Variant report

Variant	nsv933681
Chromosome Location	chr7:33169539-33185909
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:121)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:121 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:33183918-33184232	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:33168366-33169659	K562	blood:	n/a	n/a
3	BHLHE40	chr7:33183980-33184223	HepG2	liver:	n/a	n/a
4	BHLHE40	chr7:33183680-33184321	GM12878	blood:	n/a	n/a
5	CEBPB	chr7:33184795-33185097	K562	blood:	n/a	n/a
6	CEBPB	chr7:33182019-33182327	IMR90	lung:	n/a	chr7:33182139-33182150
7	CEBPB	chr7:33181993-33182305	HepG2	liver:	n/a	chr7:33182139-33182150
8	CEBPB	chr7:33176676-33176923	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:33182001-33182288	K562	blood:	n/a	chr7:33182139-33182150
10	CEBPB	chr7:33184867-33185147	K562	blood:	n/a	n/a
11	CHD2	chr7:33168610-33169651	GM12878	blood:	n/a	chr7:33168837-33168847
12	CTCF	chr7:33180764-33180828	ProgFib	skin:	n/a	n/a
13	CTCF	chr7:33183660-33183810	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr7:33183441-33183457	GM13976	blood:	n/a	n/a
15	CTCF	chr7:33183217-33183278	GM20000	blood:	n/a	n/a
16	CTCF	chr7:33169500-33169650	GM12864	blood:	n/a	n/a
17	CUX1	chr7:33183668-33184296	GM12878	blood:	n/a	n/a
18	E2F6	chr7:33168567-33169624	K562	blood:	n/a	chr7:33169126-33169141 chr7:33168839-33168848
19	EBF1	chr7:33183985-33184177	GM12878	blood:	n/a	n/a
20	EBF1	chr7:33183582-33183964	GM12878	blood:	n/a	n/a
21	EBF1	chr7:33169761-33170042	GM12878	blood:	n/a	chr7:33169903-33169914
22	EBF1	chr7:33183550-33184338	GM12878	blood:	n/a	n/a
23	EBF1	chr7:33176086-33176156	GM12878	blood:	n/a	n/a
24	ELF1	chr7:33168552-33169576	MCF-7	breast:	n/a	n/a
25	ELF1	chr7:33168424-33169653	GM12878	blood:	n/a	n/a
26	EP300	chr7:33184822-33185159	K562	blood:	n/a	chr7:33184928-33184936
27	EP300	chr7:33183659-33184357	GM12878	blood:	n/a	n/a
28	EP300	chr7:33183767-33184336	GM12878	blood:	n/a	n/a
29	FOXA2	chr7:33183997-33184227	HepG2	liver:	n/a	n/a
30	GABPA	chr7:33168436-33169673	MCF-7	breast:	n/a	chr7:33168839-33168848
31	GATA1	chr7:33184667-33185407	PBDE	blood:	n/a	chr7:33185164-33185174
32	GATA2	chr7:33168572-33169586	SH-SY5Y	brain:	n/a	chr7:33168766-33168776
33	GATA2	chr7:33169861-33170258	SH-SY5Y	brain:	n/a	chr7:33170071-33170080
34	GATA2	chr7:33169821-33170242	HUVEC	blood vessel:	n/a	chr7:33169843-33169854 chr7:33170071-33170080
35	GATA3	chr7:33172309-33172497	SH-SY5Y	brain:	n/a	chr7:33172342-33172363
36	GATA3	chr7:33169725-33170269	SH-SY5Y	brain:	n/a	chr7:33169843-33169854 chr7:33170071-33170080
37	GTF2F1	chr7:33168951-33169990	Hela-S3	cervix:	n/a	chr7:33169062-33169073
38	HCFC1	chr7:33168590-33169546	K562	blood:	n/a	n/a
39	HCFC1	chr7:33167888-33169779	Hela-S3	cervix:	n/a	n/a
40	HDAC2	chr7:33168506-33169745	MCF-7	breast:	n/a	n/a
41	HDAC2	chr7:33168430-33169866	MCF-7	breast:	n/a	n/a
42	HDAC2	chr7:33169054-33169572	HepG2	liver:	n/a	n/a
43	IKZF1	chr7:33184024-33184119	GM12878	blood:	n/a	n/a
44	IRF1	chr7:33180251-33180444	K562	blood:	n/a	n/a
45	IRF1	chr7:33183685-33183892	K562	blood:	n/a	n/a
46	JUND	chr7:33184976-33185201	K562	blood:	n/a	n/a
47	JUND	chr7:33168358-33169552	K562	blood:	n/a	n/a
48	MAFF	chr7:33171270-33171513	HepG2	liver:	n/a	n/a
49	MAFF	chr7:33184896-33185124	K562	blood:	n/a	n/a
50	MAFK	chr7:33172379-33172599	HepG2	liver:	n/a	chr7:33172490-33172504 chr7:33172491-33172502 chr7:33172491-33172502

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:33172994-33173044	HCPEpiC	choroid plexus:	n/a
2	chr7:33172994-33173044	SKMC	muscle:	n/a
3	chr7:33172994-33173044	HNPCEpiC	eye:	n/a
4	chr7:33172994-33173044	NHBE	bronchial:	n/a
5	chr7:33172994-33173044	HCF	heart:	n/a
6	chr7:33172994-33173044	HIPEpiC	eye:	n/a
7	chr7:33172994-33173044	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:33172994-33173044	SAEC	small airway:	n/a
9	chr7:33172994-33173044	GM12891	blood:	n/a
10	chr7:33172994-33173044	GM12892	blood:	n/a
11	chr7:33172994-33173044	AG09319	gingival:	n/a
12	chr7:33172994-33173044	HEK293	kidney:	embryo
13	chr7:33172994-33173044	AG04449	skin:	fetal
14	chr7:33172994-33173044	GM19239	blood:	n/a
15	chr7:33172994-33173044	HRCEpiC	kidney:	n/a
16	chr7:33172994-33173044	NT2-D1	testis:	n/a
17	chr7:33172994-33173044	SK-N-SH_RA	brain:	n/a
18	chr7:33172994-33173044	HRPEpiC	eye:	n/a
19	chr7:33172994-33173044	NHDF-neo	bronchial:	n/a
20	chr7:33172994-33173044	CMK	blood:	n/a
21	chr7:33172994-33173044	GM12878	blood:	n/a
22	chr7:33172994-33173044	GM06990	blood:	n/a
23	chr7:33172994-33173044	U87	brain:	n/a
24	chr7:33172994-33173044	NH-A	brain:	n/a
25	chr7:33172994-33173044	LNCaP	prostate:	n/a
26	chr7:33172994-33173044	ECC-1	luminal epithelium:	n/a
27	chr7:33172994-33173044	IMR90	lung:	fetal
28	chr7:33172994-33173044	HUVEC	blood vessel:	n/a
29	chr7:33172994-33173044	T-47D	breast:	n/a
30	chr7:33172994-33173044	ovcar-3	ovarian:	n/a
31	chr7:33172994-33173044	AoSMC	blood vessel:	n/a
32	chr7:33172994-33173044	MCF10A-Er-Src	breast:	n/a
