Variant report

Variant	nsv1040304
Chromosome Location	chr12:38908242-38995786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:340)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:38978937-38979254	GM12878	blood:	n/a	chr12:38978975-38978984 chr12:38979090-38979101
2	BATF	chr12:38978987-38979244	GM12878	blood:	n/a	chr12:38979090-38979101
3	BRCA1	chr12:38980636-38980915	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:38982828-38983122	HepG2	liver:	n/a	chr12:38982971-38982982
5	CEBPB	chr12:38982762-38983190	ECC-1	luminal epithelium:	n/a	chr12:38982971-38982982
6	CEBPB	chr12:38982893-38983133	MCF-7	breast:	n/a	chr12:38982971-38982982
7	CEBPB	chr12:38980570-38980873	A549	lung:	n/a	chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980712
8	CEBPB	chr12:38981442-38981823	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:38933170-38933247	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:38949928-38950461	Hela-S3	cervix:	n/a	chr12:38950417-38950428
11	CEBPB	chr12:38951464-38951704	IMR90	lung:	n/a	chr12:38951566-38951577
12	CEBPB	chr12:38982562-38983243	Hela-S3	cervix:	n/a	chr12:38982971-38982982
13	CEBPB	chr12:38980443-38981124	Hela-S3	cervix:	n/a	chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980917-38980930 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980712
14	CEBPB	chr12:38982717-38983202	ECC-1	luminal epithelium:	n/a	chr12:38982971-38982982
15	CEBPB	chr12:38950379-38950387	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:38950329-38950425	A549	lung:	n/a	n/a
17	CEBPB	chr12:38951490-38951690	A549	lung:	n/a	chr12:38951566-38951577
18	CEBPB	chr12:38951466-38951741	HepG2	liver:	n/a	chr12:38951566-38951577
19	CEBPB	chr12:38982837-38983151	H1-hESC	embryonic stem cell:	n/a	chr12:38982971-38982982
20	CEBPB	chr12:38919074-38919216	A549	lung:	n/a	n/a
21	CHD2	chr12:38980670-38980954	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr12:38910620-38910626	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr12:38938615-38938757	GM12878	blood:	n/a	n/a
24	CTCF	chr12:38938580-38938730	GM12865	blood:	n/a	n/a
25	CTCF	chr12:38938520-38938670	HRE	kidney:	n/a	n/a
26	CTCF	chr12:38949551-38949727	LNCaP	prostate:	n/a	n/a
27	CTCF	chr12:38938630-38938705	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:38938593-38938737	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr12:38938660-38938810	GM12875	blood:	n/a	n/a
30	CTCF	chr12:38949500-38949650	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr12:38938600-38938750	Caco-2	colon:	n/a	n/a
32	CTCF	chr12:38938520-38938670	NHEK	skin:	n/a	n/a
33	CTCF	chr12:38938600-38938750	GM12878	blood:	n/a	n/a
34	CTCF	chr12:38988469-38988544	GM10266	blood:	n/a	n/a
35	CTCF	chr12:38938660-38938810	BE2_C	brain:	n/a	n/a
36	CTCF	chr12:38938600-38938750	GM12869	blood:	n/a	n/a
37	CTCF	chr12:38938596-38938762	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr12:38938520-38938670	GM06990	blood:	n/a	n/a
39	CTCF	chr12:38938600-38938750	SAEC	small airway:	n/a	n/a
