Variant report

Variant	esv18831
Chromosome Location	chr7:64534085-64581674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:580)
CpG islands
(count:611)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:64541546-64541931	K562	blood:	n/a	n/a
2	ATF2	chr7:64541527-64541853	GM12878	blood:	n/a	n/a
3	ATF2	chr7:64541453-64541816	GM12878	blood:	n/a	n/a
4	ATF3	chr7:64541560-64541795	K562	blood:	n/a	n/a
5	BATF	chr7:64541643-64541950	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:64541090-64541263	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:64541395-64541827	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:64541415-64541499	K562	blood:	n/a	n/a
9	BRCA1	chr7:64541586-64541752	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:64541691-64541792	GM12878	blood:	n/a	n/a
11	BRCA1	chr7:64541526-64541924	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr7:64575969-64576353	K562	blood:	n/a	n/a
13	CBX3	chr7:64541167-64542125	K562	blood:	n/a	n/a
14	CBX3	chr7:64568683-64569067	K562	blood:	n/a	n/a
15	CBX3	chr7:64575978-64576471	K562	blood:	n/a	n/a
16	CEBPB	chr7:64541514-64542396	K562	blood:	n/a	chr7:64541668-64541676
17	CEBPB	chr7:64541591-64541839	HepG2	liver:	n/a	chr7:64541668-64541676
18	CEBPB	chr7:64541375-64542360	Hela-S3	cervix:	n/a	chr7:64541668-64541676
19	CEBPB	chr7:64541804-64542117	K562	blood:	n/a	n/a
20	CEBPB	chr7:64541555-64542417	K562	blood:	n/a	chr7:64541668-64541676
21	CEBPB	chr7:64541592-64541776	HepG2	liver:	n/a	chr7:64541668-64541676
22	CEBPB	chr7:64541600-64542303	A549	lung:	n/a	chr7:64541668-64541676
23	CEBPB	chr7:64541517-64542119	HepG2	liver:	n/a	chr7:64541668-64541676
24	CEBPB	chr7:64541534-64542126	HepG2	liver:	n/a	chr7:64541668-64541676
25	CEBPB	chr7:64541851-64541986	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:64541525-64542395	IMR90	lung:	n/a	chr7:64541668-64541676
27	CEBPB	chr7:64541848-64542012	MCF-7	breast:	n/a	n/a
28	CEBPD	chr7:64541630-64541831	HepG2	liver:	n/a	n/a
29	CEBPD	chr7:64541459-64542104	K562	blood:	n/a	n/a
30	CEBPD	chr7:64541549-64541854	HepG2	liver:	n/a	n/a
31	CHD2	chr7:64541398-64541598	HepG2	liver:	n/a	n/a
32	CHD2	chr7:64541280-64541898	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr7:64541430-64541898	GM12878	blood:	n/a	n/a
34	CREB1	chr7:64541612-64541964	GM12878	blood:	n/a	n/a
35	CREB1	chr7:64541619-64541995	GM12878	blood:	n/a	n/a
36	CREB1	chr7:64541565-64542019	HepG2	liver:	n/a	n/a
37	CREB1	chr7:64541599-64541974	K562	blood:	n/a	n/a
38	CREB1	chr7:64541623-64541938	ECC-1	luminal epithelium:	n/a	n/a
39	CREB1	chr7:64541619-64541973	HepG2	liver:	n/a	n/a
40	CREB1	chr7:64541618-64541838	K562	blood:	n/a	n/a
41	CREB1	chr7:64541611-64541983	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr7:64541611-64541822	A549	lung:	n/a	n/a
43	CREB1	chr7:64541493-64541815	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr7:64541446-64541942	A549	lung:	n/a	n/a
45	CTCF	chr7:64563217-64563324	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:64541340-64541490	GM12872	blood:	n/a	n/a
47	CTCF	chr7:64541400-64541550	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr7:64541340-64541490	GM12869	blood:	n/a	n/a
49	CTCF	chr7:64562860-64563010	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:64541300-64541450	RPTEC	kidney:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64540465-64540515	HRE	kidney:	n/a
2	chr7:64540465-64540515	HRE	kidney:	n/a
3	chr7:64541193-64541243	ProgFib	skin:	n/a
4	chr7:64540465-64540515	NH-A	brain:	n/a
5	chr7:64537871-64537921	GM19239	blood:	n/a
6	chr7:64537871-64537921	AG10803	skin:	n/a
7	chr7:64537871-64537921	GM12878	blood:	n/a
8	chr7:64537091-64537141	NT2-D1	testis:	n/a
9	chr7:64535504-64535554	RPTEC	kidney:	n/a
10	chr7:64535486-64535536	NH-A	brain:	n/a
11	chr7:64537091-64537141	U87	brain:	n/a
12	chr7:64580908-64580958	HEEpiC	esophagus:	n/a
13	chr7:64540465-64540515	A549	lung:	n/a
14	chr7:64535486-64535536	SK-N-SH	brain:	n/a
15	chr7:64541387-64541437	T-47D	breast:	n/a
16	chr7:64541923-64541973	HRCEpiC	kidney:	n/a
17	chr7:64535504-64535554	LNCaP	prostate:	n/a
18	chr7:64541387-64541437	HAEpiC	amniotic membrane:	n/a
19	chr7:64540465-64540515	U87	brain:	n/a
20	chr7:64537871-64537921	T-47D	breast:	n/a
21	chr7:64535486-64535536	NT2-D1	testis:	n/a
22	chr7:64540465-64540515	LNCaP	prostate:	n/a
23	chr7:64537871-64537921	HEEpiC	esophagus:	n/a
24	chr7:64541193-64541243	A549	lung:	n/a
25	chr7:64540465-64540515	HEEpiC	esophagus:	n/a
26	chr7:64541387-64541437	AG04450	lung:	fetal
27	chr7:64540465-64540515	NB4	blood:	n/a
28	chr7:64541923-64541973	MCF10A-Er-Src	breast:	n/a
29	chr7:64541923-64541973	HIPEpiC	eye:	n/a
30	chr7:64541387-64541437	HRPEpiC	eye:	n/a
31	chr7:64580908-64580958	AG09319	gingival:	n/a
32	chr7:64535504-64535554	CMK	blood:	n/a
33	chr7:64535486-64535536	MCF10A-Er-Src	breast:	n/a
34	chr7:64580908-64580958	IMR90	lung:	fetal
35	chr7:64535486-64535536	Hela-S3	cervix:	n/a
36	chr7:64541923-64541973	SAEC	small airway:	n/a
37	chr7:64537091-64537141	ProgFib	skin:	n/a
