Variant report

Variant	nsv464438
Chromosome Location	chr7:40193535-40350887
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	chr7:40272146-40272441	HepG2	liver:	n/a	n/a
2	ATF1	chr7:40269675-40270043	K562	blood:	n/a	n/a
3	BACH1	chr7:40335510-40335517	K562	blood:	n/a	n/a
4	BHLHE40	chr7:40269813-40270013	K562	blood:	n/a	n/a
5	BHLHE40	chr7:40280341-40280356	K562	blood:	n/a	n/a
6	BRCA1	chr7:40272097-40272467	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr7:40231639-40232007	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:40203696-40203826	A549	lung:	n/a	chr7:40203778-40203789
9	CEBPB	chr7:40255472-40255581	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:40305500-40305758	IMR90	lung:	n/a	chr7:40305633-40305644 chr7:40305631-40305644 chr7:40305631-40305644 chr7:40305631-40305644
11	CEBPB	chr7:40234363-40234668	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:40203739-40203813	HepG2	liver:	n/a	chr7:40203778-40203789
13	CEBPB	chr7:40218790-40218984	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:40240340-40240766	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:40238608-40238955	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:40233806-40233858	HepG2	liver:	n/a	chr7:40233822-40233833
17	CEBPB	chr7:40227213-40227471	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:40346853-40346935	HepG2	liver:	n/a	chr7:40346890-40346901
19	CHD2	chr7:40273928-40274040	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr7:40252879-40253271	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr7:40252773-40253365	K562	blood:	n/a	n/a
22	CTCF	chr7:40226240-40226390	GM12866	blood:	n/a	chr7:40226365-40226374
23	CTCF	chr7:40272177-40272511	MCF-7	breast:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
24	CTCF	chr7:40272227-40272424	A549	lung:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
25	CTCF	chr7:40272260-40272410	HCM	heart:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
26	CTCF	chr7:40300351-40300404	GM20000	blood:	n/a	n/a
27	CTCF	chr7:40293186-40293321	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:40293252-40293296	HepG2	liver:	n/a	n/a
29	CTCF	chr7:40272220-40272416	GM13976	blood:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
30	CTCF	chr7:40272240-40272390	HCFaa	heart:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
31	CTCF	chr7:40272180-40272330	GM12870	blood:	n/a	n/a
32	CTCF	chr7:40293040-40293190	HCT-116	colon:	n/a	n/a
33	CTCF	chr7:40272200-40272350	HFF	foreskin:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
34	CTCF	chr7:40293160-40293310	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr7:40226269-40226469	Gliobla	brain:	n/a	chr7:40226365-40226374
36	CTCF	chr7:40272041-40272620	MCF-7	breast:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
37	CTCF	chr7:40272260-40272410	Hela-S3	cervix:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
38	CTCF	chr7:40293208-40293281	LNCaP	prostate:	n/a	n/a
39	CTCF	chr7:40238940-40239090	HPAF	blood vessel:	n/a	chr7:40238989-40239010
40	CTCF	chr7:40238900-40239050	GM12871	blood:	n/a	chr7:40238989-40239010
41	CTCF	chr7:40238860-40239010	HCT-116	colon:	n/a	chr7:40238989-40239010
42	CTCF	chr7:40226270-40226458	Fibrobl	skin:	n/a	chr7:40226365-40226374
43	CTCF	chr7:40238860-40239010	K562	blood:	n/a	chr7:40238989-40239010
44	CTCF	chr7:40335780-40335930	RPTEC	kidney:	n/a	n/a
45	CTCF	chr7:40238948-40239044	Pancreas_OC	pancreas:	n/a	chr7:40238989-40239010
46	CTCF	chr7:40335820-40335970	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr7:40272360-40272510	HAc	cerebellar:	n/a	n/a
48	CTCF	chr7:40272200-40272350	HEK293	kidney:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
49	CTCF	chr7:40272240-40272390	BE2_C	brain:	n/a	chr7:40272319-40272340 chr7:40272317-40272335 chr7:40272318-40272334
50	CTCF	chr7:40226420-40226570	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40240143-40240193	RPTEC	kidney:	n/a
2	chr7:40338163-40338213	LNCaP	prostate:	n/a
3	chr7:40338163-40338213	GM12892	blood:	n/a
4	chr7:40260671-40260721	SAEC	small airway:	n/a
5	chr7:40260671-40260721	MCF10A-Er-Src	breast:	n/a
6	chr7:40240143-40240193	NHBE	bronchial:	n/a
7	chr7:40240143-40240193	HRE	kidney:	n/a
8	chr7:40260671-40260721	AoSMC	blood vessel:	n/a
9	chr7:40338163-40338213	MCF10A-Er-Src	breast:	n/a
10	chr7:40338163-40338213	RPTEC	kidney:	n/a
11	chr7:40240143-40240193	AG10803	skin:	n/a
12	chr7:40260671-40260721	GM12891	blood:	n/a
13	chr7:40260671-40260721	GM06990	blood:	n/a
14	chr7:40338163-40338213	HepG2	liver:	n/a
15	chr7:40338163-40338213	NHBE	bronchial:	n/a
16	chr7:40338163-40338213	SKMC	muscle:	n/a
17	chr7:40240143-40240193	GM12878	blood:	n/a
18	chr7:40240143-40240193	BJ	skin:	n/a
19	chr7:40260671-40260721	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:40338163-40338213	Hepatocyte	liver:	n/a
21	chr7:40338163-40338213	HNPCEpiC	eye:	n/a
22	chr7:40240143-40240193	HL-60	blood:	n/a
23	chr7:40338163-40338213	NH-A	brain:	n/a
24	chr7:40338163-40338213	ECC-1	luminal epithelium:	n/a
25	chr7:40260671-40260721	K562	blood:	n/a
26	chr7:40260671-40260721	Hepatocyte	liver:	n/a
27	chr7:40240143-40240193	BE2_C	brain:	n/a
28	chr7:40240143-40240193	LNCaP	prostate:	n/a
29	chr7:40240143-40240193	SKMC	muscle:	n/a
30	chr7:40260671-40260721	HRCEpiC	kidney:	n/a
