Variant report

Variant	nsv1029800
Chromosome Location	chr7:65309327-65367692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:540)
CpG islands
(count:550)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:540 , 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	ARID3A	chr7:65317529-65317586	HepG2	liver:	n/a	n/a
2	BACH1	chr7:65338017-65338205	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:65363733-65363930	GM12878	blood:	n/a	n/a
4	CBX3	chr7:65349978-65350321	K562	blood:	n/a	n/a
5	CBX3	chr7:65313184-65313538	K562	blood:	n/a	n/a
6	CBX3	chr7:65349953-65350396	K562	blood:	n/a	n/a
7	CCNT2	chr7:65337783-65338592	K562	blood:	n/a	chr7:65338186-65338195
8	CEBPB	chr7:65338012-65338138	A549	lung:	n/a	n/a
9	CEBPB	chr7:65337697-65338239	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr7:65317457-65317641	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:65316813-65317139	K562	blood:	n/a	chr7:65316972-65316983
12	CEBPB	chr7:65357879-65358155	K562	blood:	n/a	n/a
13	CEBPB	chr7:65332341-65332420	K562	blood:	n/a	chr7:65332396-65332407
14	CEBPB	chr7:65316853-65317020	Hela-S3	cervix:	n/a	chr7:65316972-65316983
15	CEBPB	chr7:65340770-65341035	A549	lung:	n/a	n/a
16	CEBPB	chr7:65357854-65358191	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:65334430-65334653	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:65340715-65341029	K562	blood:	n/a	n/a
19	CEBPB	chr7:65313883-65313907	IMR90	lung:	n/a	chr7:65313890-65313901
20	CEBPB	chr7:65332878-65332911	K562	blood:	n/a	chr7:65332889-65332900
21	CEBPB	chr7:65313890-65313913	HepG2	liver:	n/a	chr7:65313890-65313901
22	CEBPB	chr7:65357995-65358022	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:65338009-65338209	K562	blood:	n/a	n/a
24	CEBPB	chr7:65316917-65317009	HepG2	liver:	n/a	chr7:65316972-65316983
25	CEBPB	chr7:65337913-65338272	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:65332776-65332976	HepG2	liver:	n/a	chr7:65332889-65332900
27	CEBPB	chr7:65340839-65340967	K562	blood:	n/a	n/a
28	CEBPB	chr7:65340825-65340981	K562	blood:	n/a	n/a
29	CEBPB	chr7:65338072-65338234	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:65316843-65317061	K562	blood:	n/a	chr7:65316972-65316983
31	CEBPB	chr7:65334430-65334631	A549	lung:	n/a	n/a
32	CEBPB	chr7:65347599-65347887	K562	blood:	n/a	chr7:65347728-65347741 chr7:65347728-65347739 chr7:65347841-65347852 chr7:65347654-65347667
33	CEBPB	chr7:65337762-65338153	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:65317549-65317757	A549	lung:	n/a	n/a
35	CEBPB	chr7:65316797-65317059	K562	blood:	n/a	chr7:65316972-65316983
36	CEBPB	chr7:65319952-65320112	K562	blood:	n/a	chr7:65320028-65320039
37	CEBPB	chr7:65340848-65340966	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:65319992-65320101	HepG2	liver:	n/a	chr7:65320028-65320039
39	CEBPB	chr7:65347681-65347818	K562	blood:	n/a	chr7:65347728-65347741 chr7:65347728-65347739
40	CEBPB	chr7:65332768-65333066	IMR90	lung:	n/a	chr7:65332889-65332900
41	CEBPB	chr7:65332307-65332445	HepG2	liver:	n/a	chr7:65332396-65332407
42	CEBPB	chr7:65340761-65341049	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:65340776-65341047	IMR90	lung:	n/a	n/a
44	CEBPD	chr7:65337963-65338299	HepG2	liver:	n/a	n/a
45	CHD1	chr7:65338466-65338502	GM12878	blood:	n/a	n/a
46	CHD1	chr7:65339184-65339363	GM12878	blood:	n/a	n/a