38	chr7:64537871-64537921	HUVEC	blood vessel:	n/a
39	chr7:64580908-64580958	HCM	heart:	n/a
40	chr7:64540465-64540515	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:64541923-64541973	ovcar-3	ovarian:	n/a
42	chr7:64541923-64541973	SK-N-MC	brain:	n/a
43	chr7:64541923-64541973	SKMC	muscle:	n/a
44	chr7:64580908-64580958	NT2-D1	testis:	n/a
45	chr7:64537091-64537141	GM12891	blood:	n/a
46	chr7:64535504-64535554	AG04449	skin:	fetal
47	chr7:64541387-64541437	HepG2	liver:	n/a
48	chr7:64541193-64541243	Caco-2	colon:	n/a
49	chr7:64541923-64541973	NH-A	brain:	n/a
50	chr7:64540465-64540515	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:64540231..64542866-chr7:65234211..65237009,2	MCF-7	breast:
2	chr7:64541235..64542233-chr7:65235555..65236448,5	MCF-7	breast:
3	chr7:64499257..64501633-chr7:64540419..64543070,2	MCF-7	breast:
4	chr2:157191420..157192342-chr7:64541745..64542280,2	Hela-S3	cervix:
5	chr7:64541401..64541976-chr7:65235201..65235732,3	MCF-7	breast:
6	chr7:64541143..64541896-chr7:65235210..65235720,2	Hela-S3	cervix:
7	chr1:236958470..236959023-chr7:64541184..64541935,2	Hela-S3	cervix:
8	chr7:64541160..64542217-chr7:65235379..65236226,3	HCT-116	colon:
9	chr20:30192973..30193963-chr7:64540947..64541759,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF273-7	chr7:64544612-64544635	NONHSAT121075
2	lnc-ZNF273-7	chr7:64568773-64569143	NONHSAT121075
3	lnc-ZNF273-7	chr7:64563733-64563817	NONHSAT121075
4	lnc-ZNF273-7	chr7:64552258-64552330	NONHSAT121075

No data

Variant related genes	Relation type
ENSG00000226002	TF binding region
ENSG00000227113	TF binding region
ENSG00000226002	CpG island
ENSG00000227113	CpG island
ENSG00000116984	chromatin interactions
ENSG00000125968	chromatin interactions

Extended variants
information (count: 2000 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2000 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576003327	chr7:64534129-64534130	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs72606557	chr7:64534151-64534152	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs1799335	chr7:64534161-64534162	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs572670967	chr7:64534165-64534166	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs542376984	chr7:64534166-64534167	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561055417	chr7:64534191-64534192	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529965128	chr7:64534197-64534198	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147092229	chr7:64534207-64534208	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs59144687	chr7:64534208-64534209	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs546819293	chr7:64534223-64534224	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs560145034	chr7:64534273-64534274	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs116410932	chr7:64534370-64534371	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs551856478	chr7:64534401-64534402	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs568863014	chr7:64534426-64534427	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs537531548	chr7:64534456-64534457	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547922061	chr7:64534470-64534471	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs147141567	chr7:64534636-64534637	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs568312016	chr7:64534672-64534673	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs370313768	chr7:64534675-64534676	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs140294378	chr7:64534811-64534812	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs373071528	chr7:64535224-64535225	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs147712144	chr7:64535240-64535241	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs534087104	chr7:64535273-64535274	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs71533998	chr7:64535312-64535313	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs571029701	chr7:64535338-64535339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs370677301	chr7:64535387-64535388	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556270608	chr7:64535393-64535394	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs1852024	chr7:64535417-64535418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186827745	chr7:64535460-64535461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555852894	chr7:64535470-64535471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1799102	chr7:64535480-64535481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540016681	chr7:64535489-64535490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560314577	chr7:64535499-64535500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs5001356	chr7:64535529-64535530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs546112380	chr7:64535622-64535623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562133391	