Variant report

Variant	nsv1051524
Chromosome Location	chr12:41409977-41643387
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	ARID3A	chr12:41411864-41412129	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:41566591-41566714	K562	blood:	n/a	n/a
3	ATF1	chr12:41579594-41579660	K562	blood:	n/a	n/a
4	ATF1	chr12:41565651-41565777	K562	blood:	n/a	n/a
5	BATF	chr12:41468059-41468293	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:41411840-41412184	HepG2	liver:	n/a	n/a
7	CEBPB	chr12:41586255-41586474	K562	blood:	n/a	chr12:41586376-41586387 chr12:41586336-41586349 chr12:41586336-41586347 chr12:41586377-41586388
8	CEBPB	chr12:41586258-41586417	H1-hESC	embryonic stem cell:	n/a	chr12:41586376-41586387 chr12:41586336-41586349 chr12:41586336-41586347 chr12:41586377-41586388
9	CEBPB	chr12:41528491-41528708	H1-hESC	embryonic stem cell:	n/a	chr12:41528621-41528632
10	CEBPB	chr12:41593430-41593849	A549	lung:	n/a	n/a
11	CEBPB	chr12:41602689-41602802	HepG2	liver:	n/a	chr12:41602756-41602767 chr12:41602756-41602769 chr12:41602757-41602768
12	CEBPB	chr12:41527172-41527446	IMR90	lung:	n/a	chr12:41527285-41527296
13	CEBPB	chr12:41533773-41534082	HepG2	liver:	n/a	chr12:41533925-41533936
14	CEBPB	chr12:41497450-41497789	A549	lung:	n/a	chr12:41497608-41497619
15	CEBPB	chr12:41497428-41497791	IMR90	lung:	n/a	chr12:41497608-41497619
16	CEBPB	chr12:41545648-41545940	A549	lung:	n/a	n/a
17	CEBPB	chr12:41533752-41534008	A549	lung:	n/a	chr12:41533925-41533936
18	CEBPB	chr12:41528469-41528790	HepG2	liver:	n/a	chr12:41528621-41528632
19	CEBPB	chr12:41527133-41527407	A549	lung:	n/a	chr12:41527285-41527296
20	CEBPB	chr12:41545520-41546043	A549	lung:	n/a	n/a
21	CEBPB	chr12:41545629-41545990	A549	lung:	n/a	n/a
22	CEBPB	chr12:41528481-41528820	A549	lung:	n/a	chr12:41528621-41528632
23	CEBPB	chr12:41586208-41586501	A549	lung:	n/a	chr12:41586376-41586387 chr12:41586336-41586349 chr12:41586336-41586347 chr12:41586377-41586388
24	CEBPB	chr12:41527149-41527466	HepG2	liver:	n/a	chr12:41527285-41527296
25	CEBPB	chr12:41586172-41586527	HepG2	liver:	n/a	chr12:41586376-41586387 chr12:41586336-41586349 chr12:41586336-41586347 chr12:41586377-41586388
26	CEBPB	chr12:41629537-41629781	A549	lung:	n/a	n/a
27	CEBPB	chr12:41500689-41501018	IMR90	lung:	n/a	chr12:41500844-41500855
28	CEBPB	chr12:41411847-41412147	HepG2	liver:	n/a	chr12:41411994-41412011
29	CEBPB	chr12:41500676-41501006	A549	lung:	n/a	chr12:41500844-41500855
30	CEBPB	chr12:41497449-41497789	HepG2	liver:	n/a	chr12:41497608-41497619
31	CEBPB	chr12:41582452-41582507	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr12:41593453-41593595	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:41497452-41497751	Hela-S3	cervix:	n/a	chr12:41497608-41497619
34	CEBPB	chr12:41635579-41635806	HepG2	liver:	n/a	chr12:41635633-41635646 chr12:41635633-41635644
35	CEBPB	chr12:41500713-41501021	HepG2	liver:	n/a	chr12:41500844-41500855
36	CEBPB	chr12:41586185-41586519	IMR90	lung:	n/a	chr12:41586376-41586387 chr12:41586336-41586349 chr12:41586336-41586347 chr12:41586377-41586388
37	CEBPB	chr12:41529567-41529876	A549	lung:	n/a	chr12:41529779-41529790 chr12:41529780-41529791 chr12:41529779-41529792 chr12:41529779-41529790
38	CEBPB	chr12:41529576-41529865	HepG2	liver:	n/a	chr12:41529779-41529790 chr12:41529780-41529791 chr12:41529779-41529792 chr12:41529779-41529790
39	CEBPB	chr12:41635598-41635798	A549	lung:	n/a	chr12:41635633-41635646 chr12:41635633-41635644
40	CHD2	chr12:41583115-41583162	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr12:41581857-41582620	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr12:41461894-41462012	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:41584313-41584507	NHEK	skin:	n/a	n/a
44	CTCF	chr12:41583775-41584763	A549	lung:	n/a	n/a
45	CTCF	chr12:41500260-41500305	Fibrobl	skin:	n/a	n/a
46	CTCF	chr12:41578806-41578851	GM10248	blood:	n/a	n/a
47	CTCF	chr12:41584300-41584450	GM12867	blood:	n/a	n/a
48	CTCF	chr12:41565740-41565890	HRE	kidney:	n/a	n/a
49	CTCF	chr12:41584300-41584450	GM12874	blood:	n/a	n/a
50	CTCF	chr12:41584320-41584470	HPF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41583115-41583165	HRPEpiC	eye:	n/a
2	chr12:41583115-41583165	HRPEpiC	eye:	n/a
3	chr12:41583115-41583165	Caco-2	colon:	n/a
4	chr12:41583115-41583165	NHBE	bronchial:	n/a
5	chr12:41582362-41582412	HepG2	liver:	n/a
6	chr12:41582961-41583011	BE2_C	brain:	n/a
7	chr12:41581484-41581534	GM12878	blood:	n/a
8	chr12:41582063-41582113	HRCEpiC	kidney:	n/a
9	chr12:41582063-41582113	K562	blood:	n/a
10	chr12:41582067-41582117	CMK	blood:	n/a
11	chr12:41581414-41581464	HRE	kidney:	n/a
12	chr12:41582063-41582113	NHBE	bronchial:	n/a
13	chr12:41582362-41582412	HRE	kidney:	n/a
14	chr12:41581484-41581534	NT2-D1	testis:	n/a
15	chr12:41582349-41582399	GM12891	blood:	n/a
16	chr12:41582017-41582067	NHBE	bronchial:	n/a
17	chr12:41582063-41582113	BE2_C	brain:	n/a
18	chr12:41582362-41582412	NT2-D1	testis:	n/a
19	chr12:41583367-41583417	HAEpiC	amniotic membrane:	n/a
20	chr12:41582017-41582067	PFSK-1	brain:	n/a
21	chr12:41583367-41583417	BJ	skin:	n/a
22	chr12:41582362-41582412	H1-hESC	embryonic stem cell:	embryo
