Variant report

Variant	nsv889083
Chromosome Location	chr7:117203417-117256374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:392)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:117228213-117228911	GM12878	blood:	n/a	n/a
2	ATF2	chr7:117228256-117228885	GM12878	blood:	n/a	n/a
3	ATF3	chr7:117228178-117228937	A549	lung:	n/a	n/a
4	ATF3	chr7:117222180-117222830	A549	lung:	n/a	n/a
5	ATF3	chr7:117222102-117222912	A549	lung:	n/a	n/a
6	BACH1	chr7:117245114-117245164	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr7:117204164-117204384	GM12878	blood:	n/a	n/a
8	BATF	chr7:117228364-117228827	GM12878	blood:	n/a	chr7:117228615-117228626
9	BCL11A	chr7:117228325-117228839	GM12878	blood:	n/a	n/a
10	BCL3	chr7:117228101-117228945	A549	lung:	n/a	n/a
11	BCL3	chr7:117222144-117222940	A549	lung:	n/a	chr7:117222627-117222634
12	BCL3	chr7:117228214-117228853	A549	lung:	n/a	n/a
13	BCL3	chr7:117245619-117246225	A549	lung:	n/a	n/a
14	BCL3	chr7:117222062-117223040	A549	lung:	n/a	chr7:117222627-117222634
15	BCLAF1	chr7:117228370-117228794	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:117204094-117204536	GM12878	blood:	n/a	chr7:117204311-117204320 chr7:117204311-117204320
17	BHLHE40	chr7:117228373-117228856	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:117243779-117244031	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:117222167-117222831	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:117245834-117246047	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr7:117228113-117228980	Hela-S3	cervix:	n/a	chr7:117228650-117228657
22	CEBPB	chr7:117248027-117248377	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:117212837-117213239	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
24	CEBPB	chr7:117222054-117222935	A549	lung:	n/a	chr7:117222302-117222313
25	CEBPB	chr7:117227809-117228967	Hela-S3	cervix:	n/a	chr7:117228586-117228597
26	CEBPB	chr7:117222117-117222867	IMR90	lung:	n/a	chr7:117222302-117222313
27	CEBPB	chr7:117248001-117248434	A549	lung:	n/a	n/a
28	CEBPB	chr7:117221884-117223012	A549	lung:	n/a	chr7:117222302-117222313
29	CEBPB	chr7:117222133-117222567	HepG2	liver:	n/a	chr7:117222302-117222313
30	CEBPB	chr7:117245562-117246203	A549	lung:	n/a	n/a
31	CEBPB	chr7:117247948-117248373	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:117228349-117228788	MCF-7	breast:	n/a	chr7:117228586-117228597
33	CEBPB	chr7:117206581-117206695	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:117222032-117222940	Hela-S3	cervix:	n/a	chr7:117222302-117222313
35	CEBPB	chr7:117228431-117228821	IMR90	lung:	n/a	chr7:117228586-117228597
36	CEBPB	chr7:117228203-117228832	A549	lung:	n/a	chr7:117228586-117228597
37	CEBPB	chr7:117245738-117246078	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:117228036-117228960	A549	lung:	n/a	chr7:117228586-117228597
39	CEBPB	chr7:117222236-117222366	HepG2	liver:	n/a	chr7:117222302-117222313
40	CEBPB	chr7:117213004-117213146	A549	lung:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
41	CEBPB	chr7:117222244-117222431	K562	blood:	n/a	chr7:117222302-117222313
42	CEBPB	chr7:117212851-117213351	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
43	CEBPB	chr7:117222135-117222657	MCF-7	breast:	n/a	chr7:117222302-117222313
44	CEBPB	chr7:117252740-117253129	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:117255526-117255698	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:117252709-117253048	MCF-7	breast:	n/a	n/a
47	CEBPB	chr7:117221920-117222859	A549	lung:	n/a	chr7:117222302-117222313
48	CHD2	chr7:117228282-117228913	GM12878	blood:	n/a	n/a
49	CHD2	chr7:117222172-117222928	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr7:117204156-117204422	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:117228958-117229008	HAEpiC	amniotic membrane:	n/a
