Variant report

Variant	nsv608334
Chromosome Location	chr7:121670522-121725961
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	chr7:121704395-121704574	K562	blood:	n/a	n/a
2	ATF2	chr7:121712973-121714428	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:121712059-121714376	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:121714609-121715189	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:121713907-121713915	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:121679046-121679201	GM12878	blood:	n/a	chr7:121679117-121679128 chr7:121679111-121679119
7	BATF	chr7:121710247-121710427	GM12878	blood:	n/a	chr7:121710339-121710350
8	BATF	chr7:121679013-121679251	GM12878	blood:	n/a	chr7:121679117-121679128 chr7:121679111-121679119
9	BCL3	chr7:121717575-121717816	GM12878	blood:	n/a	n/a
10	BRCA1	chr7:121695241-121695450	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr7:121721475-121721570	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:121686435-121686763	MCF-7	breast:	n/a	n/a
13	CEBPB	chr7:121686407-121686783	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:121694814-121695046	A549	lung:	n/a	chr7:121694925-121694938 chr7:121694927-121694938 chr7:121694925-121694936
15	CEBPB	chr7:121724316-121724409	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:121686395-121686756	A549	lung:	n/a	n/a
17	CEBPB	chr7:121686536-121686762	K562	blood:	n/a	n/a
18	CEBPB	chr7:121694792-121695005	HepG2	liver:	n/a	chr7:121694925-121694938 chr7:121694927-121694938 chr7:121694925-121694936
19	CEBPB	chr7:121686438-121686728	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:121686409-121686759	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:121683862-121683937	A549	lung:	n/a	n/a
22	CEBPB	chr7:121686407-121686768	IMR90	lung:	n/a	n/a
23	CHD2	chr7:121712164-121714352	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr7:121672497-121672543	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr7:121724816-121725007	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr7:121714603-121715094	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:121683894-121683918	Lung_OC	lung:	n/a	n/a
28	CTCF	chr7:121677566-121677601	GM13976	blood:	n/a	n/a
29	E2F4	chr7:121693353-121693700	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr7:121686518-121686767	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr7:121723451-121723463	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr7:121705018-121705146	MCF10A-Er-Src	breast:	n/a	n/a
33	EBF1	chr7:121697056-121697314	GM12878	blood:	n/a	chr7:121697171-121697182
34	EP300	chr7:121697065-121697258	GM12878	blood:	n/a	n/a
35	EP300	chr7:121703676-121703677	GM12878	blood:	n/a	n/a
36	FAM48A	chr7:121672542-121672626	GM12878	blood:	n/a	n/a
37	FOS	chr7:121686433-121686825	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr7:121695143-121695521	MCF10A-Er-Src	breast:	n/a	chr7:121695322-121695334 chr7:121695322-121695333
39	FOS	chr7:121709311-121709387	MCF10A-Er-Src	breast:	n/a	chr7:121709331-121709338 chr7:121709331-121709339 chr7:121709329-121709341 chr7:121709331-121709339 chr7:121709332-121709343 chr7:121709329-121709340
40	FOS	chr7:121695180-121695509	MCF10A-Er-Src	breast:	n/a	chr7:121695322-121695334 chr7:121695322-121695333
41	FOS	chr7:121708852-121709483	HUVEC	blood vessel:	n/a	chr7:121709331-121709338 chr7:121709331-121709339 chr7:121709329-121709341 chr7:121709331-121709339 chr7:121709332-121709343 chr7:121709472-121709481 chr7:121709329-121709340
42	FOS	chr7:121686466-121686830	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr7:121694895-121695501	HUVEC	blood vessel:	n/a	chr7:121694938-121694949 chr7:121695322-121695334 chr7:121695322-121695333
44	FOS	chr7:121686452-121686844	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr7:121709252-121709436	MCF10A-Er-Src	breast:	n/a	chr7:121709331-121709338 chr7:121709331-121709339 chr7:121709329-121709341 chr7:121709331-121709339 chr7:121709332-121709343 chr7:121709329-121709340
46	FOS	chr7:121695178-121695507	MCF10A-Er-Src	breast:	n/a	chr7:121695322-121695334 chr7:121695322-121695333
47	FOS	chr7:121679091-121679328	MCF10A-Er-Src	breast:	n/a	chr7:121679263-121679271 chr7:121679114-121679126 chr7:121679261-121679273
48	FOS	chr7:121686468-121686837	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr7:121695107-121695517	MCF10A-Er-Src	breast:	n/a	chr7:121695322-121695334 chr7:121695322-121695333
50	FOXA1	chr7:121694476-121694732	T-47D	breast:	n/a	chr7:121694610-121694625

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121714135-121714185	MCF10A-Er-Src	breast:	n/a
2	chr7:121714135-121714185	ECC-1	luminal epithelium:	n/a
3	chr7:121701410-121701460	GM19239	blood:	n/a
4	chr7:121701410-121701460	HAEpiC	amniotic membrane:	n/a
5	chr7:121701410-121701460	ovcar-3	ovarian:	n/a
6	chr7:121725792-121725842	NB4	blood:	n/a
7	chr7:121725792-121725842	AG09319	gingival:	n/a
8	chr7:121701410-121701460	HRPEpiC	eye:	n/a
9	chr7:121701410-121701460	SK-N-SH_RA	brain:	n/a
10	chr7:121701410-121701460	SK-N-SH	brain:	n/a
11	chr7:121714135-121714185	IMR90	lung:	fetal
12	chr7:121714135-121714185	SK-N-MC	brain:	n/a
13	chr7:121725792-121725842	PrEC	prostate:	n/a
14	chr7:121714135-121714185	GM06990	blood:	n/a
15	chr7:121725792-121725842	SAEC	small airway:	n/a
16	chr7:121714135-121714185	AG10803	skin:	n/a
17	chr7:121725792-121725842	BJ	skin:	n/a
