12:64176316..64181928,12	K562	blood:
7	chr12:64173978..64177817-chr12:64182120..64184728,4	K562	blood:
8	chr12:64186627..64188743-chr12:64193793..64196445,3	K562	blood:
9	chr12:64172206..64174854-chr12:64184728..64186447,3	K562	blood:
10	chr12:63497370..63497928-chr12:64195474..64196377,2	MCF-7	breast:
11	chr12:64176321..64178980-chr12:64185649..64187480,3	MCF-7	breast:
12	chr12:64180929..64182540-chr12:64189836..64191999,2	MCF-7	breast:
13	chr12:64172671..64176292-chr12:64191216..64196632,5	MCF-7	breast:
14	chr12:64172631..64179011-chr12:64187703..64190145,6	MCF-7	breast:
15	chr12:64178892..64180813-chr12:64194580..64197206,2	K562	blood:
16	chr12:64189848..64191605-chr12:64194273..64195833,2	MCF-7	breast:
17	chr12:64189848..64191605-chr12:64194273..64195833,2	MCF-7	breast:
18	chr12:63497039..63497977-chr12:64195476..64196144,2	K562	blood:
19	chr12:64193892..64196710-chr12:64197339..64199038,3	K562	blood:
20	chr12:63545419..63546376-chr12:64195555..64196413,2	MCF-7	breast:
21	chr12:64186627..64188743-chr12:64193793..64196445,3	K562	blood:
22	chr12:64172633..64174907-chr12:64183878..64187539,3	MCF-7	breast:
23	chr12:64172589..64175160-chr12:64189373..64193026,5	MCF-7	breast:
24	chr12:64178892..64180813-chr12:64194580..64197206,2	K562	blood:
25	chr12:64172665..64175331-chr12:64194682..64197216,2	K562	blood:
26	chr12:64172533..64176121-chr12:64194832..64198679,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPY19L2-1	chr12:64189261-64189498	ENSG00000249753.2

No data

Variant related genes	Relation type
ENSG00000249753	TF binding region
TMEM5	TF binding region
ENSG00000249753	chromatin interactions
ENSG00000118600	chromatin interactions

Extended variants
information (count: 556 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150417042	chr12:64178796-64178797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs188655071	chr12:64178797-64178798	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369137385	chr12:64178809-64178810	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs199830732	chr12:64178811-64178812	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs570537825	chr12:64178818-64178819	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs138231365	chr12:64178833-64178834	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372764664	chr12:64178879-64178880	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560911123	chr12:64178887-64178888	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370383744	chr12:64178902-64178903	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554016278	chr12:64178947-64178948	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs181362969	chr12:64178951-64178952	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs542954491	chr12:64178974-64178975	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs530058060	chr12:64179047-64179048	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34755648	chr12:64179053-64179054	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563095821	chr12:64179069-64179070	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185251311	chr12:64179072-64179073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545074503	chr12:64179113-64179114	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564846206	chr12:64179139-64179140	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149304355	chr12:64179151-64179152	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs76948828	chr12:64179213-64179214	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs144538483	chr12:64179255-64179256	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs61935925	chr12:64179271-64179272	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs138161284	chr12:64179292-64179293	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530004486	chr12:64179446-64179447	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs550040293	chr12:64179463-64179464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528976809	chr12:64179622-64179623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550144596	chr12:64179654-64179655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569810341	chr12:64179697-64179698	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538490499	chr12:64179727-64179728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs117972385	chr12:64179744-64179745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527385243	chr12:64179746-64179747	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571670666	chr12:64179819-64179820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533891957	chr12:64179853-64179854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553740981	chr12:64179855-64179856	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs11829078	chr12:64179869-64179870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536527471	chr12:64179871-64179872	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556620548	chr12:64179927-64179928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532106376	chr12:64179939-64179940	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576546665	chr12:64180035-64180036	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs565671209	chr12:64180045-64180046	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189707388	chr12:64180138-64180139	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142661417	chr12:64180140-64180141	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572177878	chr12:64180150-64180151	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541165777	chr12:64180154-64180155	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146302106	chr12:64180172-64180173	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs529740886	chr12:64180257-64180258	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528425070	chr12:64180260-64180261	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550031839	chr12:64180288-64180289	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182650982	chr12:64180290-64180291	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34686344	chr12:64180291-64180292	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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	17899364	CNVD
Colorectal cancer	16272173	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
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	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
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64174400-64180600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:64174400-64180600	Weak transcription	Gastric	stomach
3	chr12:64174400-64184000	Weak transcription	Esophagus	oesophagus
4	chr12:64174400-64184000	Weak transcription	Lung	lung
5	chr12:64174400-64189200	Weak transcription	Pancreas	Pancrea
6	chr12:64174400-64200200	Weak transcription	Spleen	Spleen
7	chr12:64174400-64201800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:64174400-64203400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr12:64174400-64204400	Weak transcription	Small Intestine	intestine
10	chr12:64174400-64204800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:64174600-64180600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:64174600-64180600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:64174600-64180800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr12:64174600-64183800	Weak transcription	Psoas Muscle	Psoas
15	chr12:64174600-64186200	Weak transcription	Aorta	Aorta
16	chr12:64174600-64187800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr12:64174600-64199400	Weak transcription	Brain Substantia Nigra	brain
18	chr12:64174600-64200200	Weak transcription	HSMMtube	muscle
19	chr12:64174600-64200600	Weak transcription	Thymus	Thymus
20	chr12:64174600-64201000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr12:64174600-64204400	Weak transcription	Colonic Mucosa	Colon
22	chr12:64174800-64199200	Weak transcription	Stomach Mucosa	stomach
23	chr12:64174800-64208000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr12:64174800-64208000	Weak transcription	Fetal Brain Male	brain
25	chr12:64174800-64208600	Weak transcription	Fetal Brain Female	brain
26	chr12:64175000-64180800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr12:64175000-64180800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr12:64175000-64183800	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr12:64175000-64184000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr12:64175000-64184600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr12:64175000-64186000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr12:64175000-64186000	Weak transcription	Brain Germinal Matrix	brain
33	chr12:64175000-64189000	Weak transcription	Fetal Intestine Small	intestine
34	chr12:64175000-64200200	Weak transcription	Brain Anterior Caudate	brain
35	chr12:64175200-64180000	Weak transcription	NHDF-Ad	bronchial
36	chr12:64175200-64181800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:64175200-64184800	Strong transcription	Placenta	Placenta
38	chr12:64175200-64185600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr12:64175200-64199400	Weak transcription	NHLF	lung
40	chr12:64175200-64202400	Weak transcription	Fetal Heart	heart
41	chr12:64175200-64205200	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr12:64175400-64178800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr12:64175400-64178800	Strong transcription	A549	lung
44	chr12:64175400-64179000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr12:64175400-64179200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr12:64175400-64179800	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr12:64175400-64189400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr12:64175400-64200800	Weak transcription	Colon Smooth Muscle	Colon
49	chr12:64175400-64201800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr12:64175400-64202600	Weak transcription	Hela-S3	cervix

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