Variant report

Variant	esv1800675
Chromosome Location	chr7:117159386-117204462
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:103 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:117195388-117195586	K562	blood:	n/a	n/a
2	BACH1	chr7:117188133-117188349	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:117204164-117204384	GM12878	blood:	n/a	n/a
4	BHLHE40	chr7:117204094-117204536	GM12878	blood:	n/a	chr7:117204311-117204320 chr7:117204311-117204320
5	CEBPB	chr7:117200159-117200394	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:117161164-117161364	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:117198075-117198115	A549	lung:	n/a	n/a
8	CEBPB	chr7:117171679-117171984	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:117171738-117171964	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:117161167-117161444	IMR90	lung:	n/a	n/a
11	CEBPB	chr7:117171672-117172026	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:117202940-117203217	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:117202887-117203267	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:117202921-117203156	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:117200161-117200427	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr7:117170361-117170547	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:117191755-117191958	HepG2	liver:	n/a	n/a
18	CHD2	chr7:117204156-117204422	GM12878	blood:	n/a	n/a
19	CTCF	chr7:117172563-117172636	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr7:117172540-117172690	HEK293	kidney:	n/a	n/a
21	CTCF	chr7:117172360-117172510	HVMF	connective:	n/a	n/a
22	CTCF	chr7:117172860-117173010	GM12866	blood:	n/a	n/a
23	CTCF	chr7:117172569-117172651	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:117172680-117172830	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:117185640-117185790	Caco-2	colon:	n/a	n/a
26	CTCF	chr7:117163028-117163072	LNCaP	prostate:	n/a	n/a
27	CTCF	chr7:117172498-117172663	HepG2	liver:	n/a	n/a
28	CTCF	chr7:117172480-117172630	AG09319	gingival:	n/a	n/a
29	CTCF	chr7:117173244-117173262	LNCaP	prostate:	n/a	n/a
30	CTCF	chr7:117172560-117172710	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:117188020-117188170	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr7:117172560-117172710	K562	blood:	n/a	n/a
33	CTCF	chr7:117172400-117172550	RPTEC	kidney:	n/a	n/a
34	CTCF	chr7:117172500-117172650	GM06990	blood:	n/a	n/a
35	CTCF	chr7:117189178-117189209	GM10266	blood:	n/a	n/a
36	CTCF	chr7:117172620-117172770	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr7:117172460-117172610	GM12872	blood:	n/a	n/a
38	CTCF	chr7:117172180-117172330	AG09319	gingival:	n/a	n/a
39	CTCF	chr7:117172588-117172644	MCF-7	breast:	n/a	n/a
40	E2F4	chr7:117173056-117173282	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr7:117192024-117192202	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr7:117171554-117171665	MCF10A-Er-Src	breast:	n/a	n/a
43	EBF1	chr7:117190682-117191106	GM12878	blood:	n/a	chr7:117190891-117190902 chr7:117190890-117190903 chr7:117190892-117190901 chr7:117190891-117190901 chr7:117190892-117190901
44	EBF1	chr7:117190715-117191003	GM12878	blood:	n/a	chr7:117190891-117190902 chr7:117190890-117190903 chr7:117190892-117190901 chr7:117190891-117190901 chr7:117190892-117190901
45	EBF1	chr7:117174750-117175152	GM12878	blood:	n/a	chr7:117174933-117174942 chr7:117174932-117174943
46	EP300	chr7:117204175-117204516	GM12878	blood:	n/a	n/a
47	EP300	chr7:117178107-117178125	GM12878	blood:	n/a	n/a
48	EP300	chr7:117170510-117170801	GM12878	blood:	n/a	n/a
49	EP300	chr7:117204156-117204458	GM12878	blood:	n/a	n/a
50	EP300	chr7:117202914-117203222	Hela-S3	cervix:	n/a	chr7:117203075-117203089 chr7:117203080-117203088