chr7:64535630-64535631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6974079	chr7:64535631-64535632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs547784289	chr7:64535633-64535634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183277428	chr7:64535642-64535643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527407621	chr7:64535692-64535693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187604652	chr7:64535698-64535699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571059459	chr7:64535700-64535701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539737628	chr7:64535725-64535726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569632494	chr7:64535738-64535739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556864834	chr7:64535739-64535740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570368570	chr7:64535761-64535762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533444830	chr7:64535795-64535796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535806870	chr7:64535830-64535831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555811952	chr7:64535831-64535832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547246578	chr7:64535847-64535848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	17426248	CNVD
Cognitive impairment	21505072	CNVD
Schizophrenia	20967226	CNVD
Cancer	21272361	CNVD
Hodgkin''s lymphoma	17606441	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64499600-64541000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:64499800-64541000	Weak transcription	Lung	lung
3	chr7:64499800-64541000	Weak transcription	Ovary	ovary
4	chr7:64500000-64540200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr7:64500000-64541000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr7:64500200-64541000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr7:64500200-64541000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr7:64500200-64541000	Weak transcription	NH-A	brain
9	chr7:64500400-64541000	Weak transcription	Brain Germinal Matrix	brain
10	chr7:64500400-64541000	Weak transcription	Duodenum Mucosa	Duodenum
11	chr7:64500600-64541000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr7:64500600-64541000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:64500600-64541000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:64500600-64541000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:64500600-64541000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr7:64500600-64541000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr7:64500600-64541000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:64500600-64541000	Weak transcription	Hela-S3	cervix
19	chr7:64500600-64541200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr7:64500800-64541200	Weak transcription	Primary T cells from cord blood	blood
21	chr7:64501000-64541000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr7:64504800-64541000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:64507000-64541000	Weak transcription	Pancreas	Pancrea
24	chr7:64515400-64541200	Weak transcription	Aorta	Aorta
25	chr7:64515800-64541200	Weak transcription	Gastric	stomach
26	chr7:64517200-64535000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr7:64517600-64534600	Weak transcription	GM12878-XiMat	blood
28	chr7:64518600-64534800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:64518600-64541000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr7:64520200-64541200	Weak transcription	A549	lung
31	chr7:64520800-64541000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr7:64521800-64541200	Weak transcription	Spleen	Spleen
33	chr7:64522600-64541000	Weak transcription	Brain Anterior Caudate	brain
34	chr7:64522800-64541000	Weak transcription	Right Ventricle	heart
35	chr7:64522800-64541000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr7:64522800-64541200	Weak transcription	Brain Angular Gyrus	brain
37	chr7:64523000-64541000	Weak transcription	Psoas Muscle	Psoas
38	chr7:64523200-64541000	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr7:64523200-64541200	Weak transcription	Brain Hippocampus Middle	brain
40	chr7:64523600-64541000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr7:64523800-64541000	Weak transcription	Fetal Muscle Leg	muscle
42	chr7:64524200-64541000	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr7:64524200-64541000	Weak transcription	HSMM	muscle
44	chr7:64524800-64541000	Weak transcription	Liver	Liver
45	chr7:64525200-64538800	Weak transcription	K562	blood
46	chr7:64525800-64541000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr7:64525800-64541000	Weak transcription	Primary B cells from cord blood	blood
48	chr7:64526800-64541200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:64527600-64541000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:64527600-64541000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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