23	chr12:41583367-41583417	SK-N-SH_RA	brain:	n/a
24	chr12:41585373-41585423	T-47D	breast:	n/a
25	chr12:41581484-41581534	GM12891	blood:	n/a
26	chr12:41581484-41581534	SK-N-SH	brain:	n/a
27	chr12:41582961-41583011	HAEpiC	amniotic membrane:	n/a
28	chr12:41481184-41481234	HNPCEpiC	eye:	n/a
29	chr12:41585373-41585423	RPTEC	kidney:	n/a
30	chr12:41481088-41481138	Caco-2	colon:	n/a
31	chr12:41582063-41582113	NHDF-neo	bronchial:	n/a
32	chr12:41582063-41582113	SK-N-MC	brain:	n/a
33	chr12:41583367-41583417	NHBE	bronchial:	n/a
34	chr12:41583721-41583771	U87	brain:	n/a
35	chr12:41582017-41582067	HEK293	kidney:	embryo
36	chr12:41585373-41585423	HL-60	blood:	n/a
37	chr12:41481184-41481234	GM12892	blood:	n/a
38	chr12:41481184-41481234	AG04450	lung:	fetal
39	chr12:41581484-41581534	HRCEpiC	kidney:	n/a
40	chr12:41583721-41583771	BE2_C	brain:	n/a
41	chr12:41583115-41583165	HMEC	breast:	n/a
42	chr12:41583721-41583771	HRPEpiC	eye:	n/a
43	chr12:41582349-41582399	HRE	kidney:	n/a
44	chr12:41582349-41582399	AG09309	skin:	n/a
45	chr12:41582067-41582117	HAEpiC	amniotic membrane:	n/a
46	chr12:41583721-41583771	NH-A	brain:	n/a
47	chr12:41581484-41581534	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:41481184-41481234	HEK293	kidney:	embryo
49	chr12:41581484-41581534	HUVEC	blood vessel:	n/a
50	chr12:41582362-41582412	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:41588867..41591479-chr12:41595208..41596814,2	K562	blood:
2	chr12:41615335..41618133-chr12:41621079..41623279,2	K562	blood:
3	chr12:41619133..41620847-chr12:41622341..41624023,2	MCF-7	breast:
4	chr12:41449274..41451098-chr12:41453450..41455316,2	K562	blood:
5	chr12:41447343..41449022-chr12:41451324..41453086,2	K562	blood:
6	chr12:41443017..41445495-chr12:41450238..41452740,2	MCF-7	breast:
7	chr12:41443017..41445495-chr12:41450238..41452740,2	MCF-7	breast:
8	chr12:41619133..41620847-chr12:41622341..41624023,2	MCF-7	breast:
9	chr12:41495512..41497146-chr5:132296285..132299181,2	MCF-7	breast:
10	chr12:41615335..41618133-chr12:41621079..41623279,2	K562	blood:
11	chr12:41447343..41449022-chr12:41451324..41453086,2	K562	blood:
12	chr12:41588867..41591479-chr12:41595208..41596814,2	K562	blood:
13	chr12:41449274..41451098-chr12:41453450..41455316,2	K562	blood:

Variant related genes	Relation type
PDZRN4	TF binding region
CNTN1	TF binding region
PDZRN4	CpG island
CNTN1	CpG island

Extended variants
information (count: 6411 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6411 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571130571	chr12:41409986-41409987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117089828	chr12:41410085-41410086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550340628	chr12:41410096-41410097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146771507	chr12:41410097-41410098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184245861	chr12:41410107-41410108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189005728	chr12:41410117-41410118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs61924397	chr12:41410140-41410141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369070288	chr12:41410169-41410170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182129191	chr12:41410178-41410179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577129048	chr12:41410190-41410191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544576631	chr12:41410192-41410193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186328542	chr12:41410201-41410202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376370870	chr12:41410204-41410205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189994095	chr12:41410238-41410239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74893121	chr12:41410253-41410254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76096615	chr12:41410265-41410266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180708666	chr12:41410266-41410267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369138669	chr12:41410288-41410289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140458146	chr12:41410373-41410374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373509156	chr12:41410386-41410387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550159697	chr12:41410402-41410403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373530981	chr12:41410403-41410404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535903320	chr12:41410444-41410445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547883322	chr12:41410466-41410467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373871151	chr12:41410491-41410492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566695601	chr12:41410583-41410584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534419629	chr12:41410594-41410595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs267603461	chr12:41410596-41410597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34326474	chr12:41410623-41410624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538201110	chr12:41410624-41410625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199833589	