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:117171038-117171088	AG04450	lung:	fetal
2	chr7:117171038-117171088	PANC-1	pancreas:	n/a
3	chr7:117171038-117171088	ovcar-3	ovarian:	n/a
4	chr7:117171038-117171088	NT2-D1	testis:	n/a
5	chr7:117171038-117171088	HEK293	kidney:	embryo
6	chr7:117171038-117171088	SK-N-SH	brain:	n/a
7	chr7:117171038-117171088	K562	blood:	n/a
8	chr7:117171038-117171088	HMEC	breast:	n/a
9	chr7:117171038-117171088	GM12892	blood:	n/a
10	chr7:117171038-117171088	GM06990	blood:	n/a
11	chr7:117171038-117171088	NB4	blood:	n/a
12	chr7:117171038-117171088	HEEpiC	esophagus:	n/a
13	chr7:117171038-117171088	Hepatocyte	liver:	n/a
14	chr7:117171038-117171088	PrEC	prostate:	n/a
15	chr7:117171038-117171088	NHBE	bronchial:	n/a
16	chr7:117171038-117171088	AG09319	gingival:	n/a
17	chr7:117171038-117171088	PFSK-1	brain:	n/a
18	chr7:117171038-117171088	ProgFib	skin:	n/a
19	chr7:117171038-117171088	AG04449	skin:	fetal
20	chr7:117171038-117171088	U87	brain:	n/a
21	chr7:117171038-117171088	SAEC	small airway:	n/a
22	chr7:117171038-117171088	HAEpiC	amniotic membrane:	n/a
23	chr7:117171038-117171088	ECC-1	luminal epithelium:	n/a
24	chr7:117171038-117171088	BJ	skin:	n/a
25	chr7:117171038-117171088	Hela-S3	cervix:	n/a
26	chr7:117171038-117171088	CMK	blood:	n/a
27	chr7:117171038-117171088	HCM	heart:	n/a
28	chr7:117171038-117171088	HIPEpiC	eye:	n/a
29	chr7:117171038-117171088	HepG2	liver:	n/a
30	chr7:117171038-117171088	HCT-116	colon:	n/a
31	chr7:117171038-117171088	GM12891	blood:	n/a
32	chr7:117171038-117171088	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:117171038-117171088	HRPEpiC	eye:	n/a
34	chr7:117171038-117171088	AoSMC	blood vessel:	n/a
35	chr7:117171038-117171088	T-47D	breast:	n/a
36	chr7:117171038-117171088	AG09309	skin:	n/a
37	chr7:117171038-117171088	A549	lung:	n/a
38	chr7:117171038-117171088	HCF	heart:	n/a
39	chr7:117171038-117171088	Caco-2	colon:	n/a
40	chr7:117171038-117171088	H1-hESC	embryonic stem cell:	embryo
41	chr7:117171038-117171088	Jurkat	blood:	n/a
42	chr7:117171038-117171088	MCF-7	breast:	n/a
43	chr7:117171038-117171088	HRE	kidney:	n/a
44	chr7:117171038-117171088	SK-N-MC	brain:	n/a
45	chr7:117171038-117171088	RPTEC	kidney:	n/a
46	chr7:117171038-117171088	NH-A	brain:	n/a
47	chr7:117171038-117171088	SKMC	muscle:	n/a
48	chr7:117171038-117171088	HRCEpiC	kidney:	n/a
49	chr7:117171038-117171088	HNPCEpiC	eye:	n/a
50	chr7:117171038-117171088	GM19239	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:117100350-117112126..7:117167208-117172399	H1-hESC	embryonic stem cell:	embryo
2	7:117100350-117112126..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
3	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:
4	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:
5	7:117065049-117068137..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
6	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:
7	chr7:117190103..117191769-chr7:117198785..117201652,2	K562	blood:
8	chr7:117171466..117173089-chr7:117174919..117176705,2	K562	blood:
9	chr7:117173270..117176194-chr7:117177984..117179733,2	MCF-7	breast:
10	chr7:117173270..117176194-chr7:117177984..117179733,2	MCF-7	breast:
11	7:115847372-115857098..7:117179549-117182665	H1-hESC	embryonic stem cell:	embryo
12	7:115847372-115857098..7:117167208-117172399	H1-hESC	embryonic stem cell:	embryo
13	7:116604327-116608063..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
14	chr7:117171466..117173089-chr7:117174919..117176705,2	K562	blood:
15	7:115847372-115857098..7:117194433-117196955	H1-hESC	embryonic stem cell:	embryo
16	7:115890993-115892266..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
17	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASZ1-1	chr7:117200787-117200846	ENSG00000232661.1

No data

Variant related genes	Relation type
CFTR	TF binding region
CFTR	CpG island
ENSG00000001626	chromatin interactions
ENSG00000154438	chromatin interactions
ENSG00000135269	chromatin interactions
ENSG00000228368	chromatin interactions