18	chr7:121725792-121725842	GM06990	blood:	n/a
19	chr7:121714135-121714185	NHBE	bronchial:	n/a
20	chr7:121714135-121714185	ovcar-3	ovarian:	n/a
21	chr7:121725792-121725842	ProgFib	skin:	n/a
22	chr7:121701410-121701460	AG10803	skin:	n/a
23	chr7:121725792-121725842	HCF	heart:	n/a
24	chr7:121701410-121701460	HIPEpiC	eye:	n/a
25	chr7:121701410-121701460	PrEC	prostate:	n/a
26	chr7:121701410-121701460	Caco-2	colon:	n/a
27	chr7:121701410-121701460	Hela-S3	cervix:	n/a
28	chr7:121725792-121725842	H1-hESC	embryonic stem cell:	embryo
29	chr7:121714135-121714185	Hela-S3	cervix:	n/a
30	chr7:121701410-121701460	LNCaP	prostate:	n/a
31	chr7:121701410-121701460	AG04449	skin:	fetal
32	chr7:121725792-121725842	HRCEpiC	kidney:	n/a
33	chr7:121725792-121725842	HEK293	kidney:	embryo
34	chr7:121701410-121701460	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:121725792-121725842	AG04449	skin:	fetal
36	chr7:121701410-121701460	PANC-1	pancreas:	n/a
37	chr7:121714135-121714185	U87	brain:	n/a
38	chr7:121725792-121725842	HCPEpiC	choroid plexus:	n/a
39	chr7:121725792-121725842	HNPCEpiC	eye:	n/a
40	chr7:121725792-121725842	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:121701410-121701460	BE2_C	brain:	n/a
42	chr7:121701410-121701460	AG09309	skin:	n/a
43	chr7:121701410-121701460	HCT-116	colon:	n/a
44	chr7:121701410-121701460	GM12892	blood:	n/a
45	chr7:121725792-121725842	PFSK-1	brain:	n/a
46	chr7:121714135-121714185	HEEpiC	esophagus:	n/a
47	chr7:121725792-121725842	SKMC	muscle:	n/a
48	chr7:121714135-121714185	GM12891	blood:	n/a
49	chr7:121714135-121714185	NH-A	brain:	n/a
50	chr7:121714135-121714185	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:121694544..121696684-chr7:121697590..121700568,2	MCF-7	breast:
2	chr7:121689235..121689772-chrX:57477123..57477731,2	MCF-7	breast:
3	chr7:121688053..121690814-chr7:121693064..121695575,2	K562	blood:
4	chr7:121688053..121690814-chr7:121693064..121695575,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTPRZ1	hsa-miR-124-3p	chr7:121701422-121701443
2	PTPRZ1	hsa-miR-124-3p	chr7:121701436-121701442

Variant related genes	Relation type
PTPRZ1	TF binding region
AASS	TF binding region
RNU7-154P	TF binding region
PTPRZ1	CpG island
AASS	CpG island
RNU7-154P	CpG island
ENSG00000106278	chromatin interactions

Extended variants
information (count: 1918 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1147498	chr7:121670522-121670523	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532678955	chr7:121670536-121670537	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552775890	chr7:121670541-121670542	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193213494	chr7:121670547-121670548	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538004555	chr7:121670593-121670594	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201780611	chr7:121670648-121670649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184420514	chr7:121670655-121670656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17144026	chr7:121670696-121670697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147260262	chr7:121670697-121670698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140944667	chr7:121670698-121670699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577928805	chr7:121670719-121670720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573127928	chr7:121670722-121670723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553181498	chr7:121670723-121670724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574540905	chr7:121670812-121670813	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139287962	chr7:121670820-121670821	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368892276	chr7:121670826-121670827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544966801	chr7:121670849-121670850	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544049906	chr7:121670855-121670856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188184501	chr7:121670856-121670857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575517006	chr7:121670872-121670873	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142386413	chr7:121670917-121670918	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560983665	chr7:121670922-121670923	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529731333	chr7:121670944-121670945	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180791772	chr7:121670965-121670966	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1725060	chr7:121671083-121671084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540257774	chr7:121671105-121671106	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559882744	chr7:121671126-121671127	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1147497	chr7:121671127-121671128	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs552456362	chr7:121671151-121671152	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368438174	chr7:121671153-121671154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569167789	chr7:121671160-121671161	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537767994	chr7:121671164-121671165	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531803693	chr7:121671182-121671183	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151335221	