Variant report

Variant	nsv981571
Chromosome Location	chr7:116608949-116617079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:144)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:144 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:116610804-116611102	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:116610635-116610721	K562	blood:	n/a	n/a
3	ATF2	chr7:116610509-116610918	GM12878	blood:	n/a	n/a
4	ATF2	chr7:116610493-116611042	GM12878	blood:	n/a	n/a
5	BATF	chr7:116610564-116610923	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:116611264-116611533	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:116610509-116610842	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:116612095-116612258	K562	blood:	n/a	chr7:116612194-116612210
9	BHLHE40	chr7:116611353-116611600	GM12878	blood:	n/a	chr7:116611467-116611488
10	BHLHE40	chr7:116610643-116610898	GM12878	blood:	n/a	n/a
11	CHD1	chr7:116611508-116611547	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:116615433-116615471	Lung_OC	lung:	n/a	n/a
13	CTCF	chr7:116616400-116616550	GM12866	blood:	n/a	n/a
14	CTCF	chr7:116616202-116616312	GM10248	blood:	n/a	n/a
15	CUX1	chr7:116610251-116610361	K562	blood:	n/a	n/a
16	CUX1	chr7:116610556-116611043	GM12878	blood:	n/a	n/a
17	CUX1	chr7:116611546-116611557	K562	blood:	n/a	n/a
18	CUX1	chr7:116611024-116611056	K562	blood:	n/a	n/a
19	E2F4	chr7:116610646-116610816	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr7:116611280-116611474	GM12878	blood:	n/a	n/a
21	EBF1	chr7:116610664-116610858	GM12878	blood:	n/a	n/a
22	EBF1	chr7:116611243-116611497	GM12878	blood:	n/a	n/a
23	ELF1	chr7:116610360-116610737	K562	blood:	n/a	chr7:116610527-116610540
24	EP300	chr7:116610522-116610813	GM12878	blood:	n/a	n/a
25	EP300	chr7:116611357-116611494	K562	blood:	n/a	n/a
26	EP300	chr7:116610713-116610860	K562	blood:	n/a	n/a
27	EP300	chr7:116610575-116610905	GM12878	blood:	n/a	n/a
28	EP300	chr7:116610731-116610742	GM12878	blood:	n/a	n/a
29	EP300	chr7:116612027-116612219	K562	blood:	n/a	n/a
30	FOS	chr7:116610610-116610926	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr7:116610619-116610882	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr7:116610640-116610955	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr7:116610627-116610921	MCF10A-Er-Src	breast:	n/a	n/a
34	FOXA1	chr7:116610797-116611241	HepG2	liver:	n/a	n/a
35	FOXA1	chr7:116612037-116612352	HepG2	liver:	n/a	n/a
36	FOXA1	chr7:116612053-116612354	HepG2	liver:	n/a	n/a
37	FOXA1	chr7:116610777-116611268	HepG2	liver:	n/a	n/a
38	FOXA2	chr7:116612072-116612387	HepG2	liver:	n/a	n/a
39	FOXM1	chr7:116610457-116611057	GM12878	blood:	n/a	n/a
40	GATA3	chr7:116611972-116612426	MCF-7	breast:	n/a	n/a
41	HCFC1	chr7:116611720-116611746	K562	blood:	n/a	n/a
42	HCFC1	chr7:116610399-116610574	K562	blood:	n/a	n/a
43	HDAC2	chr7:116612028-116612336	HepG2	liver:	n/a	n/a
44	HEY1	chr7:116612839-116613049	K562	blood:	n/a	n/a
45	HEY1	chr7:116612856-116613073	HepG2	liver:	n/a	n/a
46	HNF4G	chr7:116612026-116612290	HepG2	liver:	n/a	chr7:116612135-116612147
47	IKZF1	chr7:116610314-116610954	GM12878	blood:	n/a	n/a
48	IRF1	chr7:116611472-116611480	K562	blood:	n/a	n/a
49	JUN	chr7:116610862-116611009	K562	blood:	n/a	n/a
50	JUND	chr7:116611302-116611390	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:116610238-116610288	HepG2	liver:	n/a
2	chr7:116610238-116610288	RPTEC	kidney:	n/a
3	chr7:116610238-116610288	HCM	heart:	n/a
4	chr7:116610238-116610288	AG09309	skin:	n/a
5	chr7:116610238-116610288	GM12878	blood:	n/a
6	chr7:116610238-116610288	T-47D	breast:	n/a
7	chr7:116610238-116610288	ovcar-3	ovarian:	n/a
8	chr7:116610238-116610288	Hepatocyte	liver:	n/a
9	chr7:116610238-116610288	NHBE	bronchial:	n/a
10	chr7:116610238-116610288	SK-N-MC	brain:	n/a
11	chr7:116610238-116610288	H1-hESC	embryonic stem cell:	embryo
12	chr7:116610238-116610288	HNPCEpiC	eye:	n/a
13	chr7:116610238-116610288	Caco-2	colon:	n/a
14	chr7:116610238-116610288	SKMC	muscle:	n/a
15	chr7:116610238-116610288	NH-A	brain:	n/a
16	chr7:116610238-116610288	AG10803	skin:	n/a
17	chr7:116610238-116610288	AG09319	gingival:	n/a
18	chr7:116610238-116610288	SAEC	small airway:	n/a
19	chr7:116610238-116610288	SK-N-SH_RA	brain:	n/a
20	chr7:116610238-116610288	MCF-7	breast:	n/a
21	chr7:116610238-116610288	U87	brain:	n/a
22	chr7:116610238-116610288	Jurkat	blood:	n/a
23	chr7:116610238-116610288	HL-60	blood:	n/a
24	chr7:116610238-116610288	HMEC	breast:	n/a
25	chr7:116610238-116610288	HCF	heart:	n/a
26	chr7:116610238-116610288	AG04450	lung:	fetal
27	chr7:116610238-116610288	HRCEpiC	kidney:	n/a
28	chr7:116610238-116610288	GM12892	blood:	n/a
29	chr7:116610238-116610288	HCT-116	colon:	n/a
30	chr7:116610238-116610288	ECC-1	luminal epithelium:	n/a
31	chr7:116610238-116610288	MCF10A-Er-Src	breast:	n/a
32	chr7:116610238-116610288	HRPEpiC	eye:	n/a
33	chr7:116610238-116610288	PFSK-1	brain:	n/a
34	chr7:116610238-116610288	K562	blood:	n/a
35	chr7:116610238-116610288	HRE	kidney:	n/a
36	chr7:116610238-116610288	PANC-1	pancreas:	n/a
37	chr7:116610238-116610288	GM19239	blood:	n/a
38	chr7:116610238-116610288	A549	lung:	n/a
39	chr7:116610238-116610288	LNCaP	prostate:	n/a
40	chr7:116610238-116610288	SK-N-SH	brain:	n/a
41	chr7:116610238-116610288	HEK293	kidney:	embryo
42	chr7:116610238-116610288	BJ	skin:	n/a
43	chr7:116610238-116610288	IMR90	lung:	fetal
44	chr7:116610238-116610288	AG04449	skin:	fetal
