Variant report

Variant	nsv889241
Chromosome Location	chr7:136976713-137038092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:136992921-136992933	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr7:137028122-137028571	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:137023922-137024163	A549	lung:	n/a	n/a
4	CEBPB	chr7:137023920-137024145	IMR90	lung:	n/a	n/a
5	CEBPB	chr7:137020635-137020980	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:137023871-137024074	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:137020688-137020924	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr7:137028267-137028479	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr7:137028095-137028618	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr7:137028861-137028958	LNCaP	prostate:	n/a	n/a
11	CTCF	chr7:137005800-137005950	K562	blood:	n/a	n/a
12	CTCF	chr7:136984100-136984250	GM06990	blood:	n/a	n/a
13	CTCF	chr7:137022800-137022950	HFF	foreskin:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
14	CTCF	chr7:137022856-137022895	GM10266	blood:	n/a	n/a
15	CTCF	chr7:137022760-137022910	MCF-7	breast:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
16	CTCF	chr7:136989540-136989690	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:137013280-137013430	BE2_C	brain:	n/a	n/a
18	CTCF	chr7:137022840-137022990	HPF	lung:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
19	CTCF	chr7:136989420-136989570	HCM	heart:	n/a	n/a
20	CTCF	chr7:137028460-137028610	AG09319	gingival:	n/a	n/a
21	CTCF	chr7:137022700-137022850	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr7:137022791-137022948	GM12878	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
23	CTCF	chr7:137022796-137022798	GM19240	blood:	n/a	n/a
24	CTCF	chr7:137028480-137028630	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr7:137022784-137022936	LNCaP	prostate:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
26	CTCF	chr7:137022780-137022930	GM12873	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
27	CTCF	chr7:137022540-137022690	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr7:137022740-137022890	AG04449	skin:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
29	CTCF	chr7:137008548-137008569	GM20000	blood:	n/a	n/a
30	CTCF	chr7:137022640-137022790	HCM	heart:	n/a	n/a
31	CTCF	chr7:136989520-136989670	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr7:136989530-136989618	HepG2	liver:	n/a	n/a
33	CTCF	chr7:137022800-137022950	HMEC	breast:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
34	CTCF	chr7:137022780-137022930	RPTEC	kidney:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
35	CTCF	chr7:137022760-137022910	RPTEC	kidney:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
36	CTCF	chr7:137022800-137022950	NHLF	lung:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
37	CTCF	chr7:137022762-137022873	Fibrobl	skin:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
38	CTCF	chr7:137022740-137022890	K562	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
39	CTCF	chr7:137022740-137022890	HL-60	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
40	CTCF	chr7:137022777-137022928	Medullo	brain:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
41	CTCF	chr7:137022760-137022910	GM12872	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
42	CTCF	chr7:136989480-136989630	HVMF	connective:	n/a	n/a
43	CTCF	chr7:137022800-137022950	GM06990	blood:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
44	CTCF	chr7:137022740-137022890	HFF-Myc	foreskin:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
45	CTCF	chr7:137022820-137022970	BJ	skin:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
46	CTCF	chr7:137022780-137022930	Caco-2	colon:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
47	CTCF	chr7:137022619-137022949	H1-hESC	embryonic stem cell:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
48	CTCF	chr7:137022760-137022910	HepG2	liver:	n/a	chr7:137022848-137022866 chr7:137022843-137022864
49	CTCF	chr7:136989400-136989550	HCM	heart:	n/a	n/a
50	CTCF	chr7:137022740-137022890	WERI-Rb-1	eye:	n/a	chr7:137022848-137022866 chr7:137022843-137022864

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137028198-137028248	PrEC	prostate:	n/a
2	chr7:137028972-137029022	HIPEpiC	eye:	n/a
3	chr7:137002261-137002311	HRPEpiC	eye:	n/a
4	chr7:137003665-137003715	AG04449	skin:	fetal
5	chr7:137027135-137027185	SAEC	small airway:	n/a
6	chr7:137028410-137028460	HRCEpiC	kidney:	n/a
7	chr7:137028617-137028667	AG09309	skin:	n/a
8	chr7:137028604-137028654	GM06990	blood:	n/a
9	chr7:137028546-137028596	HCPEpiC	choroid plexus:	n/a
10	chr7:137028165-137028215	H1-hESC	embryonic stem cell:	embryo
11	chr7:137028972-137029022	RPTEC	kidney:	n/a
12	chr7:137032114-137032164	CMK	blood:	n/a
13	chr7:137029097-137029147	HRE	kidney:	n/a
14	chr7:137028198-137028248	GM19239	blood:	n/a
15	chr7:137028442-137028492	HEEpiC	esophagus:	n/a
16	chr7:137028198-137028248	GM12878	blood:	n/a
17	chr7:137028972-137029022	HUVEC	blood vessel:	n/a
18	chr7:137013465-137013515	HRCEpiC	kidney:	n/a
19	chr7:137011196-137011246	CMK	blood:	n/a
20	chr7:137003665-137003715	ECC-1	luminal epithelium:	n/a
21	chr7:137002261-137002311	GM12891	blood:	n/a
22	chr7:137013465-137013515	NHDF-neo	bronchial:	n/a
23	chr7:137028410-137028460	HAEpiC	amniotic membrane:	n/a
24	chr7:137028546-137028596	A549	lung:	n/a
