Variant report

Variant	nsv889448
Chromosome Location	chr7:149741002-149880262
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	ARID3A	chr7:149822922-149823231	HepG2	liver:	n/a	n/a
2	ATF1	chr7:149742080-149742094	K562	blood:	n/a	n/a
3	BACH1	chr7:149746378-149746646	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:149743485-149743750	GM12878	blood:	n/a	n/a
5	BATF	chr7:149757655-149757938	GM12878	blood:	n/a	chr7:149757827-149757838
6	BCL3	chr7:149855744-149856234	GM12878	blood:	n/a	n/a
7	BCL3	chr7:149836967-149837225	GM12878	blood:	n/a	n/a
8	BCL3	chr7:149808531-149808727	GM12878	blood:	n/a	n/a
9	BCL3	chr7:149808506-149808789	GM12878	blood:	n/a	n/a
10	BCL3	chr7:149855735-149856134	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:149855946-149856146	K562	blood:	n/a	n/a
12	BHLHE40	chr7:149823075-149823280	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:149822919-149823295	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:149798171-149798831	Hela-S3	cervix:	n/a	chr7:149798497-149798510 chr7:149798497-149798508
15	CEBPB	chr7:149822945-149823293	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:149822923-149823294	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:149786230-149786562	Hela-S3	cervix:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
18	CEBPB	chr7:149786163-149786592	HepG2	liver:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
19	CEBPB	chr7:149853126-149853388	HepG2	liver:	n/a	chr7:149853311-149853324
20	CEBPB	chr7:149786189-149786644	K562	blood:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
21	CEBPB	chr7:149786165-149786549	H1-hESC	embryonic stem cell:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
22	CEBPB	chr7:149784693-149784950	HepG2	liver:	n/a	chr7:149784796-149784807
23	CEBPB	chr7:149786176-149786566	IMR90	lung:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
24	CEBPB	chr7:149875817-149875915	K562	blood:	n/a	chr7:149875881-149875894
25	CEBPB	chr7:149804465-149804596	A549	lung:	n/a	n/a
26	CEBPB	chr7:149791079-149791364	H1-hESC	embryonic stem cell:	n/a	chr7:149791213-149791222 chr7:149791213-149791224
27	CEBPB	chr7:149791162-149791277	HepG2	liver:	n/a	chr7:149791213-149791222 chr7:149791213-149791224
28	CEBPB	chr7:149822980-149823212	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:149786250-149786562	A549	lung:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
30	CHD1	chr7:149746398-149746684	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:149746382-149746488	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr7:149798413-149798689	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr7:149757620-149757770	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr7:149757526-149757945	K562	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
35	CTCF	chr7:149807805-149807923	GM19239	blood:	n/a	chr7:149807833-149807843 chr7:149807881-149807899 chr7:149807831-149807844 chr7:149807828-149807846 chr7:149807830-149807851 chr7:149807831-149807840 chr7:149807884-149807897
36	CTCF	chr7:149742487-149743058	SK-N-SH	brain:	n/a	n/a
37	CTCF	chr7:149746320-149746470	BE2_C	brain:	n/a	n/a
38	CTCF	chr7:149807819-149807898	Medullo	brain:	n/a	chr7:149807833-149807843 chr7:149807831-149807844 chr7:149807828-149807846 chr7:149807830-149807851 chr7:149807831-149807840 chr7:149807884-149807897
39	CTCF	chr7:149788372-149788482	GM20000	blood:	n/a	n/a
40	CTCF	chr7:149757626-149757919	LNCaP	prostate:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
41	CTCF	chr7:149757661-149757881	ProgFib	skin:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
42	CTCF	chr7:149742800-149742950	K562	blood:	n/a	n/a
43	CTCF	chr7:149757586-149757948	K562	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
44	CTCF	chr7:149742805-149742986	HepG2	liver:	n/a	n/a
45	CTCF	chr7:149744020-149744170	A549	lung:	n/a	n/a
46	CTCF	chr7:149807789-149807981	LNCaP	prostate:	n/a	chr7:149807833-149807843 chr7:149807881-149807899 chr7:149807831-149807844 chr7:149807828-149807846 chr7:149807830-149807851 chr7:149807831-149807840 chr7:149807884-149807897
47	CTCF	chr7:149746340-149746490	BE2_C	brain:	n/a	n/a
48	CTCF	chr7:149781880-149782030	A549	lung:	n/a	n/a
49	CTCF	chr7:149757620-149757770	K562	blood:	n/a	n/a
50	CTCF	chr7:149757620-149757770	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149744597-149744647	AG04450	lung:	fetal
2	chr7:149780548-149780598	Jurkat	blood:	n/a
3	chr7:149744041-149744091	GM12891	blood:	n/a
4	chr7:149744597-149744647	AG04450	lung:	fetal
5	chr7:149780548-149780598	Jurkat	blood:	n/a
6	chr7:149744041-149744091	GM12891	blood:	n/a
7	chr7:149749941-149749991	PrEC	prostate:	n/a
8	chr7:149745299-149745349	GM19239	blood:	n/a
9	chr7:149749941-149749991	HRCEpiC	kidney:	n/a
10	chr7:149767502-149767552	A549	lung:	n/a
11	chr7:149780548-149780598	NHBE	bronchial:	n/a
12	chr7:149744935-149744985	Caco-2	colon:	n/a
13	chr7:149780548-149780598	AoSMC	blood vessel:	n/a
14	chr7:149780548-149780598	GM12892	blood:	n/a
15	chr7:149746468-149746518	HRE	kidney:	n/a
16	chr7:149780548-149780598	Hela-S3	cervix:	n/a
17	chr7:149749941-149749991	HCF	heart:	n/a
18	chr7:149744597-149744647	BJ	skin:	n/a
19	chr7:149767828-149767878	LNCaP	prostate:	n/a
20	chr7:149767828-149767878	U87	brain:	n/a
21	chr7:149809179-149809229	HepG2	liver:	n/a
22	chr7:149746077-149746127	IMR90	lung:	fetal
23	chr7:149746077-149746127	GM12878	blood:	n/a
24	chr7:149749941-149749991	HAEpiC	amniotic membrane:	n/a
