Variant report

Variant	nsv934280
Chromosome Location	chr10:96401297-96540495
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	chr10:96440204-96440693	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:96447569-96447764	HepG2	liver:	n/a	n/a
3	ATF1	chr10:96433424-96433649	K562	blood:	n/a	n/a
4	ATF3	chr10:96433388-96433701	HCT-116	colon:	n/a	n/a
5	BCL3	chr10:96440125-96440773	A549	lung:	n/a	n/a
6	BRCA1	chr10:96440359-96440638	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr10:96438283-96438592	IMR90	lung:	n/a	chr10:96438440-96438451
8	CEBPB	chr10:96485747-96485947	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:96433362-96433720	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr10:96433387-96433694	HepG2	liver:	n/a	n/a
11	CEBPB	chr10:96452997-96453294	HepG2	liver:	n/a	chr10:96453142-96453153
12	CEBPB	chr10:96426194-96426529	A549	lung:	n/a	chr10:96426349-96426360
13	CEBPB	chr10:96440251-96440706	A549	lung:	n/a	chr10:96440500-96440511
14	CEBPB	chr10:96438306-96438602	Hela-S3	cervix:	n/a	chr10:96438440-96438451
15	CEBPB	chr10:96426231-96426446	H1-hESC	embryonic stem cell:	n/a	chr10:96426349-96426360
16	CEBPB	chr10:96437529-96437557	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr10:96407836-96408083	A549	lung:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
18	CEBPB	chr10:96453074-96453300	K562	blood:	n/a	chr10:96453142-96453153
19	CEBPB	chr10:96404195-96404419	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:96485737-96485940	A549	lung:	n/a	n/a
21	CEBPB	chr10:96433393-96433726	A549	lung:	n/a	n/a
22	CEBPB	chr10:96520913-96521049	A549	lung:	n/a	chr10:96520959-96520970 chr10:96520961-96520970 chr10:96520960-96520971 chr10:96520961-96520970 chr10:96520961-96520970 chr10:96520961-96520970
23	CEBPB	chr10:96520862-96521099	HepG2	liver:	n/a	chr10:96520959-96520970 chr10:96520961-96520970 chr10:96520960-96520971 chr10:96520961-96520970 chr10:96520961-96520970 chr10:96520961-96520970
24	CEBPB	chr10:96440358-96440615	MCF-7	breast:	n/a	chr10:96440500-96440511
25	CEBPB	chr10:96426220-96426538	HepG2	liver:	n/a	chr10:96426349-96426360
26	CEBPB	chr10:96487896-96488218	IMR90	lung:	n/a	chr10:96488055-96488066
27	CEBPB	chr10:96487954-96488117	H1-hESC	embryonic stem cell:	n/a	chr10:96488055-96488066
28	CEBPB	chr10:96436301-96436615	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr10:96433472-96433592	K562	blood:	n/a	n/a
30	CEBPB	chr10:96520891-96521011	IMR90	lung:	n/a	chr10:96520959-96520970 chr10:96520961-96520970 chr10:96520960-96520971 chr10:96520961-96520970 chr10:96520961-96520970 chr10:96520961-96520970
31	CEBPB	chr10:96407802-96408115	HepG2	liver:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
32	CEBPB	chr10:96440299-96440668	HepG2	liver:	n/a	chr10:96440500-96440511
33	CEBPB	chr10:96426245-96426536	IMR90	lung:	n/a	chr10:96426349-96426360
34	CEBPB	chr10:96487899-96488178	A549	lung:	n/a	chr10:96488055-96488066
35	CEBPB	chr10:96438271-96438623	HepG2	liver:	n/a	chr10:96438440-96438451
36	CEBPB	chr10:96440321-96440589	IMR90	lung:	n/a	chr10:96440500-96440511
37	CEBPB	chr10:96504015-96504089	HepG2	liver:	n/a	chr10:96504062-96504073
38	CEBPB	chr10:96487903-96488237	HepG2	liver:	n/a	chr10:96488055-96488066
39	CEBPB	chr10:96440242-96440692	HepG2	liver:	n/a	chr10:96440500-96440511
40	CEBPB	chr10:96433429-96433686	IMR90	lung:	n/a	n/a
41	CEBPB	chr10:96440269-96440616	HepG2	liver:	n/a	chr10:96440500-96440511
42	CEBPB	chr10:96440103-96440886	A549	lung:	n/a	chr10:96440500-96440511
43	CEBPB	chr10:96440255-96440680	Hela-S3	cervix:	n/a	chr10:96440500-96440511
44	CEBPB	chr10:96440287-96440606	MCF-7	breast:	n/a	chr10:96440500-96440511
45	CEBPB	chr10:96440299-96440699	A549	lung:	n/a	chr10:96440500-96440511
46	CEBPB	chr10:96407816-96408111	H1-hESC	embryonic stem cell:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
47	CEBPB	chr10:96438272-96438617	A549	lung:	n/a	chr10:96438440-96438451
48	CEBPB	chr10:96485885-96485913	K562	blood:	n/a	n/a
49	CEBPB	chr10:96407891-96408016	K562	blood:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
50	CEBPB	chr10:96507808-96507867	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96447464-96447514	Hepatocyte	liver:	n/a
2	chr10:96442031-96442081	PrEC	prostate:	n/a
3	chr10:96447464-96447514	Hepatocyte	liver:	n/a
4	chr10:96442031-96442081	PrEC	prostate:	n/a
5	chr10:96442674-96442724	Jurkat	blood:	n/a
6	chr10:96523347-96523397	NHBE	bronchial:	n/a
7	chr10:96523248-96523298	GM12878	blood:	n/a
8	chr10:96521152-96521202	A549	lung:	n/a
9	chr10:96447464-96447514	GM12878	blood:	n/a
10	chr10:96447464-96447514	MCF10A-Er-Src	breast:	n/a
11	chr10:96443071-96443121	NHDF-neo	bronchial:	n/a
12	chr10:96446783-96446833	SKMC	muscle:	n/a
13	chr10:96521152-96521202	HMEC	breast:	n/a
14	chr10:96447464-96447514	GM12891	blood:	n/a
15	chr10:96521086-96521136	HCPEpiC	choroid plexus:	n/a
16	chr10:96443165-96443215	SKMC	muscle:	n/a
17	chr10:96442031-96442081	ECC-1	luminal epithelium:	n/a
18	chr10:96521152-96521202	AG04450	lung:	fetal
19	chr10:96523248-96523298	AG04450	lung:	fetal