chr7:121671232-121671233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568245824	chr7:121671352-121671353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557380356	chr7:121671364-121671365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1147496	chr7:121671425-121671426	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs374236623	chr7:121671477-121671478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545784966	chr7:121671498-121671499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534135481	chr7:121671520-121671521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369001795	chr7:121671523-121671524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184288962	chr7:121671524-121671525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371023137	chr7:121671535-121671536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147762028	chr7:121671536-121671537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141147829	chr7:121671549-121671550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558904195	chr7:121671572-121671573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146937705	chr7:121671602-121671603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377400045	chr7:121671653-121671654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370493601	chr7:121671654-121671655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575579446	chr7:121671672-121671673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
small cell lung cancer	20016488	CNVD
Myxofibrosarcoma	20639860	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121634400-121706000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:121651200-121717600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:121652200-121679000	Weak transcription	NHEK	skin
4	chr7:121652400-121683200	Weak transcription	Brain Germinal Matrix	brain
5	chr7:121653800-121672600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:121653800-121673600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:121654000-121672200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:121654000-121672400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:121654000-121673200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr7:121654000-121675400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:121654000-121675600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr7:121654000-121679000	Weak transcription	Fetal Brain Female	brain
13	chr7:121654000-121679400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:121654200-121671200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:121655600-121699000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:121663800-121705600	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr7:121667400-121678000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:121667800-121696200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:121668000-121696800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
20	chr7:121668200-121697000	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr7:121669000-121672200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:121670200-121670600	Enhancers	Fetal Brain Male	brain
23	chr7:121670600-121680600	Weak transcription	Fetal Brain Male	brain
24	chr7:121670800-121671200	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr7:121671200-121681800	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr7:121671200-121696800	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr7:121672200-121673000	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr7:121672200-121697200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:121672400-121672800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr7:121672400-121678200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:121672600-121672800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:121672600-121672800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr7:121672800-121673600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:121672800-121674000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr7:121672800-121679800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:121673000-121673200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr7:121673200-121688000	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr7:121673200-121688600	Strong transcription	H1 Cell Line	embryonic stem cell
39	chr7:121673600-121675200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:121673600-121679400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:121674000-121687800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr7:121675200-121677400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:121675400-121676400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
44	chr7:121675600-121688000	Strong transcription	H9 Cell Line	embryonic stem cell
45	chr7:121676400-121677400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr7:121677400-121677800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
47	chr7:121677400-121688800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:121677800-121680400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr7:121678000-121678200	Enhancers	Fetal Muscle Leg	muscle
50	chr7:121678000-121685800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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