Variant report

Variant	nsv594846
Chromosome Location	chr4:92178715-92253926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:197)
CpG islands
(count:62)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:197 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:92191483-92191539	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr4:92246616-92246958	GM12878	blood:	n/a	n/a
3	BATF	chr4:92246684-92246980	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:92223302-92223415	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:92181253-92181489	HepG2	liver:	n/a	chr4:92181364-92181375
6	CHD2	chr4:92223402-92223554	GM12878	blood:	n/a	n/a
7	CTCF	chr4:92196766-92196816	GM10248	blood:	n/a	n/a
8	CTCF	chr4:92224307-92224326	GM10266	blood:	n/a	n/a
9	CTCF	chr4:92247480-92247630	GM12874	blood:	n/a	n/a
10	CTCF	chr4:92185520-92185670	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr4:92236120-92236270	HVMF	connective:	n/a	n/a
12	CTCF	chr4:92237937-92237962	GM20000	blood:	n/a	n/a
13	CTCF	chr4:92247623-92247698	GM13976	blood:	n/a	n/a
14	CUX1	chr4:92217982-92218053	GM12878	blood:	n/a	n/a
15	E2F4	chr4:92210264-92210314	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr4:92225103-92225323	MCF10A-Er-Src	breast:	n/a	n/a
17	EBF1	chr4:92188793-92188993	GM12878	blood:	n/a	n/a
18	EP300	chr4:92223291-92223465	GM12878	blood:	n/a	n/a
19	EP300	chr4:92246540-92246754	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr4:92246505-92247133	SK-N-SH	brain:	n/a	chr4:92246526-92246533 chr4:92246898-92246912
21	EP300	chr4:92188777-92188977	GM12878	blood:	n/a	n/a
22	EP300	chr4:92209990-92210316	GM12878	blood:	n/a	n/a
23	EP300	chr4:92223445-92223554	GM12878	blood:	n/a	n/a
24	EP300	chr4:92229381-92229386	K562	blood:	n/a	n/a
25	EP300	chr4:92210232-92210450	GM12878	blood:	n/a	n/a
26	EP300	chr4:92233652-92233790	GM12878	blood:	n/a	n/a
27	EP300	chr4:92182790-92182870	K562	blood:	n/a	n/a
28	EP300	chr4:92246620-92246949	SK-N-SH_RA	brain:	n/a	chr4:92246898-92246912
29	ESR1	chr4:92179583-92179826	T-47D	breast:	n/a	n/a
30	ESR1	chr4:92246589-92246957	ECC-1	luminal epithelium:	n/a	n/a
31	FOS	chr4:92251930-92252285	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr4:92246676-92247017	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:92251940-92252272	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:92246734-92247049	HUVEC	blood vessel:	n/a	n/a
35	FOS	chr4:92222061-92222261	MCF10A-Er-Src	breast:	n/a	chr4:92222081-92222093 chr4:92222082-92222091 chr4:92222084-92222091 chr4:92222079-92222090
36	FOS	chr4:92210191-92210306	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:92188808-92189058	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:92246688-92246996	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:92246689-92247009	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:92251930-92252300	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:92188780-92189059	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:92246671-92247017	MCF10A-Er-Src	breast:	n/a	n/a
43	FOSL2	chr4:92246687-92247125	SK-N-SH	brain:	n/a	n/a
44	FOSL2	chr4:92251826-92252389	SK-N-SH	brain:	n/a	n/a
45	FOXA1	chr4:92229620-92229870	T-47D	breast:	n/a	n/a
46	FOXA1	chr4:92201074-92201311	T-47D	breast:	n/a	n/a
47	FOXA1	chr4:92193578-92193866	T-47D	breast:	n/a	chr4:92193697-92193712
48	GATA2	chr4:92240899-92241367	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr4:92241781-92242096	T-47D	breast:	n/a	chr4:92241934-92241941 chr4:92241927-92241948 chr4:92241933-92241943 chr4:92241934-92241941 chr4:92241930-92241946 chr4:92241934-92241941
50	GATA3	chr4:92179412-92179844	T-47D	breast:	n/a	chr4:92179624-92179631

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92189705-92189755	IMR90	lung:	fetal
2	chr4:92189705-92189755	IMR90	lung:	fetal
3	chr4:92189705-92189755	U87	brain:	n/a
4	chr4:92189705-92189755	GM12891	blood:	n/a
5	chr4:92189705-92189755	RPTEC	kidney:	n/a
6	chr4:92189705-92189755	HCPEpiC	choroid plexus:	n/a
7	chr4:92189705-92189755	HL-60	blood:	n/a
8	chr4:92189705-92189755	NB4	blood:	n/a
9	chr4:92189705-92189755	MCF10A-Er-Src	breast:	n/a
10	chr4:92189705-92189755	SKMC	muscle:	n/a
11	chr4:92189705-92189755	K562	blood:	n/a
12	chr4:92189705-92189755	ECC-1	luminal epithelium:	n/a
13	chr4:92189705-92189755	HepG2	liver:	n/a
14	chr4:92189705-92189755	H1-hESC	embryonic stem cell:	embryo
15	chr4:92189705-92189755	HEK293	kidney:	embryo
16	chr4:92189705-92189755	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:92189705-92189755	GM19239	blood:	n/a
18	chr4:92189705-92189755	NT2-D1	testis:	n/a
19	chr4:92189705-92189755	PFSK-1	brain:	n/a
20	chr4:92189705-92189755	LNCaP	prostate:	n/a
21	chr4:92189705-92189755	AG04449	skin:	fetal
22	chr4:92189705-92189755	T-47D	breast:	n/a
23	chr4:92189705-92189755	Hela-S3	cervix:	n/a
24	chr4:92189705-92189755	HRPEpiC	eye:	n/a