45	chr7:116610238-116610288	NB4	blood:	n/a
46	chr7:116610238-116610288	CMK	blood:	n/a
47	chr7:116610238-116610288	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:116610238-116610288	PrEC	prostate:	n/a
49	chr7:116610238-116610288	BE2_C	brain:	n/a
50	chr7:116610238-116610288	AoSMC	blood vessel:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:116599684..116602391-chr7:116609129..116611076,2	MCF-7	breast:
2	7:116434729-116454408..7:116610596-116619447	H1-hESC	embryonic stem cell:	embryo
3	chr7:116616956..116618843-chr7:116623491..116625617,2	K562	blood:
4	chr7:116615230..116617091-chr7:116619480..116621250,2	K562	blood:
5	7:116610596-116619447..7:117114628-117119361	H1-hESC	embryonic stem cell:	embryo
6	chr7:116592500..116594356-chr7:116610942..116612554,2	K562	blood:
7	chr7:116517701..116519651-chr7:116609886..116612746,2	K562	blood:
8	7:116610596-116619447..7:116754962-116765597	GM12878	blood:
9	chr7:116595834..116597800-chr7:116612377..116614043,2	K562	blood:
10	chr7:116608803..116612859-chr7:116615821..116619025,5	K562	blood:
11	chr7:116601473..116604004-chr7:116608166..116610648,2	K562	blood:
12	chr7:116608803..116612859-chr7:116615821..116619025,5	K562	blood:
13	chr7:116590784..116596766-chr7:116599392..116609813,21	MCF-7	breast:
14	7:116610596-116619447..7:116651084-116657331	H1-hESC	embryonic stem cell:	embryo
15	7:115861595-115870968..7:116610596-116619447	GM12878	blood:
16	chr7:116614047..116614930-chr7:116624578..116625102,2	K562	blood:
17	chr7:116607594..116610667-chr7:116617183..116619569,3	MCF-7	breast:
18	chr7:116595788..116597544-chr7:116616683..116619041,2	K562	blood:
19	chr7:116569834..116572713-chr7:116615771..116619319,3	MCF-7	breast:
20	chr7:116558517..116560603-chr7:116609318..116611727,2	K562	blood:
21	7:115847372-115857098..7:116610596-116619447	H1-hESC	embryonic stem cell:	embryo
22	7:116610596-116619447..7:117432820-117434816	H1-hESC	embryonic stem cell:	embryo
23	7:116610596-116619447..7:116849860-116864942	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
TPM3P1	TF binding region
ENSG00000228368	TF binding region
TPM3P1	CpG island
ENSG00000228368	CpG island
ENSG00000004866	chromatin interactions
ENSG00000198898	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000001626	chromatin interactions
ENSG00000077063	chromatin interactions
ENSG00000227199	chromatin interactions
ENSG00000135269	chromatin interactions

Extended variants
information (count: 262 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75474009	chr7:116609029-116609030	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs576577050	chr7:116609050-116609051	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs143917224	chr7:116609097-116609098	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs368957366	chr7:116609102-116609103	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs192927768	chr7:116609112-116609113	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562315595	chr7:116609116-116609117	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs544159206	chr7:116609119-116609120	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs184227862	chr7:116609126-116609127	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs541768057	chr7:116609128-116609129	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs377644844	chr7:116609192-116609193	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs570261108	chr7:116609248-116609249	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs550508659	chr7:116609249-116609250	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs536036559	chr7:116609259-116609260	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs562838103	chr7:116609273-116609274	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs533396124	chr7:116609278-116609279	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs371982659	chr7:116609279-116609280	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs555729499	chr7:116609291-116609292	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs187097716	chr7:116609316-116609317	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs371108614	chr7:116609350-116609351	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs150088915	chr7:116609356-116609357	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs570094713	chr7:116609363-116609364	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs191807984	chr7:116609400-116609401	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs548859516	chr7:116609422-116609423	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs567478644	chr7:116609458-116609459	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs574452282	chr7:116609477-116609478	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs534582168	chr7:116609478-116609479	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs147285000	chr7:116609535-116609536	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs73714359	chr7:116609540-116609541	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs114652048	chr7:116609768-116609769	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs73472897	chr7:116609794-116609795	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575207801	chr7:116609835-116609836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542709495	chr7:116609863-116609864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555652243	