2	chr7:117228958-117229008	NT2-D1	testis:	n/a
3	chr7:117228958-117229008	MCF10A-Er-Src	breast:	n/a
4	chr7:117228958-117229008	HUVEC	blood vessel:	n/a
5	chr7:117228958-117229008	MCF-7	breast:	n/a
6	chr7:117228958-117229008	AG04449	skin:	fetal
7	chr7:117228958-117229008	U87	brain:	n/a
8	chr7:117228958-117229008	GM06990	blood:	n/a
9	chr7:117228958-117229008	NHDF-neo	bronchial:	n/a
10	chr7:117228958-117229008	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:117228958-117229008	AG04450	lung:	fetal
12	chr7:117228958-117229008	NB4	blood:	n/a
13	chr7:117228958-117229008	T-47D	breast:	n/a
14	chr7:117228958-117229008	RPTEC	kidney:	n/a
15	chr7:117228958-117229008	LNCaP	prostate:	n/a
16	chr7:117228958-117229008	Caco-2	colon:	n/a
17	chr7:117228958-117229008	IMR90	lung:	fetal
18	chr7:117228958-117229008	HRE	kidney:	n/a
19	chr7:117228958-117229008	AG09309	skin:	n/a
20	chr7:117228958-117229008	Hela-S3	cervix:	n/a
21	chr7:117228958-117229008	NHBE	bronchial:	n/a
22	chr7:117228958-117229008	HEK293	kidney:	embryo
23	chr7:117228958-117229008	PFSK-1	brain:	n/a
24	chr7:117228958-117229008	NH-A	brain:	n/a
25	chr7:117228958-117229008	SK-N-MC	brain:	n/a
26	chr7:117228958-117229008	PANC-1	pancreas:	n/a
27	chr7:117228958-117229008	BE2_C	brain:	n/a
28	chr7:117228958-117229008	HRCEpiC	kidney:	n/a
29	chr7:117228958-117229008	SK-N-SH_RA	brain:	n/a
30	chr7:117228958-117229008	ovcar-3	ovarian:	n/a
31	chr7:117228958-117229008	AoSMC	blood vessel:	n/a
32	chr7:117228958-117229008	GM19239	blood:	n/a
33	chr7:117228958-117229008	HCPEpiC	choroid plexus:	n/a
34	chr7:117228958-117229008	HRPEpiC	eye:	n/a
35	chr7:117228958-117229008	SK-N-SH	brain:	n/a
36	chr7:117228958-117229008	CMK	blood:	n/a
37	chr7:117228958-117229008	ECC-1	luminal epithelium:	n/a
38	chr7:117228958-117229008	HCM	heart:	n/a
39	chr7:117228958-117229008	HepG2	liver:	n/a
40	chr7:117228958-117229008	GM12891	blood:	n/a
41	chr7:117228958-117229008	PrEC	prostate:	n/a
42	chr7:117228958-117229008	SKMC	muscle:	n/a
43	chr7:117228958-117229008	Hepatocyte	liver:	n/a
44	chr7:117228958-117229008	BJ	skin:	n/a
45	chr7:117228958-117229008	HEEpiC	esophagus:	n/a
46	chr7:117228958-117229008	SAEC	small airway:	n/a
47	chr7:117228958-117229008	H1-hESC	embryonic stem cell:	embryo
48	chr7:117228958-117229008	AG10803	skin:	n/a
49	chr7:117228958-117229008	A549	lung:	n/a
50	chr7:117228958-117229008	GM12878	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:117100350-117112126..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
2	chr7:117255614..117259660-chr7:117261825..117265320,4	K562	blood:
3	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
4	7:116544149-116547624..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
5	chr12:58237960..58239522-chr7:117246298..117249075,2	MCF-7	breast:
6	chr7:117203452..117206266-chr7:117206487..117208495,3	MCF-7	breast:
7	chr7:117255020..117257143-chr7:117304303..117306209,2	MCF-7	breast:
8	chr7:117244166..117245859-chr7:117250473..117252926,2	MCF-7	breast:
9	7:115847372-115857098..7:117228556-117233275	H1-hESC	embryonic stem cell:	embryo
10	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
11	7:117251668-117255413..7:117341506-117356953	Hela-S3	cervix:
12	7:115861595-115870968..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
13	7:115861595-115870968..7:117216968-117220729	H1-hESC	embryonic stem cell:	embryo
14	7:116754962-116765597..7:117228556-117233275	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTTNBP2-1	chr7:117244845-117245043	ENSG00000083622.8
2	lnc-CTTNBP2-1	chr7:117256283-117256394	ENSG00000083622.8
3	lnc-ASZ1-1	chr7:117204570-117204730	ENSG00000232661.1
4	lnc-CTTNBP2-4	chr7:117226261-117226470	NONHSAT122949

