Variant report

Variant	nsv971389
Chromosome Location	chr7:65429706-65439767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:141)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:141 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:65432845-65433050	H1-hESC	embryonic stem cell:	n/a	chr7:65432936-65432950
2	CHD2	chr7:65439414-65439565	K562	blood:	n/a	n/a
3	HMGN3	chr7:65439440-65439692	K562	blood:	n/a	n/a
4	MAFF	chr7:65432882-65432965	HepG2	liver:	n/a	n/a
5	MAFF	chr7:65432782-65433074	K562	blood:	n/a	n/a
6	MAFK	chr7:65432852-65433047	IMR90	lung:	n/a	chr7:65432938-65432953 chr7:65432939-65432949 chr7:65432940-65432949
7	MAFK	chr7:65432774-65433054	HepG2	liver:	n/a	chr7:65432938-65432953 chr7:65432939-65432949 chr7:65432940-65432949
8	MAFK	chr7:65432804-65433059	HepG2	liver:	n/a	chr7:65432938-65432953 chr7:65432939-65432949 chr7:65432940-65432949
9	MAFK	chr7:65432800-65433114	K562	blood:	n/a	chr7:65432938-65432953 chr7:65432939-65432949 chr7:65432940-65432949
10	NFIC	chr7:65439387-65439749	ECC-1	luminal epithelium:	n/a	n/a
11	POLR2A	chr7:65435157-65435517	K562	blood:	n/a	n/a
12	POLR2A	chr7:65432550-65432756	GM12878	blood:	n/a	n/a
13	POLR2A	chr7:65439252-65439294	MCF-7	breast:	n/a	n/a
14	POLR2A	chr7:65438943-65439045	GM12878	blood:	n/a	n/a
15	POLR2A	chr7:65432687-65432800	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr7:65439010-65439130	HepG2	liver:	n/a	n/a
17	POLR2A	chr7:65439368-65440405	PFSK-1	brain:	n/a	n/a
18	POLR2A	chr7:65430079-65430415	K562	blood:	n/a	n/a
19	POLR2A	chr7:65433348-65433624	K562	blood:	n/a	n/a
20	POLR2A	chr7:65437512-65437999	GM12892	blood:	n/a	n/a
21	POLR2A	chr7:65430060-65430778	K562	blood:	n/a	n/a
22	POLR2A	chr7:65433738-65434151	K562	blood:	n/a	n/a
23	POLR2A	chr7:65435966-65436234	K562	blood:	n/a	n/a
24	POLR2A	chr7:65439145-65439777	K562	blood:	n/a	n/a
25	POLR2A	chr7:65438929-65439266	PFSK-1	brain:	n/a	n/a
26	POLR2A	chr7:65437635-65438182	GM12892	blood:	n/a	n/a
27	POLR2A	chr7:65432581-65432635	ProgFib	skin:	n/a	n/a
28	POLR2A	chr7:65438783-65438791	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr7:65439284-65440503	SK-N-MC	brain:	n/a	n/a
30	POLR2A	chr7:65437441-65437459	HepG2	liver:	n/a	n/a
31	POLR2A	chr7:65436193-65436207	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr7:65437117-65437392	HepG2	liver:	n/a	n/a
33	POLR2A	chr7:65429748-65430018	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:65439515-65439666	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr7:65434558-65434580	HepG2	liver:	n/a	n/a
36	POLR2A	chr7:65432491-65432988	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr7:65432481-65432742	HL-60	blood:	n/a	n/a
38	POLR2A	chr7:65437958-65438080	GM12878	blood:	n/a	n/a
39	POLR2A	chr7:65433335-65433934	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr7:65433648-65433966	HepG2	liver:	n/a	n/a
41	POLR2A	chr7:65432936-65433035	A549	lung:	n/a	n/a
42	POLR2A	chr7:65430112-65430314	HepG2	liver:	n/a	n/a
43	POLR2A	chr7:65439119-65440321	GM12878	blood:	n/a	n/a
44	POLR2A	chr7:65432598-65432731	GM12878	blood:	n/a	n/a
45	POLR2A	chr7:65439242-65439348	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr7:65438227-65438267	HepG2	liver:	n/a	n/a
47	POLR2A	chr7:65431808-65431869	ProgFib	skin:	n/a	n/a
48	POLR2A	chr7:65439003-65440498	GM12892	blood:	n/a	n/a
49	POLR2A	chr7:65429600-65430080	SK-N-MC	brain:	n/a	n/a
50	POLR2A	chr7:65433619-65433636	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65439432-65439482	GM19239	blood:	n/a
2	chr7:65439512-65439562	PANC-1	pancreas:	n/a
3	chr7:65439432-65439482	SK-N-SH_RA	brain:	n/a
4	chr7:65439512-65439562	T-47D	breast:	n/a
5	chr7:65439432-65439482	HepG2	liver:	n/a
6	chr7:65439432-65439482	HL-60	blood:	n/a
7	chr7:65439432-65439482	RPTEC	kidney:	n/a
8	chr7:65439432-65439482	GM12891	blood:	n/a
9	chr7:65439432-65439482	HRE	kidney:	n/a
10	chr7:65439512-65439562	GM12891	blood:	n/a
11	chr7:65439432-65439482	AG10803	skin:	n/a
12	chr7:65439512-65439562	PrEC	prostate:	n/a
13	chr7:65439432-65439482	HCT-116	colon:	n/a
14	chr7:65439432-65439482	LNCaP	prostate:	n/a
15	chr7:65439512-65439562	SAEC	small airway:	n/a
16	chr7:65439432-65439482	SK-N-MC	brain:	n/a
17	chr7:65439512-65439562	K562	blood:	n/a
18	chr7:65439512-65439562	HRPEpiC	eye:	n/a
19	chr7:65439432-65439482	MCF-7	breast:	n/a
20	chr7:65439432-65439482	AG09319	gingival:	n/a
21	chr7:65439432-65439482	HNPCEpiC	eye:	n/a
22	chr7:65439432-65439482	ovcar-3	ovarian:	n/a
23	chr7:65439512-65439562	HepG2	liver:	n/a
24	chr7:65439432-65439482	ECC-1	luminal epithelium:	n/a
25	chr7:65439432-65439482	AG09309	skin:	n/a
26	chr7:65439512-65439562	RPTEC	kidney:	n/a
27	chr7:65439512-65439562	HUVEC	blood vessel:	n/a
28	chr7:65439432-65439482	A549	lung:	n/a
29	chr7:65439432-65439482	PANC-1	pancreas:	n/a
30	chr7:65439512-65439562	Caco-2	colon:	n/a
31	chr7:65439432-65439482	SAEC	small airway:	n/a
32	chr7:65439432-65439482	K562	blood:	n/a
33	chr7:65439432-65439482	PFSK-1	brain:	n/a
34	chr7:65439432-65439482	U87	brain:	n/a
35	chr7:65439432-65439482	BE2_C	brain:	n/a
36	chr7:65439432-65439482	HIPEpiC	eye:	n/a
37	chr7:65439512-65439562	BE2_C	brain:	n/a
38	chr7:65439512-65439562	AG10803	skin:	n/a
39	chr7:65439512-65439562	U87	brain:	n/a
40	chr7:65439432-65439482	GM06990	blood:	n/a
41	chr7:65439432-65439482	AG04450	lung:	fetal
42	chr7:65439432-65439482	Hela-S3	cervix:	n/a
43	chr7:65439512-65439562	SK-N-SH_RA	brain:	n/a
44	chr7:65439432-65439482	T-47D	breast:	n/a
45	chr7:65439432-65439482	NT2-D1	testis:	n/a
46	chr7:65439512-65439562	CMK	blood:	n/a
47	chr7:65439432-65439482	H1-hESC	embryonic stem cell:	embryo
48	chr7:65439432-65439482	BJ	skin:	n/a
49	chr7:65439432-65439482	Caco-2	colon:	n/a
50	chr7:65439512-65439562	SKMC	muscle:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65426424..65431277-chr7:65442612..65445930,6	K562	blood:
2	chr7:65431361..65432924-chr7:65439699..65441509,2	K562	blood:
3	chr7:65425587..65427267-chr7:65432943..65434454,2	K562	blood:
4	chr7:65430936..65433654-chr7:65438028..65439679,2	MCF-7	breast:
5	chr7:65439470..65441298-chr7:65540371..65542201,2	K562	blood:
6	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
7	chr7:65431377..65432977-chr7:65445764..65448122,2	K562	blood:
8	chr7:65431361..65432924-chr7:65439699..65441509,2	K562	blood:

