Variant report

Variant	nsv1021251
Chromosome Location	chr7:146522341-146802125
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	ATF1	chr7:146554072-146554083	K562	blood:	n/a	n/a
2	BACH1	chr7:146796893-146796911	K562	blood:	n/a	n/a
3	BATF	chr7:146793808-146794055	GM12878	blood:	n/a	n/a
4	CCNT2	chr7:146578068-146578178	K562	blood:	n/a	n/a
5	CEBPB	chr7:146532369-146532435	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr7:146793958-146794294	HepG2	liver:	n/a	chr7:146794140-146794153 chr7:146794140-146794151
7	CEBPB	chr7:146571852-146572197	IMR90	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
8	CEBPB	chr7:146550317-146550587	A549	lung:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
9	CEBPB	chr7:146738575-146738797	HepG2	liver:	n/a	chr7:146738715-146738732 chr7:146738754-146738767
10	CEBPB	chr7:146769642-146769941	A549	lung:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
11	CEBPB	chr7:146547738-146547759	K562	blood:	n/a	n/a
12	CEBPB	chr7:146673718-146673968	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:146645855-146646062	A549	lung:	n/a	n/a
14	CEBPB	chr7:146650551-146650805	IMR90	lung:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
15	CEBPB	chr7:146690528-146690601	K562	blood:	n/a	chr7:146690555-146690566
16	CEBPB	chr7:146653286-146653563	HepG2	liver:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
17	CEBPB	chr7:146631945-146632234	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:146658691-146659162	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr7:146547720-146547928	HepG2	liver:	n/a	chr7:146547770-146547781
20	CEBPB	chr7:146769663-146769977	K562	blood:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
21	CEBPB	chr7:146582398-146582629	ECC-1	luminal epithelium:	n/a	chr7:146582542-146582553
22	CEBPB	chr7:146653225-146653552	A549	lung:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
23	CEBPB	chr7:146571842-146572194	H1-hESC	embryonic stem cell:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
24	CEBPB	chr7:146631955-146632230	A549	lung:	n/a	n/a
25	CEBPB	chr7:146650625-146650798	K562	blood:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
26	CEBPB	chr7:146769642-146769942	IMR90	lung:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
27	CEBPB	chr7:146571860-146572193	HepG2	liver:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
28	CEBPB	chr7:146690401-146690637	IMR90	lung:	n/a	chr7:146690555-146690566
29	CEBPB	chr7:146690433-146690694	H1-hESC	embryonic stem cell:	n/a	chr7:146690555-146690566
30	CEBPB	chr7:146769719-146769861	H1-hESC	embryonic stem cell:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
31	CEBPB	chr7:146690455-146690710	HepG2	liver:	n/a	chr7:146690555-146690566
32	CEBPB	chr7:146573237-146573380	HepG2	liver:	n/a	chr7:146573302-146573313
33	CEBPB	chr7:146794034-146794272	A549	lung:	n/a	chr7:146794140-146794153 chr7:146794140-146794151
34	CEBPB	chr7:146550344-146550639	HepG2	liver:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
35	CEBPB	chr7:146702238-146702507	HepG2	liver:	n/a	chr7:146702320-146702331 chr7:146702320-146702333
36	CEBPB	chr7:146571872-146572192	A549	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
37	CEBPB	chr7:146571827-146572187	K562	blood:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
38	CEBPB	chr7:146769619-146769984	HepG2	liver:	n/a	chr7:146769802-146769813 chr7:146769801-146769812
39	CEBPZ	chr7:146762179-146762302	HepG2	liver:	n/a	n/a
40	CREB1	chr7:146658679-146659194	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr7:146658220-146658370	HRPEpiC	eye:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
42	CTCF	chr7:146776318-146776419	ProgFib	skin:	n/a	n/a
43	CTCF	chr7:146776260-146776410	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:146658237-146658455	H1-hESC	embryonic stem cell:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
45	CTCF	chr7:146658200-146658350	MCF-7	breast:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
46	CTCF	chr7:146776340-146776490	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr7:146658075-146658460	H1-hESC	embryonic stem cell:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
48	CTCF	chr7:146657184-146657206	GM10266	blood:	n/a	n/a
49	CTCF	chr7:146658220-146658370	Caco-2	colon:	n/a	chr7:146658320-146658341 chr7:146658325-146658343 chr7:146658279-146658288
50	CTCF	chr7:146776280-146776430	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146603166-146603216	AG04449	skin:	fetal
2	chr7:146603166-146603216	AG04449	skin:	fetal
3	chr7:146635353-146635403	T-47D	breast:	n/a
4	chr7:146572638-146572688	AG09319	gingival:	n/a
5	chr7:146635353-146635403	GM19239	blood:	n/a
6	chr7:146603166-146603216	HEK293	kidney:	embryo
7	chr7:146603166-146603216	ProgFib	skin:	n/a
8	chr7:146603166-146603216	NH-A	brain:	n/a
9	chr7:146572638-146572688	AG04450	lung:	fetal
10	chr7:146635353-146635403	SK-N-MC	brain:	n/a
11	chr7:146603166-146603216	HRPEpiC	eye:	n/a
12	chr7:146635353-146635403	HepG2	liver:	n/a
13	chr7:146572638-146572688	NHDF-neo	bronchial:	n/a
14	chr7:146635353-146635403	Hela-S3	cervix:	n/a
15	chr7:146603166-146603216	AG10803	skin:	n/a
16	chr7:146603166-146603216	Hela-S3	cervix:	n/a
17	chr7:146635353-146635403	HCM	heart:	n/a
18	chr7:146603166-146603216	NHDF-neo	bronchial:	n/a
19	chr7:146572638-146572688	GM19239	blood:	n/a
20	chr7:146635353-146635403	Jurkat	blood:	n/a
21	chr7:146635353-146635403	HRE	kidney:	n/a
22	chr7:146603166-146603216	A549	lung:	n/a
23	chr7:146603166-146603216	MCF-7	breast:	n/a
24	chr7:146635353-146635403	Hepatocyte	liver:	n/a
