Variant report

Variant	nsv817332
Chromosome Location	chr7:145811034-145829299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:1040)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:145813392-145814179	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:145812851-145813178	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:145824603-145824809	K562	blood:	n/a	chr7:145824732-145824741 chr7:145824733-145824742 chr7:145824732-145824741
4	BHLHE40	chr7:145812888-145813075	K562	blood:	n/a	n/a
5	CBX3	chr7:145812871-145813165	K562	blood:	n/a	n/a
6	CBX3	chr7:145812824-145813236	K562	blood:	n/a	n/a
7	CCNT2	chr7:145813050-145813510	K562	blood:	n/a	n/a
8	CCNT2	chr7:145813815-145814042	K562	blood:	n/a	n/a
9	CEBPB	chr7:145816237-145816462	HepG2	liver:	n/a	chr7:145816401-145816412
10	CEBPB	chr7:145818808-145819059	K562	blood:	n/a	chr7:145818945-145818958
11	CHD1	chr7:145812804-145813353	H1-hESC	embryonic stem cell:	n/a	chr7:145813043-145813053
12	CHD2	chr7:145825258-145825274	GM12878	blood:	n/a	n/a
13	CHD2	chr7:145813014-145813128	K562	blood:	n/a	chr7:145813043-145813053
14	CHD2	chr7:145812779-145814147	H1-hESC	embryonic stem cell:	n/a	chr7:145813043-145813053
15	CTBP2	chr7:145812742-145814278	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr7:145828960-145829110	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr7:145826500-145826687	GM12878	blood:	n/a	n/a
18	CTCF	chr7:145826440-145826590	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr7:145813900-145814050	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr7:145812900-145813050	HCM	heart:	n/a	n/a
21	CTCF	chr7:145816220-145816370	AG09319	gingival:	n/a	n/a
22	CTCF	chr7:145816196-145816364	Medullo	brain:	n/a	n/a
23	CTCF	chr7:145813920-145814070	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr7:145812920-145813070	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr7:145828986-145829069	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:145812937-145813014	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:145813440-145813590	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr7:145812901-145813035	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:145813680-145813830	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr7:145816200-145816350	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr7:145813996-145814017	Fibrobl	skin:	n/a	n/a
32	CTCF	chr7:145828977-145829048	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:145812940-145813090	HRE	kidney:	n/a	n/a
34	CTCF	chr7:145816160-145816310	AG09319	gingival:	n/a	n/a
35	CTCF	chr7:145813900-145814050	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:145824348-145824444	K562	blood:	n/a	n/a
37	CTCF	chr7:145813880-145814030	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:145812940-145813090	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr7:145813880-145814030	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr7:145812860-145813010	HRE	kidney:	n/a	n/a
41	CTCF	chr7:145824280-145824430	HEK293	kidney:	n/a	n/a
42	CTCF	chr7:145824359-145824412	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:145824265-145824565	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr7:145812955-145813002	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:145816180-145816330	HEK293	kidney:	n/a	n/a
46	CTCF	chr7:145826481-145826596	LNCaP	prostate:	n/a	n/a
47	CTCF	chr7:145828919-145829007	ProgFib	skin:	n/a	n/a
48	CTCF	chr7:145812905-145813127	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:145828871-145829130	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr7:145812940-145813090	WERI-Rb-1	eye:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145813417-145813467	H1-hESC	embryonic stem cell:	embryo
2	chr7:145813008-145813058	NH-A	brain:	n/a
3	chr7:145813008-145813058	T-47D	breast:	n/a
4	chr7:145813417-145813467	H1-hESC	embryonic stem cell:	embryo
5	chr7:145813008-145813058	NH-A	brain:	n/a
6	chr7:145813008-145813058	T-47D	breast:	n/a
7	chr7:145812842-145812892	MCF-7	breast:	n/a
8	chr7:145813413-145813463	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:145813494-145813544	ProgFib	skin:	n/a
10	chr7:145813066-145813116	NHBE	bronchial:	n/a
11	chr7:145813432-145813482	SAEC	small airway:	n/a
12	chr7:145814003-145814053	SK-N-SH	brain:	n/a
13	chr7:145813008-145813058	SK-N-MC	brain:	n/a
14	chr7:145813432-145813482	ovcar-3	ovarian:	n/a
15	chr7:145813417-145813467	NHBE	bronchial:	n/a
16	chr7:145813437-145813487	NB4	blood:	n/a
17	chr7:145813432-145813482	NHDF-neo	bronchial:	n/a
18	chr7:145813946-145813996	GM12878	blood:	n/a
19	chr7:145812871-145812921	HepG2	liver:	n/a
20	chr7:145814152-145814202	T-47D	breast:	n/a
21	chr7:145813915-145813965	HCT-116	colon:	n/a
22	chr7:145813421-145813471	NB4	blood:	n/a
23	chr7:145813494-145813544	Caco-2	colon:	n/a
24	chr7:145813008-145813058	HCPEpiC	choroid plexus:	n/a
