Variant report

Variant	nsv482593
Chromosome Location	chr7:153480650-153633269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:390)
CpG islands
(count:1098)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:390 , 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	ARID3A	chr7:153590800-153590804	K562	blood:	n/a	n/a
2	ARID3A	chr7:153531658-153531679	HepG2	liver:	n/a	n/a
3	ATF1	chr7:153545773-153545921	K562	blood:	n/a	n/a
4	BACH1	chr7:153539559-153539602	K562	blood:	n/a	n/a
5	BACH1	chr7:153631881-153631909	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:153583560-153584651	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:153591752-153591756	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr7:153505233-153505545	GM12878	blood:	n/a	n/a
9	BCL3	chr7:153505225-153505579	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:153597667-153597672	K562	blood:	n/a	n/a
11	BHLHE40	chr7:153505233-153505431	K562	blood:	n/a	n/a
12	BRCA1	chr7:153631179-153631191	HepG2	liver:	n/a	n/a
13	BRCA1	chr7:153555396-153555505	HepG2	liver:	n/a	n/a
14	CCNT2	chr7:153538905-153539222	K562	blood:	n/a	n/a
15	CEBPB	chr7:153632851-153633134	HepG2	liver:	n/a	chr7:153632987-153632998 chr7:153632987-153633000
16	CEBPB	chr7:153632890-153633162	K562	blood:	n/a	chr7:153632987-153632998 chr7:153632987-153633000
17	CEBPB	chr7:153538062-153538353	A549	lung:	n/a	n/a
18	CEBPB	chr7:153558923-153559017	K562	blood:	n/a	chr7:153558992-153559003
19	CEBPB	chr7:153617338-153617636	K562	blood:	n/a	chr7:153617469-153617480
20	CEBPB	chr7:153538058-153538388	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:153573602-153573901	MCF-7	breast:	n/a	n/a
22	CEBPB	chr7:153558884-153559293	HepG2	liver:	n/a	chr7:153558992-153559003
23	CEBPB	chr7:153538026-153538375	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:153617320-153617608	HepG2	liver:	n/a	chr7:153617469-153617480
25	CHD2	chr7:153583801-153584156	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr7:153526890-153526941	HepG2	liver:	n/a	n/a
27	CTBP2	chr7:153583188-153584353	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:153540086-153540330	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:153529300-153529450	HVMF	connective:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
30	CTCF	chr7:153529340-153529490	BE2_C	brain:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
31	CTCF	chr7:153529327-153529521	Medullo	brain:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
32	CTCF	chr7:153533101-153533227	K562	blood:	n/a	n/a
33	CTCF	chr7:153540103-153540321	GM19239	blood:	n/a	n/a
34	CTCF	chr7:153584259-153584494	H1-hESC	embryonic stem cell:	n/a	chr7:153584294-153584307 chr7:153584297-153584310
35	CTCF	chr7:153540196-153540215	A549	lung:	n/a	n/a
36	CTCF	chr7:153529323-153529541	MCF-7	breast:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
37	CTCF	chr7:153584321-153584440	Fibrobl	skin:	n/a	n/a
38	CTCF	chr7:153529231-153529607	HepG2	liver:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
39	CTCF	chr7:153533020-153533170	BE2_C	brain:	n/a	n/a
40	CTCF	chr7:153484900-153484974	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr7:153529313-153529561	K562	blood:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
42	CTCF	chr7:153499199-153499297	LNCaP	prostate:	n/a	n/a
43	CTCF	chr7:153584296-153584382	Pancreas_OC	pancreas:	n/a	chr7:153584297-153584310
44	CTCF	chr7:153617400-153617550	AG09319	gingival:	n/a	n/a
45	CTCF	chr7:153516540-153516668	Fibrobl	skin:	n/a	n/a
46	CTCF	chr7:153584136-153584470	H1-hESC	embryonic stem cell:	n/a	chr7:153584294-153584307 chr7:153584297-153584310
47	CTCF	chr7:153532500-153532650	BE2_C	brain:	n/a	n/a
48	CTCF	chr7:153557360-153557510	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr7:153529300-153529450	K562	blood:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
50	CTCF	chr7:153532300-153532450	RPTEC	kidney:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153584416-153584466	AG10803	skin:	n/a
2	chr7:153586022-153586072	HEEpiC	esophagus:	n/a
3	chr7:153584609-153584659	HAEpiC	amniotic membrane:	n/a
4	chr7:153584748-153584798	Jurkat	blood:	n/a
5	chr7:153584609-153584659	HRCEpiC	kidney:	n/a
6	chr7:153583318-153583368	AG09309	skin:	n/a
7	chr7:153583318-153583368	LNCaP	prostate:	n/a
8	chr7:153584597-153584647	SKMC	muscle:	n/a
