Variant report

Variant	nsv889446
Chromosome Location	chr7:149722588-149806051
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	chr7:149742080-149742094	K562	blood:	n/a	n/a
2	BACH1	chr7:149746378-149746646	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:149743485-149743750	GM12878	blood:	n/a	n/a
4	BATF	chr7:149757655-149757938	GM12878	blood:	n/a	chr7:149757827-149757838
5	CEBPB	chr7:149804465-149804596	A549	lung:	n/a	n/a
6	CEBPB	chr7:149786250-149786562	A549	lung:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
7	CEBPB	chr7:149791079-149791364	H1-hESC	embryonic stem cell:	n/a	chr7:149791213-149791222 chr7:149791213-149791224
8	CEBPB	chr7:149786176-149786566	IMR90	lung:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
9	CEBPB	chr7:149784693-149784950	HepG2	liver:	n/a	chr7:149784796-149784807
10	CEBPB	chr7:149786163-149786592	HepG2	liver:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
11	CEBPB	chr7:149798171-149798831	Hela-S3	cervix:	n/a	chr7:149798497-149798510 chr7:149798497-149798508
12	CEBPB	chr7:149791162-149791277	HepG2	liver:	n/a	chr7:149791213-149791222 chr7:149791213-149791224
13	CEBPB	chr7:149786230-149786562	Hela-S3	cervix:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
14	CEBPB	chr7:149786189-149786644	K562	blood:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
15	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
16	CHD1	chr7:149746398-149746684	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr7:149746382-149746488	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr7:149798413-149798689	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr7:149757664-149757844	HepG2	liver:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
20	CTCF	chr7:149757526-149757945	K562	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
21	CTCF	chr7:149746200-149746350	HL-60	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
22	CTCF	chr7:149781960-149782110	HEK293	kidney:	n/a	n/a
23	CTCF	chr7:149781880-149782030	A549	lung:	n/a	n/a
24	CTCF	chr7:149746134-149746323	GM19240	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
25	CTCF	chr7:149742780-149742930	AG09309	skin:	n/a	n/a
26	CTCF	chr7:149749377-149749388	K562	blood:	n/a	n/a
27	CTCF	chr7:149742800-149742950	NB4	blood:	n/a	n/a
28	CTCF	chr7:149743980-149744130	BE2_C	brain:	n/a	n/a
29	CTCF	chr7:149742800-149742950	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr7:149757660-149757810	HFF	foreskin:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
31	CTCF	chr7:149757647-149757904	GM19240	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
32	CTCF	chr7:149744000-149744150	HepG2	liver:	n/a	n/a
33	CTCF	chr7:149757460-149757610	BE2_C	brain:	n/a	n/a
34	CTCF	chr7:149757523-149757948	A549	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
35	CTCF	chr7:149746070-149746366	MCF-7	breast:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
36	CTCF	chr7:149781817-149782023	K562	blood:	n/a	n/a
37	CTCF	chr7:149746200-149746350	HUVEC	blood vessel:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
38	CTCF	chr7:149757620-149757770	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr7:149757660-149757810	NB4	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
40	CTCF	chr7:149742755-149743007	IMR90	lung:	n/a	n/a
41	CTCF	chr7:149746045-149746331	A549	lung:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
42	CTCF	chr7:149742800-149742950	AG09319	gingival:	n/a	n/a
43	CTCF	chr7:149742505-149743044	A549	lung:	n/a	n/a
44	CTCF	chr7:149745920-149746070	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr7:149773913-149773991	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr7:149746077-149746362	NHEK	skin:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
47	CTCF	chr7:149746146-149746312	HUVEC	blood vessel:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
48	CTCF	chr7:149781860-149782130	HepG2	liver:	n/a	n/a
49	CTCF	chr7:149746168-149746303	GM10248	blood:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
50	CTCF	chr7:149746420-149746570	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149735729-149735779	RPTEC	kidney:	n/a
2	chr7:149738501-149738551	GM19239	blood:	n/a
3	chr7:149749941-149749991	HRPEpiC	eye:	n/a
4	chr7:149744041-149744091	HCT-116	colon:	n/a
5	chr7:149735729-149735779	RPTEC	kidney:	n/a
6	chr7:149738501-149738551	GM19239	blood:	n/a
7	chr7:149749941-149749991	HRPEpiC	eye:	n/a
8	chr7:149744041-149744091	HCT-116	colon:	n/a
9	chr7:149745299-149745349	H1-hESC	embryonic stem cell:	embryo
10	chr7:149744935-149744985	HIPEpiC	eye:	n/a
11	chr7:149735726-149735776	HepG2	liver:	n/a
12	chr7:149731742-149731792	AG04449	skin:	fetal
13	chr7:149731742-149731792	GM12892	blood:	n/a
14	chr7:149735726-149735776	GM12891	blood:	n/a
15	chr7:149744597-149744647	HIPEpiC	eye:	n/a
16	chr7:149732579-149732629	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:149744418-149744468	HNPCEpiC	eye:	n/a
18	chr7:149733103-149733153	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:149738473-149738523	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:149732847-149732897	H1-hESC	embryonic stem cell:	embryo
21	chr7:149733103-149733153	HNPCEpiC	eye:	n/a
22	chr7:149744418-149744468	NH-A	brain:	n/a
23	chr7:149767502-149767552	SK-N-SH_RA	brain:	n/a
24	chr7:149780548-149780598	ovcar-3	ovarian:	n/a
25	chr7:149742121-149742171	HAEpiC	amniotic membrane:	n/a