25	chr7:149745299-149745349	HNPCEpiC	eye:	n/a
26	chr7:149749941-149749991	BE2_C	brain:	n/a
27	chr7:149744041-149744091	NB4	blood:	n/a
28	chr7:149742121-149742171	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:149744935-149744985	LNCaP	prostate:	n/a
30	chr7:149744597-149744647	ProgFib	skin:	n/a
31	chr7:149749941-149749991	GM12892	blood:	n/a
32	chr7:149742121-149742171	HEK293	kidney:	embryo
33	chr7:149744597-149744647	H1-hESC	embryonic stem cell:	embryo
34	chr7:149744418-149744468	SK-N-SH_RA	brain:	n/a
35	chr7:149744041-149744091	AoSMC	blood vessel:	n/a
36	chr7:149767828-149767878	CMK	blood:	n/a
37	chr7:149780548-149780598	GM19239	blood:	n/a
38	chr7:149742121-149742171	HepG2	liver:	n/a
39	chr7:149744041-149744091	GM06990	blood:	n/a
40	chr7:149767502-149767552	HNPCEpiC	eye:	n/a
41	chr7:149746640-149746690	HAEpiC	amniotic membrane:	n/a
42	chr7:149746077-149746127	HL-60	blood:	n/a
43	chr7:149767828-149767878	NH-A	brain:	n/a
44	chr7:149746468-149746518	ovcar-3	ovarian:	n/a
45	chr7:149767502-149767552	SK-N-SH	brain:	n/a
46	chr7:149744418-149744468	MCF-7	breast:	n/a
47	chr7:149745299-149745349	ProgFib	skin:	n/a
48	chr7:149746077-149746127	BE2_C	brain:	n/a
49	chr7:149744597-149744647	SK-N-SH_RA	brain:	n/a
50	chr7:149746640-149746690	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:149580322..149580844-chr7:149745955..149746566,2	MCF-7	breast:
2	chr7:149757556..149758057-chr7:149919306..149919858,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0E2-2	chr7:149759178-149759348	ENSG00000241449
2	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449
3	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124091
4	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124088
5	lnc-ATP6V0E2-2	chr7:149771062-149771465	ENSG00000241449
6	lnc-ATP6V0E2-2	chr7:149774721-149774910	ucscGeneNc_uc003whi_1
7	lnc-ATP6V0E2-2	chr7:149761675-149761850	ucscGeneNc_uc003whi_1
8	lnc-ATP6V0E2-2	chr7:149775097-149776161	ucscGeneNc_uc003whi_1
9	lnc-ATP6V0E2-2	chr7:149771062-149771172	ENSG00000241449
10	lnc-ATP6V0E2-2	chr7:149773639-149773744	ENSG00000241449
11	lnc-ATP6V0E2-2	chr7:149770570-149771181	ucscGeneNc_uc003whi_1
12	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124087
13	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449

Variant related genes	Relation type
ENSG00000241449	TF binding region
ENSG00000241449	CpG island

Extended variants
information (count: 2273 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2273 , 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	rs2628670	chr7:149741002-149741003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564176404	chr7:149741012-149741013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs55818109	chr7:149741028-149741029	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs549738751	chr7:149741039-149741040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570139821	chr7:149741043-149741044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535538860	chr7:149741050-149741051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73725963	chr7:149741051-149741052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs566139458	chr7:149741052-149741053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2628671	chr7:149741180-149741181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138371924	chr7:149741213-149741214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143930985	chr7:149741218-149741219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186355172	chr7:149741221-149741222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191107983	chr7:149741237-149741238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556955047	chr7:149741263-149741264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573719113	chr7:149741278-149741279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183374944	chr7:149741300-149741301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559524608	chr7:149741358-149741359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375413193	chr7:149741366-149741367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572934096	chr7:149741479-149741480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73725964	chr7:149741645-149741646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs2628672	chr7:149741661-149741662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530672322	chr7:149741682-149741683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549774126	chr7:149741691-149741692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563525087	chr7:149741692-149741693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1140749	chr7:149741845-149741846	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs529436727	chr7:149741862-149741863	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs1063698	chr7:149741890-149741891	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs549187897	chr7:149741957-149741958	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs369060227	chr7:149741967-149741968	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs372567286	chr7:149742004-149742005	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs576640714	chr7:149742015-149742016	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs566129913	chr7:149742016-149742017	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs202213437	chr7:149742027-149742028	