Variant report

Variant	nsv609077
Chromosome Location	chr7:153522140-153654045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:415)
CpG islands
(count:1281)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:153531658-153531679	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:153590800-153590804	K562	blood:	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	BHLHE40	chr7:153597667-153597672	K562	blood:	n/a	n/a
9	BRCA1	chr7:153631179-153631191	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:153555396-153555505	HepG2	liver:	n/a	n/a
11	CCNT2	chr7:153538905-153539222	K562	blood:	n/a	n/a
12	CEBPB	chr7:153558923-153559017	K562	blood:	n/a	chr7:153558992-153559003
13	CEBPB	chr7:153573602-153573901	MCF-7	breast:	n/a	n/a
14	CEBPB	chr7:153653827-153654031	K562	blood:	n/a	chr7:153653924-153653933
15	CEBPB	chr7:153538026-153538375	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:153650331-153650429	K562	blood:	n/a	n/a
17	CEBPB	chr7:153617320-153617608	HepG2	liver:	n/a	chr7:153617469-153617480
18	CEBPB	chr7:153538062-153538353	A549	lung:	n/a	n/a
19	CEBPB	chr7:153653846-153654075	A549	lung:	n/a	chr7:153653924-153653933
20	CEBPB	chr7:153636771-153636970	K562	blood:	n/a	n/a
21	CEBPB	chr7:153649215-153649575	A549	lung:	n/a	chr7:153649388-153649399
22	CEBPB	chr7:153558884-153559293	HepG2	liver:	n/a	chr7:153558992-153559003
23	CEBPB	chr7:153632890-153633162	K562	blood:	n/a	chr7:153632987-153632998 chr7:153632987-153633000
24	CEBPB	chr7:153632851-153633134	HepG2	liver:	n/a	chr7:153632987-153632998 chr7:153632987-153633000
25	CEBPB	chr7:153617338-153617636	K562	blood:	n/a	chr7:153617469-153617480
26	CEBPB	chr7:153538058-153538388	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:153649223-153649552	HepG2	liver:	n/a	chr7:153649388-153649399
28	CHD2	chr7:153653758-153653916	HepG2	liver:	n/a	n/a
29	CHD2	chr7:153583801-153584156	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr7:153526890-153526941	HepG2	liver:	n/a	n/a
31	CTBP2	chr7:153583188-153584353	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:153529340-153529490	BE2_C	brain:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
33	CTCF	chr7:153529405-153529449	Hela-S3	cervix:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
34	CTCF	chr7:153645257-153645434	LNCaP	prostate:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
35	CTCF	chr7:153584260-153584410	BE2_C	brain:	n/a	chr7:153584294-153584307 chr7:153584297-153584310
36	CTCF	chr7:153532318-153532488	HepG2	liver:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
37	CTCF	chr7:153529312-153529558	MCF-7	breast:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
38	CTCF	chr7:153584341-153584421	NHEK	skin:	n/a	n/a
39	CTCF	chr7:153540103-153540321	GM19239	blood:	n/a	n/a
40	CTCF	chr7:153529300-153529450	HepG2	liver:	n/a	chr7:153529418-153529431 chr7:153529415-153529433
41	CTCF	chr7:153589240-153589390	GM12867	blood:	n/a	n/a
42	CTCF	chr7:153532362-153532523	MCF-7	breast:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
43	CTCF	chr7:153645260-153645410	A549	lung:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
44	CTCF	chr7:153532400-153532550	HL-60	blood:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
45	CTCF	chr7:153532360-153532510	NHEK	skin:	n/a	chr7:153532422-153532443 chr7:153532428-153532444 chr7:153532427-153532445
46	CTCF	chr7:153557360-153557510	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr7:153540159-153540165	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:153584260-153584410	SK-N-SH_RA	brain:	n/a	chr7:153584294-153584307 chr7:153584297-153584310
49	CTCF	chr7:153584320-153584470	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:153645248-153645411	Medullo	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153579447-153579497	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:153583563-153583613	Hepatocyte	liver:	n/a
3	chr7:153641307-153641357	AG09309	skin:	n/a
4	chr7:153641267-153641317	HUVEC	blood vessel:	n/a
5	chr7:153583867-153583917	GM12892	blood:	n/a
6	chr7:153641267-153641317	AoSMC	blood vessel:	n/a
7	chr7:153582285-153582335	HEEpiC	esophagus:	n/a
8	chr7:153584582-153584632	SK-N-SH_RA	brain:	n/a
9	chr7:153586207-153586257	HEK293	kidney:	embryo
10	chr7:153585368-153585418	HCF	heart:	n/a
11	chr7:153641307-153641357	MCF-7	breast:	n/a
12	chr7:153584748-153584798	BJ	skin:	n/a