40	CTCF	chr12:38938560-38938710	HRE	kidney:	n/a	n/a
41	CTCF	chr12:38938400-38938550	A549	lung:	n/a	n/a
42	CTCF	chr12:38938500-38938650	GM12878	blood:	n/a	n/a
43	CTCF	chr12:38938620-38938770	GM12873	blood:	n/a	n/a
44	CTCF	chr12:38938580-38938730	GM12869	blood:	n/a	n/a
45	CTCF	chr12:38938610-38938730	GM19240	blood:	n/a	n/a
46	CTCF	chr12:38938580-38938730	GM12873	blood:	n/a	n/a
47	CTCF	chr12:38938580-38938730	GM12874	blood:	n/a	n/a
48	CTCF	chr12:38938600-38938750	HepG2	liver:	n/a	n/a
49	CTCF	chr12:38938620-38938770	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr12:38938626-38938738	LNCaP	prostate:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:38984007-38984057	GM12891	blood:	n/a
2	chr12:38984007-38984057	SK-N-MC	brain:	n/a
3	chr12:38938054-38938104	MCF-7	breast:	n/a
4	chr12:38984007-38984057	AoSMC	blood vessel:	n/a
5	chr12:38984007-38984057	GM19239	blood:	n/a
6	chr12:38984007-38984057	PrEC	prostate:	n/a
7	chr12:38984007-38984057	AG10803	skin:	n/a
8	chr12:38984007-38984057	T-47D	breast:	n/a
9	chr12:38938054-38938104	BE2_C	brain:	n/a
10	chr12:38938054-38938104	GM12892	blood:	n/a
11	chr12:38984007-38984057	HRPEpiC	eye:	n/a
12	chr12:38984007-38984057	HRCEpiC	kidney:	n/a
13	chr12:38938054-38938104	LNCaP	prostate:	n/a
14	chr12:38938054-38938104	GM19239	blood:	n/a
15	chr12:38938054-38938104	BJ	skin:	n/a
16	chr12:38938054-38938104	SK-N-SH	brain:	n/a
17	chr12:38938054-38938104	GM06990	blood:	n/a
18	chr12:38984007-38984057	HAEpiC	amniotic membrane:	n/a
19	chr12:38938054-38938104	HNPCEpiC	eye:	n/a
20	chr12:38938054-38938104	HL-60	blood:	n/a
21	chr12:38938054-38938104	HepG2	liver:	n/a
22	chr12:38938054-38938104	HEK293	kidney:	embryo
23	chr12:38984007-38984057	HNPCEpiC	eye:	n/a
24	chr12:38984007-38984057	AG09319	gingival:	n/a
25	chr12:38938054-38938104	HEEpiC	esophagus:	n/a
26	chr12:38984007-38984057	GM06990	blood:	n/a
27	chr12:38938054-38938104	Hepatocyte	liver:	n/a
28	chr12:38984007-38984057	MCF10A-Er-Src	breast:	n/a
29	chr12:38984007-38984057	U87	brain:	n/a
30	chr12:38984007-38984057	Hepatocyte	liver:	n/a
31	chr12:38938054-38938104	K562	blood:	n/a
32	chr12:38984007-38984057	PFSK-1	brain:	n/a
33	chr12:38938054-38938104	CMK	blood:	n/a
34	chr12:38938054-38938104	Caco-2	colon:	n/a
35	chr12:38938054-38938104	NT2-D1	testis:	n/a
36	chr12:38984007-38984057	HUVEC	blood vessel:	n/a
37	chr12:38984007-38984057	Caco-2	colon:	n/a
38	chr12:38984007-38984057	IMR90	lung:	fetal
39	chr12:38938054-38938104	HCT-116	colon:	n/a
40	chr12:38984007-38984057	AG04449	skin:	fetal
41	chr12:38984007-38984057	RPTEC	kidney:	n/a
42	chr12:38938054-38938104	AG04449	skin:	fetal
43	chr12:38938054-38938104	NB4	blood:	n/a
44	chr12:38938054-38938104	AoSMC	blood vessel:	n/a
45	chr12:38938054-38938104	GM12878	blood:	n/a
46	chr12:38938054-38938104	HRCEpiC	kidney:	n/a
47	chr12:38938054-38938104	IMR90	lung:	fetal
48	chr12:38984007-38984057	GM12878	blood:	n/a
49	chr12:38984007-38984057	HCT-116	colon:	n/a
50	chr12:38984007-38984057	H1-hESC	embryonic stem cell:	embryo