33	chr7:33172994-33173044	Hepatocyte	liver:	n/a
34	chr7:33172994-33173044	HAEpiC	amniotic membrane:	n/a
35	chr7:33172994-33173044	HL-60	blood:	n/a
36	chr7:33172994-33173044	AG10803	skin:	n/a
37	chr7:33172994-33173044	Jurkat	blood:	n/a
38	chr7:33172994-33173044	HepG2	liver:	n/a
39	chr7:33172994-33173044	NB4	blood:	n/a
40	chr7:33172994-33173044	BE2_C	brain:	n/a
41	chr7:33172994-33173044	PrEC	prostate:	n/a
42	chr7:33172994-33173044	K562	blood:	n/a
43	chr7:33172994-33173044	A549	lung:	n/a
44	chr7:33172994-33173044	RPTEC	kidney:	n/a
45	chr7:33172994-33173044	PANC-1	pancreas:	n/a
46	chr7:33172994-33173044	PFSK-1	brain:	n/a
47	chr7:33172994-33173044	AG04450	lung:	fetal
48	chr7:33172994-33173044	MCF-7	breast:	n/a
49	chr7:33172994-33173044	SK-N-SH	brain:	n/a
50	chr7:33172994-33173044	Caco-2	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:33179137..33181368-chr7:33185643..33187342,2	MCF-7	breast:
2	chr7:33147764..33149683-chr7:33167457..33170052,3	MCF-7	breast:
3	chr7:33173373..33176159-chr7:33177718..33179831,2	K562	blood:
4	chr7:33168317..33169892-chr7:33174441..33176886,2	MCF-7	breast:
5	chr7:33179137..33181368-chr7:33185643..33187342,2	MCF-7	breast:
6	chr7:33169914..33172476-chr7:33187197..33189119,2	MCF-7	breast:
7	chr7:33168152..33172039-chr7:33180833..33185691,4	K562	blood:
8	chr7:33167291..33169895-chr7:33178548..33180361,2	K562	blood:
9	chr7:33179229..33183198-chr7:33185335..33188130,3	K562	blood:
10	chr7:33173373..33176159-chr7:33177718..33179831,2	K562	blood:
11	chr7:33179229..33183198-chr7:33185335..33188130,3	K562	blood:
12	chr7:33183803..33185518-chr7:33185914..33189355,3	MCF-7	breast:
13	chr7:33174121..33176456-chr7:33182217..33185074,2	K562	blood:
14	chr7:33174121..33176456-chr7:33182217..33185074,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228015	TF binding region
ENSG00000228015	CpG island
ENSG00000164610	chromatin interactions
ENSG00000122507	chromatin interactions
ENSG00000228015	chromatin interactions

Extended variants
information (count: 592 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561911089	chr7:33169613-33169614	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs529087676	chr7:33169644-33169645	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs1468797	chr7:33169660-33169661	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs79503896	chr7:33169670-33169671	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs539403348	chr7:33169725-33169726	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528712776	chr7:33169746-33169747	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs551379434	chr7:33169770-33169771	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs187411516	chr7:33169776-33169777	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs533107422	chr7:33169820-33169821	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs538533135	chr7:33169834-33169835	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs367580425	chr7:33169851-33169852	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115819560	chr7:33169860-33169861	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs138980339	chr7:33169918-33169919	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192208478	chr7:33169938-33169939	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs554206992	chr7:33169980-33169981	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572433106	chr7:33169997-33169998	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs545922345	chr7:33170042-33170043	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs369355769	chr7:33170047-33170048	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562339521	chr7:33170066-33170067	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs184744333	chr7:33170068-33170069	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs551356916	chr7:33170094-33170095	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs1569239	chr7:33170104-33170105	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs543272963	chr7:33170125-33170126	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs561838247	chr7:33170134-33170135	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs529055658	chr7:33170160-33170161	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs189478477	chr7:33170166-33170167	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs559530856	chr7:33170236-33170237	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376200718	chr7:33170306-33170307	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs533035839	chr7:33170317-33170318	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs77901428	chr7:33170321-33170322	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs567096206	chr7:33170347-33170348	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs150570189	chr7:33170348-33170349	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs534013721	chr7:33170358-33170359	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs551544849	chr7:33170361-33170362	