No data

Variant related genes	Relation type
CFTR	TF binding region
ENSG00000234001	TF binding region
ENSG00000232661	TF binding region
CFTR	CpG island
ENSG00000234001	CpG island
ENSG00000232661	CpG island
ENSG00000001626	chromatin interactions
ENSG00000135269	chromatin interactions
ENSG00000004866	chromatin interactions
ENSG00000175215	chromatin interactions
ENSG00000232661	chromatin interactions

Extended variants
information (count: 2118 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2118 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs213952	chr7:117203417-117203418	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34042174	chr7:117203421-117203422	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs557644752	chr7:117203427-117203428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528997024	chr7:117203436-117203437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375157863	chr7:117203474-117203475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563936089	chr7:117203486-117203487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566976127	chr7:117203493-117203494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144602234	chr7:117203499-117203500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534409137	chr7:117203549-117203550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs4148707	chr7:117203575-117203576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs397843648	chr7:117203576-117203577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552633158	chr7:117203615-117203616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571156010	chr7:117203690-117203691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569571527	chr7:117203739-117203740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555743791	chr7:117203891-117203892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556605646	chr7:117203898-117203899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148484513	chr7:117203944-117203945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190692691	chr7:117204016-117204017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554223558	chr7:117204027-117204028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572188888	chr7:117204066-117204067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142249127	chr7:117204167-117204168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73715574	chr7:117204322-117204323	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575943791	chr7:117204348-117204349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543280932	chr7:117204369-117204370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117720522	chr7:117204393-117204394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573562444	chr7:117204443-117204444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10281281	chr7:117204462-117204463	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs563123419	chr7:117204498-117204499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559387526	chr7:117204532-117204533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182813527	chr7:117204577-117204578	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs187152693	chr7:117204581-117204582	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs191747007	chr7:117204617-117204618	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs532059220	chr7:117204638-117204639	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs529090312	chr7:117204677-117204678	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs550467867	chr7:117204679-117204680	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs372728734	chr7:117204703-117204704	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs17140169	chr7:117204713-117204714	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146793783	chr7:117204805-117204806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140579556	chr7:117204806-117204807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184637962	chr7:117204808-117204809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557545445	chr7:117204819-117204820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78835416	chr7:117204919-117204920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575802687	chr7:117204921-117204922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536974064	chr7:117204928-117204929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555229276	chr7:117204953-117204954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369723046	chr7:117204958-117204959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573598093	chr7:117205002-117205003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541021057	chr7:117205007-117205008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534808764	chr7:117205044-117205045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375955322	chr7:117205073-117205074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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	22286061	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:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117173000-117208000	Weak transcription	Pancreas	Pancrea
2	chr7:117181400-117213400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:117185800-117203600	Weak transcription	Fetal Intestine Large	intestine
4	chr7:117187000-117205200	Weak transcription	Stomach Mucosa	stomach
5	chr7:117193400-117205200	Weak transcription	Fetal Intestine Small	intestine
6	chr7:117195800-117206000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr7:117196000-117203800	Weak transcription	Dnd41	blood
8	chr7:117202400-117212600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr7:117202600-117204800	Enhancers	Fetal Heart	heart
10	chr7:117203200-117204000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr7:117203600-117207000	Enhancers	Fetal Intestine Large	intestine
12	chr7:117203800-117204800	Enhancers	Dnd41	blood
13	chr7:117204000-117205600	Enhancers	Placenta Amnion	Placenta Amnion
14	chr7:117204200-117205400	Enhancers	A549	lung
15	chr7:117204200-117207000	Enhancers	Liver	Liver
16	chr7:117205200-117206400	Enhancers	Fetal Intestine Small	intestine
17	chr7:117205200-117207000	Enhancers	Stomach Mucosa	stomach
18	chr7:117205600-117206400	Enhancers	Small Intestine	intestine
19	chr7:117206000-117206600	Enhancers	Duodenum Mucosa	Duodenum
20	chr7:117206400-117208400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:117206400-117211600	Weak transcription	Fetal Intestine Small	intestine
22	chr7:117206400-117216800	Weak transcription	Small Intestine	intestine
23	chr7:117206600-117207000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:117206600-117217600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr7:117207000-117211400	Weak transcription	Fetal Intestine Large	intestine
26	chr7:117207000-117212200	Weak transcription	Stomach Mucosa	stomach
27	chr7:117208000-117208600	Strong transcription	Pancreas	Pancrea
28	chr7:117208600-117232400	Weak transcription	Pancreas	Pancrea
29	chr7:117211400-117214200	Enhancers	Fetal Intestine Large	intestine
30	chr7:117211600-117214200	Enhancers	Fetal Intestine Small	intestine
31	chr7:117212200-117212600	Enhancers	Stomach Mucosa	stomach
32	chr7:117212600-117212800	Active TSS	A549	lung
33	chr7:117212600-117213800	Enhancers	Fetal Lung	lung
34	chr7:117212600-117213800	Weak transcription	Stomach Mucosa	stomach
35	chr7:117212600-117214000	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr7:117212600-117214200	Enhancers	Fetal Heart	heart
37	chr7:117212800-117213000	Flanking Active TSS	A549	lung
38	chr7:117213000-117213600	Enhancers	A549	lung
39	chr7:117213400-117214400	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr7:117213600-117220400	Weak transcription	A549	lung
41	chr7:117213800-117214800	Enhancers	Stomach Mucosa	stomach
42	chr7:117214000-117228000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr7:117214200-117216200	Weak transcription	Fetal Intestine Small	intestine
44	chr7:117214200-117216600	Weak transcription	Fetal Intestine Large	intestine
45	chr7:117214400-117228000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr7:117216200-117217800	Enhancers	Fetal Intestine Small	intestine
47	chr7:117216600-117217400	Enhancers	Fetal Intestine Large	intestine
48	chr7:117216600-117218200	Enhancers	Dnd41	blood
49	chr7:117216800-117217000	Enhancers	Fetal Heart	heart
50	chr7:117216800-117217000	Enhancers	Small Intestine	intestine

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