26	chr7:149746640-149746690	SK-N-SH	brain:	n/a
27	chr7:149767828-149767878	NB4	blood:	n/a
28	chr7:149731767-149731817	HRPEpiC	eye:	n/a
29	chr7:149749941-149749991	GM06990	blood:	n/a
30	chr7:149734481-149734531	NB4	blood:	n/a
31	chr7:149746077-149746127	Hela-S3	cervix:	n/a
32	chr7:149767502-149767552	NT2-D1	testis:	n/a
33	chr7:149749941-149749991	HEK293	kidney:	embryo
34	chr7:149744418-149744468	HCF	heart:	n/a
35	chr7:149731742-149731792	HepG2	liver:	n/a
36	chr7:149732579-149732629	GM19239	blood:	n/a
37	chr7:149767502-149767552	HNPCEpiC	eye:	n/a
38	chr7:149746468-149746518	BJ	skin:	n/a
39	chr7:149746468-149746518	HEK293	kidney:	embryo
40	chr7:149767502-149767552	GM19239	blood:	n/a
41	chr7:149732847-149732897	ProgFib	skin:	n/a
42	chr7:149732847-149732897	GM19239	blood:	n/a
43	chr7:149734481-149734531	RPTEC	kidney:	n/a
44	chr7:149745299-149745349	HCF	heart:	n/a
45	chr7:149767828-149767878	GM12892	blood:	n/a
46	chr7:149735729-149735779	PFSK-1	brain:	n/a
47	chr7:149733103-149733153	LNCaP	prostate:	n/a
48	chr7:149746077-149746127	ProgFib	skin:	n/a
49	chr7:149745299-149745349	BJ	skin:	n/a
50	chr7:149732847-149732897	HEEpiC	esophagus:	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	chr7:149732185-149732207	NONHSAT124087
2	lnc-ATP6V0E2-2	chr7:149737556-149737743	NONHSAT124091
3	lnc-ATP6V0E2-2	chr7:149771062-149771172	ENSG00000241449
4	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124087
5	lnc-ATP6V0E2-2	chr7:149773639-149773744	ENSG00000241449
6	lnc-ATP6V0E2-2	chr7:149738452-149738550	ENSG00000241449
7	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124088
8	lnc-ATP6V0E2-2	chr7:149774721-149774910	ucscGeneNc_uc003whi_1
9	lnc-ATP6V0E2-2	chr7:149735636-149735802	NONHSAT124088
10	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124091
11	lnc-ATP6V0E2-2	chr7:149770570-149771181	ucscGeneNc_uc003whi_1
12	lnc-ATP6V0E2-2	chr7:149761675-149761850	ucscGeneNc_uc003whi_1
13	lnc-ATP6V0E2-2	chr7:149771062-149771465	ENSG00000241449
14	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449
15	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449
16	lnc-ATP6V0E2-2	chr7:149737610-149737743	ENSG00000241449
17	lnc-ATP6V0E2-2	chr7:149775097-149776161	ucscGeneNc_uc003whi_1
18	lnc-ATP6V0E2-2	chr7:149738452-149738550	NONHSAT124091
19	lnc-ATP6V0E2-2	chr7:149759178-149759348	ENSG00000241449

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

Extended variants
information (count: 2892 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2892 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2450034	chr7:149722588-149722589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547625406	chr7:149722600-149722601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs66947840	chr7:149722603-149722604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190962643	chr7:149722624-149722625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533397881	chr7:149722640-149722641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540035162	chr7:149722694-149722695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2449737	chr7:149722697-149722698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs6979976	chr7:149722715-149722716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535752304	chr7:149722733-149722734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555590550	chr7:149722735-149722736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565382827	chr7:149722771-149722772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143856136	chr7:149722801-149722802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557600761	chr7:149722857-149722858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183397821	chr7:149722871-149722872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543123503	chr7:149722921-149722922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111640969	chr7:149722965-149722966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2626783	chr7:149722997-149722998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573841210	chr7:149723017-149723018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374315534	chr7:149723020-149723021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2626785	chr7:149723021-149723022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527728145	chr7:149723045-149723046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184987546	chr7:149723059-149723060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564292342	chr7:149723073-149723074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190951822	chr7:149723085-149723086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562510482	chr7:149723150-149723151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549821109	chr7:149723195-149723196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569916325	chr7:149723196-149723197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532955890	chr7:149723213-149723214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549305999	chr7:149723242-149723243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566346993	chr7:149723297-149723298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534350002	chr7:149723404-149723405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368755022	chr7:149723405-149723406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28375502	chr7:149723423-149723424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs183227837	