Variant report

Variant	nsv981772
Chromosome Location	chr7:56009678-56020897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:551)
CpG islands
(count:856)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:551 , 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	ARID3A	chr7:56019388-56019761	HepG2	liver:	n/a	n/a
2	ATF1	chr7:56019350-56020014	K562	blood:	n/a	n/a
3	ATF2	chr7:56019342-56019791	GM12878	blood:	n/a	n/a
4	ATF2	chr7:56019461-56019764	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:56019330-56019830	GM12878	blood:	n/a	n/a
6	ATF2	chr7:56019351-56019751	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr7:56019402-56019762	K562	blood:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
8	ATF3	chr7:56019416-56019701	HepG2	liver:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
9	ATF3	chr7:56019467-56019655	GM12878	blood:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
10	ATF3	chr7:56019371-56019733	H1-hESC	embryonic stem cell:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
11	ATF3	chr7:56019336-56019783	GM12878	blood:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
12	ATF3	chr7:56019395-56019775	K562	blood:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
13	ATF3	chr7:56019294-56019732	H1-hESC	embryonic stem cell:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
14	ATF3	chr7:56019386-56019741	K562	blood:	n/a	chr7:56019562-56019582 chr7:56019561-56019572
15	BACH1	chr7:56019432-56019700	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:56015104-56015127	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr7:56019441-56019875	A549	lung:	n/a	n/a
18	BCL3	chr7:56019355-56019856	A549	lung:	n/a	n/a
19	BCL3	chr7:56014422-56014601	GM12878	blood:	n/a	n/a
20	BCLAF1	chr7:56019280-56019855	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:56019377-56020244	K562	blood:	n/a	chr7:56019863-56019879
22	BHLHE40	chr7:56019380-56019884	HepG2	liver:	n/a	chr7:56019863-56019879
23	BHLHE40	chr7:56019340-56019922	GM12878	blood:	n/a	chr7:56019863-56019879
24	BRCA1	chr7:56019415-56019778	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr7:56019367-56019859	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr7:56019416-56019752	HepG2	liver:	n/a	n/a
27	BRCA1	chr7:56019370-56019995	GM12878	blood:	n/a	n/a
28	CBX3	chr7:56019245-56020236	K562	blood:	n/a	n/a
29	CBX3	chr7:56019433-56019722	K562	blood:	n/a	n/a
30	CCNT2	chr7:56019384-56019852	K562	blood:	n/a	chr7:56019431-56019440
31	CEBPB	chr7:56019368-56020010	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:56019347-56020040	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:56019331-56019592	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:56019341-56019741	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:56019368-56019770	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr7:56019392-56019744	K562	blood:	n/a	n/a
37	CEBPB	chr7:56019428-56019713	A549	lung:	n/a	n/a
38	CEBPD	chr7:56019325-56019573	HepG2	liver:	n/a	n/a
39	CEBPD	chr7:56019247-56019761	HepG2	liver:	n/a	n/a
40	CHD1	chr7:56019516-56019883	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr7:56019446-56020007	GM12878	blood:	n/a	n/a
42	CHD2	chr7:56019348-56019989	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr7:56019428-56020087	K562	blood:	n/a	n/a
44	CHD2	chr7:56019404-56020016	HepG2	liver:	n/a	n/a
45	CHD2	chr7:56019334-56020151	GM12878	blood:	n/a	n/a
46	CHD2	chr7:56019402-56020004	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr7:56019308-56020245	HepG2	liver:	n/a	chr7:56019560-56019573
48	CREB1	chr7:56019276-56020148	GM12878	blood:	n/a	chr7:56019560-56019573
49	CREB1	chr7:56019364-56019725	A549	lung:	n/a	chr7:56019560-56019573
50	CREB1	chr7:56019278-56020179	H1-hESC	embryonic stem cell:	n/a	chr7:56019560-56019573

