Variant report

Variant	esv1794817
Chromosome Location	chr10:18827828-18888369
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:630)
CpG islands
(count:427)
Chromatin interactive
region (count:10)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:18855015-18855499	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:18883708-18883996	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:18871855-18872156	K562	blood:	n/a	n/a
4	ARID3A	chr10:18854097-18854130	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:18847006-18847183	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:18850803-18851483	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:18843485-18843910	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:18872609-18872929	K562	blood:	n/a	n/a
9	ARID3A	chr10:18852867-18853155	HepG2	liver:	n/a	n/a
10	ATF1	chr10:18871829-18872244	K562	blood:	n/a	n/a
11	BHLHE40	chr10:18883841-18883953	K562	blood:	n/a	n/a
12	BRCA1	chr10:18860126-18860500	GM12878	blood:	n/a	n/a
13	BRCA1	chr10:18848238-18848611	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr10:18860127-18860500	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr10:18866717-18867121	K562	blood:	n/a	n/a
16	CBX3	chr10:18866819-18867030	K562	blood:	n/a	n/a
17	CEBPB	chr10:18884993-18885181	A549	lung:	n/a	chr10:18885082-18885095
18	CEBPB	chr10:18855132-18855383	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr10:18854245-18854618	K562	blood:	n/a	n/a
20	CEBPB	chr10:18872595-18872894	K562	blood:	n/a	n/a
21	CHD2	chr10:18860126-18860500	GM12878	blood:	n/a	n/a
22	CHD2	chr10:18854418-18854541	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr10:18872640-18872790	GM12872	blood:	n/a	n/a
24	CTCF	chr10:18883920-18884070	AG09319	gingival:	n/a	n/a
25	CTCF	chr10:18883800-18883950	BE2_C	brain:	n/a	n/a
26	CTCF	chr10:18872560-18872710	GM12864	blood:	n/a	n/a
27	CTCF	chr10:18883860-18884010	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr10:18883880-18884030	HCT-116	colon:	n/a	n/a
29	CTCF	chr10:18883820-18883970	HAc	cerebellar:	n/a	n/a
30	CTCF	chr10:18883880-18884030	HCM	heart:	n/a	n/a
31	CTCF	chr10:18883616-18883717	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr10:18872880-18873030	HepG2	liver:	n/a	n/a
33	CTCF	chr10:18883860-18884010	GM12875	blood:	n/a	n/a
34	CTCF	chr10:18883820-18883970	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr10:18872640-18872790	GM12878	blood:	n/a	n/a
36	CTCF	chr10:18883592-18883789	MCF-7	breast:	n/a	n/a
37	CTCF	chr10:18872520-18872670	RPTEC	kidney:	n/a	n/a
38	CTCF	chr10:18872540-18872690	GM12874	blood:	n/a	n/a
39	CTCF	chr10:18883660-18883810	SAEC	small airway:	n/a	n/a
40	CTCF	chr10:18883840-18883990	HepG2	liver:	n/a	n/a
41	CTCF	chr10:18883540-18883690	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr10:18883517-18884137	HepG2	liver:	n/a	n/a
43	CTCF	chr10:18887483-18887512	Fibrobl	skin:	n/a	n/a
44	CTCF	chr10:18872620-18872770	GM12864	blood:	n/a	n/a
45	CTCF	chr10:18883560-18883710	GM06990	blood:	n/a	n/a
46	CTCF	chr10:18883655-18883713	LNCaP	prostate:	n/a	n/a
47	CTCF	chr10:18883903-18884009	GM20000	blood:	n/a	n/a
48	CTCF	chr10:18872620-18872770	GM12878	blood:	n/a	n/a
49	CTCF	chr10:18872615-18872770	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr10:18883840-18883990	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:18828426-18828476	GM12892	blood:	n/a
2	chr10:18875548-18875598	HCPEpiC	choroid plexus:	n/a
3	chr10:18875473-18875523	AG09309	skin:	n/a
4	chr10:18875381-18875431	MCF10A-Er-Src	breast:	n/a
5	chr10:18875381-18875431	HCF	heart:	n/a
6	chr10:18875473-18875523	Hepatocyte	liver:	n/a
7	chr10:18875381-18875431	MCF-7	breast:	n/a
8	chr10:18875473-18875523	BE2_C	brain:	n/a
9	chr10:18828426-18828476	HCM	heart:	n/a
10	chr10:18875548-18875598	NB4	blood:	n/a
11	chr10:18875473-18875523	U87	brain:	n/a
12	chr10:18877005-18877055	Hepatocyte	liver:	n/a
13	chr10:18875548-18875598	HCT-116	colon:	n/a
14	chr10:18828426-18828476	AG10803	skin:	n/a
15	chr10:18875473-18875523	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:18877005-18877055	HEK293	kidney:	embryo
17	chr10:18875473-18875523	HRPEpiC	eye:	n/a
18	chr10:18875473-18875523	K562	blood:	n/a
19	chr10:18828486-18828536	HNPCEpiC	eye:	n/a
20	chr10:18877005-18877055	AG04449	skin:	fetal
21	chr10:18875473-18875523	HUVEC	blood vessel:	n/a
22	chr10:18877005-18877055	HNPCEpiC	eye:	n/a
23	chr10:18828426-18828476	NH-A	brain:	n/a
24	chr10:18875473-18875523	SAEC	small airway:	n/a
25	chr10:18877005-18877055	HRPEpiC	eye:	n/a
26	chr10:18877005-18877055	HCM	heart:	n/a
27	chr10:18875381-18875431	HEK293	kidney:	embryo
28	chr10:18875381-18875431	SK-N-SH_RA	brain:	n/a
29	chr10:18875473-18875523	NB4	blood:	n/a
30	chr10:18828486-18828536	ovcar-3	ovarian:	n/a
31	chr10:18828426-18828476	Caco-2	colon:	n/a
32	chr10:18875381-18875431	ovcar-3	ovarian:	n/a
33	chr10:18828340-18828390	NT2-D1	testis:	n/a
34	chr10:18828426-18828476	NB4	blood:	n/a
35	chr10:18877005-18877055	HL-60	blood:	n/a
36	chr10:18875548-18875598	K562	blood:	n/a
37	chr10:18875548-18875598	HCM	heart:	n/a
38	chr10:18877005-18877055	ovcar-3	ovarian:	n/a
39	chr10:18828486-18828536	NT2-D1	testis:	n/a
