Variant report

Variant	nsv889442
Chromosome Location	chr7:149687123-149838371
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	chr7:149700297-149700734	K562	blood:	n/a	n/a
3	ATF1	chr7:149742080-149742094	K562	blood:	n/a	n/a
4	BACH1	chr7:149746378-149746646	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:149743485-149743750	GM12878	blood:	n/a	n/a
6	BATF	chr7:149757655-149757938	GM12878	blood:	n/a	chr7:149757827-149757838
7	BCL3	chr7:149808531-149808727	GM12878	blood:	n/a	n/a
8	BCL3	chr7:149808506-149808789	GM12878	blood:	n/a	n/a
9	BCL3	chr7:149836967-149837225	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:149823075-149823280	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:149784693-149784950	HepG2	liver:	n/a	chr7:149784796-149784807
12	CEBPB	chr7:149701346-149701464	A549	lung:	n/a	n/a
13	CEBPB	chr7:149786176-149786566	IMR90	lung:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
14	CEBPB	chr7:149713771-149714042	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:149822923-149823294	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:149786230-149786562	Hela-S3	cervix:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
17	CEBPB	chr7:149786189-149786644	K562	blood:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
18	CEBPB	chr7:149822945-149823293	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:149786163-149786592	HepG2	liver:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
20	CEBPB	chr7:149822980-149823212	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:149701434-149701491	K562	blood:	n/a	n/a
22	CEBPB	chr7:149791162-149791277	HepG2	liver:	n/a	chr7:149791213-149791222 chr7:149791213-149791224
23	CEBPB	chr7:149804465-149804596	A549	lung:	n/a	n/a
24	CEBPB	chr7:149701451-149701643	IMR90	lung:	n/a	n/a
25	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
26	CEBPB	chr7:149786250-149786562	A549	lung:	n/a	chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786322-149786331 chr7:149786321-149786332 chr7:149786322-149786331
27	CEBPB	chr7:149791079-149791364	H1-hESC	embryonic stem cell:	n/a	chr7:149791213-149791222 chr7:149791213-149791224
28	CEBPB	chr7:149798171-149798831	Hela-S3	cervix:	n/a	chr7:149798497-149798510 chr7:149798497-149798508
29	CEBPB	chr7:149822919-149823295	HepG2	liver:	n/a	n/a
30	CHD1	chr7:149746398-149746684	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:149798413-149798689	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr7:149746382-149746488	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:149742820-149742970	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr7:149757648-149757908	MCF-7	breast:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
35	CTCF	chr7:149757660-149757810	GM12870	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
36	CTCF	chr7:149698460-149698610	GM12866	blood:	n/a	n/a
37	CTCF	chr7:149700640-149700790	GM12870	blood:	n/a	n/a
38	CTCF	chr7:149757660-149757810	AG04450	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
39	CTCF	chr7:149757620-149757770	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr7:149698297-149698558	A549	lung:	n/a	n/a
41	CTCF	chr7:149742800-149742950	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr7:149781900-149782086	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr7:149746082-149746379	Medullo	brain:	n/a	chr7:149746208-149746221 chr7:149746248-149746261
44	CTCF	chr7:149781940-149782090	NB4	blood:	n/a	n/a
45	CTCF	chr7:149782080-149782230	GM12872	blood:	n/a	n/a
46	CTCF	chr7:149698440-149698590	GM12870	blood:	n/a	n/a
47	CTCF	chr7:149742780-149742930	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr7:149757561-149757916	A549	lung:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790
49	CTCF	chr7:149722346-149722414	NHEK	skin:	n/a	chr7:149722360-149722381 chr7:149722365-149722383
50	CTCF	chr7:149757644-149757901	GM12891	blood:	n/a	chr7:149757768-149757784 chr7:149757767-149757785 chr7:149757770-149757783 chr7:149757769-149757790

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149744418-149744468	HNPCEpiC	eye:	n/a
2	chr7:149738501-149738551	HIPEpiC	eye:	n/a
3	chr7:149746077-149746127	RPTEC	kidney:	n/a
4	chr7:149744418-149744468	HNPCEpiC	eye:	n/a
5	chr7:149738501-149738551	HIPEpiC	eye:	n/a
6	chr7:149746077-149746127	RPTEC	kidney:	n/a
7	chr7:149732847-149732897	HRPEpiC	eye:	n/a
8	chr7:149780548-149780598	HUVEC	blood vessel:	n/a
9	chr7:149767502-149767552	BJ	skin:	n/a
10	chr7:149738501-149738551	A549	lung:	n/a
11	chr7:149745299-149745349	Hepatocyte	liver:	n/a
12	chr7:149746077-149746127	K562	blood:	n/a
13	chr7:149745299-149745349	HIPEpiC	eye:	n/a
14	chr7:149809179-149809229	PANC-1	pancreas:	n/a
15	chr7:149744597-149744647	RPTEC	kidney:	n/a
16	chr7:149733821-149733871	CMK	blood:	n/a
17	chr7:149732847-149732897	SAEC	small airway:	n/a
18	chr7:149745299-149745349	GM06990	blood:	n/a
19	chr7:149738501-149738551	NB4	blood:	n/a
20	chr7:149780548-149780598	HCF	heart:	n/a
21	chr7:149742121-149742171	BE2_C	brain:	n/a
22	chr7:149780548-149780598	HCPEpiC	choroid plexus:	n/a
23	chr7:149734481-149734531	SK-N-SH_RA	brain:	n/a
24	chr7:149738473-149738523	MCF-7	breast:	n/a
25	chr7:149744935-149744985	NH-A	brain:	n/a
26	chr7:149736127-149736177	NHDF-neo	bronchial:	n/a
27	chr7:149744418-149744468	AG04449	skin:	fetal
28	chr7:149738501-149738551	ECC-1	luminal epithelium:	n/a
29	chr7:149735726-149735776	HRE	kidney:	n/a
30	chr7:149745299-149745349	PFSK-1	brain:	n/a
31	chr7:149744041-149744091	K562	blood:	n/a