25	chr7:146603166-146603216	AG09309	skin:	n/a
26	chr7:146572638-146572688	AG09309	skin:	n/a
27	chr7:146603166-146603216	Caco-2	colon:	n/a
28	chr7:146572638-146572688	HRE	kidney:	n/a
29	chr7:146572638-146572688	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:146572638-146572688	NHBE	bronchial:	n/a
31	chr7:146603166-146603216	SK-N-SH_RA	brain:	n/a
32	chr7:146635353-146635403	H1-hESC	embryonic stem cell:	embryo
33	chr7:146635353-146635403	Caco-2	colon:	n/a
34	chr7:146603166-146603216	Jurkat	blood:	n/a
35	chr7:146572638-146572688	ProgFib	skin:	n/a
36	chr7:146603166-146603216	AG04450	lung:	fetal
37	chr7:146635353-146635403	RPTEC	kidney:	n/a
38	chr7:146635353-146635403	HRCEpiC	kidney:	n/a
39	chr7:146635353-146635403	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:146572638-146572688	NH-A	brain:	n/a
41	chr7:146572638-146572688	HCPEpiC	choroid plexus:	n/a
42	chr7:146603166-146603216	HCPEpiC	choroid plexus:	n/a
43	chr7:146635353-146635403	CMK	blood:	n/a
44	chr7:146635353-146635403	HEK293	kidney:	embryo
45	chr7:146635353-146635403	AG04450	lung:	fetal
46	chr7:146603166-146603216	HNPCEpiC	eye:	n/a
47	chr7:146603166-146603216	MCF10A-Er-Src	breast:	n/a
48	chr7:146635353-146635403	SK-N-SH	brain:	n/a
49	chr7:146635353-146635403	HEEpiC	esophagus:	n/a
50	chr7:146572638-146572688	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
2	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
3	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
4	chr7:146728137..146729642-chr7:146730753..146732443,2	K562	blood:
5	chr7:146715781..146717659-chr7:146720196..146724156,3	K562	blood:
6	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
7	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
8	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
9	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
10	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
11	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
12	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
13	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
14	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
15	chr7:146500988..146503359-chr7:146527735..146530660,2	K562	blood:
16	chr7:146761282..146763181-chr7:146763573..146765951,2	K562	blood:
17	chr11:86510283..86512929-chr7:146532947..146535829,2	MCF-7	breast:
18	chr7:146761282..146763181-chr7:146763573..146765951,2	K562	blood:
19	chr7:146771218..146771738-chrX:153626554..153627086,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EZH2-4	chr7:146782785-146782914	ENSG00000236795.1
2	lnc-EZH2-4	chr7:146794524-146794701	ENSG00000236795.1
3	lnc-EZH2-4	chr7:146779632-146780313	ENSG00000236795.1
4	lnc-EZH2-4	chr7:146778026-146779180	ENSG00000236795.1

Variant related genes	Relation type
ENSG00000236795	TF binding region
ENSG00000221766	TF binding region
ENSG00000236795	CpG island
ENSG00000221766	CpG island
ENSG00000147403	chromatin interactions
ENSG00000150687	chromatin interactions

Extended variants
information (count: 4326 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4326 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532411407	chr7:146522346-146522347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs151185190	chr7:146522351-146522352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569039212	chr7:146522356-146522357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537934330	chr7:146522361-146522362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140287213	chr7:146522385-146522386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185287072	chr7:146522416-146522417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113212187	chr7:146522469-146522470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534231306	chr7:146522501-146522502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554407558	chr7:146522507-146522508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62481404	chr7:146522528-146522529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150022496	chr7:146522532-146522533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190046231	chr7:146522535-146522536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145237382	chr7:146522537-146522538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544259546	chr7:146522567-146522568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567137396	chr7:146522574-146522575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182298299	chr7:146522587-146522588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368180139	chr7:146522623-146522624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574528357	chr7:146522658-146522659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552052160	chr7:146522663-146522664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7809945	chr7:146522667-146522668	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs549356019	chr7:146522752-146522753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142367315	chr7:146522789-146522790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531737764	chr7:146522806-146522807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550105068	chr7:146522808-146522809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545828282	chr7:146522849-146522850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562509973	chr7:146522869-146522870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146308209	chr7:146522895-146522896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548619278	chr7:146522920-146522921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139369327	