Variant report

Variant	nsv981505
Chromosome Location	chr7:65428348-65445874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:65445769-65446159	K562	blood:	n/a	n/a
2	ATF2	chr7:65445713-65446255	GM12878	blood:	n/a	n/a
3	ATF2	chr7:65445705-65446301	GM12878	blood:	n/a	n/a
4	BACH1	chr7:65432845-65433050	H1-hESC	embryonic stem cell:	n/a	chr7:65432936-65432950
5	BCL11A	chr7:65445804-65446185	GM12878	blood:	n/a	n/a
6	BCLAF1	chr7:65445700-65446344	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:65445579-65446242	K562	blood:	n/a	n/a
8	BHLHE40	chr7:65445743-65446248	GM12878	blood:	n/a	n/a
9	CBX3	chr7:65445617-65446294	K562	blood:	n/a	n/a
10	CCNT2	chr7:65445729-65446235	K562	blood:	n/a	n/a
11	CEBPB	chr7:65442107-65442335	K562	blood:	n/a	n/a
12	CEBPB	chr7:65445614-65446288	GM12878	blood:	n/a	n/a
13	CHD1	chr7:65445638-65446195	GM12878	blood:	n/a	n/a
14	CHD2	chr7:65439959-65440009	K562	blood:	n/a	n/a
15	CHD2	chr7:65445752-65446128	GM12878	blood:	n/a	n/a
16	CHD2	chr7:65439414-65439565	K562	blood:	n/a	n/a
17	CREB1	chr7:65445614-65446332	GM12878	blood:	n/a	n/a
18	CTCF	chr7:65440880-65441030	K562	blood:	n/a	n/a
19	CTCF	chr7:65440900-65441050	HEK293	kidney:	n/a	n/a
20	CTCF	chr7:65440920-65441022	GM19238	blood:	n/a	n/a
21	CTCF	chr7:65440880-65441030	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr7:65440920-65441070	GM12874	blood:	n/a	n/a
23	CTCF	chr7:65440880-65441030	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr7:65440860-65441010	BE2_C	brain:	n/a	n/a
25	CTCF	chr7:65440857-65441108	HepG2	liver:	n/a	n/a
26	CTCF	chr7:65440925-65440956	GM10266	blood:	n/a	n/a
27	CTCF	chr7:65440894-65441024	HepG2	liver:	n/a	n/a
28	CTCF	chr7:65440891-65441015	GM12878	blood:	n/a	n/a
29	CTCF	chr7:65440920-65441070	GM12872	blood:	n/a	n/a
30	CTCF	chr7:65440820-65440970	HCT-116	colon:	n/a	n/a
31	CTCF	chr7:65440920-65441070	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr7:65440840-65440990	A549	lung:	n/a	n/a
33	CTCF	chr7:65440860-65441010	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:65440896-65441047	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:65440880-65441030	GM12872	blood:	n/a	n/a
36	CTCF	chr7:65440840-65440990	GM12866	blood:	n/a	n/a
37	CTCF	chr7:65440899-65441027	GM12891	blood:	n/a	n/a
38	CTCF	chr7:65440940-65441090	RPTEC	kidney:	n/a	n/a
39	CTCF	chr7:65440820-65440970	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:65440880-65441030	RPTEC	kidney:	n/a	n/a
41	CTCF	chr7:65440860-65441010	GM12873	blood:	n/a	n/a
42	CTCF	chr7:65440920-65441070	GM12868	blood:	n/a	n/a
43	CTCF	chr7:65440909-65441041	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:65440925-65441015	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:65440860-65441010	HepG2	liver:	n/a	n/a
46	CTCF	chr7:65440820-65440970	HRE	kidney:	n/a	n/a
47	CTCF	chr7:65440800-65440950	HEK293	kidney:	n/a	n/a
48	CTCF	chr7:65440840-65440990	GM12878	blood:	n/a	n/a
49	CTCF	chr7:65440880-65441030	HepG2	liver:	n/a	n/a
50	CTCF	chr7:65440880-65441030	HFF	foreskin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65439512-65439562	RPTEC	kidney:	n/a
2	chr7:65445384-65445434	ECC-1	luminal epithelium:	n/a
3	chr7:65444356-65444406	SK-N-SH_RA	brain:	n/a
4	chr7:65439432-65439482	HRE	kidney:	n/a
