Variant report

Variant	nsv830972
Chromosome Location	chr7:40814709-40945917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:40890683-40890970	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:40817590-40817869	GM12878	blood:	n/a	n/a
3	BRCA1	chr7:40910014-40910049	GM12878	blood:	n/a	n/a
4	BRCA1	chr7:40872900-40872908	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr7:40829656-40829661	GM12878	blood:	n/a	n/a
6	BRCA1	chr7:40938804-40939224	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr7:40945608-40945732	HepG2	liver:	n/a	chr7:40945677-40945688
8	CEBPB	chr7:40888411-40889134	IMR90	lung:	n/a	chr7:40888591-40888602 chr7:40888592-40888603 chr7:40888593-40888602 chr7:40888591-40888604 chr7:40888593-40888602 chr7:40888593-40888602 chr7:40888982-40888995 chr7:40888591-40888604 chr7:40888591-40888602 chr7:40888593-40888602 chr7:40888982-40888993 chr7:40888591-40888604
9	CEBPB	chr7:40888419-40889093	Hela-S3	cervix:	n/a	chr7:40888591-40888602 chr7:40888592-40888603 chr7:40888593-40888602 chr7:40888591-40888604 chr7:40888593-40888602 chr7:40888593-40888602 chr7:40888982-40888995 chr7:40888591-40888604 chr7:40888591-40888602 chr7:40888593-40888602 chr7:40888982-40888993 chr7:40888591-40888604
10	CEBPB	chr7:40815997-40816043	IMR90	lung:	n/a	n/a
11	CEBPB	chr7:40926771-40927111	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:40871844-40872172	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:40909807-40910061	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:40882285-40882593	IMR90	lung:	n/a	chr7:40882419-40882430 chr7:40882419-40882428 chr7:40882417-40882430 chr7:40882417-40882428
15	CEBPB	chr7:40945543-40945840	IMR90	lung:	n/a	chr7:40945677-40945688
16	CEBPB	chr7:40888446-40889101	HepG2	liver:	n/a	chr7:40888591-40888602 chr7:40888592-40888603 chr7:40888593-40888602 chr7:40888591-40888604 chr7:40888593-40888602 chr7:40888593-40888602 chr7:40888982-40888995 chr7:40888591-40888604 chr7:40888591-40888602 chr7:40888593-40888602 chr7:40888982-40888993 chr7:40888591-40888604
17	CEBPB	chr7:40945637-40945767	Hela-S3	cervix:	n/a	chr7:40945677-40945688
18	CEBPB	chr7:40842154-40842458	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:40871958-40872119	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:40882294-40882522	HepG2	liver:	n/a	chr7:40882419-40882430 chr7:40882419-40882428 chr7:40882417-40882430 chr7:40882417-40882428
21	CEBPB	chr7:40875867-40876101	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:40938683-40939561	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:40875828-40876163	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:40865931-40866299	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:40847973-40848479	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:40871913-40872210	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:40875845-40876145	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:40875866-40876065	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:40871849-40872123	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:40888483-40888753	K562	blood:	n/a	chr7:40888591-40888602 chr7:40888592-40888603 chr7:40888593-40888602 chr7:40888591-40888604 chr7:40888593-40888602 chr7:40888593-40888602 chr7:40888591-40888604 chr7:40888591-40888602 chr7:40888593-40888602 chr7:40888591-40888604
31	CHD2	chr7:40938722-40939630	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr7:40906340-40906490	NHEK	skin:	n/a	n/a
33	CTCF	chr7:40934909-40934937	LNCaP	prostate:	n/a	n/a
34	CTCF	chr7:40873500-40873650	RPTEC	kidney:	n/a	n/a
35	CTCF	chr7:40873540-40873690	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr7:40873411-40873757	GM12878	blood:	n/a	n/a
37	CTCF	chr7:40906320-40906470	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr7:40873520-40873670	AG10803	skin:	n/a	n/a
39	CTCF	chr7:40906320-40906470	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr7:40873480-40873630	NHLF	lung:	n/a	n/a
41	CTCF	chr7:40873540-40873690	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr7:40873540-40873690	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr7:40906350-40906395	GM12878	blood:	n/a	n/a
44	CTCF	chr7:40873540-40873690	HCM	heart:	n/a	n/a
45	CTCF	chr7:40906320-40906470	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr7:40873520-40873670	AG09309	skin:	n/a	n/a
47	CTCF	chr7:40873184-40873763	IMR90	lung:	n/a	n/a
48	CTCF	chr7:40906280-40906430	HMF	breast:	n/a	n/a
49	CTCF	chr7:40873540-40873690	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr7:40873520-40873670	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:40866195-40866245	BE2_C	brain:	n/a
2	chr7:40866195-40866245	BE2_C	brain:	n/a
3	chr7:40819169-40819219	AG04449	skin:	fetal
4	chr7:40939069-40939119	HCPEpiC	choroid plexus:	n/a
5	chr7:40819169-40819219	RPTEC	kidney:	n/a
6	chr7:40819169-40819219	MCF10A-Er-Src	breast:	n/a
7	chr7:40937922-40937972	Hela-S3	cervix:	n/a
8	chr7:40855639-40855689	GM12891	blood:	n/a
9	chr7:40866195-40866245	NT2-D1	testis:	n/a
10	chr7:40873953-40874003	NH-A	brain:	n/a
11	chr7:40873953-40874003	HIPEpiC	eye:	n/a
12	chr7:40866195-40866245	HRCEpiC	kidney:	n/a
13	chr7:40819169-40819219	NH-A	brain:	n/a
14	chr7:40937922-40937972	SK-N-MC	brain:	n/a
15	chr7:40873953-40874003	SKMC	muscle:	n/a
16	chr7:40855639-40855689	HCM	heart:	n/a
