Variant report

Variant	nsv975787
Chromosome Location	chr10:99048466-99061224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:765)
CpG islands
(count:917)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:765 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:99052299-99052770	K562	blood:	n/a	n/a
2	ARID3A	chr10:99051614-99052821	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:99053811-99054111	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:99057363-99057743	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:99057466-99058100	K562	blood:	n/a	n/a
6	ARID3A	chr10:99053920-99054039	K562	blood:	n/a	n/a
7	ATF1	chr10:99057474-99058065	K562	blood:	n/a	n/a
8	ATF1	chr10:99052266-99052723	K562	blood:	n/a	n/a
9	ATF2	chr10:99052194-99052756	GM12878	blood:	n/a	n/a
10	BACH1	chr10:99052348-99052837	K562	blood:	n/a	chr10:99052752-99052766
11	BACH1	chr10:99051579-99051818	K562	blood:	n/a	n/a
12	BCLAF1	chr10:99052363-99052864	GM12878	blood:	n/a	n/a
13	BCLAF1	chr10:99051689-99052353	GM12878	blood:	n/a	chr10:99052184-99052197 chr10:99052097-99052110
14	BHLHE40	chr10:99057702-99057972	K562	blood:	n/a	n/a
15	BHLHE40	chr10:99051944-99052578	HepG2	liver:	n/a	n/a
16	BHLHE40	chr10:99051765-99052726	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:99057423-99057534	HepG2	liver:	n/a	n/a
18	BHLHE40	chr10:99051884-99052413	K562	blood:	n/a	n/a
19	BRCA1	chr10:99052170-99052216	HepG2	liver:	n/a	n/a
20	BRCA1	chr10:99051994-99052658	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr10:99051745-99052768	K562	blood:	n/a	n/a
22	CBX3	chr10:99057566-99058055	K562	blood:	n/a	n/a
23	CCNT2	chr10:99057509-99058010	K562	blood:	n/a	n/a
24	CCNT2	chr10:99051900-99052431	K562	blood:	n/a	n/a
25	CEBPB	chr10:99057276-99057587	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:99057315-99057445	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr10:99057205-99057918	K562	blood:	n/a	n/a
28	CEBPB	chr10:99057248-99057676	HepG2	liver:	n/a	n/a
29	CEBPB	chr10:99051672-99052054	K562	blood:	n/a	n/a
30	CEBPB	chr10:99057269-99057525	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr10:99051701-99052649	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr10:99057203-99058031	K562	blood:	n/a	n/a
33	CEBPB	chr10:99057230-99057761	A549	lung:	n/a	n/a
34	CEBPB	chr10:99057240-99057531	IMR90	lung:	n/a	n/a
35	CEBPB	chr10:99053204-99053404	K562	blood:	n/a	n/a
36	CEBPB	chr10:99057255-99057571	K562	blood:	n/a	n/a
37	CEBPB	chr10:99057249-99057566	MCF-7	breast:	n/a	n/a
38	CEBPB	chr10:99057191-99057593	A549	lung:	n/a	n/a
39	CEBPB	chr10:99057250-99057537	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:99057237-99057538	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:99057027-99057729	A549	lung:	n/a	n/a
42	CEBPB	chr10:99051576-99052610	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:99052314-99052569	K562	blood:	n/a	n/a
44	CEBPB	chr10:99051545-99052583	A549	lung:	n/a	n/a
45	CEBPB	chr10:99051845-99052575	HepG2	liver:	n/a	n/a
46	CEBPD	chr10:99051888-99052643	HepG2	liver:	n/a	n/a
47	CEBPD	chr10:99057337-99058040	K562	blood:	n/a	n/a
48	CEBPD	chr10:99057253-99058178	K562	blood:	n/a	n/a
49	CHD1	chr10:99052048-99052367	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr10:99051640-99052635	GM12878	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99053150-99053200	AG04449	skin:	fetal
2	chr10:99049020-99049070	HMEC	breast:	n/a
3	chr10:99053150-99053200	AG04449	skin:	fetal
4	chr10:99049020-99049070	HMEC	breast:	n/a
5	chr10:99052555-99052605	AG04450	lung:	fetal
6	chr10:99055765-99055815	ECC-1	luminal epithelium:	n/a
7	chr10:99052545-99052595	RPTEC	kidney:	n/a
8	chr10:99052468-99052518	ovcar-3	ovarian:	n/a
9	chr10:99052215-99052265	AG10803	skin:	n/a
10	chr10:99052489-99052539	HEK293	kidney:	embryo
11	chr10:99053150-99053200	NT2-D1	testis:	n/a
12	chr10:99052215-99052265	SAEC	small airway:	n/a
13	chr10:99052215-99052265	H1-hESC	embryonic stem cell:	embryo
14	chr10:99052489-99052539	HRPEpiC	eye:	n/a
15	chr10:99052472-99052522	SKMC	muscle:	n/a
16	chr10:99052653-99052703	ProgFib	skin:	n/a
17	chr10:99052509-99052559	RPTEC	kidney:	n/a