25	chr4:92189705-92189755	MCF-7	breast:	n/a
26	chr4:92189705-92189755	ProgFib	skin:	n/a
27	chr4:92189705-92189755	HCT-116	colon:	n/a
28	chr4:92189705-92189755	HCF	heart:	n/a
29	chr4:92189705-92189755	ovcar-3	ovarian:	n/a
30	chr4:92189705-92189755	AG09309	skin:	n/a
31	chr4:92189705-92189755	BE2_C	brain:	n/a
32	chr4:92189705-92189755	HMEC	breast:	n/a
33	chr4:92189705-92189755	Jurkat	blood:	n/a
34	chr4:92189705-92189755	GM12878	blood:	n/a
35	chr4:92189705-92189755	AG04450	lung:	fetal
36	chr4:92189705-92189755	HRE	kidney:	n/a
37	chr4:92189705-92189755	BJ	skin:	n/a
38	chr4:92189705-92189755	HUVEC	blood vessel:	n/a
39	chr4:92189705-92189755	A549	lung:	n/a
40	chr4:92189705-92189755	HEEpiC	esophagus:	n/a
41	chr4:92189705-92189755	AoSMC	blood vessel:	n/a
42	chr4:92189705-92189755	GM12892	blood:	n/a
43	chr4:92189705-92189755	NH-A	brain:	n/a
44	chr4:92189705-92189755	SK-N-SH_RA	brain:	n/a
45	chr4:92189705-92189755	SAEC	small airway:	n/a
46	chr4:92189705-92189755	NHBE	bronchial:	n/a
47	chr4:92189705-92189755	PANC-1	pancreas:	n/a
48	chr4:92189705-92189755	Hepatocyte	liver:	n/a
49	chr4:92189705-92189755	AG10803	skin:	n/a
50	chr4:92189705-92189755	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:92176022..92178505-chr4:92180113..92182729,2	K562	blood:
2	chr4:92249209..92252138-chr4:92252795..92255607,2	MCF-7	breast:
3	chr4:92228930..92230474-chr4:92239556..92242007,2	K562	blood:
4	chr4:92228930..92230474-chr4:92239556..92242007,2	K562	blood:
5	chr4:92249209..92252138-chr4:92252795..92255607,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000249049	TF binding region
ENSG00000249049	CpG island

Extended variants
information (count: 856 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6836730	chr4:92178715-92178716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545740341	chr4:92178718-92178719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111449183	chr4:92178838-92178839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375994393	chr4:92178842-92178843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556367402	chr4:92178861-92178862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56788276	chr4:92178900-92178901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs375881784	chr4:92178922-92178923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545556269	chr4:92178947-92178948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13151372	chr4:92178955-92178956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs186787533	chr4:92179015-92179016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541056307	chr4:92179046-92179047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561633455	chr4:92179052-92179053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200862978	chr4:92179054-92179055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28628384	chr4:92179066-92179067	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs550943362	chr4:92179097-92179098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191873582	chr4:92179116-92179117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563504896	chr4:92179117-92179118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371427380	chr4:92179180-92179181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184105989	chr4:92179188-92179189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185943749	chr4:92188056-92188057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375924949	chr4:92188087-92188088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139728791	chr4:92188098-92188099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559218538	chr4:92188118-92188119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149353301	chr4:92188144-92188145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144660949	chr4:92188166-92188167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576157345	chr4:92188246-92188247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561869086	chr4:92188258-92188259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531001133	chr4:92188291-92188292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550783237	chr4:92188293-92188294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369637802	chr4:92188296-92188297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543764884	chr4:92188326-92188327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564534057	chr4:92188339-92188340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189623501	chr4:92188353-92188354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143601798	chr4:92188377-92188378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372216912	chr4:92188380-92188381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547360291	chr4:92188425-92188426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567131899	