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs569657948	chr7:33170411-33170412	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs530526584	chr7:33170442-33170443	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs193149028	chr7:33170531-33170532	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs34922240	chr7:33170548-33170549	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs555710967	chr7:33170549-33170550	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs567813985	chr7:33170557-33170558	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs115180620	chr7:33170593-33170594	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs554052022	chr7:33170603-33170604	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs5883385	chr7:33170630-33170631	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs184430464	chr7:33170636-33170637	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs1548880	chr7:33170658-33170659	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557841036	chr7:33170741-33170742	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs569732348	chr7:33170768-33170769	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs189304534	chr7:33170798-33170799	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs139421307	chr7:33170808-33170809	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs113416823	chr7:33170817-33170818	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Williams-beuren syndrome	18553513	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33168000-33169600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:33168000-33169800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:33168000-33170000	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr7:33168000-33170200	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr7:33168200-33169600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:33168200-33169600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:33168200-33169600	Active TSS	Brain Substantia Nigra	brain
8	chr7:33168200-33169600	Active TSS	Duodenum Mucosa	Duodenum
9	chr7:33168200-33169600	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr7:33168200-33169600	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr7:33168200-33169800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr7:33168200-33169800	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr7:33168200-33169800	Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr7:33168200-33169800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:33168200-33169800	Active TSS	Muscle Satellite Cultured Cells	--
16	chr7:33168200-33169800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:33168200-33169800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:33168200-33169800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:33168200-33169800	Active TSS	Colon Smooth Muscle	Colon
20	chr7:33168200-33169800	Active TSS	Fetal Brain Female	brain
21	chr7:33168200-33169800	Active TSS	Fetal Kidney	kidney
22	chr7:33168200-33169800	Active TSS	Placenta Amnion	Placenta Amnion
23	chr7:33168200-33169800	Active TSS	Stomach Smooth Muscle	stomach
24	chr7:33168200-33169800	Active TSS	GM12878-XiMat	blood
25	chr7:33168200-33170000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:33168200-33170000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:33168200-33170000	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr7:33168200-33170000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:33168200-33170000	Active TSS	Brain Cingulate Gyrus	brain
30	chr7:33168200-33170000	Active TSS	Fetal Intestine Large	intestine
31	chr7:33168200-33170200	Active TSS	H1 Cell Line	embryonic stem cell
32	chr7:33168200-33170200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:33168200-33170200	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr7:33168200-33170200	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr7:33168200-33170200	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr7:33168200-33170600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:33168400-33169600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr7:33168400-33169600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:33168400-33169600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
40	chr7:33168400-33169600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:33168400-33169600	Active TSS	Liver	Liver
42	chr7:33168400-33169600	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr7:33168400-33169600	ZNF genes & repeats	Fetal Brain Male	brain
44	chr7:33168400-33169600	Active TSS	Fetal Intestine Small	intestine
45	chr7:33168400-33169600	Active TSS	Fetal Lung	lung
46	chr7:33168400-33169600	Active TSS	Fetal Thymus	thymus
47	chr7:33168400-33169600	Active TSS	Stomach Mucosa	stomach
48	chr7:33168400-33169600	Active TSS	Thymus	Thymus
49	chr7:33168400-33169600	Active TSS	Hela-S3	cervix
50	chr7:33168400-33169600	Active TSS	HMEC	breast

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