Variant report

Variant	nsv889527
Chromosome Location	chr7:153495423-153638248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:1099)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 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	chr7:153631881-153631909	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:153539559-153539602	K562	blood:	n/a	n/a
6	BACH1	chr7:153591752-153591756	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:153583560-153584651	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	chr7:153505233-153505431	K562	blood:	n/a	n/a
11	BHLHE40	chr7:153597667-153597672	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	chr7:153558923-153559017	K562	blood:	n/a	chr7:153558992-153559003
17	CEBPB	chr7:153636771-153636970	K562	blood:	n/a	n/a
18	CEBPB	chr7:153538026-153538375	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:153538062-153538353	A549	lung:	n/a	n/a
20	CEBPB	chr7:153573602-153573901	MCF-7	breast:	n/a	n/a
21	CEBPB	chr7:153538058-153538388	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:153632890-153633162	K562	blood:	n/a	chr7:153632987-153632998 chr7:153632987-153633000
23	CEBPB	chr7:153617338-153617636	K562	blood:	n/a	chr7:153617469-153617480
24	CEBPB	chr7:153558884-153559293	HepG2	liver:	n/a	chr7:153558992-153559003
25	CEBPB	chr7:153617320-153617608	HepG2	liver:	n/a	chr7:153617469-153617480
26	CHD2	chr7:153583801-153584156	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr7:153526890-153526941	HepG2	liver:	n/a	n/a
28	CTBP2	chr7:153583188-153584353	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:153532600-153532750	RPTEC	kidney:	n/a	n/a
30	CTCF	chr7:153533101-153533227	K562	blood:	n/a	n/a
31	CTCF	chr7:153532360-153532510	HMEC	breast:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
32	CTCF	chr7:153529320-153529470	BE2_C	brain:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
33	CTCF	chr7:153584312-153584413	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:153495955-153496030	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr7:153584259-153584494	H1-hESC	embryonic stem cell:	n/a	chr7:153584294-153584307 chr7:153584297-153584310
36	CTCF	chr7:153540196-153540215	A549	lung:	n/a	n/a
37	CTCF	chr7:153532380-153532530	K562	blood:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
38	CTCF	chr7:153540304-153540349	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:153557380-153557530	K562	blood:	n/a	n/a
40	CTCF	chr7:153529413-153529466	LNCaP	prostate:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
41	CTCF	chr7:153540103-153540321	GM19239	blood:	n/a	n/a
42	CTCF	chr7:153529340-153529490	A549	lung:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
43	CTCF	chr7:153532353-153532483	Kidney_OC	kidney:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
44	CTCF	chr7:153532332-153532530	LNCaP	prostate:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
45	CTCF	chr7:153557400-153557536	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr7:153532337-153532504	H1-hESC	embryonic stem cell:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
47	CTCF	chr7:153529231-153529607	HepG2	liver:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
48	CTCF	chr7:153540159-153540165	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:153532380-153532530	BE2_C	brain:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
50	CTCF	chr7:153578710-153578739	Lung_OC	lung:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153584609-153584659	NHBE	bronchial:	n/a
2	chr7:153584609-153584659	NHBE	bronchial:	n/a
3	chr7:153584609-153584659	SAEC	small airway:	n/a
4	chr7:153579447-153579497	Jurkat	blood:	n/a
5	chr7:153583867-153583917	ProgFib	skin:	n/a
6	chr7:153584597-153584647	AG04450	lung:	fetal
7	chr7:153586207-153586257	PANC-1	pancreas:	n/a
8	chr7:153582285-153582335	AG09319	gingival:	n/a
9	chr7:153584582-153584632	Jurkat	blood:	n/a
10	chr7:153586592-153586642	SAEC	small airway:	n/a
11	chr7:153586592-153586642	U87	brain:	n/a
12	chr7:153583867-153583917	BE2_C	brain:	n/a
13	chr7:153584416-153584466	HCM	heart:	n/a
14	chr7:153584416-153584466	AoSMC	blood vessel:	n/a
15	chr7:153584416-153584466	ECC-1	luminal epithelium:	n/a
16	chr7:153586592-153586642	HCPEpiC	choroid plexus:	n/a
17	chr7:153584839-153584889	MCF10A-Er-Src	breast:	n/a
18	chr7:153584839-153584889	A549	lung:	n/a