31	chr7:40240143-40240193	Jurkat	blood:	n/a
32	chr7:40240143-40240193	NH-A	brain:	n/a
33	chr7:40260671-40260721	SK-N-MC	brain:	n/a
34	chr7:40240143-40240193	SAEC	small airway:	n/a
35	chr7:40338163-40338213	SK-N-MC	brain:	n/a
36	chr7:40338163-40338213	NB4	blood:	n/a
37	chr7:40260671-40260721	HRPEpiC	eye:	n/a
38	chr7:40260671-40260721	HEK293	kidney:	embryo
39	chr7:40260671-40260721	PFSK-1	brain:	n/a
40	chr7:40240143-40240193	PFSK-1	brain:	n/a
41	chr7:40240143-40240193	SK-N-MC	brain:	n/a
42	chr7:40260671-40260721	HEEpiC	esophagus:	n/a
43	chr7:40338163-40338213	HRE	kidney:	n/a
44	chr7:40338163-40338213	IMR90	lung:	fetal
45	chr7:40260671-40260721	MCF-7	breast:	n/a
46	chr7:40260671-40260721	U87	brain:	n/a
47	chr7:40338163-40338213	HCT-116	colon:	n/a
48	chr7:40338163-40338213	Jurkat	blood:	n/a
49	chr7:40240143-40240193	HMEC	breast:	n/a
50	chr7:40260671-40260721	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:40271921..40272777-chr7:40766227..40766815,2	MCF-7	breast:
2	chr7:40271945..40272762-chr7:40522914..40523878,2	MCF-7	breast:
3	chr1:6483244..6484243-chr7:40333894..40334600,2	MCF-7	breast:
4	chr7:40250465..40252237-chr7:40254677..40256213,2	K562	blood:
5	chr7:40334583..40336119-chr7:40353617..40356349,2	K562	blood:
6	chr7:40259840..40262064-chr7:40262266..40264754,2	K562	blood:
7	chr7:40250465..40252237-chr7:40254677..40256213,2	K562	blood:
8	chr7:40345049..40347172-chr7:40349979..40352115,2	K562	blood:
9	chr7:40241300..40243620-chr7:40251162..40253022,2	K562	blood:
10	chr7:40344397..40346549-chr7:40349560..40351479,2	K562	blood:
11	chr7:40345049..40347172-chr7:40349979..40352115,2	K562	blood:
12	chr7:40259840..40262064-chr7:40262266..40264754,2	K562	blood:
13	chr7:40241300..40243620-chr7:40251162..40253022,2	K562	blood:
14	chr7:40344397..40346549-chr7:40349560..40351479,2	K562	blood:
15	chr7:40348620..40350328-chr7:40353767..40356702,2	K562	blood:
16	chr7:40271902..40272542-chr7:40644343..40645096,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf11-8	chr7:40333941-40333997	NONHSAT120249
2	lnc-C7orf10-3	chr7:40220547-40220597	NONHSAT120247
3	lnc-CDK13-4	chr7:40192631-40193750	NONHSAT120248
4	lnc-C7orf10-3	chr7:40221555-40221615	NONHSAT120247
5	lnc-C7orf11-8	chr7:40279515-40279605	NONHSAT120249
6	lnc-C7orf11-8	chr7:40264706-40264758	NONHSAT120249
7	lnc-C7orf11-8	chr7:40291369-40291524	NONHSAT120249
8	lnc-C7orf11-8	chr7:40336722-40336813	NONHSAT120249

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

Extended variants
information (count: 5743 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:5743 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11760739	chr7:40193535-40193536	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76783401	chr7:40193574-40193575	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs183305831	chr7:40193588-40193589	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs146454228	chr7:40193591-40193592	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs116511992	chr7:40193605-40193606	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs139889641	chr7:40193653-40193654	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs552645663	chr7:40193664-40193665	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs572527202	chr7:40193665-40193666	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs534951419	chr7:40193668-40193669	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs550847725	chr7:40193722-40193723	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs558064487	chr7:40193734-40193735	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs577794632	chr7:40193785-40193786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76889732	chr7:40193791-40193792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541709472	chr7:40193818-40193819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9690073	chr7:40193843-40193844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs574010980	chr7:40193861-40193862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548599138	chr7:40193867-40193868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117995657	chr7:40193883-40193884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71560174	chr7:40193914-40193915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372425224	chr7:40193915-40193916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71769803	chr7:40193929-40193930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs3046488	chr7:40193933-40193934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142108240	chr7:40193948-40193949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151151561	chr7:40194019-40194020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372726758	chr7:40194043-40194044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545298430	chr7:40194063-40194064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565223260	chr7:40194074-40194075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373498131	chr7:40194187-40194188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550461214	chr7:40194207-40194208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375895495	chr7:40194250-40194251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2024200	