Variant report

Variant	nsv1029363
Chromosome Location	chr7:140567136-140594073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:223)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:223 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:140587968-140588207	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:140591144-140591252	K562	blood:	n/a	n/a
3	ATF1	chr7:140589590-140589816	K562	blood:	n/a	n/a
4	ATF2	chr7:140581221-140581671	GM12878	blood:	n/a	n/a
5	ATF2	chr7:140576473-140577115	GM12878	blood:	n/a	n/a
6	ATF2	chr7:140576444-140576996	GM12878	blood:	n/a	n/a
7	BATF	chr7:140576508-140576810	GM12878	blood:	n/a	chr7:140576683-140576694
8	BATF	chr7:140581255-140581651	GM12878	blood:	n/a	n/a
9	BATF	chr7:140581246-140581721	GM12878	blood:	n/a	n/a
10	BATF	chr7:140576489-140576848	GM12878	blood:	n/a	chr7:140576683-140576694
11	BCL11A	chr7:140576510-140576778	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:140581398-140581599	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:140581364-140581658	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:140573434-140573480	K562	blood:	n/a	n/a
15	BHLHE40	chr7:140581379-140581795	GM12878	blood:	n/a	n/a
16	CCNT2	chr7:140589534-140589980	K562	blood:	n/a	chr7:140589659-140589668
17	CEBPB	chr7:140587967-140588273	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:140577007-140577309	HepG2	liver:	n/a	chr7:140577116-140577127
19	CEBPB	chr7:140576579-140577334	IMR90	lung:	n/a	chr7:140577116-140577127
20	CEBPB	chr7:140576658-140577357	Hela-S3	cervix:	n/a	chr7:140577116-140577127
21	CEBPB	chr7:140576961-140577313	A549	lung:	n/a	chr7:140577116-140577127
22	CEBPB	chr7:140576935-140577314	HepG2	liver:	n/a	chr7:140577116-140577127
23	CEBPB	chr7:140576774-140577341	H1-hESC	embryonic stem cell:	n/a	chr7:140577116-140577127
24	CEBPB	chr7:140576809-140577467	HCT-116	colon:	n/a	chr7:140577116-140577127
25	CEBPB	chr7:140587993-140588245	K562	blood:	n/a	n/a
26	CEBPB	chr7:140589395-140589913	K562	blood:	n/a	n/a
27	CEBPB	chr7:140576899-140577399	A549	lung:	n/a	chr7:140577116-140577127
28	CEBPB	chr7:140576904-140577282	MCF-7	breast:	n/a	chr7:140577116-140577127
29	CEBPB	chr7:140576891-140577387	ECC-1	luminal epithelium:	n/a	chr7:140577116-140577127
30	CEBPB	chr7:140576982-140577243	K562	blood:	n/a	chr7:140577116-140577127
31	CEBPB	chr7:140587966-140588235	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:140587982-140588232	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:140588531-140588625	HepG2	liver:	n/a	chr7:140588585-140588596
34	CEBPB	chr7:140576884-140577434	A549	lung:	n/a	chr7:140577116-140577127
35	CEBPB	chr7:140576958-140577430	MCF-7	breast:	n/a	chr7:140577116-140577127
36	CEBPB	chr7:140576834-140577323	HCT-116	colon:	n/a	chr7:140577116-140577127
37	CEBPB	chr7:140576983-140577209	HepG2	liver:	n/a	chr7:140577116-140577127
38	CEBPB	chr7:140588035-140588258	A549	lung:	n/a	n/a
39	CEBPB	chr7:140588473-140588671	K562	blood:	n/a	chr7:140588585-140588596
40	CEBPB	chr7:140576821-140577433	ECC-1	luminal epithelium:	n/a	chr7:140577116-140577127
41	CEBPB	chr7:140576908-140577346	K562	blood:	n/a	chr7:140577116-140577127
42	CEBPB	chr7:140589484-140589865	K562	blood:	n/a	n/a
43	CEBPB	chr7:140576665-140577587	K562	blood:	n/a	chr7:140577116-140577127
44	CEBPD	chr7:140576962-140577246	HepG2	liver:	n/a	n/a
45	CHD2	chr7:140589599-140589710	K562	blood:	n/a	n/a
46	CREB1	chr7:140576607-140576951	GM12878	blood:	n/a	n/a
47	CTCF	chr7:140576628-140576670	GM12878	blood:	n/a	n/a
48	CTCF	chr7:140581512-140581780	GM12878	blood:	n/a	n/a
49	CTCF	chr7:140571870-140571977	Fibrobl	skin:	n/a	n/a
50	CUX1	chr7:140583309-140583379	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140567399-140567449	AG04450	lung:	fetal
2	chr7:140567399-140567449	AG09309	skin:	n/a
3	chr7:140567399-140567449	HCT-116	colon:	n/a
4	chr7:140567399-140567449	T-47D	breast:	n/a
5	chr7:140567399-140567449	Hepatocyte	liver:	n/a
6	chr7:140567399-140567449	CMK	blood:	n/a
7	chr7:140567399-140567449	MCF-7	breast:	n/a
8	chr7:140567399-140567449	PANC-1	pancreas:	n/a
9	chr7:140567399-140567449	HCF	heart:	n/a
10	chr7:140567399-140567449	ovcar-3	ovarian:	n/a
11	chr7:140567399-140567449	RPTEC	kidney:	n/a
12	chr7:140567399-140567449	HepG2	liver:	n/a
13	chr7:140567399-140567449	HEK293	kidney:	embryo
14	chr7:140567399-140567449	NHDF-neo	bronchial:	n/a
15	chr7:140567399-140567449	NHBE	bronchial:	n/a
16	chr7:140567399-140567449	SK-N-SH	brain:	n/a
17	chr7:140567399-140567449	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:140567399-140567449	BJ	skin:	n/a
19	chr7:140567399-140567449	AG09319	gingival:	n/a
20	chr7:140567399-140567449	ECC-1	luminal epithelium:	n/a
21	chr7:140567399-140567449	GM06990	blood:	n/a
22	chr7:140567399-140567449	HAEpiC	amniotic membrane:	n/a
23	chr7:140567399-140567449	SKMC	muscle:	n/a
24	chr7:140567399-140567449	NT2-D1	testis:	n/a
25	chr7:140567399-140567449	NB4	blood:	n/a
26	chr7:140567399-140567449	GM12878	blood:	n/a
27	chr7:140567399-140567449	GM12891	blood:	n/a
28	chr7:140567399-140567449	HRCEpiC	kidney:	n/a
29	chr7:140567399-140567449	HRPEpiC	eye:	n/a
30	chr7:140567399-140567449	AoSMC	blood vessel:	n/a
31	chr7:140567399-140567449	AG04449	skin:	fetal
32	chr7:140567399-140567449	HL-60	blood:	n/a
33	chr7:140567399-140567449	MCF10A-Er-Src	breast:	n/a
34	chr7:140567399-140567449	HCM	heart:	n/a
35	chr7:140567399-140567449	PFSK-1	brain:	n/a
36	chr7:140567399-140567449	HNPCEpiC	eye:	n/a