chr12:41410625-41410626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567330815	chr12:41410666-41410667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1056020	chr12:41410691-41410692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199617690	chr12:41410716-41410717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs56236911	chr12:41410763-41410764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs113295313	chr12:41410786-41410787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547267666	chr12:41410815-41410816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554326095	chr12:41410821-41410822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572484804	chr12:41410851-41410852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540401296	chr12:41410871-41410872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73116992	chr12:41410877-41410878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373134797	chr12:41411019-41411020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373539116	chr12:41411022-41411023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532429590	chr12:41411029-41411030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571885319	chr12:41411080-41411081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115786333	chr12:41411095-41411096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138189250	chr12:41411096-41411097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538621523	chr12:41411100-41411101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185315559	chr12:41411132-41411133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149170261	chr12:41411138-41411139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41405200-41429800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr12:41405400-41417600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:41405600-41423000	Weak transcription	Ovary	ovary
4	chr12:41407000-41425200	Weak transcription	Brain Angular Gyrus	brain
5	chr12:41408000-41413000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:41408200-41426400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:41408200-41449800	Weak transcription	Brain Anterior Caudate	brain
8	chr12:41408400-41421400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr12:41408800-41428000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:41409000-41435000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr12:41409600-41416800	Weak transcription	A549	lung
12	chr12:41410000-41424800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:41413000-41413600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:41413600-41416400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:41416400-41417400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:41417000-41427400	Weak transcription	Fetal Lung	lung
17	chr12:41417200-41417800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr12:41417600-41417800	Enhancers	Aorta	Aorta
19	chr12:41417600-41418000	Enhancers	Brain Cingulate Gyrus	brain
20	chr12:41417800-41423000	Weak transcription	Aorta	Aorta
21	chr12:41418000-41424600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr12:41418600-41422800	Weak transcription	Brain Substantia Nigra	brain
23	chr12:41419600-41422200	Weak transcription	Brain Hippocampus Middle	brain
24	chr12:41421000-41423600	Weak transcription	Fetal Kidney	kidney
25	chr12:41421400-41421800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
26	chr12:41421800-41426200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr12:41422800-41423000	Active TSS	Brain Substantia Nigra	brain
28	chr12:41422800-41423200	ZNF genes & repeats	Fetal Brain Male	brain
29	chr12:41423000-41423200	Enhancers	Aorta	Aorta
30	chr12:41426000-41426600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:41426000-41426800	Enhancers	Placenta	Placenta
32	chr12:41426200-41426600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr12:41428000-41429000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:41428200-41429200	Enhancers	NHEK	skin
35	chr12:41428600-41428800	Enhancers	Colon Smooth Muscle	Colon
36	chr12:41428600-41428800	Enhancers	Rectal Smooth Muscle	rectum
37	chr12:41428600-41429000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:41428600-41429000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:41428600-41429200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:41428800-41429400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr12:41428800-41430000	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:41429000-41469600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:41430000-41430800	Enhancers	Colon Smooth Muscle	Colon
44	chr12:41435800-41446000	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr12:41438200-41439800	Enhancers	Rectal Smooth Muscle	rectum
46	chr12:41438200-41445800	Weak transcription	A549	lung
47	chr12:41438400-41439800	Enhancers	Colon Smooth Muscle	Colon
48	chr12:41439200-41439800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr12:41439800-41442800	Weak transcription	Colon Smooth Muscle	Colon
50	chr12:41439800-41446000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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