25	chr7:145813066-145813116	Jurkat	blood:	n/a
26	chr7:145812871-145812921	H1-hESC	embryonic stem cell:	embryo
27	chr7:145813031-145813081	SKMC	muscle:	n/a
28	chr7:145814306-145814356	Hepatocyte	liver:	n/a
29	chr7:145813439-145813489	NB4	blood:	n/a
30	chr7:145813417-145813467	SAEC	small airway:	n/a
31	chr7:145812842-145812892	HMEC	breast:	n/a
32	chr7:145813008-145813058	HIPEpiC	eye:	n/a
33	chr7:145812871-145812921	NB4	blood:	n/a
34	chr7:145813066-145813116	PrEC	prostate:	n/a
35	chr7:145813432-145813482	RPTEC	kidney:	n/a
36	chr7:145814152-145814202	HCT-116	colon:	n/a
37	chr7:145812842-145812892	CMK	blood:	n/a
38	chr7:145813066-145813116	HRE	kidney:	n/a
39	chr7:145813413-145813463	HNPCEpiC	eye:	n/a
40	chr7:145813031-145813081	H1-hESC	embryonic stem cell:	embryo
41	chr7:145813432-145813482	HCT-116	colon:	n/a
42	chr7:145812842-145812892	GM12891	blood:	n/a
43	chr7:145813439-145813489	ovcar-3	ovarian:	n/a
44	chr7:145813915-145813965	SK-N-SH_RA	brain:	n/a
45	chr7:145812871-145812921	HRPEpiC	eye:	n/a
46	chr7:145814003-145814053	U87	brain:	n/a
47	chr7:145813417-145813467	ProgFib	skin:	n/a
48	chr7:145813915-145813965	HMEC	breast:	n/a
49	chr7:145813432-145813482	HMEC	breast:	n/a
50	chr7:145813008-145813058	GM12878	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:145800703..145803223-chr7:145808125..145812343,3	K562	blood:
2	chr7:145816235..145818075-chr7:145818635..145820633,2	K562	blood:
3	chr7:118909733..118910708-chr7:145816212..145816735,2	MCF-7	breast:
4	chr7:145816235..145818075-chr7:145818635..145820633,2	K562	blood:
5	chr7:145805690..145807503-chr7:145809091..145811939,2	K562	blood:

No data

Variant related genes	Relation type
CNTNAP2	TF binding region
CNTNAP2	CpG island

Extended variants
information (count: 210 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:210 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373814623	chr7:145811323-145811324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs189996161	chr7:145811348-145811349	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569629012	chr7:145811378-145811379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs538196683	chr7:145811398-145811399	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs4109905	chr7:145811836-145811837	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs548823041	chr7:145811856-145811857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs74712482	chr7:145811896-145811897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372314447	chr7:145811944-145811945	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs142882223	chr7:145811956-145811957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs370614964	chr7:145811960-145811961	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs538170002	chr7:145811971-145811972	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs376580158	chr7:145811986-145811987	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141261972	chr7:145812036-145812037	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs185418476	chr7:145812079-145812080	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs550222829	chr7:145812083-145812084	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568770932	chr7:145812117-145812118	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs143392658	chr7:145812149-145812150	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs548058646	chr7:145812176-145812177	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs533839071	chr7:145812200-145812201	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs377282467	chr7:145812230-145812231	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs118010185	chr7:145812269-145812270	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539947078	chr7:145812308-145812309	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7779642	chr7:145812354-145812355	Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs576378696	chr7:145812396-145812397	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs112088549	chr7:145812408-145812409	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs116731157	chr7:145812409-145812410	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs368913518	chr7:145812455-145812456	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs555463983	chr7:145812494-145812495	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs571264636	chr7:145812507-145812508	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs189929274	chr7:145812583-145812584	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs148364685	chr7:145812651-145812652	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs559164717	chr7:145812654-145812655	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs527816894	chr7:145812664-145812665	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs141581820	chr7:145812670-145812671	