chr7:40194260-40194261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs529725068	chr7:40194268-40194269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186471140	chr7:40194271-40194272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566115077	chr7:40194302-40194303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538275532	chr7:40194339-40194340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140068213	chr7:40194398-40194399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571649035	chr7:40194480-40194481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537759960	chr7:40194484-40194485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150382873	chr7:40194623-40194624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574200567	chr7:40194651-40194652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189801018	chr7:40194687-40194688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183120020	chr7:40194695-40194696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553542511	chr7:40194712-40194713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147632977	chr7:40194749-40194750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142180266	chr7:40194752-40194753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556383743	chr7:40194753-40194754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574791301	chr7:40194770-40194771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1269104	chr7:40194788-40194789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1267272	chr7:40194808-40194809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563825483	chr7:40194815-40194816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40181200-40202400	Weak transcription	HSMMtube	muscle
2	chr7:40190200-40202200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:40192000-40196000	Weak transcription	Fetal Intestine Large	intestine
4	chr7:40192200-40196000	Weak transcription	Fetal Intestine Small	intestine
5	chr7:40192200-40196000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:40192200-40196200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr7:40196000-40196200	Enhancers	Duodenum Mucosa	Duodenum
8	chr7:40196000-40196200	Enhancers	Fetal Intestine Large	intestine
9	chr7:40196000-40196200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr7:40196000-40196400	Enhancers	Fetal Intestine Small	intestine
11	chr7:40196200-40196400	Flanking Active TSS	Fetal Intestine Large	intestine
12	chr7:40196200-40196400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
13	chr7:40196200-40196600	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr7:40196200-40196600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
15	chr7:40196200-40196600	Enhancers	Rectal Smooth Muscle	rectum
16	chr7:40196200-40197000	Active TSS	Colon Smooth Muscle	Colon
17	chr7:40196400-40197000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:40196400-40197000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:40196400-40197200	Active TSS	Fetal Intestine Large	intestine
20	chr7:40196400-40197200	Active TSS	Fetal Intestine Small	intestine
21	chr7:40196400-40197200	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr7:40196600-40197000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:40196600-40197000	Active TSS	Rectal Mucosa Donor 31	rectum
24	chr7:40196600-40197000	Active TSS	Rectal Smooth Muscle	rectum
25	chr7:40196600-40197200	Active TSS	Duodenum Mucosa	Duodenum
26	chr7:40197200-40197400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
27	chr7:40197200-40198200	Enhancers	Fetal Intestine Large	intestine
28	chr7:40197200-40206800	Weak transcription	Fetal Intestine Small	intestine
29	chr7:40197400-40197600	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr7:40198200-40207000	Weak transcription	Fetal Intestine Large	intestine
31	chr7:40202000-40202600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr7:40202200-40202400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:40202200-40202600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:40202200-40202600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:40202200-40202600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr7:40202200-40202600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr7:40202400-40202800	Enhancers	HSMMtube	muscle
38	chr7:40204600-40205000	Enhancers	Fetal Stomach	stomach
39	chr7:40206800-40209200	Enhancers	Fetal Intestine Small	intestine
40	chr7:40207000-40209800	Enhancers	Fetal Intestine Large	intestine
41	chr7:40209800-40222200	Weak transcription	Fetal Intestine Large	intestine
42	chr7:40210400-40210600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:40210600-40212000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr7:40210800-40211400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:40212000-40212400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr7:40215000-40215800	Enhancers	Liver	Liver
47	chr7:40215200-40215400	Enhancers	HSMMtube	muscle
48	chr7:40215200-40215600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:40215200-40216200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr7:40215400-40215600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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