17	chr7:40905203-40905253	LNCaP	prostate:	n/a
18	chr7:40855639-40855689	GM06990	blood:	n/a
19	chr7:40855639-40855689	NH-A	brain:	n/a
20	chr7:40939069-40939119	GM12891	blood:	n/a
21	chr7:40855639-40855689	MCF-7	breast:	n/a
22	chr7:40866195-40866245	SK-N-SH_RA	brain:	n/a
23	chr7:40855639-40855689	AG09319	gingival:	n/a
24	chr7:40905203-40905253	IMR90	lung:	fetal
25	chr7:40937922-40937972	H1-hESC	embryonic stem cell:	embryo
26	chr7:40819169-40819219	HIPEpiC	eye:	n/a
27	chr7:40855639-40855689	ECC-1	luminal epithelium:	n/a
28	chr7:40939069-40939119	AG09309	skin:	n/a
29	chr7:40866195-40866245	HCF	heart:	n/a
30	chr7:40866195-40866245	BJ	skin:	n/a
31	chr7:40873953-40874003	ProgFib	skin:	n/a
32	chr7:40866195-40866245	SKMC	muscle:	n/a
33	chr7:40905203-40905253	HL-60	blood:	n/a
34	chr7:40905203-40905253	HCF	heart:	n/a
35	chr7:40939069-40939119	Hepatocyte	liver:	n/a
36	chr7:40819169-40819219	CMK	blood:	n/a
37	chr7:40866195-40866245	AG04449	skin:	fetal
38	chr7:40905203-40905253	NHDF-neo	bronchial:	n/a
39	chr7:40819169-40819219	Caco-2	colon:	n/a
40	chr7:40855639-40855689	HCF	heart:	n/a
41	chr7:40855639-40855689	ovcar-3	ovarian:	n/a
42	chr7:40905203-40905253	Hepatocyte	liver:	n/a
43	chr7:40905203-40905253	HCT-116	colon:	n/a
44	chr7:40873953-40874003	HCT-116	colon:	n/a
45	chr7:40939069-40939119	HRCEpiC	kidney:	n/a
46	chr7:40939069-40939119	ovcar-3	ovarian:	n/a
47	chr7:40937922-40937972	LNCaP	prostate:	n/a
48	chr7:40866195-40866245	HEEpiC	esophagus:	n/a
49	chr7:40873953-40874003	AG09309	skin:	n/a
50	chr7:40873953-40874003	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr7:40944502..40946618-chr7:40947507..40949025,2	MCF-7	breast:
2	chr7:40873081..40874051-chr7:41750669..41751620,2	MCF-7	breast:
3	chr7:40939613..40941276-chr7:40941813..40943599,2	K562	blood:
4	chr7:40820053..40822689-chr7:40827136..40828898,2	K562	blood:
5	chr7:40839610..40841601-chr7:40845220..40847169,2	MCF-7	breast:
6	chr7:40939613..40941276-chr7:40941813..40943599,2	K562	blood:
7	chr7:40820053..40822689-chr7:40827136..40828898,2	K562	blood:
8	chr7:40883101..40886053-chr7:40887057..40889418,2	K562	blood:
9	chr7:40818449..40820320-chr7:40826991..40829099,2	K562	blood:
10	chr7:40883101..40886053-chr7:40887057..40889418,2	K562	blood:
11	chr7:40818449..40820320-chr7:40826991..40829099,2	K562	blood:
12	chr7:40839610..40841601-chr7:40845220..40847169,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDK13-2	chr7:40822188-40822311	ENSG00000227658.1
2	lnc-CDK13-8	chr7:40847756-40848013	NONHSAT120254
3	lnc-CDK13-2	chr7:40824783-40824816	ENSG00000227658.1
4	lnc-CDK13-2	chr7:40815157-40815308	ENSG00000227658.1
5	lnc-CDK13-8	chr7:40899915-40900108	NONHSAT120254
6	lnc-CDK13-2	chr7:40823116-40823186	ENSG00000227658.1

Variant related genes	Relation type
SUGCT	TF binding region
ENSG00000227658	TF binding region
SUGCT	CpG island
ENSG00000227658	CpG island

Extended variants
information (count: 4545 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4545 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555497825	chr7:40814724-40814725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11769562	chr7:40814840-40814841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567510197	chr7:40814961-40814962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117274279	chr7:40814966-40814967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556416398	chr7:40814982-40814983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17530165	chr7:40815025-40815026	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114926963	chr7:40815062-40815063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557488812	chr7:40815074-40815075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189462003	chr7:40815200-40815201	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs539962021	chr7:40815311-40815312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143073051	chr7:40815342-40815343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576576523	chr7:40815355-40815356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529097898	chr7:40815414-40815415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35523967	chr7:40815500-40815501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544448335	chr7:40815537-40815538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181053119	chr7:40815593-40815594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148195383	chr7:40815594-40815595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551725641	chr7:40815691-40815692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111837824	chr7:40815748-40815749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530760153	chr7:40815825-40815826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549059151	chr7:40815835-40815836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368228395	chr7:40815844-40815845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527723152	chr7:40815845-40815846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17530213	chr7:40815895-40815896	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs116582634	chr7:40815970-40815971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150381965	chr7:40815971-40815972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186043880	