20	chr10:96523248-96523298	GM12891	blood:	n/a
21	chr10:96443195-96443245	PrEC	prostate:	n/a
22	chr10:96523347-96523397	MCF10A-Er-Src	breast:	n/a
23	chr10:96523347-96523397	HUVEC	blood vessel:	n/a
24	chr10:96521086-96521136	HCF	heart:	n/a
25	chr10:96443383-96443433	NHDF-neo	bronchial:	n/a
26	chr10:96443165-96443215	AG10803	skin:	n/a
27	chr10:96443383-96443433	GM12891	blood:	n/a
28	chr10:96443195-96443245	MCF-7	breast:	n/a
29	chr10:96521152-96521202	HCF	heart:	n/a
30	chr10:96442031-96442081	CMK	blood:	n/a
31	chr10:96523347-96523397	U87	brain:	n/a
32	chr10:96442674-96442724	PrEC	prostate:	n/a
33	chr10:96521086-96521136	AoSMC	blood vessel:	n/a
34	chr10:96442031-96442081	HAEpiC	amniotic membrane:	n/a
35	chr10:96446783-96446833	HCM	heart:	n/a
36	chr10:96523248-96523298	HCF	heart:	n/a
37	chr10:96442674-96442724	H1-hESC	embryonic stem cell:	embryo
38	chr10:96523248-96523298	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:96443165-96443215	LNCaP	prostate:	n/a
40	chr10:96443383-96443433	GM06990	blood:	n/a
41	chr10:96442154-96442204	GM12878	blood:	n/a
42	chr10:96442674-96442724	SK-N-SH	brain:	n/a
43	chr10:96522433-96522483	HCPEpiC	choroid plexus:	n/a
44	chr10:96522433-96522483	PrEC	prostate:	n/a
45	chr10:96521152-96521202	AG09319	gingival:	n/a
46	chr10:96521152-96521202	LNCaP	prostate:	n/a
47	chr10:96446783-96446833	HEK293	kidney:	embryo
48	chr10:96521086-96521136	HRE	kidney:	n/a
49	chr10:96522433-96522483	NT2-D1	testis:	n/a
50	chr10:96523347-96523397	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:96429982..96431947-chr10:96435733..96437659,2	K562	blood:
2	chr10:96429982..96431947-chr10:96435733..96437659,2	K562	blood:
3	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:
4	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:

Variant related genes	Relation type
CYP2C18	TF binding region
CYP2C19	TF binding region
CTBP2P2	TF binding region
MTND4P19	TF binding region
CYP2C18	CpG island
CYP2C19	CpG island
CTBP2P2	CpG island
MTND4P19	CpG island

Extended variants
information (count: 5648 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5648 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543303772	chr10:96401344-96401345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556520840	chr10:96401369-96401370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17110170	chr10:96401371-96401372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545225335	chr10:96401387-96401388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139595443	chr10:96401393-96401394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149740230	chr10:96401523-96401524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541065499	chr10:96401535-96401536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560848518	chr10:96401576-96401577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529987388	chr10:96401577-96401578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190163639	chr10:96401621-96401622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12774450	chr10:96401654-96401655	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs532337312	chr10:96401660-96401661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112296416	chr10:96401701-96401702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145662453	chr10:96401709-96401710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534012563	chr10:96401725-96401726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187252144	chr10:96401773-96401774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567642528	chr10:96401816-96401817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543379062	chr10:96401844-96401845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189219362	chr10:96401852-96401853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34564477	chr10:96401855-96401856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556819872	chr10:96401900-96401901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569597930	chr10:96401927-96401928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545601605	chr10:96401943-96401944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536430129	chr10:96401975-96401976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529695880	chr10:96402023-96402024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559182348	chr10:96402034-96402035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572202317	chr10:96402040-96402041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541571040	chr10:96402041-96402042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541121101	chr10:96402086-96402087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560904088	chr10:96402115-96402116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148486701	chr10:96402229-96402230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114594804	chr10:96402269-96402270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375507887	chr10:96402297-96402298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370649636	