Variant report

Variant	nsv549767
Chromosome Location	chr10:1064940-1073684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:856)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr10:1066397-1066874	A549	lung:	n/a	n/a
2	BCL3	chr10:1066604-1067072	A549	lung:	n/a	n/a
3	BCLAF1	chr10:1066352-1066772	GM12878	blood:	n/a	n/a
4	BCLAF1	chr10:1065120-1065685	GM12878	blood:	n/a	n/a
5	BCLAF1	chr10:1066403-1066750	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:1068528-1068714	HepG2	liver:	n/a	n/a
7	CCNT2	chr10:1070541-1070630	K562	blood:	n/a	n/a
8	CHD2	chr10:1066605-1066663	K562	blood:	n/a	n/a
9	CHD2	chr10:1066926-1066982	K562	blood:	n/a	n/a
10	CHD2	chr10:1065766-1065910	K562	blood:	n/a	n/a
11	CTCF	chr10:1068420-1068570	HRPEpiC	eye:	n/a	n/a
12	CTCF	chr10:1068440-1068590	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr10:1068520-1068670	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr10:1068460-1068610	HVMF	connective:	n/a	n/a
15	CUX1	chr10:1072731-1072787	K562	blood:	n/a	n/a
16	EP300	chr10:1066602-1066739	HepG2	liver:	n/a	n/a
17	EP300	chr10:1070469-1070882	K562	blood:	n/a	n/a
18	EP300	chr10:1072997-1073735	SK-N-SH	brain:	n/a	n/a
19	FOSL2	chr10:1066414-1067244	HepG2	liver:	n/a	n/a
20	GATA2	chr10:1071705-1072069	SH-SY5Y	brain:	n/a	chr10:1071864-1071871 chr10:1071783-1071790
21	GATA2	chr10:1073108-1073393	SH-SY5Y	brain:	n/a	n/a
22	GATA3	chr10:1071659-1072077	SH-SY5Y	brain:	n/a	chr10:1071864-1071871 chr10:1071783-1071790
23	GATA3	chr10:1073087-1073638	SH-SY5Y	brain:	n/a	n/a
24	HMGN3	chr10:1067015-1067106	K562	blood:	n/a	n/a
25	IRF1	chr10:1065836-1066034	K562	blood:	n/a	n/a
26	JUND	chr10:1066348-1067222	A549	lung:	n/a	n/a
27	MTA3	chr10:1066405-1067580	GM12878	blood:	n/a	n/a
28	MXI1	chr10:1068604-1068622	H1-hESC	embryonic stem cell:	n/a	n/a
29	MXI1	chr10:1066767-1066890	Hela-S3	cervix:	n/a	n/a
30	NFATC1	chr10:1065276-1065981	GM12878	blood:	n/a	n/a
31	NFATC1	chr10:1066390-1066818	GM12878	blood:	n/a	n/a
32	PML	chr10:1065197-1065827	K562	blood:	n/a	n/a
33	POLR2A	chr10:1066416-1066792	HepG2	liver:	n/a	n/a
34	POLR2A	chr10:1065025-1065812	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr10:1065359-1065699	GM12878	blood:	n/a	n/a
36	POLR2A	chr10:1066346-1067246	K562	blood:	n/a	n/a
37	POLR2A	chr10:1067149-1067293	A549	lung:	n/a	n/a
38	POLR2A	chr10:1066948-1067245	HepG2	liver:	n/a	n/a
39	POLR2A	chr10:1066870-1067277	A549	lung:	n/a	n/a
40	POLR2A	chr10:1069501-1069757	A549	lung:	n/a	n/a
41	POLR2A	chr10:1066011-1066033	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr10:1066270-1067309	GM12891	blood:	n/a	n/a
43	POLR2A	chr10:1066857-1067138	GM12891	blood:	n/a	n/a
44	POLR2A	chr10:1066291-1067431	PFSK-1	brain:	n/a	n/a
45	POLR2A	chr10:1067230-1067734	PFSK-1	brain:	n/a	n/a
46	POLR2A	chr10:1064657-1066260	GM12892	blood:	n/a	n/a
47	POLR2A	chr10:1066465-1066759	U87	brain:	n/a	n/a
48	POLR2A	chr10:1066354-1066831	HL-60	blood:	n/a	n/a
49	POLR2A	chr10:1064706-1065855	GM12891	blood:	n/a	n/a
50	POLR2A	chr10:1066439-1067127	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:1068567-1068617	HL-60	blood:	n/a
2	chr10:1068528-1068578	U87	brain:	n/a
3	chr10:1068567-1068617	HL-60	blood:	n/a
4	chr10:1068528-1068578	U87	brain:	n/a
5	chr10:1072690-1072740	HRCEpiC	kidney:	n/a
6	chr10:1068703-1068753	A549	lung:	n/a
7	chr10:1067538-1067588	RPTEC	kidney:	n/a
8	chr10:1067372-1067422	HL-60	blood:	n/a
9	chr10:1067538-1067588	NHBE	bronchial:	n/a
10	chr10:1071085-1071135	HUVEC	blood vessel:	n/a
11	chr10:1071902-1071952	RPTEC	kidney:	n/a
12	chr10:1068703-1068753	AG04450	lung:	fetal
13	chr10:1068763-1068813	HEEpiC	esophagus:	n/a
14	chr10:1071902-1071952	CMK	blood:	n/a
15	chr10:1071902-1071952	HCT-116	colon:	n/a
16	chr10:1068490-1068540	GM12891	blood:	n/a
17	chr10:1071902-1071952	HepG2	liver:	n/a
18	chr10:1064919-1064969	HRPEpiC	eye:	n/a
19	chr10:1067420-1067470	SK-N-SH	brain:	n/a
20	chr10:1071573-1071623	H1-hESC	embryonic stem cell:	embryo
21	chr10:1072690-1072740	HUVEC	blood vessel:	n/a
22	chr10:1068528-1068578	GM12892	blood:	n/a
23	chr10:1068567-1068617	U87	brain:	n/a
24	chr10:1068667-1068717	RPTEC	kidney:	n/a
25	chr10:1068528-1068578	AG09319	gingival:	n/a
26	chr10:1064919-1064969	T-47D	breast:	n/a
27	chr10:1064919-1064969	AG09319	gingival:	n/a
28	chr10:1067420-1067470	HNPCEpiC	eye:	n/a
29	chr10:1068667-1068717	NH-A	brain:	n/a
30	chr10:1068567-1068617	HNPCEpiC	eye:	n/a
31	chr10:1071573-1071623	BE2_C	brain:	n/a
32	chr10:1071902-1071952	GM12891	blood:	n/a
33	chr10:1071085-1071135	NB4	blood:	n/a
34	chr10:1072690-1072740	SK-N-SH	brain:	n/a
35	chr10:1071085-1071135	HL-60	blood:	n/a
36	chr10:1067538-1067588	ECC-1	luminal epithelium:	n/a
37	chr10:1068490-1068540	NB4	blood:	n/a
38	chr10:1068490-1068540	NHBE	bronchial:	n/a
39	chr10:1064919-1064969	AG09309	skin:	n/a
40	chr10:1068528-1068578	IMR90	lung:	fetal
41	chr10:1071902-1071952	HRCEpiC	kidney:	n/a
42	chr10:1067372-1067422	HAEpiC	amniotic membrane:	n/a