chr7:146522931-146522932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527930256	chr7:146522982-146522983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532606386	chr7:146523038-146523039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547668849	chr7:146523040-146523041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571187676	chr7:146523059-146523060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188606006	chr7:146523061-146523062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371606410	chr7:146523087-146523088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377297305	chr7:146523088-146523089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568841508	chr7:146523115-146523116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537546881	chr7:146523144-146523145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554607916	chr7:146523168-146523169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574445283	chr7:146523211-146523212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73459336	chr7:146523239-146523240	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs567614715	chr7:146523245-146523246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141805669	chr7:146523260-146523261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs9969182	chr7:146523381-146523382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76085799	chr7:146523387-146523388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562544464	chr7:146523400-146523401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192351253	chr7:146523408-146523409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541846356	chr7:146523442-146523443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371304299	chr7:146523533-146523534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566528069	chr7:146523554-146523555	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Glioma	20126413	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146522000-146523800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:146522400-146525000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:146522600-146523800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr7:146522600-146523800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr7:146522800-146523000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr7:146522800-146523800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:146522800-146523800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr7:146522800-146524200	Enhancers	Brain Germinal Matrix	brain
9	chr7:146523000-146523600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:146523000-146523800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:146523200-146523800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:146523200-146523800	Enhancers	Fetal Brain Female	brain
13	chr7:146523600-146523800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:146525000-146525800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:146525800-146526000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:146525800-146526000	Enhancers	Fetal Lung	lung
17	chr7:146526200-146526800	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr7:146529200-146529400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:146529400-146537800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:146536800-146537000	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:146546400-146547200	Enhancers	Brain Germinal Matrix	brain
22	chr7:146557400-146557600	Enhancers	Brain Germinal Matrix	brain
23	chr7:146557600-146558200	Weak transcription	Brain Germinal Matrix	brain
24	chr7:146558200-146558400	Enhancers	Brain Germinal Matrix	brain
25	chr7:146558400-146559600	Weak transcription	Brain Germinal Matrix	brain
26	chr7:146558800-146560200	Enhancers	Fetal Brain Male	brain
27	chr7:146559000-146560200	Enhancers	Fetal Brain Female	brain
28	chr7:146559400-146559600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:146559400-146559800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr7:146559600-146560600	Enhancers	Brain Germinal Matrix	brain
31	chr7:146561400-146561800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:146561400-146561800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:146561800-146562800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr7:146562800-146563000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr7:146571800-146573200	Enhancers	Fetal Brain Male	brain
36	chr7:146571800-146573800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:146572000-146572800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:146572000-146572800	Enhancers	Brain Germinal Matrix	brain
39	chr7:146572000-146573400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:146572000-146573400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:146572000-146574000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:146572000-146574200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:146572200-146572800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr7:146572200-146573400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:146572200-146573600	Enhancers	Fetal Brain Female	brain
46	chr7:146572400-146573400	Enhancers	Fetal Stomach	stomach
47	chr7:146572600-146573400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr7:146572600-146573400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr7:146572600-146573600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:146572800-146573200	Enhancers	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links