Variant report

Variant	nsv520941
Chromosome Location	chr10:5903518-5904918
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	ARID3A	chr10:5903253-5903873	HepG2	liver:	n/a	chr10:5903606-5903622
2	ATF2	chr10:5904094-5905203	GM12878	blood:	n/a	n/a
3	ATF2	chr10:5904071-5905027	GM12878	blood:	n/a	n/a
4	BATF	chr10:5904143-5905100	GM12878	blood:	n/a	n/a
5	BATF	chr10:5904206-5904991	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:5904162-5905104	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:5904278-5904614	GM12878	blood:	n/a	n/a
8	BCL3	chr10:5903292-5903542	GM12878	blood:	n/a	chr10:5903433-5903442
9	BCL3	chr10:5904200-5904748	GM12878	blood:	n/a	n/a
10	BCLAF1	chr10:5904038-5904983	GM12878	blood:	n/a	n/a
11	BCLAF1	chr10:5904086-5905107	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:5904170-5904892	GM12878	blood:	n/a	n/a
13	CBX3	chr10:5903296-5903685	HCT-116	colon:	n/a	n/a
14	CBX3	chr10:5902840-5903782	HCT-116	colon:	n/a	n/a
15	CEBPB	chr10:5904144-5904329	HepG2	liver:	n/a	n/a
16	CEBPB	chr10:5904286-5904770	GM12878	blood:	n/a	n/a
17	CEBPB	chr10:5904056-5904980	GM12878	blood:	n/a	n/a
18	CHD1	chr10:5904267-5904867	GM12878	blood:	n/a	n/a
19	CHD2	chr10:5904177-5905077	GM12878	blood:	n/a	n/a
20	CREB1	chr10:5904117-5905044	GM12878	blood:	n/a	n/a
21	CREB1	chr10:5904075-5905144	GM12878	blood:	n/a	n/a
22	CTCF	chr10:5904483-5905254	GM12878	blood:	n/a	n/a
23	CUX1	chr10:5904260-5904824	GM12878	blood:	n/a	n/a
24	E2F4	chr10:5903259-5903609	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr10:5904188-5905055	GM12878	blood:	n/a	n/a
26	EBF1	chr10:5904081-5905014	GM12878	blood:	n/a	n/a
27	EBF1	chr10:5904140-5904870	GM12878	blood:	n/a	n/a
28	EGR1	chr10:5904393-5904659	GM12878	blood:	n/a	n/a
29	EGR1	chr10:5904399-5904649	GM12878	blood:	n/a	n/a
30	ELF1	chr10:5904152-5904932	GM12878	blood:	n/a	n/a
31	ELK1	chr10:5904248-5904512	GM12878	blood:	n/a	n/a
32	EP300	chr10:5904186-5905099	GM12878	blood:	n/a	n/a
33	EP300	chr10:5904184-5905009	GM12878	blood:	n/a	n/a
34	EP300	chr10:5903323-5903568	HepG2	liver:	n/a	chr10:5903433-5903442
35	EP300	chr10:5904235-5904738	GM12878	blood:	n/a	n/a
36	EP300	chr10:5903215-5903603	HepG2	liver:	n/a	chr10:5903433-5903442
37	ESRRA	chr10:5904023-5905341	GM12878	blood:	n/a	n/a
38	FOS	chr10:5903247-5903678	MCF10A-Er-Src	breast:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903390-5903401 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903431-5903442 chr10:5903433-5903440 chr10:5903433-5903441
39	FOS	chr10:5903253-5903630	MCF10A-Er-Src	breast:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903390-5903401 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903431-5903442 chr10:5903433-5903440 chr10:5903433-5903441
40	FOS	chr10:5903211-5903627	MCF10A-Er-Src	breast:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903390-5903401 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903431-5903442 chr10:5903433-5903440 chr10:5903433-5903441
41	FOS	chr10:5903244-5903698	HUVEC	blood vessel:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903390-5903401 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903431-5903442 chr10:5903433-5903440 chr10:5903433-5903441
42	FOS	chr10:5903244-5903659	MCF10A-Er-Src	breast:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903390-5903401 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903431-5903442 chr10:5903433-5903440 chr10:5903433-5903441
43	FOSL1	chr10:5903237-5903557	K562	blood:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903433-5903440 chr10:5903433-5903441
44	FOSL1	chr10:5903084-5903919	HCT-116	colon:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903433-5903440 chr10:5903433-5903441
45	FOSL1	chr10:5903294-5903752	HCT-116	colon:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903433-5903440 chr10:5903433-5903441
46	FOSL2	chr10:5903301-5903720	MCF-7	breast:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903391-5903402 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903430-5903441 chr10:5903433-5903440 chr10:5903433-5903441
47	FOSL2	chr10:5903162-5903609	HepG2	liver:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903391-5903402 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903430-5903441 chr10:5903433-5903440 chr10:5903433-5903441
48	FOSL2	chr10:5903232-5903680	SK-N-SH	brain:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903391-5903402 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903430-5903441 chr10:5903433-5903440 chr10:5903433-5903441
49	FOSL2	chr10:5903299-5903553	A549	lung:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903391-5903402 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903430-5903441 chr10:5903433-5903440 chr10:5903433-5903441
50	FOSL2	chr10:5903112-5903684	A549	lung:	n/a	chr10:5903432-5903443 chr10:5903432-5903442 chr10:5903391-5903402 chr10:5903434-5903445 chr10:5903433-5903441 chr10:5903430-5903441 chr10:5903433-5903440 chr10:5903433-5903441

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5904561-5904611	GM19239	blood:	n/a
2	chr10:5904561-5904611	NT2-D1	testis:	n/a
3	chr10:5904561-5904611	ECC-1	luminal epithelium:	n/a
4	chr10:5904561-5904611	HRCEpiC	kidney:	n/a
5	chr10:5904561-5904611	MCF10A-Er-Src	breast:	n/a
6	chr10:5904561-5904611	SK-N-SH_RA	brain:	n/a