chr7:149723482-149723483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2626786	chr7:149723483-149723484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28738073	chr7:149723517-149723518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs139891394	chr7:149723524-149723525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143778030	chr7:149723532-149723533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188014627	chr7:149723587-149723588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200121048	chr7:149723629-149723630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201525725	chr7:149723647-149723648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573073168	chr7:149723690-149723691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544938019	chr7:149723731-149723732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193017430	chr7:149723752-149723753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199661886	chr7:149723761-149723762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183105277	chr7:149723807-149723808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549282012	chr7:149723828-149723829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187748419	chr7:149723841-149723842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192456307	chr7:149723870-149723871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2626790	chr7:149723876-149723877	Weak transcription	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
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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149701000-149727800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:149727800-149730200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr7:149729600-149730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:149730200-149744000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr7:149730600-149731000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:149733000-149744000	Weak transcription	Right Atrium	heart
7	chr7:149737000-149737200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr7:149741800-149742000	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr7:149742200-149742400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr7:149742200-149742600	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr7:149742600-149743000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:149743000-149743200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr7:149743000-149743200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr7:149743000-149743200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr7:149743000-149743200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:149743200-149744000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr7:149743200-149744000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr7:149743400-149743600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
19	chr7:149743400-149743600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:149743400-149744800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr7:149743400-149745200	Weak transcription	Colon Smooth Muscle	Colon
22	chr7:149743600-149743800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr7:149743600-149744000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr7:149743800-149744000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
25	chr7:149743800-149744400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:149743800-149746600	Active TSS	Brain Anterior Caudate	brain
27	chr7:149744000-149744200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr7:149744000-149744200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:149744000-149744200	Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr7:149744000-149744200	Enhancers	Fetal Brain Male	brain
31	chr7:149744000-149744400	Active TSS	Brain Germinal Matrix	brain
32	chr7:149744000-149744600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chr7:149744000-149745600	Active TSS	Right Atrium	heart
34	chr7:149744000-149745800	Active TSS	Stomach Smooth Muscle	stomach
35	chr7:149744000-149746200	Active TSS	Brain Hippocampus Middle	brain
36	chr7:149744000-149746400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
37	chr7:149744000-149746400	Active TSS	Fetal Brain Female	brain
38	chr7:149744000-149746400	Active TSS	HepG2	liver
39	chr7:149744000-149746600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
40	chr7:149744000-149746600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
41	chr7:149744000-149746600	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr7:149744000-149746800	Active TSS	H9 Cell Line	embryonic stem cell
43	chr7:149744000-149746800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
44	chr7:149744000-149746800	Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr7:149744200-149744400	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr7:149744200-149744400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
47	chr7:149744200-149744400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:149744200-149744600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:149744200-149744600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr7:149744200-149745800	Active TSS	Primary T helper naive cells fromperipheralblood	blood

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