13	chr7:153586207-153586257	BJ	skin:	n/a
14	chr7:153641307-153641357	NHBE	bronchial:	n/a
15	chr7:153584873-153584923	HUVEC	blood vessel:	n/a
16	chr7:153641267-153641317	HepG2	liver:	n/a
17	chr7:153582285-153582335	HCPEpiC	choroid plexus:	n/a
18	chr7:153586207-153586257	GM19239	blood:	n/a
19	chr7:153586130-153586180	NHDF-neo	bronchial:	n/a
20	chr7:153586022-153586072	K562	blood:	n/a
21	chr7:153586592-153586642	PANC-1	pancreas:	n/a
22	chr7:153586592-153586642	HEK293	kidney:	embryo
23	chr7:153579447-153579497	HCM	heart:	n/a
24	chr7:153582285-153582335	Caco-2	colon:	n/a
25	chr7:153586207-153586257	MCF10A-Er-Src	breast:	n/a
26	chr7:153584839-153584889	HRPEpiC	eye:	n/a
27	chr7:153585368-153585418	K562	blood:	n/a
28	chr7:153582285-153582335	MCF10A-Er-Src	breast:	n/a
29	chr7:153584416-153584466	SKMC	muscle:	n/a
30	chr7:153584609-153584659	HIPEpiC	eye:	n/a
31	chr7:153586022-153586072	Jurkat	blood:	n/a
32	chr7:153579447-153579497	SKMC	muscle:	n/a
33	chr7:153584839-153584889	GM12878	blood:	n/a
34	chr7:153584597-153584647	LNCaP	prostate:	n/a
35	chr7:153584416-153584466	HRPEpiC	eye:	n/a
36	chr7:153584873-153584923	ProgFib	skin:	n/a
37	chr7:153586022-153586072	HNPCEpiC	eye:	n/a
38	chr7:153641267-153641317	HIPEpiC	eye:	n/a
39	chr7:153586130-153586180	K562	blood:	n/a
40	chr7:153584582-153584632	HCT-116	colon:	n/a
41	chr7:153583563-153583613	H1-hESC	embryonic stem cell:	embryo
42	chr7:153641307-153641357	T-47D	breast:	n/a
43	chr7:153583867-153583917	HRPEpiC	eye:	n/a
44	chr7:153586130-153586180	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:153589306-153589356	ProgFib	skin:	n/a
46	chr7:153585368-153585418	CMK	blood:	n/a
47	chr7:153584748-153584798	HL-60	blood:	n/a
48	chr7:153579447-153579497	HRE	kidney:	n/a
49	chr7:153584597-153584647	NT2-D1	testis:	n/a
50	chr7:153584416-153584466	AoSMC	blood vessel:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:153528031..153530118-chr7:153531328..153534242,3	K562	blood:
2	chr7:153527409..153529713-chr7:153538152..153540890,2	K562	blood:
3	chr7:153103586..153106568-chr7:153587349..153589344,2	K562	blood:
4	chr7:153522857..153524871-chr7:153525129..153529297,3	K562	blood:
5	chr7:152591605..152592124-chr7:153532194..153532836,2	MCF-7	breast:
6	chr7:153577342..153579521-chr7:153583996..153586013,2	K562	blood:
7	chr7:153608416..153610606-chr7:153614763..153616522,2	K562	blood:
8	chr7:153630679..153632497-chr7:153633918..153635661,2	K562	blood:
9	chr7:153106936..153109083-chr7:153612449..153615319,2	K562	blood:
10	chr7:153102450..153104761-chr7:153532927..153535675,2	K562	blood:
11	chr7:153528295..153530118-chr7:153531328..153534242,2	K562	blood:
12	chr7:153103492..153105797-chr7:153617476..153620137,2	K562	blood:
13	chr7:153636605..153638915-chr7:153643180..153645983,3	K562	blood:
14	chr7:153646257..153648420-chr7:153652652..153654403,2	K562	blood:
15	chr7:153636379..153638876-chr7:153641967..153644697,4	K562	blood:
16	chr7:153528031..153530118-chr7:153531328..153534242,3	K562	blood:
17	chr7:153613840..153616509-chr7:153617529..153619976,2	K562	blood:
18	chr7:153524674..153526933-chr7:153539368..153541510,2	K562	blood:
19	chr7:153078275..153079219-chr7:153531525..153532699,6	MCF-7	breast:
20	chr7:153608416..153610606-chr7:153614763..153616522,2	K562	blood:
21	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
22	chr7:153576130..153578324-chr7:153580213..153583011,2	MCF-7	breast:
23	chr7:153524674..153526933-chr7:153539368..153541510,2	K562	blood:
24	chr7:153525347..153527049-chr7:153542550..153545512,2	K562	blood:
25	chr7:153535667..153538318-chr7:153542041..153544226,2	K562	blood:
26	chr7:153528295..153530118-chr7:153531328..153534242,2	K562	blood:
27	chr7:153646257..153648420-chr7:153652652..153654403,2	K562	blood:
28	chr7:153608416..153611349-chr7:153614803..153616522,2	K562	blood:
29	chr7:153535667..153538318-chr7:153542041..153544226,2	K562	blood:
30	chr7:153103427..153106418-chr7:153612695..153615251,3	K562	blood:
31	chr7:153524660..153527227-chr7:153530341..153532970,2	K562	blood:
32	chr7:153636605..153638915-chr7:153643180..153645983,3	K562	blood:
33	chr7:153522857..153524871-chr7:153525129..153529297,3	K562	blood:
34	chr7:153613840..153616509-chr7:153617529..153619976,2	K562	blood:
35	chr7:153078567..153079314-chr7:153528933..153530177,7	MCF-7	breast:
36	chr7:153608416..153611349-chr7:153614803..153616522,2	K562	blood:
37	chr7:153636379..153638876-chr7:153641967..153644697,4	K562	blood:
38	chr7:152890055..152890585-chr7:153532359..153532887,2	MCF-7	breast:
39	chr7:153527409..153529713-chr7:153538152..153540890,2	K562	blood:
40	chr7:153524660..153527227-chr7:153530341..153532970,2	K562	blood:
41	chr7:153576130..153578324-chr7:153580213..153583011,2	MCF-7	breast:
42	chr7:153630679..153632497-chr7:153633918..153635661,2	K562	blood:
43	chr7:153104450..153106704-chr7:153631945..153634979,3	K562	blood:

No data

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

Extended variants
information (count: 3434 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3434 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562817551	chr7:153523211-153523212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577850114	chr7:153523232-153523233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78250995	chr7:153523237-153523238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150680030	chr7:153523239-153523240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527452040	chr7:153523272-153523273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549079141	chr7:153523294-153523295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555711199	chr7:153523312-153523313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561003571	chr7:153523313-153523314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531597745	chr7:153523341-153523342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17173793	chr7:153523345-153523346	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371926051	chr7:153523362-153523363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571945672	chr7:153523390-153523391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138948634	chr7:153523415-153523416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182586838	chr7:153523477-153523478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187715288	chr7:153523622-153523623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530149705	chr7:153523629-153523630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536802822	chr7:153523664-153523665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114086692	chr7:153523668-153523669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191243173	chr7:153523684-153523685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149394168	chr7:153523688-153523689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530716344	chr7:153523771-153523772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73161588	chr7:153523776-153523777	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs11975315	chr7:153523785-153523786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577895454	chr7:153523829-153523830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544995199	chr7:153523833-153523834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553998345	chr7:153523860-153523861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572154280	chr7:153523861-153523862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183154011	chr7:153523876-153523877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2538418	chr7:153523926-153523927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377291151	chr7:153523937-153523938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368505906	chr7:153523938-153523939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372550242	chr7:153523939-153523940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71757738	chr7:153523940-153523941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200897108	chr7:153523950-153523951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529060243	chr7:153526807-153526808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140360660	chr7:153526817-153526818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569251097	chr7:153526907-153526908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539863539	chr7:153526919-153526920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184831844	chr7:153526920-153526921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6969368	chr7:153526957-153526958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368572477	chr7:153526987-153526988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567182537	