5	chr7:65439512-65439562	NB4	blood:	n/a
6	chr7:65439432-65439482	HepG2	liver:	n/a
7	chr7:65445384-65445434	NH-A	brain:	n/a
8	chr7:65439512-65439562	HRE	kidney:	n/a
9	chr7:65439432-65439482	AG04450	lung:	fetal
10	chr7:65444356-65444406	HEEpiC	esophagus:	n/a
11	chr7:65444356-65444406	U87	brain:	n/a
12	chr7:65439512-65439562	HMEC	breast:	n/a
13	chr7:65439432-65439482	RPTEC	kidney:	n/a
14	chr7:65444356-65444406	SK-N-SH	brain:	n/a
15	chr7:65445384-65445434	HAEpiC	amniotic membrane:	n/a
16	chr7:65439512-65439562	HRCEpiC	kidney:	n/a
17	chr7:65439512-65439562	AG09319	gingival:	n/a
18	chr7:65439512-65439562	SKMC	muscle:	n/a
19	chr7:65439432-65439482	AG04449	skin:	fetal
20	chr7:65439432-65439482	HCPEpiC	choroid plexus:	n/a
21	chr7:65439512-65439562	AG04450	lung:	fetal
22	chr7:65439512-65439562	Caco-2	colon:	n/a
23	chr7:65439512-65439562	PrEC	prostate:	n/a
24	chr7:65445384-65445434	CMK	blood:	n/a
25	chr7:65445384-65445434	A549	lung:	n/a
26	chr7:65445384-65445434	NT2-D1	testis:	n/a
27	chr7:65439432-65439482	LNCaP	prostate:	n/a
28	chr7:65439432-65439482	HCF	heart:	n/a
29	chr7:65445384-65445434	GM12878	blood:	n/a
30	chr7:65445384-65445434	NHBE	bronchial:	n/a
31	chr7:65439512-65439562	AoSMC	blood vessel:	n/a
32	chr7:65439512-65439562	NHBE	bronchial:	n/a
33	chr7:65439512-65439562	HCF	heart:	n/a
34	chr7:65439432-65439482	HEK293	kidney:	embryo
35	chr7:65444356-65444406	H1-hESC	embryonic stem cell:	embryo
36	chr7:65444356-65444406	NHBE	bronchial:	n/a
37	chr7:65444356-65444406	NB4	blood:	n/a
38	chr7:65439432-65439482	SK-N-MC	brain:	n/a
39	chr7:65445384-65445434	H1-hESC	embryonic stem cell:	embryo
40	chr7:65439432-65439482	Jurkat	blood:	n/a
41	chr7:65444356-65444406	BJ	skin:	n/a
42	chr7:65439512-65439562	HCT-116	colon:	n/a
43	chr7:65445384-65445434	HNPCEpiC	eye:	n/a
44	chr7:65445384-65445434	MCF-7	breast:	n/a
45	chr7:65439432-65439482	SK-N-SH	brain:	n/a
46	chr7:65439512-65439562	ProgFib	skin:	n/a
47	chr7:65444356-65444406	SK-N-MC	brain:	n/a
48	chr7:65444356-65444406	HL-60	blood:	n/a
49	chr7:65445384-65445434	PrEC	prostate:	n/a
50	chr7:65439512-65439562	K562	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65425587..65427267-chr7:65432943..65434454,2	K562	blood:
2	chr7:65441240..65443607-chr7:65444690..65447035,2	MCF-7	breast:
3	chr7:65431377..65432977-chr7:65445764..65448122,2	K562	blood:
4	chr7:65426424..65431277-chr7:65442612..65445930,6	K562	blood:
5	chr7:65337864..65339398-chr7:65445758..65448693,2	K562	blood:
6	chr7:65431361..65432924-chr7:65439699..65441509,2	K562	blood:
7	chr7:65445709..65448649-chr7:65579782..65581390,2	K562	blood:
8	chr7:65439784..65442429-chr7:65442521..65444614,2	MCF-7	breast:
9	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
10	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
11	chr7:65421351..65423087-chr7:65426463..65428555,2	K562	blood:
12	chr7:65431377..65432977-chr7:65445764..65448122,2	K562	blood:
13	chr7:65431361..65432924-chr7:65439699..65441509,2	K562	blood:
14	chr7:65419242..65420839-chr7:65426993..65428588,2	MCF-7	breast:
15	chr7:65430936..65433654-chr7:65438028..65439679,2	MCF-7	breast:
16	chr7:65439470..65441298-chr7:65540371..65542201,2	K562	blood:
17	chr7:65439784..65442429-chr7:65442521..65444614,2	MCF-7	breast:

No data

Variant related genes	Relation type
GUSB	TF binding region
GUSB	CpG island
ENSG00000241258	chromatin interactions
ENSG00000196715	chromatin interactions
ENSG00000126522	chromatin interactions
ENSG00000169919	chromatin interactions

Extended variants
information (count: 806 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566484251	chr7:65428385-65428386	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs569761256	chr7:65428394-65428395	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535089733	chr7:65428396-65428397	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535495432	chr7:65428421-65428422	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377141676	chr7:65428435-65428436	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs937108	chr7:65428452-65428453	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs139154566	chr7:65428512-65428513	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs541279650	chr7:65428525-65428526	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200764498	chr7:65428557-65428558	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138500657	chr7:65428558-65428559	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372318856	chr7:65428577-65428578	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376851856	chr7:65428578-65428579	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs118189608	chr7:65428650-65428651	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
14	rs577805780	chr7:65428716-65428717	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544037785	chr7:65428770-65428771	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563606899	chr7:65428771-65428772	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529422118	chr7:65428784-65428785	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs736270	chr7:65428822-65428823	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs191815431	chr7:65428867-65428868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528506120	chr7:65428902-65428903	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs144081458	chr7:65428903-65428904	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148304965	chr7:65428953-65428954	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372680218	chr7:65428993-65428994	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533141692	chr7:65429006-65429007	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549986044	chr7:65429007-65429008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2008188	chr7:65429013-65429014	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs77390147	chr7:65429024-65429025	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146479736	chr7:65429037-65429038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141149199	chr7:65429051-65429052	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183816559	chr7:65429077-65429078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188360855	chr7:65429078-65429079	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560072634	chr7:65429081-65429082	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577945597	chr7:65429101-65429102	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543638816	chr7:65429107-65429108	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369415664	chr7:65429115-65429116	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574171529	chr7:65429119-65429120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs190212577	chr7:65429176-65429177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs559928132	chr7:65429246-65429247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529250251	chr7:65429249-65429250	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs182474035	chr7:65429280-65429281	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368958999	chr7:65429293-65429294	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545446158	chr7:65429301-65429302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564360146	chr7:65429320-65429321	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113059520	chr7:65429322-65429323	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200228580	chr7:65429329-65429330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs141430018	chr7:65429347-65429348	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373819742	chr7:65429353-65429354	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs150304382	chr7:65429358-65429359	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1061361	chr7:65429359-65429360	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs121918183	chr7:65429369-65429370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	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
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Chronic myeloid leukemia	18641042	CNVD

Chromatin state (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65417800-65432400	Weak transcription	Stomach Mucosa	stomach
2	chr7:65417800-65441600	Strong transcription	Primary T cells from cord blood	blood
3	chr7:65417800-65445400	Weak transcription	Fetal Heart	heart
4	chr7:65418000-65445400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr7:65418200-65434400	Strong transcription	A549	lung
6	chr7:65418400-65442400	Strong transcription	Adipose Nuclei	Adipose
7	chr7:65418400-65445200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:65418800-65442400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:65418800-65444000	Strong transcription	Dnd41	blood
10	chr7:65418800-65445200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:65418800-65445400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:65418800-65445600	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:65418800-65446000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr7:65419000-65440200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr7:65419000-65440600	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr7:65419000-65442400	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr7:65419000-65442400	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr7:65419000-65442600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:65419000-65445200	Strong transcription	Fetal Muscle Trunk	muscle
20	chr7:65419000-65445400	Strong transcription	Fetal Thymus	thymus
21	chr7:65419000-65445400	Strong transcription	Thymus	Thymus
22	chr7:65419200-65445200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:65419400-65445200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr7:65419600-65442400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:65419600-65444800	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr7:65419800-65445400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:65420200-65445200	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr7:65420400-65442200	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr7:65420600-65442400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:65420600-65442400	Strong transcription	Fetal Brain Female	brain
31	chr7:65422400-65444800	Strong transcription	Brain Germinal Matrix	brain
32	chr7:65422400-65445600	Weak transcription	Right Atrium	heart
33	chr7:65422600-65442400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr7:65422800-65440600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:65423000-65433000	Strong transcription	Primary B cells from cord blood	blood
36	chr7:65423000-65441200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr7:65423000-65441200	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr7:65423000-65442400	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:65423000-65442400	Strong transcription	Stomach Smooth Muscle	stomach
40	chr7:65423000-65444800	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr7:65423000-65445600	Strong transcription	Fetal Intestine Large	intestine
42	chr7:65423200-65442400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:65423400-65442200	Strong transcription	Primary T helper cells PMA-I stimulated	--
44	chr7:65423400-65442400	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr7:65423600-65429600	Strong transcription	HMEC	breast
46	chr7:65423600-65442200	Strong transcription	Duodenum Mucosa	Duodenum
47	chr7:65423600-65442400	Strong transcription	Right Ventricle	heart
48	chr7:65423600-65445000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:65423600-65445400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:65423600-65445400	Strong transcription	Fetal Muscle Leg	muscle

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