37	chr7:140567399-140567449	HIPEpiC	eye:	n/a
38	chr7:140567399-140567449	HCPEpiC	choroid plexus:	n/a
39	chr7:140567399-140567449	HUVEC	blood vessel:	n/a
40	chr7:140567399-140567449	BE2_C	brain:	n/a
41	chr7:140567399-140567449	LNCaP	prostate:	n/a
42	chr7:140567399-140567449	HMEC	breast:	n/a
43	chr7:140567399-140567449	HRE	kidney:	n/a
44	chr7:140567399-140567449	Caco-2	colon:	n/a
45	chr7:140567399-140567449	U87	brain:	n/a
46	chr7:140567399-140567449	NH-A	brain:	n/a
47	chr7:140567399-140567449	PrEC	prostate:	n/a
48	chr7:140567399-140567449	H1-hESC	embryonic stem cell:	embryo
49	chr7:140567399-140567449	Jurkat	blood:	n/a
50	chr7:140567399-140567449	A549	lung:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:140588144..140589724-chr7:140618968..140621680,2	K562	blood:
2	chr7:140566130..140568402-chr7:140568584..140570185,2	MCF-7	breast:
3	chr7:140589437..140591945-chr7:140623059..140625802,2	K562	blood:
4	chr7:140559226..140564238-chr7:140566941..140572115,8	K562	blood:
5	chr7:140589226..140590844-chr7:140624439..140626444,2	MCF-7	breast:
6	chr7:140588302..140590134-chr7:140608160..140610912,2	K562	blood:
7	chr7:140567539..140569746-chr7:140571900..140574839,2	MCF-7	breast:
8	chr7:140557460..140561593-chr7:140571056..140573621,3	K562	blood:
9	chr7:140581979..140583708-chr7:140590896..140592469,2	K562	blood:
10	chr7:140581979..140583708-chr7:140590896..140592469,2	K562	blood:
11	chr7:140555946..140559478-chr7:140574386..140576522,3	MCF-7	breast:
12	chr7:140586780..140588546-chr7:140616185..140618447,2	K562	blood:
13	chr7:140576301..140578300-chr7:140622207..140624826,3	MCF-7	breast:
14	chr7:140560224..140564238-chr7:140566941..140570656,4	K562	blood:
15	chr7:140571783..140574857-chr7:140622852..140625165,3	K562	blood:
16	chr7:140572911..140575551-chr7:140622620..140624458,2	MCF-7	breast:
17	chr7:140566130..140568402-chr7:140568584..140570185,2	MCF-7	breast:
18	chr7:140585371..140588493-chr7:140589347..140593837,4	K562	blood:
19	chr7:140585371..140588493-chr7:140589347..140593837,4	K562	blood:
20	chr7:140567539..140569746-chr7:140571900..140574839,2	MCF-7	breast:
21	chr7:140583613..140585330-chr7:140588993..140590809,2	K562	blood:
22	chr7:140559633..140561782-chr7:140587885..140590240,2	MCF-7	breast:
23	chr7:140574947..140577128-chr7:140708628..140711066,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271932	TF binding region
ENSG00000271932	CpG island
ENSG00000090263	chromatin interactions
ENSG00000157764	chromatin interactions
ENSG00000271932	chromatin interactions

Extended variants
information (count: 944 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180750449	chr7:140567250-140567251	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs34485101	chr7:140567265-140567266	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs560493084	chr7:140567283-140567284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs376287810	chr7:140567302-140567303	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs569978765	chr7:140567325-140567326	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs574606365	chr7:140567328-140567329	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs201417249	chr7:140567329-140567330	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs397946427	chr7:140567339-140567340	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs373365004	chr7:140567416-140567417	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs527638856	chr7:140567439-140567440	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs7798324	chr7:140567452-140567453	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs556151127	chr7:140567457-140567458	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs564736048	chr7:140567515-140567516	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs531970248	chr7:140567523-140567524	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs550087385	chr7:140567575-140567576	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs369080213	chr7:140567581-140567582	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs568982604	chr7:140567636-140567637	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs145155599	chr7:140567678-140567679	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs543227301	chr7:140567685-140567686	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545494223	chr7:140567705-140567706	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs538767129	chr7:140567713-140567714	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs566151062	chr7:140567777-140567778	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs372501877	chr7:140567782-140567783	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs10275204	chr7:140567823-140567824	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138962248	chr7:140567866-140567867	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs143018389	chr7:140567893-140567894	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs564367458	chr7:140567895-140567896	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs576703995	chr7:140567948-140567949	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs538089752	chr7:140567953-140567954	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs556074341	chr7:140567956-140567957	Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs574532744	chr7:140568034-140568035	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541962934	