18	chr10:99051975-99052025	ECC-1	luminal epithelium:	n/a
19	chr10:99051975-99052025	AG09309	skin:	n/a
20	chr10:99051975-99052025	AG04449	skin:	fetal
21	chr10:99052468-99052518	SAEC	small airway:	n/a
22	chr10:99050413-99050463	ProgFib	skin:	n/a
23	chr10:99051975-99052025	Hepatocyte	liver:	n/a
24	chr10:99052545-99052595	HMEC	breast:	n/a
25	chr10:99052509-99052559	HepG2	liver:	n/a
26	chr10:99052472-99052522	AG10803	skin:	n/a
27	chr10:99051840-99051890	ovcar-3	ovarian:	n/a
28	chr10:99052555-99052605	HEK293	kidney:	embryo
29	chr10:99052509-99052559	SKMC	muscle:	n/a
30	chr10:99052618-99052668	MCF-7	breast:	n/a
31	chr10:99052472-99052522	HCT-116	colon:	n/a
32	chr10:99052653-99052703	HRPEpiC	eye:	n/a
33	chr10:99052618-99052668	GM12878	blood:	n/a
34	chr10:99052509-99052559	HIPEpiC	eye:	n/a
35	chr10:99049020-99049070	PrEC	prostate:	n/a
36	chr10:99052653-99052703	BE2_C	brain:	n/a
37	chr10:99052468-99052518	IMR90	lung:	fetal
38	chr10:99052509-99052559	SK-N-MC	brain:	n/a
39	chr10:99052509-99052559	NHBE	bronchial:	n/a
40	chr10:99053150-99053200	NH-A	brain:	n/a
41	chr10:99052489-99052539	HCT-116	colon:	n/a
42	chr10:99049020-99049070	HCT-116	colon:	n/a
43	chr10:99053150-99053200	HRCEpiC	kidney:	n/a
44	chr10:99052509-99052559	BJ	skin:	n/a
45	chr10:99052489-99052539	SKMC	muscle:	n/a
46	chr10:99050413-99050463	GM06990	blood:	n/a
47	chr10:99053150-99053200	Caco-2	colon:	n/a
48	chr10:99052653-99052703	HCPEpiC	choroid plexus:	n/a
49	chr10:99051975-99052025	LNCaP	prostate:	n/a
50	chr10:99052468-99052518	MCF10A-Er-Src	breast:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:99048545..99053546-chr10:99092341..99096465,6	K562	blood:
2	chr10:99050766..99052270-chr10:99085293..99087979,2	MCF-7	breast:
3	chr10:99051705..99053713-chr10:99056526..99058710,2	MCF-7	breast:
4	chr10:99044514..99046643-chr10:99048334..99050746,3	K562	blood:
5	chr10:99059557..99062005-chr10:99076805..99079632,3	K562	blood:
6	chr10:99052531..99053031-chr12:32259435..32260354,2	Hela-S3	cervix:
7	chr10:99051058..99054984-chr10:99078319..99082092,7	MCF-7	breast:
8	chr10:99051045..99053385-chr10:99092824..99094336,2	MCF-7	breast:
9	chr10:99051532..99052217-chr11:65270337..65271200,2	Hela-S3	cervix:
10	chr10:99050239..99051953-chr10:99089208..99091250,2	K562	blood:
11	chr10:99051863..99052445-chr4:76439211..76440158,2	HCT-116	colon:
12	chr10:99051590..99052388-chr10:101380641..101381344,2	Hela-S3	cervix:
13	chr10:99051546..99052354-chr2:55843946..55844595,2	Hela-S3	cervix:
14	chr10:99052581..99054143-chr10:99054832..99057681,2	K562	blood:
15	chr10:99051582..99055310-chr10:99077169..99083058,6	K562	blood:
16	chr10:99051571..99052405-chr19:12273845..12274393,2	Hela-S3	cervix:
17	chr10:99040697..99043641-chr10:99044330..99048505,4	K562	blood:
18	chr10:99052064..99052648-chr10:99078773..99079491,2	NB4	blood:
19	chr10:99050343..99055587-chr10:99077475..99082102,7	MCF-7	breast:
20	chr10:99050912..99053751-chr10:99091766..99095025,5	MCF-7	breast:
21	chr10:99055451..99057876-chr10:99084798..99087346,2	MCF-7	breast:
22	chr10:99052215..99054143-chr10:99055411..99058552,4	K562	blood:
23	chr10:99049975..99053832-chr10:99093402..99096465,5	K562	blood:
24	chr10:99051582..99054067-chr10:99077169..99079188,3	K562	blood:
25	chr10:99052282..99052884-chr5:41870193..41871067,2	Hela-S3	cervix:
26	chr10:99055592..99059898-chr10:99091799..99094514,4	K562	blood:
27	chr10:99057981..99059481-chr10:99078317..99080380,2	K562	blood:
28	chr10:99052581..99054143-chr10:99054832..99057681,2	K562	blood:
29	chr10:99050735..99053520-chr16:284621..286236,2	MCF-7	breast:

No data

Variant related genes	Relation type
ARHGAP19	TF binding region
ARHGAP19-SLIT1	TF binding region
ARHGAP19	CpG island
ARHGAP19-SLIT1	CpG island
ENSG00000213390	chromatin interactions
ENSG00000151746	chromatin interactions
ENSG00000163743	chromatin interactions
ENSG00000165879	chromatin interactions
ENSG00000260475	chromatin interactions
ENSG00000225850	chromatin interactions
ENSG00000181274	chromatin interactions
ENSG00000083720	chromatin interactions
ENSG00000174796	chromatin interactions
ENSG00000196646	chromatin interactions
ENSG00000167930	chromatin interactions