47	CHD2	chr7:65337705-65338547	Hela-S3	cervix:	n/a	n/a
48	CREB1	chr7:65337935-65338206	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr7:65337861-65338372	K562	blood:	n/a	n/a
50	CREB1	chr7:65337827-65338529	HepG2	liver:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65338716-65338766	H1-hESC	embryonic stem cell:	embryo
2	chr7:65338716-65338766	H1-hESC	embryonic stem cell:	embryo
3	chr7:65338708-65338758	HRE	kidney:	n/a
4	chr7:65315216-65315266	IMR90	lung:	fetal
5	chr7:65338427-65338477	SK-N-SH_RA	brain:	n/a
6	chr7:65338427-65338477	A549	lung:	n/a
7	chr7:65315216-65315266	HEEpiC	esophagus:	n/a
8	chr7:65338716-65338766	AG10803	skin:	n/a
9	chr7:65315216-65315266	A549	lung:	n/a
10	chr7:65338427-65338477	NT2-D1	testis:	n/a
11	chr7:65338427-65338477	BE2_C	brain:	n/a
12	chr7:65338427-65338477	HEEpiC	esophagus:	n/a
13	chr7:65337895-65337945	U87	brain:	n/a
14	chr7:65337924-65337974	NH-A	brain:	n/a
15	chr7:65315216-65315266	Caco-2	colon:	n/a
16	chr7:65338716-65338766	AG04449	skin:	fetal
17	chr7:65337895-65337945	NT2-D1	testis:	n/a
18	chr7:65338708-65338758	AG09319	gingival:	n/a
19	chr7:65315216-65315266	BJ	skin:	n/a
20	chr7:65340693-65340743	AG09309	skin:	n/a
21	chr7:65338708-65338758	NHDF-neo	bronchial:	n/a
22	chr7:65338708-65338758	HCM	heart:	n/a
23	chr7:65338708-65338758	GM12878	blood:	n/a
24	chr7:65315216-65315266	GM19239	blood:	n/a
25	chr7:65338055-65338105	Jurkat	blood:	n/a
26	chr7:65337924-65337974	GM06990	blood:	n/a
27	chr7:65338427-65338477	H1-hESC	embryonic stem cell:	embryo
28	chr7:65338427-65338477	AG04449	skin:	fetal
29	chr7:65338055-65338105	CMK	blood:	n/a
30	chr7:65338427-65338477	K562	blood:	n/a
31	chr7:65337895-65337945	PANC-1	pancreas:	n/a
32	chr7:65334477-65334527	BJ	skin:	n/a
33	chr7:65337924-65337974	SAEC	small airway:	n/a
34	chr7:65337924-65337974	LNCaP	prostate:	n/a
35	chr7:65337924-65337974	HUVEC	blood vessel:	n/a
36	chr7:65334477-65334527	NH-A	brain:	n/a
37	chr7:65340693-65340743	LNCaP	prostate:	n/a
38	chr7:65338055-65338105	HCPEpiC	choroid plexus:	n/a
39	chr7:65338716-65338766	BJ	skin:	n/a
40	chr7:65338427-65338477	HCF	heart:	n/a
41	chr7:65334477-65334527	H1-hESC	embryonic stem cell:	embryo
42	chr7:65315216-65315266	U87	brain:	n/a
43	chr7:65338708-65338758	PrEC	prostate:	n/a
44	chr7:65337895-65337945	GM19239	blood:	n/a
45	chr7:65338708-65338758	HCT-116	colon:	n/a
46	chr7:65338708-65338758	GM12891	blood:	n/a
47	chr7:65338708-65338758	Caco-2	colon:	n/a
48	chr7:65315216-65315266	Jurkat	blood:	n/a
49	chr7:65340693-65340743	PANC-1	pancreas:	n/a
50	chr7:65338708-65338758	HepG2	liver:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:64498559..64499288-chr7:65338067..65339051,2	NB4	blood:
2	chr7:65303936..65305643-chr7:65310020..65312064,2	MCF-7	breast:
3	chr11:62609016..62609720-chr7:65338341..65338852,2	Hela-S3	cervix:
4	chr7:65214366..65217502-chr7:65337041..65339664,3	MCF-7	breast:
5	chr7:64498619..64500351-chr7:65337220..65338727,3	MCF-7	breast:
6	chr7:65337864..65339398-chr7:65445758..65448693,2	K562	blood:
7	chr7:65341116..65343693-chr7:65343761..65346299,3	K562	blood:
8	chr7:65341116..65343693-chr7:65343761..65346299,3	K562	blood:
9	chr7:65366932..65368571-chr7:65372098..65374403,2	K562	blood:
10	chr7:65337072..65340818-chr7:65346369..65349456,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VKORC1L1-4	chr7:65318013-65318060	NONHSAT121122