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56019372-56019422	Caco-2	colon:	n/a
2	chr7:56018486-56018536	NHBE	bronchial:	n/a
3	chr7:56019372-56019422	Caco-2	colon:	n/a
4	chr7:56018486-56018536	NHBE	bronchial:	n/a
5	chr7:56018561-56018611	HCPEpiC	choroid plexus:	n/a
6	chr7:56019451-56019501	RPTEC	kidney:	n/a
7	chr7:56019566-56019616	SK-N-SH	brain:	n/a
8	chr7:56020011-56020061	HRPEpiC	eye:	n/a
9	chr7:56018561-56018611	AG04450	lung:	fetal
10	chr7:56020011-56020061	HEEpiC	esophagus:	n/a
11	chr7:56020011-56020061	A549	lung:	n/a
12	chr7:56019978-56020028	Jurkat	blood:	n/a
13	chr7:56018486-56018536	GM12891	blood:	n/a
14	chr7:56019384-56019434	SK-N-MC	brain:	n/a
15	chr7:56019566-56019616	HRE	kidney:	n/a
16	chr7:56019517-56019567	LNCaP	prostate:	n/a
17	chr7:56018486-56018536	AG10803	skin:	n/a
18	chr7:56019978-56020028	NH-A	brain:	n/a
19	chr7:56019384-56019434	GM12878	blood:	n/a
20	chr7:56019372-56019422	NHDF-neo	bronchial:	n/a
21	chr7:56019838-56019888	AG09319	gingival:	n/a
22	chr7:56019579-56019629	RPTEC	kidney:	n/a
23	chr7:56019475-56019525	BJ	skin:	n/a
24	chr7:56018561-56018611	SAEC	small airway:	n/a
25	chr7:56019978-56020028	GM12878	blood:	n/a
26	chr7:56019384-56019434	LNCaP	prostate:	n/a
27	chr7:56019574-56019624	GM19239	blood:	n/a
28	chr7:56018561-56018611	NB4	blood:	n/a
29	chr7:56018561-56018611	HRCEpiC	kidney:	n/a
30	chr7:56019372-56019422	BE2_C	brain:	n/a
31	chr7:56019517-56019567	HRCEpiC	kidney:	n/a
32	chr7:56019566-56019616	HUVEC	blood vessel:	n/a
33	chr7:56016941-56016991	HNPCEpiC	eye:	n/a
34	chr7:56020011-56020061	ovcar-3	ovarian:	n/a
35	chr7:56018486-56018536	RPTEC	kidney:	n/a
36	chr7:56019566-56019616	IMR90	lung:	fetal
37	chr7:56019517-56019567	RPTEC	kidney:	n/a
38	chr7:56019579-56019629	SK-N-SH	brain:	n/a
39	chr7:56019574-56019624	K562	blood:	n/a
40	chr7:56018561-56018611	ECC-1	luminal epithelium:	n/a
41	chr7:56019566-56019616	PANC-1	pancreas:	n/a
42	chr7:56020011-56020061	SK-N-SH	brain:	n/a
43	chr7:56019574-56019624	HNPCEpiC	eye:	n/a
44	chr7:56018486-56018536	K562	blood:	n/a
45	chr7:56019579-56019629	GM19239	blood:	n/a
46	chr7:56019384-56019434	AoSMC	blood vessel:	n/a
47	chr7:56020011-56020061	NB4	blood:	n/a
48	chr7:56019579-56019629	CMK	blood:	n/a
49	chr7:56019838-56019888	U87	brain:	n/a
50	chr7:56019384-56019434	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:56013802..56016565-chr7:56019386..56021893,2	MCF-7	breast:
2	chr7:56011972..56013876-chr7:56018047..56020877,2	K562	blood:
3	chr7:55955038..55957405-chr7:56008424..56010815,2	MCF-7	breast:
4	chr7:56018165..56022272-chr7:56129856..56132253,4	K562	blood:
5	chr7:56017145..56021503-chr7:56030472..56033942,8	MCF-7	breast:
6	chr7:56018437..56023114-chr7:56029023..56035214,11	K562	blood:
7	chr7:56017138..56022365-chr7:56030961..56033857,7	MCF-7	breast:
8	chr7:56013492..56017574-chr7:56017951..56020421,4	K562	blood:
9	chr7:56018384..56020889-chr7:56129856..56132224,2	K562	blood:

No data

Variant related genes	Relation type
MRPS17	TF binding region
GBAS	TF binding region
MRPS17	CpG island
GBAS	CpG island
ENSG00000129103	chromatin interactions
ENSG00000146729	chromatin interactions
ENSG00000239789	chromatin interactions
ENSG00000146731	chromatin interactions
ENSG00000178665	chromatin interactions