32	chr7:149735726-149735776	GM12878	blood:	n/a
33	chr7:149744597-149744647	PANC-1	pancreas:	n/a
34	chr7:149809179-149809229	NHDF-neo	bronchial:	n/a
35	chr7:149744041-149744091	Hepatocyte	liver:	n/a
36	chr7:149744041-149744091	SAEC	small airway:	n/a
37	chr7:149735729-149735779	AG10803	skin:	n/a
38	chr7:149742121-149742171	U87	brain:	n/a
39	chr7:149742121-149742171	HCF	heart:	n/a
40	chr7:149744597-149744647	NT2-D1	testis:	n/a
41	chr7:149744418-149744468	HCT-116	colon:	n/a
42	chr7:149731767-149731817	HUVEC	blood vessel:	n/a
43	chr7:149746640-149746690	HepG2	liver:	n/a
44	chr7:149767502-149767552	NH-A	brain:	n/a
45	chr7:149731742-149731792	NHBE	bronchial:	n/a
46	chr7:149732579-149732629	HEEpiC	esophagus:	n/a
47	chr7:149746077-149746127	HCF	heart:	n/a
48	chr7:149732847-149732897	HCPEpiC	choroid plexus:	n/a
49	chr7:149745299-149745349	HNPCEpiC	eye:	n/a
50	chr7:149767502-149767552	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:149757556..149758057-chr7:149919306..149919858,2	MCF-7	breast:
2	chr7:149580322..149580844-chr7:149745955..149746566,2	MCF-7	breast:
3	chr7:149699024..149700856-chr7:153788710..153791500,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V0E2-2	chr7:149735636-149735802	NONHSAT124088
2	lnc-ATP6V0E2-1	chr7:149701497-149702213	ENSG00000249583
3	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124087
4	lnc-ATP6V0E2-2	chr7:149771062-149771465	ENSG00000241449
5	lnc-ATP6V0E2-2	chr7:149770570-149771181	ucscGeneNc_uc003whi_1
6	lnc-ZNF467-4	chr7:149699986-149700449	NONHSAT124086
7	lnc-ATP6V0E2-1	chr7:149697841-149700167	ENSG00000249583
8	lnc-ATP6V0E2-2	chr7:149761675-149761850	ucscGeneNc_uc003whi_1
9	lnc-ATP6V0E2-2	chr7:149732185-149732207	NONHSAT124087
10	lnc-ATP6V0E2-2	chr7:149738452-149738550	NONHSAT124091
11	lnc-ATP6V0E2-2	chr7:149771062-149771172	ENSG00000241449
12	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449
13	lnc-ATP6V0E2-2	chr7:149737610-149737743	ENSG00000241449
14	lnc-ZNF467-4	chr7:149700614-149701513	NONHSAT124086
15	lnc-ATP6V0E2-2	chr7:149737556-149737743	NONHSAT124091
16	lnc-ATP6V0E2-2	chr7:149738452-149738550	ENSG00000241449
17	lnc-ATP6V0E2-2	chr7:149770706-149770828	ENSG00000241449
18	lnc-ATP6V0E2-2	chr7:149773639-149773744	ENSG00000241449
19	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124088
20	lnc-ATP6V0E2-2	chr7:149774721-149774910	ucscGeneNc_uc003whi_1
21	lnc-ATP6V0E2-2	chr7:149741839-149742195	NONHSAT124091
22	lnc-ATP6V0E2-2	chr7:149775097-149776161	ucscGeneNc_uc003whi_1
23	lnc-ATP6V0E2-2	chr7:149759178-149759348	ENSG00000241449
24	lnc-ATP6V0E2-8	chr7:149697081-149697368	expReg_chr7_12098_+

Variant related genes	Relation type
ENSG00000241449	TF binding region
ENSG00000260555	TF binding region
ENSG00000241449	CpG island
ENSG00000260555	CpG island
SOCS2	miRNA target sites
JPH1	miRNA target sites

Extended variants
information (count: 4911 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4911 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192478246	chr7:149688409-149688410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185673481	chr7:149688420-149688421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4015815	chr7:149688447-149688448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149808398	chr7:149688470-149688471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71534042	chr7:149688477-149688478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557563404	chr7:149688517-149688518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189451167	chr7:149688523-149688524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537218128	chr7:149688524-149688525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142143365	chr7:149688560-149688561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71534043	chr7:149688571-149688572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs71534044	chr7:149688586-149688587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147837523	chr7:149688609-149688610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10807977	chr7:149688629-149688630	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs537481972	chr7:149688641-149688642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71534045	chr7:149688680-149688681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192475996	chr7:149688701-149688702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs71534046	chr7:149688707-149688708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541516569	chr7:149688719-149688720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184711808	chr7:149688752-149688753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372348379	chr7:149688822-149688823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533376109	chr7:149688835-149688836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543955176	chr7:149688838-149688839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188549207	chr7:149688906-149688907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7791827	chr7:149688922-149688923	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs548606607	chr7:149688923-149688924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150106805	chr7:149688938-149688939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528199515	chr7:149688963-149688964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551078340	chr7:149688989-149688990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181432679	