40	chr10:18828340-18828390	HMEC	breast:	n/a
41	chr10:18828426-18828476	K562	blood:	n/a
42	chr10:18828340-18828390	HEEpiC	esophagus:	n/a
43	chr10:18875548-18875598	RPTEC	kidney:	n/a
44	chr10:18877005-18877055	HAEpiC	amniotic membrane:	n/a
45	chr10:18828426-18828476	PFSK-1	brain:	n/a
46	chr10:18875381-18875431	A549	lung:	n/a
47	chr10:18828426-18828476	GM12891	blood:	n/a
48	chr10:18877005-18877055	RPTEC	kidney:	n/a
49	chr10:18875548-18875598	T-47D	breast:	n/a
50	chr10:18828486-18828536	NH-A	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:18881247..18884169-chr10:18946476..18949026,2	K562	blood:
2	chr10:18871041..18872755-chr10:18938799..18941399,2	K562	blood:
3	chr10:18832497..18833999-chr10:18887489..18889225,2	K562	blood:
4	chr10:18881247..18884193-chr10:18945949..18949026,3	K562	blood:
5	chr10:18872028..18874928-chr10:18946049..18948722,4	K562	blood:
6	chr10:18824996..18829139-chr10:18831210..18835804,4	K562	blood:
7	chr10:18883515..18884111-chr10:18904979..18905887,2	MCF-7	breast:
8	chr1:1025004..1026004-chr10:18883636..18884321,2	MCF-7	breast:
9	chr10:18882733..18884546-chr10:18887488..18889531,2	MCF-7	breast:
10	chr10:18882733..18884546-chr10:18887488..18889531,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NSUN6-1	chr10:18830515-18831106	ENSG00000240291.1
2	lnc-NSUN6-1	chr10:18830098-18830177	ENSG00000240291.1
3	lnc-NSUN6-1	chr10:18834394-18834580	ENSG00000240291.1
4	lnc-NSUN6-1	chr10:18830998-18831106	ENSG00000240291.1
5	lnc-NSUN6-1	chr10:18833253-18833316	ENSG00000240291.1
6	lnc-NSUN6-1	chr10:18828123-18828228	ENSG00000240291.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CACNB2	hsa-miR-26b-5p	chr10:18828922-18828928

Variant related genes	Relation type
NSUN6	TF binding region
ENSG00000240291	TF binding region
NSUN6	CpG island
ENSG00000240291	CpG island
ENSG00000240291	chromatin interactions
ENSG00000241058	chromatin interactions
ENSG00000152487	chromatin interactions
ENSG00000165997	chromatin interactions

Extended variants
information (count: 3313 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:3313 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6482515	chr10:18827828-18827829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11014733	chr10:18827829-18827830	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571326795	chr10:18827834-18827835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75924947	chr10:18827837-18827838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75258286	chr10:18827838-18827839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78812809	chr10:18827865-18827866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557547790	chr10:18827885-18827886	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs76540339	chr10:18827886-18827887	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs369813065	chr10:18827892-18827893	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201160034	chr10:18827909-18827910	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11419902	chr10:18827910-18827911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527723625	chr10:18827911-18827912	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs536581600	chr10:18827947-18827948	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs555785761	chr10:18827951-18827952	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140646827	chr10:18827962-18827963	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11597316	chr10:18827964-18827965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556752057	chr10:18828013-18828014	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114462890	chr10:18828019-18828020	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145808514	chr10:18828027-18828028	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545253616	chr10:18828059-18828060	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138454982	chr10:18828060-18828061	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs193210073	chr10:18828061-18828062	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183067087	chr10:18828070-18828071	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561250296	chr10:18828111-18828112	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200220986	chr10:18828132-18828133	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs369426925	chr10:18828133-18828134	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs371134499	chr10:18828147-18828148	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs557859826	chr10:18828151-18828152	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs143326262	chr10:18828181-18828182	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs111250176	chr10:18828186-18828187	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs532262049	chr10:18828187-18828188	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs34813638	chr10:18828188-18828189	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs143060134	chr10:18828191-18828192	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs191856144	chr10:18828209-18828210	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs370018033	chr10:18828220-18828221	