25	chr7:136989898-136989948	H1-hESC	embryonic stem cell:	embryo
26	chr7:137028442-137028492	Caco-2	colon:	n/a
27	chr7:137028604-137028654	NH-A	brain:	n/a
28	chr7:137028198-137028248	AG10803	skin:	n/a
29	chr7:137032114-137032164	BJ	skin:	n/a
30	chr7:137028198-137028248	HL-60	blood:	n/a
31	chr7:137028410-137028460	HCM	heart:	n/a
32	chr7:137028546-137028596	HEK293	kidney:	embryo
33	chr7:137028198-137028248	NHBE	bronchial:	n/a
34	chr7:137002261-137002311	HEEpiC	esophagus:	n/a
35	chr7:137029097-137029147	PANC-1	pancreas:	n/a
36	chr7:137028617-137028667	IMR90	lung:	fetal
37	chr7:137029097-137029147	NB4	blood:	n/a
38	chr7:137002261-137002311	HCT-116	colon:	n/a
39	chr7:136989898-136989948	LNCaP	prostate:	n/a
40	chr7:137028442-137028492	RPTEC	kidney:	n/a
41	chr7:137028389-137028439	K562	blood:	n/a
42	chr7:137029097-137029147	Hepatocyte	liver:	n/a
43	chr7:137028389-137028439	Hepatocyte	liver:	n/a
44	chr7:137028442-137028492	K562	blood:	n/a
45	chr7:137013465-137013515	AoSMC	blood vessel:	n/a
46	chr7:137028410-137028460	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:137003665-137003715	SK-N-SH	brain:	n/a
48	chr7:137032114-137032164	NH-A	brain:	n/a
49	chr7:137028972-137029022	CMK	blood:	n/a
50	chr7:137028972-137029022	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:136853684..136854424-chr7:137022605..137023178,2	MCF-7	breast:
2	chr7:137026451..137029166-chr7:137034024..137036129,2	K562	blood:
3	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
4	chr7:136853636..136854568-chr7:137022322..137023760,5	MCF-7	breast:
5	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:
6	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTN-1	chr7:137037223-137037354	NONHSAT123582
2	lnc-PTN-1	chr7:137029676-137029876	XLOC_006620
3	lnc-PTN-1	chr7:137029676-137029876	ENSG00000228031.2
4	lnc-PTN-1	chr7:137037223-137037354	XLOC_006620
5	lnc-PTN-1	chr7:137035099-137035212	NONHSAT123582
6	lnc-CHRM2-1	chr7:137010132-137011700	ENSG00000231114
7	lnc-CHRM2-1	chr7:137003339-137003604	ENSG00000231114
8	lnc-PTN-1	chr7:137035115-137035216	XLOC_006620
9	lnc-PTN-1	chr7:137035115-137035212	ENSG00000228031.2
10	lnc-PTN-1	chr7:137037223-137037354	ENSG00000228031.2

Variant related genes	Relation type
PTN	TF binding region
ENSG00000231114	TF binding region
PTN	CpG island
ENSG00000231114	CpG island
ENSG00000105894	chromatin interactions
NSF	miRNA target sites
SEC61A1	miRNA target sites
ADARB1	miRNA target sites

Extended variants
information (count: 2264 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2264 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10248429	chr7:136976713-136976714	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147983721	chr7:136976718-136976719	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377520837	chr7:136976774-136976775	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190917156	chr7:136976798-136976799	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536665705	chr7:136976856-136976857	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556472449	chr7:136976865-136976866	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142315775	chr7:136976878-136976879	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545732740	chr7:136976897-136976898	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181724323	chr7:136976906-136976907	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555179651	chr7:136976917-136976918	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185944796	chr7:136976933-136976934	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541193356	chr7:136976943-136976944	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560673073	chr7:136977018-136977019	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529695857	chr7:136977053-136977054	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543059412	chr7:136977081-136977082	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563335154	chr7:136977102-136977103	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35756146	chr7:136977133-136977134	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1835534	chr7:136977138-136977139	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs552473107	chr7:136977154-136977155	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs322258	chr7:136977163-136977164	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs1835536	chr7:136977203-136977204	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs201368570	chr7:136977240-136977241	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548374882	chr7:136977249-136977250	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567763049	chr7:136977250-136977251	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536795703	chr7:136977268-136977269	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569347347	chr7:136977269-136977270	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570062532	chr7:136977311-136977312	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538644371	chr7:136977420-136977421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559219296	chr7:136977429-136977430	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572376921	chr7:136977449-136977450	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556530367	chr7:136977487-136977488	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138492528	