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38954957..38957532-chr12:38958850..38960983,2	K562	blood:
2	chr12:38917479..38920369-chr12:38920412..38922084,2	K562	blood:
3	chr12:38917479..38920369-chr12:38920412..38922084,2	K562	blood:
4	chr12:38990179..38991129-chr4:2331691..2332483,2	Hela-S3	cervix:
5	chr12:38954957..38957532-chr12:38958850..38960983,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPNE8-1	chr12:38938130-38938378	ENSG00000258119
2	lnc-CPNE8-1	chr12:38940187-38940310	ENSG00000258119
3	lnc-CPNE8-1	chr12:38983517-38983614	ENSG00000258119
4	lnc-CPNE8-1	chr12:38937979-38938333	ENSG00000258119
5	lnc-CPNE8-1	chr12:38983132-38983232	ENSG00000258119
6	lnc-CPNE8-1	chr12:38937980-38938333	XLOC_010050
7	lnc-CPNE8-1	chr12:38983132-38983232	XLOC_010050
8	lnc-CPNE8-1	chr12:38940187-38940279	ENSG00000258119
9	lnc-CPNE8-1	chr12:38983517-38983614	XLOC_010050
10	lnc-CPNE8-1	chr12:38940187-38940310	XLOC_010050

No data

Variant related genes	Relation type
ENSG00000258119	TF binding region
ENSG00000257645	TF binding region
ENSG00000258119	CpG island
ENSG00000257645	CpG island
SLC39A11	miRNA target sites
C1D	miRNA target sites
NSF	miRNA target sites
GREB1	miRNA target sites
SLC39A10	miRNA target sites
HECTD3	miRNA target sites
ZFP1	miRNA target sites
SLC39A14	miRNA target sites

Extended variants
information (count: 737 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:737 , 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	rs34294292	chr12:38908623-38908624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527491008	chr12:38908654-38908655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369520964	chr12:38908752-38908753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181460662	chr12:38908766-38908767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562133764	chr12:38908809-38908810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530779489	chr12:38908836-38908837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184963324	chr12:38908875-38908876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564413854	chr12:38908963-38908964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189349080	chr12:38908973-38908974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117859427	chr12:38909024-38909025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546803449	chr12:38909059-38909060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144432793	chr12:38909108-38909109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529565536	chr12:38909113-38909114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs61401280	chr12:38909114-38909115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs58050693	chr12:38909115-38909116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7304213	chr12:38909195-38909196	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs115100549	chr12:38909200-38909201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561069581	chr12:38909223-38909224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531421245	chr12:38909252-38909253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568518639	chr12:38909277-38909278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575143882	chr12:38909372-38909373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73096757	chr12:38909391-38909392	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs557226079	chr12:38909398-38909399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114147660	chr12:38909434-38909435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560162710	chr12:38909496-38909497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539627782	chr12:38909519-38909520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181844041	chr12:38909546-38909547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371544841	chr12:38909557-38909558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186123448	chr12:38909595-38909596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114625135	chr12:38909673-38909674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552040217	chr12:38909685-38909686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7957185	chr12:38909710-38909711	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs58499540	chr12:38909748-38909749	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12306901	chr12:38909863-38909864	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs200716393	chr12:38909867-38909868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546444506	chr12:38909892-38909893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4631924	chr12:38909937-38909938	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs34561864	chr12:38910000-38910001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528937396	chr12:38910003-38910004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549074189	chr12:38910004-38910005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs60560098	chr12:38910005-38910006	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs12307003	chr12:38910078-38910079	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs550994213	chr12:38910161-38910162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570772850	chr12:38910219-38910220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540146854	chr12:38910229-38910230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371961067	chr12:38910231-38910232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375465539	chr12:38910258-38910259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138897308	chr12:38910275-38910276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567064114	chr12:38910298-38910299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548079824	chr12:38910307-38910308	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	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
Breast cancer	21364760	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38908600-38911000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:38909000-38910400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:38909400-38910800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr12:38909600-38910000	Enhancers	Rectal Smooth Muscle	rectum
5	chr12:38909600-38910800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr12:38909600-38910800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:38909800-38910200	Enhancers	Brain Anterior Caudate	brain
8	chr12:38909800-38910400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:38909800-38910600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr12:38909800-38910600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr12:38909800-38910600	Enhancers	Colon Smooth Muscle	Colon
12	chr12:38909800-38910600	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr12:38909800-38910800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr12:38909800-38910800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr12:38909800-38910800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr12:38909800-38910800	Enhancers	Liver	Liver
17	chr12:38919800-38922000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:38921400-38921800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr12:38936000-38936600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:38936000-38938000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr12:38936000-38938400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr12:38936200-38936400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:38936200-38936800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr12:38936200-38938400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr12:38936400-38937200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:38936400-38937600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr12:38936400-38938600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr12:38936400-38939000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr12:38936400-38939000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:38936600-38937200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:38936800-38937200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr12:38936800-38937400	Enhancers	Hela-S3	cervix
33	chr12:38936800-38939000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr12:38936800-38939000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr12:38937200-38937400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:38937200-38938000	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr12:38937200-38938600	Enhancers	H9 Cell Line	embryonic stem cell
38	chr12:38937200-38938600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr12:38937200-38939000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:38937400-38939000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:38937400-38941000	Weak transcription	Hela-S3	cervix
42	chr12:38937600-38938200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr12:38937800-38939000	Enhancers	Colon Smooth Muscle	Colon
44	chr12:38938000-38938200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr12:38938000-38938400	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr12:38938200-38938400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr12:38938200-38938600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:38938200-38938600	Enhancers	Rectal Smooth Muscle	rectum
49	chr12:38938200-38938800	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr12:38938400-38938600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum

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