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs150320948	chr10:18828221-18828222	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs138060429	chr10:18828223-18828224	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs200297403	chr10:18828228-18828229	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs150280879	chr10:18828230-18828231	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147142811	chr10:18828233-18828234	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs202152674	chr10:18828261-18828262	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184280124	chr10:18828262-18828263	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs121917812	chr10:18828274-18828275	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571637787	chr10:18828295-18828296	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs140576104	chr10:18828305-18828306	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377657305	chr10:18828310-18828311	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149330185	chr10:18828320-18828321	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs137886839	chr10:18828340-18828341	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2228646	chr10:18828341-18828342	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs199714857	chr10:18828351-18828352	Strong transcription ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:41)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Olfactory neuroblastoma	18408657	CNVD

Chromatin state (count:1476 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18802600-18828000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr10:18802600-18828200	Weak transcription	Lung	lung
3	chr10:18807400-18828000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr10:18808000-18828000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:18810400-18828000	Weak transcription	Brain Angular Gyrus	brain
6	chr10:18810600-18828200	Weak transcription	Aorta	Aorta
7	chr10:18810800-18828000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr10:18814000-18828000	Weak transcription	Esophagus	oesophagus
9	chr10:18815200-18843600	Weak transcription	A549	lung
10	chr10:18815800-18828000	Weak transcription	K562	blood
11	chr10:18816400-18830400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:18816400-18841800	Strong transcription	Liver	Liver
13	chr10:18816800-18829600	Weak transcription	HSMMtube	muscle
14	chr10:18817400-18829000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr10:18818800-18828000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr10:18818800-18828400	Weak transcription	Fetal Thymus	thymus
17	chr10:18819600-18828000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:18819800-18829800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr10:18820000-18828400	Weak transcription	Fetal Muscle Leg	muscle
20	chr10:18820000-18829800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr10:18820800-18841600	Weak transcription	Hela-S3	cervix
22	chr10:18822000-18840400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr10:18822000-18848000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr10:18822200-18830400	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr10:18822400-18829600	Weak transcription	HSMM	muscle
26	chr10:18822400-18833600	Strong transcription	Primary T cells from cord blood	blood
27	chr10:18822600-18829000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr10:18822600-18830600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr10:18822800-18830600	Strong transcription	Left Ventricle	heart
30	chr10:18822800-18841800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr10:18823200-18831200	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr10:18823400-18830400	Strong transcription	Stomach Smooth Muscle	stomach
33	chr10:18823400-18830600	Strong transcription	Fetal Lung	lung
34	chr10:18823400-18834800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr10:18823600-18831000	Strong transcription	Rectal Mucosa Donor 31	rectum
36	chr10:18823600-18836600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr10:18823800-18830400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr10:18824000-18830600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr10:18824200-18829800	Weak transcription	Placenta	Placenta
40	chr10:18824200-18830600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr10:18824200-18831200	Strong transcription	Fetal Stomach	stomach
42	chr10:18824200-18831600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr10:18824200-18834800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr10:18824200-18846200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr10:18824200-18850600	Weak transcription	NHLF	lung
46	chr10:18824400-18828200	Weak transcription	GM12878-XiMat	blood
47	chr10:18824400-18829600	Weak transcription	Fetal Kidney	kidney
48	chr10:18824800-18829600	Weak transcription	HepG2	liver
49	chr10:18825000-18830400	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr10:18825000-18835800	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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