43	chr10:1067372-1067422	T-47D	breast:	n/a
44	chr10:1068528-1068578	HCPEpiC	choroid plexus:	n/a
45	chr10:1067372-1067422	HCT-116	colon:	n/a
46	chr10:1068667-1068717	HEEpiC	esophagus:	n/a
47	chr10:1067372-1067422	HCF	heart:	n/a
48	chr10:1068528-1068578	MCF10A-Er-Src	breast:	n/a
49	chr10:1071902-1071952	BJ	skin:	n/a
50	chr10:1067538-1067588	LNCaP	prostate:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:1072369..1076230-chr10:1093946..1096059,3	MCF-7	breast:
2	chr10:1069342..1071751-chr10:1093662..1096280,2	MCF-7	breast:
3	chr10:1065509..1068424-chr10:1086745..1089649,3	K562	blood:
4	chr10:1066230..1068078-chr10:1069655..1072615,2	K562	blood:
5	chr10:1061106..1063843-chr10:1063922..1066024,3	K562	blood:
6	chr10:1039567..1041272-chr10:1064973..1067031,2	K562	blood:
7	chr10:1071929..1076596-chr10:1081976..1085253,4	K562	blood:
8	chr10:1073140..1076758-chr10:1088109..1092485,5	K562	blood:
9	chr10:1068741..1070265-chr10:1070445..1072536,2	MCF-7	breast:
10	chr10:968239..971005-chr10:1062615..1065271,2	MCF-7	breast:
11	chr10:1073124..1075286-chr10:1080099..1081711,2	MCF-7	breast:
12	chr10:1066057..1068191-chr10:1094760..1097466,2	MCF-7	breast:
13	chr10:1057974..1060737-chr10:1065282..1067560,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTPBP4-1	chr10:1068608-1068723	ENSG00000232656.3
2	lnc-GTPBP4-1	chr10:1068614-1068723	ENSG00000232656.3

No data

Variant related genes	Relation type
IDI2	TF binding region
IDI2-AS1	TF binding region
IDI2	CpG island
IDI2-AS1	CpG island
ENSG00000047056	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000148377	chromatin interactions
ENSG00000107937	chromatin interactions

Extended variants
information (count: 494 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2170142	chr10:1064940-1064941	Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150913808	chr10:1064941-1064942	Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs546476769	chr10:1064946-1064947	Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs1051451	chr10:1064947-1064948	Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs183675741	chr10:1064954-1064955	Strong transcription Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs76090504	chr10:1064982-1064983	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs533568845	chr10:1064990-1064991	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs190658894	chr10:1064998-1064999	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568529702	chr10:1064999-1065000	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs181957524	chr10:1065013-1065014	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs547769363	chr10:1065054-1065055	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs2127607	chr10:1065132-1065133	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs74669000	chr10:1065167-1065168	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs558384193	chr10:1065183-1065184	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs185457666	chr10:1065184-1065185	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs17221491	chr10:1065191-1065192	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs3214941	chr10:1065204-1065205	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs397840030	chr10:1065208-1065209	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs189984608	chr10:1065245-1065246	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs10159989	chr10:1065250-1065251	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs539888600	chr10:1065291-1065292	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149879492	chr10:1065327-1065328	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs576714741	chr10:1065343-1065344	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs557918948	chr10:1065346-1065347	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs181293230	chr10:1065366-1065367	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs41294966	chr10:1065395-1065396	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371366202	chr10:1065399-1065400	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs41260144	chr10:1065406-1065407	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs368911024	chr10:1065440-1065441	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201116307	chr10:1065442-1065443	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs578143320	chr10:1065456-1065457	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs41314629	chr10:1065457-1065458	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs17851563	chr10:1065458-1065459	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376276027	chr10:1065463-1065464	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs527537227	chr10:1065490-1065491	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564510161	chr10:1065493-1065494	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs370074580	chr10:1065498-1065499	