Variant report

Variant	nsv970554
Chromosome Location	chr7:97489362-97500692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:118)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:118 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97494404-97494584	K562	blood:	n/a	n/a
2	ATF1	chr7:97492217-97492269	K562	blood:	n/a	n/a
3	BHLHE40	chr7:97493254-97493256	K562	blood:	n/a	n/a
4	BHLHE40	chr7:97499597-97499610	K562	blood:	n/a	n/a
5	CCNT2	chr7:97494912-97494960	K562	blood:	n/a	n/a
6	CEBPB	chr7:97498201-97498448	K562	blood:	n/a	n/a
7	CTCF	chr7:97492779-97492821	ProgFib	skin:	n/a	n/a
8	CTCF	chr7:97498245-97498442	T-47D	breast:	n/a	n/a
9	CTCF	chr7:97495521-97495578	GM10248	blood:	n/a	n/a
10	CUX1	chr7:97493814-97493891	K562	blood:	n/a	n/a
11	CUX1	chr7:97499497-97499498	K562	blood:	n/a	n/a
12	CUX1	chr7:97490911-97490960	GM12878	blood:	n/a	n/a
13	CUX1	chr7:97500406-97500519	K562	blood:	n/a	n/a
14	EP300	chr7:97495017-97495104	K562	blood:	n/a	n/a
15	EP300	chr7:97498277-97498371	GM12878	blood:	n/a	n/a
16	EP300	chr7:97493869-97493882	K562	blood:	n/a	n/a
17	FOS	chr7:97500598-97500982	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr7:97500636-97500976	MCF10A-Er-Src	breast:	n/a	n/a
19	GATA3	chr7:97491005-97491105	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr7:97491987-97492053	SH-SY5Y	brain:	n/a	n/a
21	HCFC1	chr7:97493849-97493851	K562	blood:	n/a	n/a
22	HMGN3	chr7:97494826-97494885	K562	blood:	n/a	n/a
23	IRF1	chr7:97494411-97494424	K562	blood:	n/a	n/a
24	IRF1	chr7:97499903-97500009	K562	blood:	n/a	n/a
25	IRF1	chr7:97493696-97493898	K562	blood:	n/a	chr7:97493816-97493830 chr7:97493813-97493824 chr7:97493819-97493830 chr7:97493817-97493830 chr7:97493811-97493831 chr7:97493813-97493827 chr7:97493817-97493830 chr7:97493814-97493825 chr7:97493815-97493829 chr7:97493817-97493830 chr7:97493818-97493835 chr7:97493812-97493826
26	JUND	chr7:97500611-97500658	K562	blood:	n/a	n/a
27	MAFF	chr7:97497683-97498291	K562	blood:	n/a	n/a
28	MAFK	chr7:97497862-97497878	Hela-S3	cervix:	n/a	n/a
29	MAFK	chr7:97497811-97497903	HepG2	liver:	n/a	n/a
30	MAFK	chr7:97497719-97497978	K562	blood:	n/a	n/a
31	MXI1	chr7:97500676-97502096	IMR90	lung:	n/a	n/a
32	MXI1	chr7:97499796-97502607	SK-N-SH	brain:	n/a	n/a
33	MYC	chr7:97492745-97492902	H1-hESC	embryonic stem cell:	n/a	n/a
34	MYC	chr7:97500446-97500588	K562	blood:	n/a	n/a
35	MYC	chr7:97492849-97492865	MCF-7	breast:	n/a	n/a
36	MYC	chr7:97492879-97492965	MCF-7	breast:	n/a	n/a
37	MYC	chr7:97492837-97492841	MCF-7	breast:	n/a	n/a
38	POLR2A	chr7:97494443-97495276	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr7:97494581-97494900	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr7:97480607-97497455	K562	blood:	n/a	n/a
41	POLR2A	chr7:97492514-97492541	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr7:97492349-97493397	K562	blood:	n/a	n/a
43	POLR2A	chr7:97493643-97494059	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr7:97496035-97496211	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr7:97497154-97497450	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr7:97492535-97493330	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr7:97494966-97495230	K562	blood:	n/a	n/a
48	POLR2A	chr7:97497906-97498637	HL-60	blood:	n/a	n/a