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs551956223	chr7:149742046-149742047	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs571977703	chr7:149742059-149742060	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs1132163	chr7:149742082-149742083	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs11973827	chr7:149742083-149742084	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs117603654	chr7:149742084-149742085	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs2628673	chr7:149742106-149742107	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs536378176	chr7:149742122-149742123	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs552811199	chr7:149742142-149742143	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs572578420	chr7:149742143-149742144	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs4993339	chr7:149742242-149742243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544808826	chr7:149742252-149742253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201990691	chr7:149742286-149742287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200318155	chr7:149742289-149742290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1860504	chr7:149742316-149742317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558291648	chr7:149742346-149742347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529781651	chr7:149742361-149742362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575191469	chr7:149742371-149742372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	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
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149730200-149744000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:149733000-149744000	Weak transcription	Right Atrium	heart
3	chr7:149741800-149742000	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr7:149742200-149742400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr7:149742200-149742600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr7:149742600-149743000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr7:149743000-149743200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr7:149743000-149743200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
9	chr7:149743000-149743200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr7:149743000-149743200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:149743200-149744000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr7:149743200-149744000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:149743400-149743600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
14	chr7:149743400-149743600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:149743400-149744800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr7:149743400-149745200	Weak transcription	Colon Smooth Muscle	Colon
17	chr7:149743600-149743800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr7:149743600-149744000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr7:149743800-149744000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr7:149743800-149744400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:149743800-149746600	Active TSS	Brain Anterior Caudate	brain
22	chr7:149744000-149744200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr7:149744000-149744200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:149744000-149744200	Active TSS	Cortex derived primary cultured neurospheres	brain
25	chr7:149744000-149744200	Enhancers	Fetal Brain Male	brain
26	chr7:149744000-149744400	Active TSS	Brain Germinal Matrix	brain
27	chr7:149744000-149744600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
28	chr7:149744000-149745600	Active TSS	Right Atrium	heart
29	chr7:149744000-149745800	Active TSS	Stomach Smooth Muscle	stomach
30	chr7:149744000-149746200	Active TSS	Brain Hippocampus Middle	brain
31	chr7:149744000-149746400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
32	chr7:149744000-149746400	Active TSS	Fetal Brain Female	brain
33	chr7:149744000-149746400	Active TSS	HepG2	liver
34	chr7:149744000-149746600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
35	chr7:149744000-149746600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr7:149744000-149746600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr7:149744000-149746800	Active TSS	H9 Cell Line	embryonic stem cell
38	chr7:149744000-149746800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
39	chr7:149744000-149746800	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr7:149744200-149744400	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr7:149744200-149744400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
42	chr7:149744200-149744400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:149744200-149744600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:149744200-149744600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr7:149744200-149745800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr7:149744200-149745800	Weak transcription	Fetal Brain Male	brain
47	chr7:149744200-149746400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
48	chr7:149744200-149746400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:149744200-149746600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
50	chr7:149744200-149746600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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