Extended variants
information (count: 1770 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561402337	chr7:117159400-117159401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547700111	chr7:117159446-117159447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs193922507	chr7:117159451-117159452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530255043	chr7:117159488-117159489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377631629	chr7:117159496-117159497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150306187	chr7:117159534-117159535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs36143091	chr7:117159561-117159562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527973665	chr7:117159585-117159586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190257222	chr7:117159602-117159603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570687096	chr7:117159614-117159615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570764516	chr7:117159654-117159655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35766024	chr7:117159656-117159657	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs550028191	chr7:117159676-117159677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568531203	chr7:117159739-117159740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181503450	chr7:117159754-117159755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535680293	chr7:117159758-117159759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553989159	chr7:117159760-117159761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566027857	chr7:117159822-117159823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533392288	chr7:117159839-117159840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557991627	chr7:117159873-117159874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567732504	chr7:117159898-117159899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552235739	chr7:117159968-117159969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543380204	chr7:117160011-117160012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185047879	chr7:117160105-117160106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35682006	chr7:117160136-117160137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573388502	chr7:117160154-117160155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34403015	chr7:117160176-117160177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530986124	chr7:117160235-117160236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568902225	chr7:117160263-117160264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34280233	chr7:117160297-117160298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200994526	chr7:117160320-117160321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542063561	chr7:117160357-117160358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560303562	chr7:117160364-117160365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527842253	chr7:117160380-117160381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13220943	chr7:117160385-117160386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376996814	chr7:117160441-117160442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564773392	chr7:117160535-117160536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537843654	chr7:117160580-117160581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs137964931	chr7:117160620-117160621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117161414	chr7:117160627-117160628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568596215	chr7:117160694-117160695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529403756	chr7:117160724-117160725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189558666	chr7:117160760-117160761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538437702	chr7:117160814-117160815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149489885	chr7:117160927-117160928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565891560	chr7:117160953-117160954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12538252	chr7:117160988-117160989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs577960097	chr7:117161045-117161046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551410973	chr7:117161069-117161070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371841409	chr7:117161091-117161092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Squamous cell cancer	20885788	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117151800-117172600	Weak transcription	Pancreas	Pancrea
2	chr7:117154400-117169600	Weak transcription	Fetal Intestine Large	intestine
3	chr7:117154400-117170800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr7:117154400-117174400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr7:117154600-117164200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr7:117155400-117163400	Weak transcription	Fetal Intestine Small	intestine
7	chr7:117163400-117163800	Strong transcription	Fetal Intestine Small	intestine
8	chr7:117163800-117170000	Weak transcription	Fetal Intestine Small	intestine
9	chr7:117164200-117164400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
10	chr7:117164400-117177600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr7:117169600-117171200	Enhancers	Fetal Intestine Large	intestine
12	chr7:117170000-117172400	Enhancers	Fetal Intestine Small	intestine
13	chr7:117170800-117173000	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr7:117171000-117171200	Enhancers	Colonic Mucosa	Colon
15	chr7:117171000-117172400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:117171200-117172000	Enhancers	Dnd41	blood
17	chr7:117171200-117172200	Enhancers	Hela-S3	cervix
18	chr7:117171200-117172400	Weak transcription	Fetal Intestine Large	intestine
19	chr7:117171400-117171800	Enhancers	HUVEC	blood vessel
20	chr7:117171600-117177400	Weak transcription	Colonic Mucosa	Colon
21	chr7:117172000-117174800	Weak transcription	Dnd41	blood
22	chr7:117172400-117172800	Weak transcription	Fetal Intestine Small	intestine
23	chr7:117172400-117173000	Enhancers	Fetal Intestine Large	intestine
24	chr7:117172600-117173000	Genic enhancers	Pancreas	Pancrea
25	chr7:117172600-117173400	Enhancers	Gastric	stomach
26	chr7:117172800-117173000	Enhancers	Fetal Intestine Small	intestine
27	chr7:117172800-117173000	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr7:117172800-117173000	Enhancers	Stomach Mucosa	stomach
29	chr7:117172800-117173400	Enhancers	A549	lung
30	chr7:117173000-117174000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr7:117173000-117174400	Weak transcription	Fetal Intestine Large	intestine
32	chr7:117173000-117174400	Weak transcription	Fetal Intestine Small	intestine
33	chr7:117173000-117174400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr7:117173000-117208000	Weak transcription	Pancreas	Pancrea
35	chr7:117173400-117178800	Weak transcription	Gastric	stomach
36	chr7:117174000-117179200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr7:117174400-117174600	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr7:117174400-117175400	Enhancers	Fetal Intestine Large	intestine
39	chr7:117174400-117175400	Enhancers	Fetal Intestine Small	intestine
40	chr7:117174400-117175600	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr7:117174600-117178800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:117174800-117175600	Enhancers	Dnd41	blood
43	chr7:117175000-117175400	Enhancers	Stomach Mucosa	stomach
44	chr7:117175400-117176200	Weak transcription	Stomach Mucosa	stomach
45	chr7:117175400-117177800	Weak transcription	Fetal Intestine Large	intestine
46	chr7:117175400-117177800	Weak transcription	Fetal Intestine Small	intestine
47	chr7:117175600-117176000	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr7:117176000-117177800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr7:117176200-117176400	Enhancers	Stomach Mucosa	stomach
50	chr7:117177400-117178000	Enhancers	Colonic Mucosa	Colon

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