chr7:149689017-149689018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62492317	chr7:149689071-149689072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557119140	chr7:149689072-149689073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62492318	chr7:149689074-149689075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62492319	chr7:149689075-149689076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371072638	chr7:149689085-149689086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7385909	chr7:149689110-149689111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7384773	chr7:149689115-149689116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4725858	chr7:149689145-149689146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572496213	chr7:149689147-149689148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541401704	chr7:149689151-149689152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370405590	chr7:149689211-149689212	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs558290873	chr7:149689232-149689233	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs554140709	chr7:149689244-149689245	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs538897325	chr7:149689268-149689269	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs117195744	chr7:149689275-149689276	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs73725947	chr7:149689286-149689287	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs370071809	chr7:149689289-149689290	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs189068714	chr7:149689294-149689295	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs386719326	chr7:149689306-149689307	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs113892191	chr7:149689309-149689310	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs149651274	chr7:149689312-149689313	Weak transcription Enhancers Bivalent Enhancer	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149688400-149688600	Enhancers	Gastric	stomach
2	chr7:149688600-149688800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr7:149688600-149696000	Weak transcription	Gastric	stomach
4	chr7:149689200-149690000	Enhancers	Pancreas	Pancrea
5	chr7:149689200-149690000	Bivalent Enhancer	Stomach Mucosa	stomach
6	chr7:149692000-149700600	Weak transcription	Right Atrium	heart
7	chr7:149692400-149692600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:149692600-149700400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr7:149692800-149693000	Enhancers	Brain Angular Gyrus	brain
10	chr7:149693000-149700400	Weak transcription	Brain Angular Gyrus	brain
11	chr7:149694800-149700200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr7:149694800-149700400	Weak transcription	Ovary	ovary
13	chr7:149696000-149696200	Enhancers	Brain Anterior Caudate	brain
14	chr7:149696000-149696600	Enhancers	Gastric	stomach
15	chr7:149696200-149698000	Weak transcription	Pancreas	Pancrea
16	chr7:149696200-149700400	Weak transcription	Brain Anterior Caudate	brain
17	chr7:149696600-149700400	Weak transcription	Gastric	stomach
18	chr7:149697800-149698600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr7:149698000-149698200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr7:149698000-149698200	Enhancers	Pancreas	Pancrea
21	chr7:149698200-149700400	Weak transcription	Pancreas	Pancrea
22	chr7:149698400-149702000	Weak transcription	Brain Hippocampus Middle	brain
23	chr7:149698600-149700400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr7:149698800-149700400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr7:149698800-149700400	Weak transcription	Colon Smooth Muscle	Colon
26	chr7:149699000-149700400	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:149699000-149700800	Weak transcription	Fetal Brain Female	brain
28	chr7:149699200-149704000	Weak transcription	Liver	Liver
29	chr7:149699800-149701200	Weak transcription	HepG2	liver
30	chr7:149700000-149700400	Weak transcription	Brain Substantia Nigra	brain
31	chr7:149700200-149700400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr7:149700200-149700600	Weak transcription	Colonic Mucosa	Colon
33	chr7:149700200-149701000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
34	chr7:149700200-149701000	ZNF genes & repeats	Fetal Brain Male	brain
35	chr7:149700200-149701000	ZNF genes & repeats	Fetal Kidney	kidney
36	chr7:149700400-149700600	Enhancers	Right Ventricle	heart
37	chr7:149700400-149700600	Bivalent/Poised TSS	Stomach Mucosa	stomach
38	chr7:149700400-149700600	Bivalent Enhancer	K562	blood
39	chr7:149700400-149700800	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
40	chr7:149700400-149700800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
41	chr7:149700400-149700800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
42	chr7:149700400-149700800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
43	chr7:149700400-149700800	ZNF genes & repeats	Fetal Heart	heart
44	chr7:149700400-149700800	ZNF genes & repeats	Fetal Intestine Large	intestine
45	chr7:149700400-149700800	ZNF genes & repeats	Ovary	ovary
46	chr7:149700400-149700800	Active TSS	NHDF-Ad	bronchial
47	chr7:149700400-149701000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
48	chr7:149700400-149701000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:149700400-149701000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:149700400-149701000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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