chr7:40815999-40816000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138093493	chr7:40816023-40816024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142648228	chr7:40816028-40816029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146014435	chr7:40816037-40816038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185345518	chr7:40816062-40816063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572742903	chr7:40816127-40816128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540278553	chr7:40816181-40816182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555480176	chr7:40816190-40816191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191022007	chr7:40816226-40816227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544389398	chr7:40816332-40816333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112188170	chr7:40816344-40816345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577824330	chr7:40816346-40816347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544962680	chr7:40816349-40816350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1921742	chr7:40816393-40816394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4460274	chr7:40816439-40816440	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs559317887	chr7:40816442-40816443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571806507	chr7:40816447-40816448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539229452	chr7:40816462-40816463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2329877	chr7:40816465-40816466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs67368543	chr7:40816516-40816517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149591262	chr7:40816552-40816553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144261808	chr7:40816554-40816555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17530234	chr7:40816580-40816581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs372283193	chr7:40816602-40816603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40812000-40817200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:40812400-40820000	Weak transcription	Aorta	Aorta
3	chr7:40817200-40817800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:40817200-40821200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr7:40817400-40817800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:40817600-40817800	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr7:40817600-40817800	Enhancers	Fetal Stomach	stomach
8	chr7:40817600-40818000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:40817800-40818600	Weak transcription	Fetal Stomach	stomach
10	chr7:40817800-40821400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr7:40818000-40822000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:40818600-40818800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:40818600-40818800	Enhancers	Stomach Smooth Muscle	stomach
14	chr7:40818600-40821400	Enhancers	Fetal Stomach	stomach
15	chr7:40818800-40819400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:40818800-40819400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr7:40819200-40821000	Enhancers	Fetal Lung	lung
18	chr7:40819400-40819600	Enhancers	Stomach Smooth Muscle	stomach
19	chr7:40819400-40819800	Enhancers	HSMMtube	muscle
20	chr7:40819400-40820200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:40819400-40820200	Enhancers	Ovary	ovary
22	chr7:40819600-40820200	Enhancers	HepG2	liver
23	chr7:40819600-40820800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr7:40819800-40822000	Weak transcription	HSMMtube	muscle
25	chr7:40820000-40820200	Enhancers	Aorta	Aorta
26	chr7:40820000-40820800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:40820000-40820800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:40820000-40821400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:40820200-40820800	Weak transcription	Aorta	Aorta
30	chr7:40820200-40825400	Weak transcription	Ovary	ovary
31	chr7:40820400-40821000	Enhancers	Fetal Heart	heart
32	chr7:40820800-40821200	Enhancers	Stomach Smooth Muscle	stomach
33	chr7:40820800-40821400	Active TSS	Aorta	Aorta
34	chr7:40821000-40823200	Weak transcription	Fetal Heart	heart
35	chr7:40821200-40823800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:40821400-40823000	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr7:40821400-40827400	Weak transcription	Aorta	Aorta
38	chr7:40822000-40822800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:40822000-40822800	Enhancers	HSMMtube	muscle
40	chr7:40822000-40823000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:40822000-40823000	Enhancers	Osteobl	bone
42	chr7:40822000-40823600	Enhancers	Dnd41	blood
43	chr7:40822400-40822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:40822400-40823000	Enhancers	Primary B cells from cord blood	blood
45	chr7:40822400-40823000	Enhancers	Primary hematopoietic stem cells	blood
46	chr7:40823200-40824400	Enhancers	Fetal Heart	heart
47	chr7:40823800-40824400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:40823800-40824600	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr7:40825400-40825600	Enhancers	Ovary	ovary
50	chr7:40827400-40827800	Strong transcription	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links