49	POLR2A	chr7:97493657-97493890	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr7:97494972-97495339	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97498451-97498501	GM12891	blood:	n/a
2	chr7:97498451-97498501	HMEC	breast:	n/a
3	chr7:97498451-97498501	T-47D	breast:	n/a
4	chr7:97498451-97498501	HCM	heart:	n/a
5	chr7:97498451-97498501	NHBE	bronchial:	n/a
6	chr7:97498451-97498501	Hepatocyte	liver:	n/a
7	chr7:97498451-97498501	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:97498451-97498501	GM12878	blood:	n/a
9	chr7:97498451-97498501	GM12892	blood:	n/a
10	chr7:97498451-97498501	HCPEpiC	choroid plexus:	n/a
11	chr7:97498451-97498501	AG10803	skin:	n/a
12	chr7:97498451-97498501	NH-A	brain:	n/a
13	chr7:97498451-97498501	ProgFib	skin:	n/a
14	chr7:97498451-97498501	NHDF-neo	bronchial:	n/a
15	chr7:97498451-97498501	HCT-116	colon:	n/a
16	chr7:97498451-97498501	NT2-D1	testis:	n/a
17	chr7:97498451-97498501	SK-N-MC	brain:	n/a
18	chr7:97498451-97498501	PFSK-1	brain:	n/a
19	chr7:97498451-97498501	AG09319	gingival:	n/a
20	chr7:97498451-97498501	ovcar-3	ovarian:	n/a
21	chr7:97498451-97498501	HNPCEpiC	eye:	n/a
22	chr7:97498451-97498501	HAEpiC	amniotic membrane:	n/a
23	chr7:97498451-97498501	K562	blood:	n/a
24	chr7:97498451-97498501	BJ	skin:	n/a
25	chr7:97498451-97498501	HUVEC	blood vessel:	n/a
26	chr7:97498451-97498501	Hela-S3	cervix:	n/a
27	chr7:97498451-97498501	HL-60	blood:	n/a
28	chr7:97498451-97498501	H1-hESC	embryonic stem cell:	embryo
29	chr7:97498451-97498501	AoSMC	blood vessel:	n/a
30	chr7:97498451-97498501	AG04449	skin:	fetal
31	chr7:97498451-97498501	ECC-1	luminal epithelium:	n/a
32	chr7:97498451-97498501	CMK	blood:	n/a
33	chr7:97498451-97498501	Caco-2	colon:	n/a
34	chr7:97498451-97498501	HCF	heart:	n/a
35	chr7:97498451-97498501	HRPEpiC	eye:	n/a
36	chr7:97498451-97498501	HEK293	kidney:	embryo
37	chr7:97498451-97498501	SK-N-SH	brain:	n/a
38	chr7:97498451-97498501	SAEC	small airway:	n/a
39	chr7:97498451-97498501	HEEpiC	esophagus:	n/a
40	chr7:97498451-97498501	SK-N-SH_RA	brain:	n/a
41	chr7:97498451-97498501	BE2_C	brain:	n/a
42	chr7:97498451-97498501	AG04450	lung:	fetal
43	chr7:97498451-97498501	U87	brain:	n/a
44	chr7:97498451-97498501	IMR90	lung:	fetal
45	chr7:97498451-97498501	RPTEC	kidney:	n/a
46	chr7:97498451-97498501	SKMC	muscle:	n/a
47	chr7:97498451-97498501	HRE	kidney:	n/a
48	chr7:97498451-97498501	PANC-1	pancreas:	n/a
49	chr7:97498451-97498501	HepG2	liver:	n/a
50	chr7:97498451-97498501	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97481488..97486650-chr7:97486817..97491260,8	K562	blood:
2	chr7:97477704..97479355-chr7:97492611..97494448,2	K562	blood:
3	chr7:97499263..97502446-chr7:97599755..97603082,5	K562	blood:
4	chr7:97499971..97501829-chr7:97601279..97602819,2	MCF-7	breast:
5	chr18:46519407..46519908-chr7:97495184..97495684,2	Hela-S3	cervix:
6	chr7:97499263..97501796-chr7:97600194..97603082,4	K562	blood:
7	chr7:97498933..97501538-chr7:115850035..115852126,2	K562	blood:
8	chr7:97488155..97489772-chr7:97499944..97501920,2	MCF-7	breast:
9	chr7:97496316..97498581-chr7:97499278..97501918,3	MCF-7	breast:
10	chr7:97496316..97498581-chr7:97499278..97501918,3	MCF-7	breast:
11	chr7:97495363..97496869-chr8:47517938..47519464,2	K562	blood:
12	chr7:97494814..97497659-chr7:97498780..97501384,2	MCF-7	breast:
13	chr7:97499747..97502097-chr7:97599134..97602634,6	MCF-7	breast:

No data

Variant related genes	Relation type
ASNS	TF binding region
ENSG00000226744	TF binding region
ASNS	CpG island
ENSG00000226744	CpG island
ENSG00000135269	chromatin interactions
ENSG00000243554	chromatin interactions
ENSG00000070669	chromatin interactions
ENSG00000226744	chromatin interactions

Extended variants
information (count: 501 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563155245	chr7:97489387-97489388	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201067447	chr7:97489413-97489414	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs1017070	chr7:97489430-97489431	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs143289933	chr7:97489503-97489504	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs111330195	chr7:97489534-97489535	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs548735979	chr7:97489545-97489546	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568489388	chr7:97489546-97489547	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs114080878	chr7:97489549-97489550	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs111724238	chr7:97489553-97489554	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs12704947	chr7:97489563-97489564	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs17169184	chr7:97489623-97489624	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs539798891	chr7:97489694-97489695	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs17169185	chr7:97489701-97489702	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs529392312	chr7:97489807-97489808	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs17169186	chr7:97489866-97489867	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs147144679	chr7:97489889-97489890	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs13239311	chr7:97489911-97489912	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs373746349	chr7:97490003-97490004	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs17345286	chr7:97490022-97490023	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs557383620	chr7:97490029-97490030	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs199766359	chr7:97490079-97490080	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11768092	chr7:97490080-97490081	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs79921982	chr7:97490116-97490117	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs115812818	chr7:97490117-97490118	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs73396242	chr7:97490146-97490147	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs537734491	chr7:97490169-97490170	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs545704343	chr7:97490335-97490336	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs386410785	chr7:97490336-97490337	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs386410786	chr7:97490350-97490351	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74858809	chr7:97490351-97490352	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs71108240	chr7:97490352-97490353	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs80131662	chr7:97490353-97490354	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs542091994	chr7:97490355-97490356	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562260330	chr7:97490387-97490388	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140256756	chr7:97490392-97490393	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547915847	chr7:97490395-97490396	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs10231594	chr7:97490403-97490404	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533383542	chr7:97490420-97490421	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574683206	chr7:97490479-97490480	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs10261245	chr7:97490482-97490483	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569882582	chr7:97490495-97490496	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs180816896	chr7:97490505-97490506	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548953251	chr7:97490514-97490515	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565541521	chr7:97490515-97490516	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs553854685	chr7:97490535-97490536	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs10261265	chr7:97490557-97490558	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs577291529	chr7:97490570-97490571	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs148424919	chr7:97490575-97490576	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556901489	chr7:97490577-97490578	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187418552	chr7:97490617-97490618	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97475000-97492800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:97477600-97500600	Weak transcription	Thymus	Thymus
3	chr7:97479000-97501000	Weak transcription	Fetal Intestine Large	intestine
4	chr7:97479200-97500800	Weak transcription	Right Ventricle	heart
5	chr7:97479400-97501000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:97479400-97501000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr7:97479600-97501000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:97479800-97500200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr7:97480000-97491800	Weak transcription	Stomach Mucosa	stomach
10	chr7:97480200-97500600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr7:97480600-97489600	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr7:97480600-97498200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:97480600-97498200	Strong transcription	K562	blood
14	chr7:97480600-97498600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr7:97480800-97490000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr7:97480800-97490600	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr7:97480800-97491000	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr7:97480800-97491000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:97480800-97491600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:97480800-97498400	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:97481000-97500600	Weak transcription	NHDF-Ad	bronchial
22	chr7:97481200-97498000	Weak transcription	Fetal Brain Male	brain
23	chr7:97481400-97500600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:97481400-97500600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr7:97481400-97500600	Weak transcription	Colon Smooth Muscle	Colon
26	chr7:97481400-97501000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr7:97481800-97489600	Weak transcription	Fetal Thymus	thymus
28	chr7:97481800-97492600	Weak transcription	Esophagus	oesophagus
29	chr7:97481800-97500800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:97481800-97501000	Weak transcription	Fetal Intestine Small	intestine
31	chr7:97481800-97501000	Weak transcription	Gastric	stomach
32	chr7:97481800-97501000	Weak transcription	Pancreas	Pancrea
33	chr7:97481800-97501000	Weak transcription	Spleen	Spleen
34	chr7:97482000-97498200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr7:97482200-97497800	Weak transcription	HMEC	breast
36	chr7:97482800-97500800	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr7:97483400-97490200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr7:97483600-97500600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr7:97483600-97500800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr7:97483800-97500800	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr7:97484000-97500400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr7:97484200-97493600	Weak transcription	GM12878-XiMat	blood
43	chr7:97484200-97500600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:97484200-97501000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr7:97484600-97501000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:97485800-97492400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr7:97485800-97497000	Weak transcription	Hela-S3	cervix
48	chr7:97486200-97500800	Weak transcription	Primary hematopoietic stem cells	blood
49	chr7:97486200-97501000	Weak transcription	Fetal Lung	lung
50	chr7:97486400-97492600	Weak transcription	HSMMtube	muscle

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