chr10:96402308-96402309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs398046181	chr10:96402321-96402322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76377581	chr10:96402322-96402323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563621241	chr10:96402325-96402326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532271291	chr10:96402327-96402328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551988035	chr10:96402346-96402347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180684684	chr10:96402390-96402391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527821992	chr10:96402394-96402395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547495134	chr10:96402427-96402428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548779260	chr10:96402548-96402549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536673483	chr10:96402549-96402550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549874868	chr10:96402580-96402581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143974386	chr10:96402613-96402614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369500797	chr10:96402621-96402622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539319257	chr10:96402634-96402635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559243709	chr10:96402767-96402768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374000581	chr10:96402771-96402772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oligozoospermia	20877625	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96393800-96403400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:96398200-96401600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:96400400-96407200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:96401000-96401400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr10:96401400-96401600	Enhancers	Placenta Amnion	Placenta Amnion
6	chr10:96401400-96402000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr10:96401600-96401800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr10:96404200-96404600	Enhancers	Liver	Liver
9	chr10:96404200-96405800	Enhancers	GM12878-XiMat	blood
10	chr10:96407200-96407400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr10:96407400-96413000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:96411400-96412000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr10:96422200-96423800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr10:96422600-96423000	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr10:96422600-96423400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr10:96422600-96423600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr10:96422600-96423800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr10:96422800-96423600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr10:96422800-96423800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr10:96422800-96423800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr10:96423000-96423200	Enhancers	Gastric	stomach
22	chr10:96423000-96423400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr10:96423000-96424000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr10:96423200-96423600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr10:96423200-96424200	Weak transcription	Gastric	stomach
26	chr10:96423400-96423600	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr10:96423400-96423800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr10:96423400-96424000	Enhancers	Stomach Mucosa	stomach
29	chr10:96423600-96426200	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr10:96423800-96424200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr10:96424000-96426200	Weak transcription	Stomach Mucosa	stomach
32	chr10:96424200-96424400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr10:96424200-96424600	Enhancers	Gastric	stomach
34	chr10:96424400-96424600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:96424600-96424800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr10:96424600-96434200	Weak transcription	Gastric	stomach
37	chr10:96426000-96426600	Enhancers	Fetal Intestine Large	intestine
38	chr10:96426200-96426400	Enhancers	Duodenum Mucosa	Duodenum
39	chr10:96426200-96426600	Enhancers	Fetal Intestine Small	intestine
40	chr10:96426200-96426800	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr10:96426200-96426800	Enhancers	Stomach Mucosa	stomach
42	chr10:96426200-96433400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr10:96426800-96430400	Weak transcription	Stomach Mucosa	stomach
44	chr10:96430400-96431800	Enhancers	Stomach Mucosa	stomach
45	chr10:96431800-96433400	Weak transcription	Stomach Mucosa	stomach
46	chr10:96433400-96433800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr10:96433400-96438200	Enhancers	Stomach Mucosa	stomach
48	chr10:96433800-96434000	Enhancers	Fetal Intestine Small	intestine
49	chr10:96434000-96436400	Weak transcription	Fetal Intestine Small	intestine
50	chr10:96434200-96434400	Enhancers	Gastric	stomach

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