chr4:92188445-92188446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144558701	chr4:92188446-92188447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368950952	chr4:92188464-92188465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78783072	chr4:92188541-92188542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181844266	chr4:92188580-92188581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549568266	chr4:92188708-92188709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568076946	chr4:92188776-92188777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537183032	chr4:92188814-92188815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144542951	chr4:92188834-92188835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576817943	chr4:92188908-92188909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539037774	chr4:92188923-92188924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552851080	chr4:92188943-92188944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572773364	chr4:92188991-92188992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541639371	chr4:92189025-92189026	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Esophageal cancer	21851588	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92178600-92179000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:92179000-92179200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:92188000-92190600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:92188200-92189600	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr4:92188200-92190000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:92188600-92189600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:92188600-92190000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:92188600-92190800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr4:92188600-92191000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:92188800-92189000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:92188800-92189600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:92189000-92189200	Enhancers	Fetal Intestine Large	intestine
13	chr4:92189000-92189400	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr4:92189000-92190400	Enhancers	Stomach Mucosa	stomach
15	chr4:92189000-92190600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:92189200-92190200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:92189200-92190200	Weak transcription	Fetal Intestine Large	intestine
18	chr4:92189200-92190400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:92189600-92190000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:92189600-92190600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr4:92190000-92190200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:92190000-92190400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr4:92190000-92190400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr4:92190000-92190400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr4:92190200-92190600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:92190200-92190600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:92190200-92190600	Enhancers	Fetal Intestine Large	intestine
28	chr4:92190200-92191000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr4:92190400-92190800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:92190400-92192000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr4:92190600-92191000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr4:92190600-92191200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:92190800-92191000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:92190800-92191200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr4:92191000-92191400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr4:92191000-92191800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr4:92191200-92192000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:92191400-92192000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:92201200-92201600	Enhancers	Left Ventricle	heart
40	chr4:92201200-92201800	Enhancers	Colonic Mucosa	Colon
41	chr4:92201400-92201800	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr4:92201400-92202000	Enhancers	Right Ventricle	heart
43	chr4:92201400-92202200	Enhancers	Pancreas	Pancrea
44	chr4:92201600-92202200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:92201800-92204400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr4:92202200-92202400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:92202600-92205000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:92203400-92203800	Enhancers	Stomach Mucosa	stomach
49	chr4:92204400-92205800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr4:92204800-92205800	Enhancers	Fetal Intestine Large	intestine

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