19	chr7:153584416-153584466	RPTEC	kidney:	n/a
20	chr7:153584416-153584466	Hepatocyte	liver:	n/a
21	chr7:153579447-153579497	HNPCEpiC	eye:	n/a
22	chr7:153584416-153584466	NHDF-neo	bronchial:	n/a
23	chr7:153583563-153583613	HCF	heart:	n/a
24	chr7:153584748-153584798	HCT-116	colon:	n/a
25	chr7:153586207-153586257	SAEC	small airway:	n/a
26	chr7:153583867-153583917	K562	blood:	n/a
27	chr7:153579447-153579497	BJ	skin:	n/a
28	chr7:153584609-153584659	HEEpiC	esophagus:	n/a
29	chr7:153586022-153586072	Caco-2	colon:	n/a
30	chr7:153584597-153584647	SK-N-SH_RA	brain:	n/a
31	chr7:153584582-153584632	Hepatocyte	liver:	n/a
32	chr7:153584609-153584659	IMR90	lung:	fetal
33	chr7:153586022-153586072	AG09309	skin:	n/a
34	chr7:153583318-153583368	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:153585368-153585418	MCF-7	breast:	n/a
36	chr7:153583867-153583917	HepG2	liver:	n/a
37	chr7:153582285-153582335	GM12891	blood:	n/a
38	chr7:153579447-153579497	HL-60	blood:	n/a
39	chr7:153584839-153584889	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:153584873-153584923	SAEC	small airway:	n/a
41	chr7:153582285-153582335	HCPEpiC	choroid plexus:	n/a
42	chr7:153586022-153586072	HCM	heart:	n/a
43	chr7:153584416-153584466	HNPCEpiC	eye:	n/a
44	chr7:153586592-153586642	MCF-7	breast:	n/a
45	chr7:153583318-153583368	GM06990	blood:	n/a
46	chr7:153586207-153586257	GM12878	blood:	n/a
47	chr7:153584597-153584647	PFSK-1	brain:	n/a
48	chr7:153586130-153586180	GM12892	blood:	n/a
49	chr7:153586592-153586642	SK-N-SH_RA	brain:	n/a
50	chr7:153583318-153583368	MCF-7	breast:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:153535667..153538318-chr7:153542041..153544226,2	K562	blood:
2	chr7:153522857..153524871-chr7:153525129..153529297,3	K562	blood:
3	chr7:153613840..153616509-chr7:153617529..153619976,2	K562	blood:
4	chr7:153528295..153530118-chr7:153531328..153534242,2	K562	blood:
5	chr7:153528031..153530118-chr7:153531328..153534242,3	K562	blood:
6	chr7:153576130..153578324-chr7:153580213..153583011,2	MCF-7	breast:
7	chr7:153524660..153527227-chr7:153530341..153532970,2	K562	blood:
8	chr7:153636379..153638876-chr7:153641967..153644697,4	K562	blood:
9	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
10	chr7:153106936..153109083-chr7:153612449..153615319,2	K562	blood:
11	chr7:153528295..153530118-chr7:153531328..153534242,2	K562	blood:
12	chr7:153527409..153529713-chr7:153538152..153540890,2	K562	blood:
13	chr7:153524674..153526933-chr7:153539368..153541510,2	K562	blood:
14	chr7:153613840..153616509-chr7:153617529..153619976,2	K562	blood:
15	chr7:153524660..153527227-chr7:153530341..153532970,2	K562	blood:
16	chr7:153535667..153538318-chr7:153542041..153544226,2	K562	blood:
17	chr7:153608416..153610606-chr7:153614763..153616522,2	K562	blood:
18	chr7:153522857..153524871-chr7:153525129..153529297,3	K562	blood:
19	chr7:153636605..153638915-chr7:153643180..153645983,3	K562	blood:
20	chr7:153524674..153526933-chr7:153539368..153541510,2	K562	blood:
21	chr7:152591605..152592124-chr7:153532194..153532836,2	MCF-7	breast:
22	chr7:153078567..153079314-chr7:153528933..153530177,7	MCF-7	breast:
23	chr7:153103586..153106568-chr7:153587349..153589344,2	K562	blood:
24	chr7:153528031..153530118-chr7:153531328..153534242,3	K562	blood:
25	chr7:153527409..153529713-chr7:153538152..153540890,2	K562	blood:
26	chr7:153630679..153632497-chr7:153633918..153635661,2	K562	blood:
27	chr7:153103427..153106418-chr7:153612695..153615251,3	K562	blood:
28	chr7:153608416..153610606-chr7:153614763..153616522,2	K562	blood:
29	chr7:153630679..153632497-chr7:153633918..153635661,2	K562	blood:
30	chr7:153102450..153104761-chr7:153532927..153535675,2	K562	blood:
31	chr7:153103492..153105797-chr7:153617476..153620137,2	K562	blood:
32	chr7:153608416..153611349-chr7:153614803..153616522,2	K562	blood:
33	chr7:153576130..153578324-chr7:153580213..153583011,2	MCF-7	breast:
34	chr7:153608416..153611349-chr7:153614803..153616522,2	K562	blood:
35	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
36	chr7:153577342..153579521-chr7:153583996..153586013,2	K562	blood:
37	chr7:153078275..153079219-chr7:153531525..153532699,6	MCF-7	breast:
38	chr7:153104450..153106704-chr7:153631945..153634979,3	K562	blood:
39	chr7:152890055..152890585-chr7:153532359..153532887,2	MCF-7	breast:

No data

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

Extended variants
information (count: 3108 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3108 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531813909	chr7:153497201-153497202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551429084	chr7:153497204-153497205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71545622	chr7:153497217-153497218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111848796	chr7:153497220-153497221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71545623	chr7:153497225-153497226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568648987	chr7:153497258-153497259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71545624	chr7:153497266-153497267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548056047	chr7:153497302-153497303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs71545625	chr7:153497321-153497322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71545626	chr7:153497334-153497335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2622105	chr7:153497337-153497338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533807543	chr7:153497372-153497373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552963736	chr7:153497385-153497386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566306373	chr7:153497401-153497402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534112300	chr7:153497423-153497424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183655384	chr7:153497455-153497456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186475920	chr7:153497467-153497468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538073551	chr7:153497477-153497478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191782813	chr7:153497492-153497493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556389673	chr7:153497523-153497524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578146358	chr7:153497535-153497536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545131063	chr7:153497541-153497542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554151737	chr7:153497574-153497575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184755169	chr7:153497576-153497577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142363402	chr7:153497581-153497582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542983618	chr7:153497608-153497609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561278647	chr7:153497609-153497610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531870942	chr7:153497614-153497615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535602928	chr7:153497641-153497642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2928838	chr7:153497642-153497643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2928839	chr7:153497653-153497654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2928840	chr7:153497670-153497671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2928841	chr7:153497687-153497688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2622106	chr7:153497688-153497689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535515460	chr7:153497724-153497725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533059617	chr7:153497756-153497757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551157319	chr7:153497798-153497799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566485542	chr7:153497832-153497833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2538462	chr7:153497853-153497854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112573038	chr7:153497895-153497896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369188480	chr7:153497904-153497905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567607850	chr7:153498011-153498012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117928518	chr7:153498026-153498027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114834325	chr7:153498087-153498088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571320255	chr7:153498212-153498213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539143412	chr7:153498220-153498221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554001030	chr7:153498228-153498229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572485278	chr7:153498286-153498287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190135765	chr7:153498325-153498326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554537572	chr7:153498343-153498344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Autism	22102821	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
small cell lung cancer	20016488	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:316 , 50 per page) page: 1 2 3 4 5 6 7

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

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