7	chr10:5904561-5904611	SKMC	muscle:	n/a
8	chr10:5904561-5904611	HMEC	breast:	n/a
9	chr10:5904561-5904611	HCPEpiC	choroid plexus:	n/a
10	chr10:5904561-5904611	H1-hESC	embryonic stem cell:	embryo
11	chr10:5904561-5904611	CMK	blood:	n/a
12	chr10:5904561-5904611	AG04449	skin:	fetal
13	chr10:5904561-5904611	Hepatocyte	liver:	n/a
14	chr10:5904561-5904611	RPTEC	kidney:	n/a
15	chr10:5904561-5904611	K562	blood:	n/a
16	chr10:5904561-5904611	Jurkat	blood:	n/a
17	chr10:5904561-5904611	IMR90	lung:	fetal
18	chr10:5904561-5904611	HCT-116	colon:	n/a
19	chr10:5904561-5904611	GM06990	blood:	n/a
20	chr10:5904561-5904611	NH-A	brain:	n/a
21	chr10:5904561-5904611	NHBE	bronchial:	n/a
22	chr10:5904561-5904611	ProgFib	skin:	n/a
23	chr10:5904561-5904611	AoSMC	blood vessel:	n/a
24	chr10:5904561-5904611	HUVEC	blood vessel:	n/a
25	chr10:5904561-5904611	HRE	kidney:	n/a
26	chr10:5904561-5904611	LNCaP	prostate:	n/a
27	chr10:5904561-5904611	GM12891	blood:	n/a
28	chr10:5904561-5904611	HRPEpiC	eye:	n/a
29	chr10:5904561-5904611	HNPCEpiC	eye:	n/a
30	chr10:5904561-5904611	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:5904561-5904611	PANC-1	pancreas:	n/a
32	chr10:5904561-5904611	SK-N-SH	brain:	n/a
33	chr10:5904561-5904611	AG04450	lung:	fetal
34	chr10:5904561-5904611	GM12878	blood:	n/a
35	chr10:5904561-5904611	HepG2	liver:	n/a
36	chr10:5904561-5904611	PrEC	prostate:	n/a
37	chr10:5904561-5904611	A549	lung:	n/a
38	chr10:5904561-5904611	NHDF-neo	bronchial:	n/a
39	chr10:5904561-5904611	Caco-2	colon:	n/a
40	chr10:5904561-5904611	T-47D	breast:	n/a
41	chr10:5904561-5904611	HIPEpiC	eye:	n/a
42	chr10:5904561-5904611	AG09319	gingival:	n/a
43	chr10:5904561-5904611	U87	brain:	n/a
44	chr10:5904561-5904611	ovcar-3	ovarian:	n/a
45	chr10:5904561-5904611	AG09309	skin:	n/a
46	chr10:5904561-5904611	BJ	skin:	n/a
47	chr10:5904561-5904611	HL-60	blood:	n/a
48	chr10:5904561-5904611	PFSK-1	brain:	n/a
49	chr10:5904561-5904611	NB4	blood:	n/a
50	chr10:5904561-5904611	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:5853453..5856522-chr10:5901378..5904221,3	K562	blood:
2	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:
3	chr10:5853575..5857221-chr10:5900529..5905112,5	MCF-7	breast:
4	chr10:5904346..5907644-chr10:5928919..5931742,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDI2-2	chr10:5904161-5904557	NONHSAT011187
2	lnc-GDI2-2	chr10:5903768-5903859	NONHSAT011187

Variant related genes	Relation type
ENSG00000240180	TF binding region
ENSG00000240180	CpG island
ENSG00000134461	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000272764	chromatin interactions

Extended variants
information (count: 67 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:67 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7071536	chr10:5903518-5903519	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs199621997	chr10:5903523-5903524	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs555043080	chr10:5903528-5903529	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs74729956	chr10:5903532-5903533	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs538115053	chr10:5903542-5903543	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs568321147	chr10:5903543-5903544	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs112464642	chr10:5903562-5903563	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs577786846	chr10:5903566-5903567	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs545209845	chr10:5903568-5903569	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs536765466	chr10:5903604-5903605	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs200871268	chr10:5903639-5903640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs79136570	chr10:5903676-5903677	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs572183544	chr10:5903684-5903685	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs150058153	chr10:5903717-5903718	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs201147492	chr10:5903723-5903724	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs67091121	chr10:5903837-5903838	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531743366	chr10:5903855-5903856	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs201502478	chr10:5903860-5903861	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs71388490	chr10:5903861-5903862	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs398054074	chr10:5903871-5903872	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs575657614	chr10:5903887-5903888	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs112060825	chr10:5903895-5903896	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs559429641	chr10:5903909-5903910	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs572991597	chr10:5903925-5903926	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs533126755	chr10:5903933-5903934	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs113859716	chr10:5903988-5903989	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs3209527	chr10:5903993-5903994	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs3209526	chr10:5904003-5904004	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs566703330	chr10:5904009-5904010	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs539593608	