ENSG00000269891	chromatin interactions
ENSG00000248668	chromatin interactions

Extended variants
information (count: 516 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554292352	chr10:99048534-99048535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369982182	chr10:99048567-99048568	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189104588	chr10:99048592-99048593	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs113233072	chr10:99048672-99048673	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376611973	chr10:99048693-99048694	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs11189104	chr10:99048760-99048761	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548056684	chr10:99048796-99048797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558549431	chr10:99048864-99048865	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs577089907	chr10:99048870-99048871	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs544042595	chr10:99048873-99048874	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs370636911	chr10:99048911-99048912	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374313511	chr10:99048933-99048934	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs192817151	chr10:99048974-99048975	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs10786323	chr10:99049010-99049011	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs11814748	chr10:99049024-99049025	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs542338082	chr10:99049028-99049029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560606881	chr10:99049029-99049030	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs567339222	chr10:99049054-99049055	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs185290065	chr10:99049094-99049095	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552627794	chr10:99049219-99049220	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs12359643	chr10:99049235-99049236	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553057993	chr10:99049256-99049257	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs1253399	chr10:99049413-99049414	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs118162612	chr10:99049417-99049418	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188554774	chr10:99049420-99049421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs563764977	chr10:99049437-99049438	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113347300	chr10:99049477-99049478	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs370100914	chr10:99049499-99049500	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558496539	chr10:99049504-99049505	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs575477337	chr10:99049531-99049532	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547864937	chr10:99049546-99049547	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs1253400	chr10:99049566-99049567	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533516689	chr10:99049592-99049593	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs11304186	chr10:99049610-99049611	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs200731885	chr10:99049633-99049634	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs191743002	chr10:99049657-99049658	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs80118573	chr10:99049662-99049663	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs538142847	chr10:99049674-99049675	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs540293071	chr10:99049731-99049732	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs77689715	chr10:99049757-99049758	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs532292513	chr10:99049778-99049779	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545562727	chr10:99049799-99049800	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs75563080	chr10:99049802-99049803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560544819	chr10:99049808-99049809	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs371381817	chr10:99049848-99049849	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572590399	chr10:99049850-99049851	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565218720	chr10:99049877-99049878	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564510142	chr10:99049917-99049918	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184290957	chr10:99049930-99049931	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188197362	chr10:99049988-99049989	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98978600-99051800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:98987200-99051200	Weak transcription	Pancreas	Pancrea