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs138894690	chr10:1065514-1065515	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs533129607	chr10:1065517-1065518	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs200869545	chr10:1065521-1065522	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376118683	chr10:1065523-1065524	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs140484326	chr10:1065532-1065533	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs41299208	chr10:1065538-1065539	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs548356090	chr10:1065542-1065543	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs370782776	chr10:1065549-1065550	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs138472250	chr10:1065557-1065558	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs41294968	chr10:1065574-1065575	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs201575182	chr10:1065580-1065581	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs574093260	chr10:1065586-1065587	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs113442797	chr10:1065603-1065604	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	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
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
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1035000-1094000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:1035800-1066200	Strong transcription	NH-A	brain
3	chr10:1036000-1066800	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr10:1036800-1066000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr10:1036800-1066800	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr10:1036800-1066800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:1036800-1066800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:1037000-1066000	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr10:1037000-1066200	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr10:1037200-1066800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:1037200-1067200	Strong transcription	NHEK	skin
12	chr10:1038000-1066200	Strong transcription	HUVEC	blood vessel
13	chr10:1038000-1066200	Strong transcription	Osteobl	bone
14	chr10:1038000-1067200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:1038200-1067000	Strong transcription	HSMM	muscle
16	chr10:1038200-1067200	Strong transcription	Muscle Satellite Cultured Cells	--
17	chr10:1038200-1067400	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr10:1038400-1065600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr10:1038400-1065600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr10:1038400-1066000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
21	chr10:1038400-1066200	Strong transcription	Duodenum Mucosa	Duodenum
22	chr10:1038400-1066200	Strong transcription	Stomach Smooth Muscle	stomach
23	chr10:1038400-1066800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr10:1038400-1066800	Strong transcription	HMEC	breast
25	chr10:1038600-1066200	Strong transcription	Brain Angular Gyrus	brain
26	chr10:1038600-1066800	Strong transcription	Fetal Thymus	thymus
27	chr10:1038600-1066800	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr10:1038600-1067000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr10:1038600-1067200	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr10:1038600-1068000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:1038800-1065800	Strong transcription	Brain Anterior Caudate	brain
32	chr10:1038800-1066600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
33	chr10:1038800-1067000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr10:1038800-1067400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:1038800-1067800	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr10:1040600-1065600	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr10:1041200-1067800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:1046400-1066000	Strong transcription	HSMMtube	muscle
39	chr10:1046800-1068600	Weak transcription	Right Atrium	heart
40	chr10:1047600-1067400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr10:1048200-1066200	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr10:1048200-1066800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr10:1048200-1066800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr10:1048600-1066800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr10:1048600-1067200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr10:1048800-1067200	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr10:1049000-1065200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr10:1049000-1066200	Strong transcription	Liver	Liver
49	chr10:1049000-1066600	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr10:1049000-1066800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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