9	chr7:153584748-153584798	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:153583563-153583613	SKMC	muscle:	n/a
11	chr7:153586022-153586072	HIPEpiC	eye:	n/a
12	chr7:153589306-153589356	GM12878	blood:	n/a
13	chr7:153584873-153584923	HUVEC	blood vessel:	n/a
14	chr7:153583867-153583917	NHDF-neo	bronchial:	n/a
15	chr7:153589306-153589356	AoSMC	blood vessel:	n/a
16	chr7:153585368-153585418	T-47D	breast:	n/a
17	chr7:153584416-153584466	NB4	blood:	n/a
18	chr7:153584416-153584466	Jurkat	blood:	n/a
19	chr7:153584873-153584923	GM12892	blood:	n/a
20	chr7:153586207-153586257	GM19239	blood:	n/a
21	chr7:153584609-153584659	AG04450	lung:	fetal
22	chr7:153583563-153583613	HRPEpiC	eye:	n/a
23	chr7:153579447-153579497	NB4	blood:	n/a
24	chr7:153584748-153584798	SK-N-SH_RA	brain:	n/a
25	chr7:153584609-153584659	SK-N-MC	brain:	n/a
26	chr7:153584597-153584647	MCF-7	breast:	n/a
27	chr7:153584597-153584647	SAEC	small airway:	n/a
28	chr7:153582285-153582335	LNCaP	prostate:	n/a
29	chr7:153583563-153583613	CMK	blood:	n/a
30	chr7:153583867-153583917	U87	brain:	n/a
31	chr7:153584873-153584923	HRCEpiC	kidney:	n/a
32	chr7:153584582-153584632	HEEpiC	esophagus:	n/a
33	chr7:153586022-153586072	ProgFib	skin:	n/a
34	chr7:153589306-153589356	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:153583563-153583613	NB4	blood:	n/a
36	chr7:153584748-153584798	HUVEC	blood vessel:	n/a
37	chr7:153584416-153584466	GM19239	blood:	n/a
38	chr7:153586592-153586642	GM12878	blood:	n/a
39	chr7:153583318-153583368	Hepatocyte	liver:	n/a
40	chr7:153584839-153584889	HCT-116	colon:	n/a
41	chr7:153582285-153582335	HRCEpiC	kidney:	n/a
42	chr7:153589306-153589356	NHBE	bronchial:	n/a
43	chr7:153584416-153584466	AoSMC	blood vessel:	n/a
44	chr7:153583563-153583613	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:153586130-153586180	SK-N-MC	brain:	n/a
46	chr7:153584839-153584889	HMEC	breast:	n/a
47	chr7:153579447-153579497	GM12891	blood:	n/a
48	chr7:153586130-153586180	SAEC	small airway:	n/a
49	chr7:153584873-153584923	LNCaP	prostate:	n/a
50	chr7:153584873-153584923	HepG2	liver:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:153103586..153106568-chr7:153587349..153589344,2	K562	blood:
2	chr7:153103427..153106418-chr7:153612695..153615251,3	K562	blood:
3	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
4	chr7:153524660..153527227-chr7:153530341..153532970,2	K562	blood:
5	chr7:153577342..153579521-chr7:153583996..153586013,2	K562	blood:
6	chr7:153576130..153578324-chr7:153580213..153583011,2	MCF-7	breast:
7	chr7:153535667..153538318-chr7:153542041..153544226,2	K562	blood:
8	chr7:153576130..153578324-chr7:153580213..153583011,2	MCF-7	breast:
9	chr7:153608416..153610606-chr7:153614763..153616522,2	K562	blood:
10	chr7:153528031..153530118-chr7:153531328..153534242,3	K562	blood:
11	chr7:153522857..153524871-chr7:153525129..153529297,3	K562	blood:
12	chr7:153102450..153104761-chr7:153532927..153535675,2	K562	blood:
13	chr7:153522857..153524871-chr7:153525129..153529297,3	K562	blood:
14	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
15	chr7:152890055..152890585-chr7:153532359..153532887,2	MCF-7	breast:
16	chr7:153104450..153106704-chr7:153631945..153634979,3	K562	blood:
17	chr7:153528295..153530118-chr7:153531328..153534242,2	K562	blood:
18	chr7:152591605..152592124-chr7:153532194..153532836,2	MCF-7	breast:
19	chr7:153524660..153527227-chr7:153530341..153532970,2	K562	blood:
20	chr7:153528295..153530118-chr7:153531328..153534242,2	K562	blood:
21	chr7:153608416..153610606-chr7:153614763..153616522,2	K562	blood:
22	chr7:153535667..153538318-chr7:153542041..153544226,2	K562	blood:
23	chr7:153608416..153611349-chr7:153614803..153616522,2	K562	blood:
24	chr7:153528031..153530118-chr7:153531328..153534242,3	K562	blood:
25	chr7:153527409..153529713-chr7:153538152..153540890,2	K562	blood:
26	chr7:153613840..153616509-chr7:153617529..153619976,2	K562	blood:
27	chr7:153527409..153529713-chr7:153538152..153540890,2	K562	blood:
28	chr7:153630679..153632497-chr7:153633918..153635661,2	K562	blood:
29	chr7:153613840..153616509-chr7:153617529..153619976,2	K562	blood:
30	chr7:153524674..153526933-chr7:153539368..153541510,2	K562	blood:
31	chr7:153524674..153526933-chr7:153539368..153541510,2	K562	blood:
32	chr7:153608416..153611349-chr7:153614803..153616522,2	K562	blood:
33	chr7:153078567..153079314-chr7:153528933..153530177,7	MCF-7	breast:
34	chr7:153078275..153079219-chr7:153531525..153532699,6	MCF-7	breast:
35	chr7:153106936..153109083-chr7:153612449..153615319,2	K562	blood:
36	chr7:153103492..153105797-chr7:153617476..153620137,2	K562	blood:

No data

Variant related genes	Relation type
DPP6	TF binding region
DPP6	CpG island
ENSG00000130226	chromatin interactions

Extended variants
information (count: 2905 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2905 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556874584	chr7:153486425-153486426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193197256	chr7:153486448-153486449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372911163	chr7:153486467-153486468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374205479	chr7:153486473-153486474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565931399	chr7:153486524-153486525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184576875	chr7:153486532-153486533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377497522	chr7:153486535-153486536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555399646	chr7:153486538-153486539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188897625	chr7:153486579-153486580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200395135	chr7:153486592-153486593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370756733	chr7:153486615-153486616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2622168	chr7:153486641-153486642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555871694	chr7:153486669-153486670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577909712	chr7:153486677-153486678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2622167	chr7:153486704-153486705	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554015741	chr7:153486720-153486721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572233025	chr7:153486744-153486745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543161101	chr7:153486756-153486757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs59640374	chr7:153486776-153486777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575737250	chr7:153486803-153486804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561403930	chr7:153486848-153486849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543123643	chr7:153486874-153486875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531687826	chr7:153486891-153486892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117436189	chr7:153486897-153486898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71278486	chr7:153486904-153486905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2622166	chr7:153486905-153486906	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs532714180	chr7:153486975-153486976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547637163	chr7:153486976-153486977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376544926	chr7:153486989-153486990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530197066	chr7:153486999-153487000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531813909	chr7:153497201-153497202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551429084	chr7:153497204-153497205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71545622	chr7:153497217-153497218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111848796	chr7:153497220-153497221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71545623	chr7:153497225-153497226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568648987	chr7:153497258-153497259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs71545624	chr7:153497266-153497267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548056047	chr7:153497302-153497303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs71545625	chr7:153497321-153497322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71545626	chr7:153497334-153497335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2622105	chr7:153497337-153497338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533807543	chr7:153497372-153497373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552963736	chr7:153497385-153497386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566306373	chr7:153497401-153497402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534112300	chr7:153497423-153497424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183655384	chr7:153497455-153497456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186475920	chr7:153497467-153497468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538073551	chr7:153497477-153497478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191782813	chr7:153497492-153497493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556389673	chr7:153497523-153497524	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