chr10:5904056-5904057	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs549070110	chr10:5904064-5904065	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs145241615	chr10:5904070-5904071	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs3209525	chr10:5904071-5904072	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs537868576	chr10:5904079-5904080	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs561873700	chr10:5904087-5904088	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs111564843	chr10:5904102-5904103	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs183780638	chr10:5904113-5904114	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs553941220	chr10:5904115-5904116	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs112416163	chr10:5904120-5904121	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs113295435	chr10:5904129-5904130	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs140526685	chr10:5904156-5904157	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs7919286	chr10:5904261-5904262	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7913112	chr10:5904300-5904301	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187318065	chr10:5904301-5904302	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs565314162	chr10:5904323-5904324	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs145857114	chr10:5904348-5904349	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs76610235	chr10:5904371-5904372	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs560347702	chr10:5904423-5904424	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs527483004	chr10:5904437-5904438	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs557822825	chr10:5904455-5904456	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5888800-5904400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:5894600-5908600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:5894600-5908600	Weak transcription	K562	blood
4	chr10:5894600-5916800	Weak transcription	Spleen	Spleen
5	chr10:5896200-5912200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr10:5896400-5918200	Weak transcription	Fetal Lung	lung
7	chr10:5896600-5903800	Weak transcription	Fetal Stomach	stomach
8	chr10:5897000-5903800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr10:5899000-5904200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr10:5899800-5904200	Weak transcription	Ovary	ovary
11	chr10:5899800-5905000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr10:5900000-5904000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:5900000-5916600	Weak transcription	Pancreas	Pancrea
14	chr10:5900400-5916200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr10:5900600-5916200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr10:5900800-5910600	Weak transcription	Brain Germinal Matrix	brain
17	chr10:5901000-5904200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:5901000-5916600	Weak transcription	Gastric	stomach
19	chr10:5901200-5904200	Weak transcription	Brain Angular Gyrus	brain
20	chr10:5901200-5918200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:5901400-5905000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr10:5901400-5915200	Weak transcription	Brain Hippocampus Middle	brain
23	chr10:5901600-5904200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr10:5901600-5912600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr10:5901600-5915600	Weak transcription	Brain Anterior Caudate	brain
26	chr10:5901800-5904200	Weak transcription	Fetal Intestine Small	intestine
27	chr10:5901800-5910800	Weak transcription	Fetal Brain Female	brain
28	chr10:5902000-5904000	Enhancers	GM12878-XiMat	blood
29	chr10:5902000-5904800	Enhancers	Placenta	Placenta
30	chr10:5902200-5904600	Enhancers	NHDF-Ad	bronchial
31	chr10:5902200-5905000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr10:5902200-5912600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr10:5902400-5904400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr10:5902400-5905000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr10:5902400-5908600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr10:5902400-5918200	Weak transcription	Primary T cells from cord blood	blood
37	chr10:5902600-5904600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr10:5902600-5910200	Weak transcription	Fetal Muscle Leg	muscle
39	chr10:5902800-5903600	Weak transcription	NHLF	lung
40	chr10:5902800-5916200	Weak transcription	Fetal Intestine Large	intestine
41	chr10:5902800-5916600	Weak transcription	Brain Substantia Nigra	brain
42	chr10:5902800-5918000	Weak transcription	Lung	lung
43	chr10:5903000-5903800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:5903000-5903800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr10:5903000-5904400	Enhancers	HSMM	muscle
46	chr10:5903000-5904600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr10:5903000-5905200	Enhancers	HepG2	liver
48	chr10:5903000-5912400	Weak transcription	Fetal Heart	heart
49	chr10:5903000-5915400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr10:5903200-5903600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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