No data

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

Extended variants
information (count: 437 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574169660	chr7:65429719-65429720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs558214758	chr7:65429758-65429759	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs193095656	chr7:65429777-65429778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185406376	chr7:65429791-65429792	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs573411597	chr7:65429824-65429825	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189020496	chr7:65429833-65429834	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565254126	chr7:65429847-65429848	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148813284	chr7:65429873-65429874	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs201838878	chr7:65430015-65430016	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181502657	chr7:65430049-65430050	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs139007306	chr7:65430057-65430058	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560915826	chr7:65430061-65430062	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150686465	chr7:65430062-65430063	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566818214	chr7:65430067-65430068	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545028138	chr7:65430078-65430079	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs548280038	chr7:65430079-65430080	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs184247705	chr7:65430135-65430136	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188482275	chr7:65430150-65430151	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs73372623	chr7:65430155-65430156	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528140837	chr7:65430212-65430213	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143506896	chr7:65430252-65430253	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370320201	chr7:65430296-65430297	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35197523	chr7:65430299-65430300	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571175222	chr7:65430310-65430311	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs568911405	chr7:65430391-65430392	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs180928677	chr7:65430424-65430425	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551254055	chr7:65430452-65430453	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567893184	chr7:65430455-65430456	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536826720	chr7:65430483-65430484	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs553573309	chr7:65430487-65430488	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78010058	chr7:65430492-65430493	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs376268079	chr7:65430527-65430528	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10229667	chr7:65430607-65430608	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111790613	chr7:65430621-65430622	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs4717280	chr7:65430703-65430704	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs143992176	chr7:65430705-65430706	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575583258	chr7:65430719-65430720	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61210523	chr7:65430723-65430724	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs57050110	chr7:65430725-65430726	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544324767	chr7:65430743-65430744	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs58924261	chr7:65430757-65430758	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs7800210	chr7:65430809-65430810	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs573886177	chr7:65430879-65430880	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542528491	chr7:65430886-65430887	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs112402002	chr7:65430895-65430896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559092755	chr7:65430929-65430930	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs28628473	chr7:65430938-65430939	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs28460798	chr7:65430945-65430946	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs28667742	chr7:65430946-65430947	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs28669341	chr7:65430955-65430956	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:255 , 50 per page) page: 1 2 3 4 5 6

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	chr7:65423600-65442200	Strong transcription	Duodenum Mucosa	Duodenum
46	chr7:65423600-65442400	Strong transcription	Right Ventricle	heart
47	chr7:65423600-65445000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr7:65423600-65445400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:65423600-65445400	Strong transcription	Fetal Muscle Leg	muscle
50	chr7:65423800-65431200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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