Wilms tumour	21544195	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Breast cancer	21509527	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Autism	22102821	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153486400-153487000	Enhancers	Colon Smooth Muscle	Colon
2	chr7:153497200-153497400	Enhancers	Colon Smooth Muscle	Colon
3	chr7:153497400-153505200	Weak transcription	Colon Smooth Muscle	Colon
4	chr7:153505200-153505600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:153505200-153505600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:153505200-153505600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:153505200-153505600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
8	chr7:153505200-153505600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:153505200-153505600	Enhancers	Colon Smooth Muscle	Colon
10	chr7:153505200-153505600	Enhancers	Esophagus	oesophagus
11	chr7:153505200-153505600	Active TSS	Gastric	stomach
12	chr7:153505200-153505600	ZNF genes & repeats	Pancreas	Pancrea
13	chr7:153523200-153524000	Enhancers	Fetal Brain Male	brain
14	chr7:153526800-153527000	Enhancers	Colon Smooth Muscle	Colon
15	chr7:153526800-153527600	Enhancers	Rectal Smooth Muscle	rectum
16	chr7:153527000-153532000	Weak transcription	Colon Smooth Muscle	Colon
17	chr7:153527600-153528400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr7:153528400-153529600	Enhancers	Rectal Smooth Muscle	rectum
19	chr7:153529600-153530800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr7:153529800-153530000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr7:153530800-153531400	Enhancers	Rectal Smooth Muscle	rectum
22	chr7:153531000-153531200	Enhancers	Stomach Smooth Muscle	stomach
23	chr7:153531200-153532800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr7:153531400-153531800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:153531800-153532400	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr7:153531800-153533400	Enhancers	Rectal Smooth Muscle	rectum
27	chr7:153532000-153532400	Enhancers	Fetal Kidney	kidney
28	chr7:153532000-153532800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:153532000-153533000	Enhancers	Brain Anterior Caudate	brain
30	chr7:153532000-153533200	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr7:153532000-153533600	Enhancers	Colon Smooth Muscle	Colon
32	chr7:153532400-153532600	Enhancers	Adipose Nuclei	Adipose
33	chr7:153532400-153533200	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr7:153532400-153540000	Weak transcription	Fetal Kidney	kidney
35	chr7:153532600-153533000	Flanking Active TSS	Adipose Nuclei	Adipose
36	chr7:153532600-153533000	Enhancers	Brain Angular Gyrus	brain
37	chr7:153532600-153533000	Enhancers	Brain Hippocampus Middle	brain
38	chr7:153532600-153533200	Enhancers	Fetal Muscle Leg	muscle
39	chr7:153532800-153533400	Enhancers	Stomach Smooth Muscle	stomach
40	chr7:153533000-153533400	Enhancers	Adipose Nuclei	Adipose
41	chr7:153533200-153533400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr7:153533400-153534000	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:153534000-153535600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr7:153535200-153535400	Enhancers	Stomach Smooth Muscle	stomach
45	chr7:153535600-153536000	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:153536000-153537800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr7:153537800-153538200	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr7:153538200-153538800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr7:153538800-153539000	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr7:153540000-153540400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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