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs117686361	chr7:145812731-145812732	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563367982	chr7:145812732-145812733	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs183263834	chr7:145812736-145812737	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs548989906	chr7:145812760-145812761	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs187427008	chr7:145812781-145812782	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs529653865	chr7:145812814-145812815	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs191393434	chr7:145812822-145812823	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs566277105	chr7:145812909-145812910	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs372665264	chr7:145812914-145812915	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs551596077	chr7:145812940-145812941	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs570168834	chr7:145812962-145812963	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs537129598	chr7:145812977-145812978	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs555780056	chr7:145812990-145812991	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs183848565	chr7:145813031-145813032	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs150447075	chr7:145813047-145813048	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs552802046	chr7:145813052-145813053	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145812000-145812600	Enhancers	Brain Germinal Matrix	brain
2	chr7:145812000-145813600	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr7:145812200-145812600	Enhancers	Fetal Brain Male	brain
4	chr7:145812200-145813600	Active TSS	Brain Anterior Caudate	brain
5	chr7:145812200-145815200	Active TSS	Brain Angular Gyrus	brain
6	chr7:145812400-145812600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:145812400-145812600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr7:145812400-145812600	Enhancers	Fetal Lung	lung
9	chr7:145812400-145812800	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:145812400-145813600	Active TSS	Brain Hippocampus Middle	brain
11	chr7:145812400-145815200	Active TSS	Fetal Brain Female	brain
12	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
13	chr7:145812600-145812800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:145812600-145812800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
16	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
17	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
18	chr7:145812600-145812800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:145812600-145812800	Enhancers	Primary hematopoietic stem cells	blood
20	chr7:145812600-145812800	Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr7:145812600-145812800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
22	chr7:145812600-145812800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:145812600-145812800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:145812600-145812800	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr7:145812600-145812800	Flanking Active TSS	Brain Substantia Nigra	brain
27	chr7:145812600-145812800	Enhancers	Fetal Heart	heart
28	chr7:145812600-145812800	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
29	chr7:145812600-145812800	Enhancers	Fetal Muscle Trunk	muscle
30	chr7:145812600-145812800	Enhancers	Fetal Muscle Leg	muscle
31	chr7:145812600-145812800	Active TSS	Fetal Stomach	stomach
32	chr7:145812600-145812800	Enhancers	Ovary	ovary
33	chr7:145812600-145812800	Enhancers	Pancreas	Pancrea
34	chr7:145812600-145813000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:145812600-145813000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:145812600-145813000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:145812600-145813000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:145812600-145813000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:145812600-145813000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr7:145812600-145813000	Flanking Active TSS	Fetal Lung	lung
41	chr7:145812600-145813000	Bivalent Enhancer	Fetal Thymus	thymus
42	chr7:145812600-145813400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:145812600-145813400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:145812600-145813400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:145812600-145813800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr7:145812600-145814000	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr7:145812600-145814000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:145812600-145814000	Active TSS	Brain Cingulate Gyrus	brain
49	chr7:145812600-145814000	Active TSS	Fetal Brain Male	brain
50	chr7:145812600-145814200	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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