chr7:136977558-136977559	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577981428	chr7:136977561-136977562	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574681000	chr7:136977565-136977566	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543549336	chr7:136977605-136977606	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562680746	chr7:136977617-136977618	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563215743	chr7:136977668-136977669	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532167246	chr7:136977727-136977728	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547906866	chr7:136977741-136977742	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113561497	chr7:136977753-136977754	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150679486	chr7:136977781-136977782	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528345863	chr7:136977838-136977839	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368652308	chr7:136977856-136977857	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116431528	chr7:136977861-136977862	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371826379	chr7:136977969-136977970	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548411939	chr7:136977979-136977980	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139832470	chr7:136978000-136978001	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371506009	chr7:136978033-136978034	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530599277	chr7:136978068-136978069	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564520189	chr7:136978070-136978071	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136938200-136980600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:136961400-136980600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:136968600-136989600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:136972000-136978400	Weak transcription	Brain Substantia Nigra	brain
5	chr7:136972200-136978000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr7:136972200-136979400	Weak transcription	Brain Angular Gyrus	brain
7	chr7:136972200-136990400	Weak transcription	Fetal Stomach	stomach
8	chr7:136972800-136978800	Weak transcription	Brain Hippocampus Middle	brain
9	chr7:136974000-136977200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:136974600-136982600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr7:136974600-136983600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:136975200-136977200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:136975200-136982600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:136975200-136991000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:136976200-136977000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr7:136976200-136979200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
17	chr7:136976600-136991000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr7:136977000-136977400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr7:136977200-136980000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:136977200-136980600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:136977400-136978200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr7:136978000-136978200	Enhancers	Brain Cingulate Gyrus	brain
23	chr7:136978200-136979000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:136978200-136983400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr7:136978400-136979400	Enhancers	Brain Substantia Nigra	brain
26	chr7:136978800-136981200	Enhancers	Brain Hippocampus Middle	brain
27	chr7:136979000-136979400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr7:136979000-136981000	Enhancers	Brain Cingulate Gyrus	brain
29	chr7:136979200-136979600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr7:136979200-136989800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr7:136979400-136979800	Enhancers	Brain Angular Gyrus	brain
32	chr7:136979400-136980400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr7:136979400-136980600	Weak transcription	Brain Substantia Nigra	brain
34	chr7:136979400-136990800	Enhancers	Brain Anterior Caudate	brain
35	chr7:136979600-136982200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:136979800-136982200	Weak transcription	Brain Angular Gyrus	brain
37	chr7:136980000-136981000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:136980000-136981600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:136980400-136984200	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr7:136980600-136980800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:136980600-136980800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:136980600-136980800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:136980600-136981200	Enhancers	Brain Substantia Nigra	brain
44	chr7:136980600-136981600	Enhancers	Fetal Lung	lung
45	chr7:136980600-136982000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:136980600-136982200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:136980600-136982800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr7:136980600-136983800	Enhancers	Fetal Heart	heart
49	chr7:136980600-136984600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:136980800-136981000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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