No data

Variant related genes	Relation type
RNU6-973P	TF binding region
VKORC1L1	TF binding region
RNU6-973P	CpG island
VKORC1L1	CpG island
ENSG00000133316	chromatin interactions
ENSG00000228409	chromatin interactions
ENSG00000236529	chromatin interactions
ENSG00000234585	chromatin interactions
ENSG00000196715	chromatin interactions
ENSG00000169919	chromatin interactions
ENSG00000239985	chromatin interactions

Extended variants
information (count: 1757 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1757 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4454721	chr7:65309327-65309328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76598184	chr7:65309331-65309332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62470863	chr7:65309335-65309336	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs76738965	chr7:65309348-65309349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367585757	chr7:65309383-65309384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75720727	chr7:65309384-65309385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76308912	chr7:65309388-65309389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78182993	chr7:65309397-65309398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188298462	chr7:65309407-65309408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74510084	chr7:65309411-65309412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73138202	chr7:65309426-65309427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71875169	chr7:65309480-65309481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201841922	chr7:65309496-65309497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180912428	chr7:65309497-65309498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200342506	chr7:65309499-65309500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148450646	chr7:65309500-65309501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76135604	chr7:65309561-65309562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75784242	chr7:65309637-65309638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570888536	chr7:65309645-65309646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78037340	chr7:65309649-65309650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74390406	chr7:65309650-65309651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566564447	chr7:65309652-65309653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114580232	chr7:65309658-65309659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368704499	chr7:65309722-65309723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552277118	chr7:65309731-65309732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569006063	chr7:65309736-65309737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs151178396	chr7:65309757-65309758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537828979	chr7:65309791-65309792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199640260	chr7:65309817-65309818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554610288	chr7:65309944-65309945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568698162	chr7:65309945-65309946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371207886	chr7:65309959-65309960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201950951	chr7:65309964-65309965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112418960	chr7:65310070-65310071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200853360	chr7:65310139-65310140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150998430	chr7:65310181-65310182	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs112709970	chr7:65310193-65310194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs374602547	chr7:65310203-65310204	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs74634677	chr7:65310236-65310237	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540059897	chr7:65310237-65310238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs556231930	chr7:65310274-65310275	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141973593	chr7:65310283-65310284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542203600	chr7:65310380-65310381	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541773580	chr7:65310383-65310384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs77778285	chr7:65310397-65310398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201669230	chr7:65310406-65310407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556110509	chr7:65310416-65310417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs561755391	chr7:65310417-65310418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs145732929	chr7:65310440-65310441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575865860	chr7:65310442-65310443	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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

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	chr7:65264000-65310800	Weak transcription	Fetal Intestine Small	intestine
2	chr7:65266800-65311000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:65297400-65311000	Weak transcription	Liver	Liver
4	chr7:65302200-65311000	Weak transcription	Right Ventricle	heart
5	chr7:65304000-65311000	Weak transcription	Pancreas	Pancrea
6	chr7:65304600-65310600	Weak transcription	Fetal Intestine Large	intestine
7	chr7:65305800-65311000	Weak transcription	Stomach Mucosa	stomach
8	chr7:65310600-65311800	Enhancers	Fetal Intestine Large	intestine
9	chr7:65310800-65311200	Enhancers	K562	blood
10	chr7:65310800-65312000	Enhancers	Fetal Intestine Small	intestine
11	chr7:65311000-65311200	Enhancers	Pancreas	Pancrea
12	chr7:65311000-65311200	Enhancers	Right Ventricle	heart
13	chr7:65311000-65311400	Enhancers	Liver	Liver
14	chr7:65311000-65311600	Enhancers	Stomach Mucosa	stomach
15	chr7:65311000-65311800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:65311200-65311800	Enhancers	Adipose Nuclei	Adipose
17	chr7:65311800-65313200	Weak transcription	Adipose Nuclei	Adipose
18	chr7:65316000-65317400	Weak transcription	Adipose Nuclei	Adipose
19	chr7:65317400-65317800	Enhancers	Adipose Nuclei	Adipose
20	chr7:65317400-65318800	Enhancers	HepG2	liver
21	chr7:65317800-65321800	Weak transcription	Adipose Nuclei	Adipose
22	chr7:65318800-65319200	Active TSS	HepG2	liver
23	chr7:65319000-65319800	Enhancers	K562	blood
24	chr7:65319200-65319400	Flanking Active TSS	HepG2	liver
25	chr7:65319400-65320400	Enhancers	HepG2	liver
26	chr7:65320400-65322800	Weak transcription	HepG2	liver
27	chr7:65321800-65322400	Enhancers	Adipose Nuclei	Adipose
28	chr7:65322000-65322200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:65322200-65322800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:65322400-65323000	Weak transcription	Adipose Nuclei	Adipose
31	chr7:65322800-65323200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:65322800-65323200	Enhancers	Liver	Liver
33	chr7:65322800-65323200	Enhancers	HepG2	liver
34	chr7:65323000-65323200	Enhancers	Adipose Nuclei	Adipose
35	chr7:65330800-65338200	Weak transcription	Right Atrium	heart
36	chr7:65334200-65334800	Enhancers	NHLF	lung
37	chr7:65334400-65334600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:65334400-65334600	Enhancers	HUVEC	blood vessel
39	chr7:65334400-65334800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:65334600-65334800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:65334600-65334800	Enhancers	HSMMtube	muscle
42	chr7:65334600-65338400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:65334800-65335800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr7:65334800-65337400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:65334800-65337800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:65334800-65338200	Weak transcription	NHLF	lung
47	chr7:65335800-65336000	Enhancers	Primary B cells from cord blood	blood
48	chr7:65335800-65336000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:65335800-65336400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr7:65335800-65336600	Enhancers	Fetal Muscle Trunk	muscle

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