chr7:153527029-153527030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111255400	chr7:153527043-153527044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372344260	chr7:153527053-153527054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555604744	chr7:153527077-153527078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34386054	chr7:153527099-153527100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538257018	chr7:153527105-153527106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374333326	chr7:153527107-153527108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs58772168	chr7:153527150-153527151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76515213	chr7:153527182-153527183	Weak transcription Enhancers	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:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153523200-153524000	Enhancers	Fetal Brain Male	brain
2	chr7:153526800-153527000	Enhancers	Colon Smooth Muscle	Colon
3	chr7:153526800-153527600	Enhancers	Rectal Smooth Muscle	rectum
4	chr7:153527000-153532000	Weak transcription	Colon Smooth Muscle	Colon
5	chr7:153527600-153528400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr7:153528400-153529600	Enhancers	Rectal Smooth Muscle	rectum
7	chr7:153529600-153530800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:153529800-153530000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr7:153530800-153531400	Enhancers	Rectal Smooth Muscle	rectum
10	chr7:153531000-153531200	Enhancers	Stomach Smooth Muscle	stomach
11	chr7:153531200-153532800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr7:153531400-153531800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr7:153531800-153532400	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:153531800-153533400	Enhancers	Rectal Smooth Muscle	rectum
15	chr7:153532000-153532400	Enhancers	Fetal Kidney	kidney
16	chr7:153532000-153532800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr7:153532000-153533000	Enhancers	Brain Anterior Caudate	brain
18	chr7:153532000-153533200	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr7:153532000-153533600	Enhancers	Colon Smooth Muscle	Colon
20	chr7:153532400-153532600	Enhancers	Adipose Nuclei	Adipose
21	chr7:153532400-153533200	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr7:153532400-153540000	Weak transcription	Fetal Kidney	kidney
23	chr7:153532600-153533000	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr7:153532600-153533000	Enhancers	Brain Angular Gyrus	brain
25	chr7:153532600-153533000	Enhancers	Brain Hippocampus Middle	brain
26	chr7:153532600-153533200	Enhancers	Fetal Muscle Leg	muscle
27	chr7:153532800-153533400	Enhancers	Stomach Smooth Muscle	stomach
28	chr7:153533000-153533400	Enhancers	Adipose Nuclei	Adipose
29	chr7:153533200-153533400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr7:153533400-153534000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:153534000-153535600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr7:153535200-153535400	Enhancers	Stomach Smooth Muscle	stomach
33	chr7:153535600-153536000	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr7:153536000-153537800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr7:153537800-153538200	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr7:153538200-153538800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr7:153538800-153539000	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr7:153540000-153540400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:153540000-153540400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:153540000-153540400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:153540000-153540400	Enhancers	Esophagus	oesophagus
42	chr7:153540000-153540400	ZNF genes & repeats	Fetal Kidney	kidney
43	chr7:153540000-153540400	Enhancers	Gastric	stomach
44	chr7:153540000-153540400	ZNF genes & repeats	Pancreas	Pancrea
45	chr7:153540200-153540400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:153540200-153540600	Active TSS	Fetal Heart	heart
47	chr7:153540400-153541000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:153545000-153545200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr7:153547400-153547600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:153554000-153556200	Enhancers	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links