chr7:116610022-116610023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574192267	chr7:116610084-116610085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183935811	chr7:116610089-116610090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560113912	chr7:116610117-116610118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12672497	chr7:116610141-116610142	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs143823862	chr7:116610177-116610178	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs7797217	chr7:116610237-116610238	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs563705954	chr7:116610238-116610239	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs530882634	chr7:116610339-116610340	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs141541032	chr7:116610351-116610352	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369218917	chr7:116610352-116610353	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs180887046	chr7:116610390-116610391	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs79826049	chr7:116610499-116610500	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs546488241	chr7:116610551-116610552	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs185568212	chr7:116610564-116610565	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs538553801	chr7:116610603-116610604	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs550259629	chr7:116610613-116610614	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs568856827	chr7:116610625-116610626	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Breast cancer	16397240	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	22291905	CNVD
Lung cancer	21911935	CNVD
Squamous cell cancer	20885788	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	21569311	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116595200-116621600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:116595600-116617200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:116596400-116616600	Weak transcription	Osteobl	bone
4	chr7:116596400-116622200	Weak transcription	Fetal Intestine Large	intestine
5	chr7:116596600-116612000	Weak transcription	Fetal Intestine Small	intestine
6	chr7:116596600-116617400	Weak transcription	Fetal Muscle Leg	muscle
7	chr7:116596800-116609600	Weak transcription	Right Atrium	heart
8	chr7:116596800-116609600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr7:116596800-116617200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:116597000-116641600	Weak transcription	Ovary	ovary
11	chr7:116597200-116610000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:116597800-116610200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:116598400-116610400	Weak transcription	HepG2	liver
14	chr7:116598400-116617600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:116598800-116609800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr7:116598800-116609800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:116598800-116610400	Weak transcription	Left Ventricle	heart
18	chr7:116598800-116630400	Weak transcription	Aorta	Aorta
19	chr7:116599200-116611800	Weak transcription	Right Ventricle	heart
20	chr7:116599600-116609600	Weak transcription	K562	blood
21	chr7:116600600-116613400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:116600600-116620200	Weak transcription	Lung	lung
23	chr7:116603400-116617800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:116603600-116610600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:116604600-116609400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:116604600-116609600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:116604800-116610200	Weak transcription	Liver	Liver
28	chr7:116606600-116611000	Enhancers	Fetal Heart	heart
29	chr7:116607000-116609400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:116607400-116610400	Weak transcription	NHDF-Ad	bronchial
31	chr7:116607600-116609400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr7:116607600-116609400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr7:116607600-116609400	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr7:116607600-116609600	Weak transcription	Pancreas	Pancrea
35	chr7:116607600-116610200	Weak transcription	Psoas Muscle	Psoas
36	chr7:116607600-116610200	Weak transcription	Hela-S3	cervix
37	chr7:116607600-116610600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:116607600-116611800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr7:116607600-116614000	Weak transcription	Brain Anterior Caudate	brain
40	chr7:116607600-116618000	Weak transcription	Spleen	Spleen
41	chr7:116607600-116622200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr7:116607600-116632400	Weak transcription	Gastric	stomach
43	chr7:116607800-116612600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:116608000-116612800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:116608200-116609400	Weak transcription	GM12878-XiMat	blood
46	chr7:116608600-116609000	Enhancers	Fetal Brain Male	brain
47	chr7:116608600-116610400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:116608600-116610800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr7:116608600-116611000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr7:116608800-116609000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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