chr7:140568141-140568142	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560543663	chr7:140568146-140568147	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376548840	chr7:140568193-140568194	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553584226	chr7:140568345-140568346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572489893	chr7:140568381-140568382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185968607	chr7:140568457-140568458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201750339	chr7:140568460-140568461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564801572	chr7:140568476-140568477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531911579	chr7:140568489-140568490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572274364	chr7:140568514-140568515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189690831	chr7:140568530-140568531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370594148	chr7:140568600-140568601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181435497	chr7:140568603-140568604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529460250	chr7:140568711-140568712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373553548	chr7:140568762-140568763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149457583	chr7:140568763-140568764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143897370	chr7:140568774-140568775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527314324	chr7:140568786-140568787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551751931	chr7:140568792-140568793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD

Chromatin state (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140475000-140580200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:140524400-140567800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr7:140525200-140567400	Weak transcription	Right Ventricle	heart
4	chr7:140527600-140573200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:140530600-140573200	Weak transcription	Gastric	stomach
6	chr7:140534600-140567600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:140534600-140570200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr7:140546000-140567600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr7:140546600-140567200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:140547000-140573200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:140547200-140567600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr7:140547200-140567600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr7:140547200-140573200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:140547200-140573400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr7:140547200-140582400	Weak transcription	Fetal Stomach	stomach
16	chr7:140547400-140572400	Weak transcription	Fetal Muscle Leg	muscle
17	chr7:140547800-140567600	Weak transcription	Thymus	Thymus
18	chr7:140548200-140576400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:140549000-140567600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:140549000-140567600	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:140549000-140567600	Weak transcription	Liver	Liver
22	chr7:140549000-140594400	Weak transcription	Fetal Thymus	thymus
23	chr7:140549200-140567600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:140549200-140569000	Weak transcription	Fetal Intestine Large	intestine
25	chr7:140549200-140569800	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr7:140549400-140579000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:140549600-140572400	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr7:140552200-140567600	Weak transcription	Psoas Muscle	Psoas
29	chr7:140552200-140573200	Weak transcription	Left Ventricle	heart
30	chr7:140557000-140567600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr7:140557200-140574200	Weak transcription	Fetal Lung	lung
32	chr7:140557400-140567200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr7:140557400-140567600	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr7:140560600-140576200	Weak transcription	NH-A	brain
35	chr7:140561400-140573000	Weak transcription	Right Atrium	heart
36	chr7:140562000-140567400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr7:140562000-140567600	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr7:140562000-140576600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr7:140563600-140567800	Weak transcription	Esophagus	oesophagus
40	chr7:140563600-140571000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr7:140563600-140573200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:140563600-140576400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:140563600-140586000	Weak transcription	K562	blood
44	chr7:140564200-140567400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr7:140564400-140567400	Weak transcription	Primary B cells from cord blood	blood
46	chr7:140564400-140567800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr7:140564400-140569600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr7:140564400-140569800	Weak transcription	Primary hematopoietic stem cells	blood
49	chr7:140564800-140567400	Weak transcription	Primary T cells from cord blood	blood
50	chr7:140564800-140567800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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