3	chr10:99019400-99050000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr10:99019400-99051600	Weak transcription	Ovary	ovary
5	chr10:99021400-99051000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr10:99023600-99051200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr10:99024000-99050800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr10:99024400-99050000	Weak transcription	Spleen	Spleen
9	chr10:99024800-99051200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr10:99025800-99050800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr10:99026000-99051200	Weak transcription	Primary T cells from cord blood	blood
12	chr10:99028600-99051200	Weak transcription	Small Intestine	intestine
13	chr10:99031400-99050400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr10:99038000-99050400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr10:99038800-99051200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr10:99038800-99051200	Weak transcription	Brain Germinal Matrix	brain
17	chr10:99038800-99051200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr10:99038800-99051200	Weak transcription	NH-A	brain
19	chr10:99038800-99051400	Weak transcription	Brain Angular Gyrus	brain
20	chr10:99039000-99050600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr10:99039000-99050800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr10:99039000-99051200	Weak transcription	Colon Smooth Muscle	Colon
23	chr10:99039000-99051200	Weak transcription	HUVEC	blood vessel
24	chr10:99039000-99051400	Weak transcription	Brain Anterior Caudate	brain
25	chr10:99039400-99051200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr10:99039400-99051200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:99039400-99051200	Weak transcription	NHEK	skin
28	chr10:99039400-99051400	Weak transcription	Adipose Nuclei	Adipose
29	chr10:99039600-99050200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr10:99039600-99050800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr10:99039600-99051000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr10:99039600-99051000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr10:99039600-99051200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr10:99039800-99050800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:99039800-99051200	Weak transcription	NHDF-Ad	bronchial
36	chr10:99040400-99050400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr10:99041200-99051600	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr10:99042000-99051000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr10:99042400-99050800	Weak transcription	GM12878-XiMat	blood
40	chr10:99042600-99051400	Weak transcription	Brain Cingulate Gyrus	brain
41	chr10:99043600-99051200	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr10:99044400-99051600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr10:99045000-99051200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr10:99045800-99051200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr10:99045800-99051600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr10:99046000-99049400	Strong transcription	Fetal Stomach	stomach
47	chr10:99046200-99049600	Strong transcription	Fetal Intestine Small	intestine
48	chr10:99046400-99051400	Weak transcription	Right Ventricle	heart
49	chr10:99046800-99049600	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr10:99047000-99048600	Strong transcription	Monocytes-CD14+_RO01746	blood

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