Extended variants
information (count: 431 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:431 , 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	rs543112536	chr7:56009697-56009698	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375320602	chr7:56009726-56009727	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs549379124	chr7:56009738-56009739	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568383439	chr7:56009788-56009789	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs6593291	chr7:56009863-56009864	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs541080563	chr7:56009884-56009885	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554305084	chr7:56009893-56009894	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572594940	chr7:56009906-56009907	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs539921887	chr7:56009907-56009908	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558313374	chr7:56009919-56009920	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs150937448	chr7:56009944-56009945	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543805200	chr7:56009951-56009952	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs71561980	chr7:56009958-56009959	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140765852	chr7:56009963-56009964	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574634746	chr7:56010034-56010035	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4548132	chr7:56010063-56010064	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs185445638	chr7:56010071-56010072	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs4443615	chr7:56010082-56010083	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs545475161	chr7:56010083-56010084	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368897990	chr7:56010104-56010105	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563801289	chr7:56010190-56010191	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs531324556	chr7:56010200-56010201	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs549316328	chr7:56010207-56010208	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567975907	chr7:56010228-56010229	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561863677	chr7:56010242-56010243	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs71015133	chr7:56010258-56010259	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11765531	chr7:56010287-56010288	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547824933	chr7:56010376-56010377	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112284520	chr7:56010386-56010387	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113011815	chr7:56010405-56010406	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566243675	chr7:56010420-56010421	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs189755962	chr7:56010540-56010541	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140366334	chr7:56010552-56010553	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs144018461	chr7:56010574-56010575	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532268029	chr7:56010594-56010595	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs570137118	chr7:56010610-56010611	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150347392	chr7:56010611-56010612	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs182833566	chr7:56010661-56010662	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138105238	chr7:56010712-56010713	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187936753	chr7:56010734-56010735	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs117285203	chr7:56010752-56010753	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs4606016	chr7:56010754-56010755	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545563891	chr7:56010774-56010775	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563940466	chr7:56010799-56010800	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35222204	chr7:56010834-56010835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376573356	chr7:56010851-56010852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531263454	chr7:56010882-56010883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543156326	chr7:56010891-56010892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370993678	chr7:56010892-56010893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530899927	chr7:56010923-56010924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Esophageal squamous carcinoma	21637470	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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Breast cancer	17142309	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56004000-56010600	ZNF genes & repeats	Liver	Liver
2	chr7:56007600-56010000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:56007600-56013800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr7:56007600-56019000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:56007800-56010400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:56007800-56019200	Weak transcription	Ovary	ovary
7	chr7:56007800-56019400	Weak transcription	Fetal Brain Male	brain
8	chr7:56008400-56019000	Weak transcription	Brain Germinal Matrix	brain
9	chr7:56008400-56019000	Weak transcription	Fetal Muscle Leg	muscle
10	chr7:56008600-56019000	Weak transcription	Fetal Brain Female	brain
11	chr7:56009000-56009800	Weak transcription	Fetal Stomach	stomach
12	chr7:56009400-56010600	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr7:56009400-56018600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr7:56009400-56019200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:56009600-56019200	Weak transcription	Fetal Lung	lung
16	chr7:56009800-56010800	Strong transcription	Fetal Stomach	stomach
17	chr7:56010400-56010600	ZNF genes & repeats	Brain Hippocampus Middle	brain
18	chr7:56010400-56010800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:56010400-56010800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
20	chr7:56010600-56019200	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr7:56010600-56019200	Weak transcription	Brain Hippocampus Middle	brain
22	chr7:56010800-56011800	Weak transcription	Fetal Stomach	stomach
23	chr7:56011000-56011600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr7:56011400-56019200	Weak transcription	Pancreas	Pancrea
25	chr7:56011800-56012200	ZNF genes & repeats	Fetal Stomach	stomach
26	chr7:56012200-56019200	Weak transcription	Fetal Stomach	stomach
27	chr7:56012400-56012800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:56012800-56019000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:56014000-56014800	Weak transcription	Brain Substantia Nigra	brain
30	chr7:56017200-56019200	Weak transcription	Right Atrium	heart
31	chr7:56018000-56018400	Enhancers	HepG2	liver
32	chr7:56018400-56019600	Active TSS	HepG2	liver
33	chr7:56018400-56020000	Active TSS	Placenta	Placenta
34	chr7:56018400-56020400	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr7:56018600-56018800	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr7:56018600-56019000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr7:56018600-56019000	Enhancers	Gastric	stomach
38	chr7:56018600-56019000	Enhancers	Dnd41	blood
39	chr7:56018600-56020600	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr7:56018600-56020800	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr7:56018800-56019000	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr7:56018800-56019200	Enhancers	Primary T cells fromperipheralblood	blood
43	chr7:56018800-56019800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr7:56019000-56019200	Enhancers	Primary B cells from cord blood	blood
45	chr7:56019000-56019200	Enhancers	Primary B cells from peripheral blood	blood
46	chr7:56019000-56019400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr7:56019000-56019400	Active TSS	Fetal Muscle Trunk	muscle
48	chr7:56019000-56019600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr7:56019000-56019600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:56019000-56019600	Active TSS	Adipose Nuclei	Adipose

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