Variant report

Variant	nsv948159
Chromosome Location	chr10:99238067-99240236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:99239602-99240078	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr10:99239623-99240073	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr10:99239509-99239539	GM20000	blood:	n/a	n/a
4	EP300	chr10:99239635-99239974	H1-hESC	embryonic stem cell:	n/a	n/a
5	FOS	chr10:99239246-99239432	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr10:99239288-99239488	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr10:99239226-99239433	MCF10A-Er-Src	breast:	n/a	n/a
8	FOSL2	chr10:99239129-99239594	HepG2	liver:	n/a	n/a
9	FOSL2	chr10:99239221-99239652	HepG2	liver:	n/a	n/a
10	FOXA1	chr10:99239041-99239534	HepG2	liver:	n/a	n/a
11	FOXA1	chr10:99239101-99239463	HepG2	liver:	n/a	n/a
12	FOXA1	chr10:99239138-99239408	HepG2	liver:	n/a	n/a
13	FOXA1	chr10:99239099-99239569	HepG2	liver:	n/a	n/a
14	HEY1	chr10:99239123-99239477	HepG2	liver:	n/a	n/a
15	JUND	chr10:99239188-99239467	HepG2	liver:	n/a	n/a
16	JUND	chr10:99239235-99239454	HepG2	liver:	n/a	n/a
17	MAX	chr10:99239817-99239933	NB4	blood:	n/a	n/a
18	MAX	chr10:99239709-99239953	MCF-7	breast:	n/a	n/a
19	MAX	chr10:99239686-99239874	K562	blood:	n/a	n/a
20	MAX	chr10:99239558-99240088	ECC-1	luminal epithelium:	n/a	n/a
21	MAX	chr10:99239649-99240063	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAX	chr10:99239639-99240116	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAX	chr10:99239746-99240004	K562	blood:	n/a	n/a
24	MAX	chr10:99239644-99240034	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAX	chr10:99239667-99240094	ECC-1	luminal epithelium:	n/a	n/a
26	MXI1	chr10:99239788-99239883	K562	blood:	n/a	n/a
27	MXI1	chr10:99239653-99240015	H1-hESC	embryonic stem cell:	n/a	n/a
28	MYC	chr10:99239599-99240172	H1-hESC	embryonic stem cell:	n/a	n/a
29	NANOG	chr10:99239668-99239938	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr10:99239386-99239426	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr10:99239284-99239390	HepG2	liver:	n/a	n/a
32	POLR2A	chr10:99239716-99240189	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr10:99238996-99239022	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr10:99239830-99240189	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr10:99239675-99240092	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr10:99239408-99239498	HepG2	liver:	n/a	n/a
37	POLR2A	chr10:99239531-99239642	HepG2	liver:	n/a	n/a
38	POLR2A	chr10:99239433-99239541	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr10:99238660-99238946	PFSK-1	brain:	n/a	n/a
40	POLR2A	chr10:99239606-99240394	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr10:99239677-99240200	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr10:99238965-99238989	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr10:99239093-99239162	HepG2	liver:	n/a	n/a
44	POLR2A	chr10:99239031-99239089	HepG2	liver:	n/a	n/a
45	POU2F2	chr10:99239633-99240078	GM12878	blood:	n/a	chr10:99239861-99239874
46	POU2F2	chr10:99239652-99240091	GM12891	blood:	n/a	chr10:99239861-99239874
47	POU2F2	chr10:99239709-99240075	GM12891	blood:	n/a	chr10:99239861-99239874
48	POU5F1	chr10:99239568-99240043	H1-hESC	embryonic stem cell:	n/a	chr10:99239861-99239874
49	RAD21	chr10:99238998-99239288	H1-hESC	embryonic stem cell:	n/a	n/a
50	RAD21	chr10:99239058-99239364	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99240234-99240284	AG10803	skin:	n/a
2	chr10:99240234-99240284	HRPEpiC	eye:	n/a
3	chr10:99240234-99240284	NHBE	bronchial:	n/a
4	chr10:99240234-99240284	NB4	blood:	n/a
5	chr10:99240234-99240284	HCF	heart:	n/a
6	chr10:99240234-99240284	HL-60	blood:	n/a
7	chr10:99240234-99240284	NHDF-neo	bronchial:	n/a
8	chr10:99240234-99240284	HEEpiC	esophagus:	n/a
9	chr10:99240234-99240284	BE2_C	brain:	n/a
10	chr10:99240234-99240284	GM19239	blood:	n/a
11	chr10:99240234-99240284	U87	brain:	n/a
12	chr10:99240234-99240284	BJ	skin:	n/a
13	chr10:99240234-99240284	HNPCEpiC	eye:	n/a
14	chr10:99240234-99240284	HPAEpiC	pulmonary alveolar:	n/a
15	chr10:99240234-99240284	T-47D	breast:	n/a
16	chr10:99240234-99240284	GM12878	blood:	n/a
17	chr10:99240234-99240284	HCM	heart:	n/a
18	chr10:99240234-99240284	GM06990	blood:	n/a
19	chr10:99240234-99240284	SK-N-MC	brain:	n/a
20	chr10:99240234-99240284	Caco-2	colon:	n/a
21	chr10:99240234-99240284	ECC-1	luminal epithelium:	n/a
22	chr10:99240234-99240284	AoSMC	blood vessel:	n/a
23	chr10:99240234-99240284	PANC-1	pancreas:	n/a
24	chr10:99240234-99240284	PFSK-1	brain:	n/a
25	chr10:99240234-99240284	MCF-7	breast:	n/a
26	chr10:99240234-99240284	HEK293	kidney:	embryo
27	chr10:99240234-99240284	ProgFib	skin:	n/a
28	chr10:99240234-99240284	SK-N-SH_RA	brain:	n/a
29	chr10:99240234-99240284	CMK	blood:	n/a
30	chr10:99240234-99240284	AG09309	skin:	n/a
31	chr10:99240234-99240284	HCT-116	colon:	n/a
32	chr10:99240234-99240284	AG04450	lung:	fetal
33	chr10:99240234-99240284	GM12892	blood:	n/a
34	chr10:99240234-99240284	Hela-S3	cervix:	n/a
35	chr10:99240234-99240284	SK-N-SH	brain:	n/a
36	chr10:99240234-99240284	GM12891	blood:	n/a
37	chr10:99240234-99240284	HRE	kidney:	n/a
38	chr10:99240234-99240284	PrEC	prostate:	n/a
39	chr10:99240234-99240284	HAEpiC	amniotic membrane:	n/a
40	chr10:99240234-99240284	HRCEpiC	kidney:	n/a
41	chr10:99240234-99240284	HIPEpiC	eye:	n/a
42	chr10:99240234-99240284	HepG2	liver:	n/a
43	chr10:99240234-99240284	H1-hESC	embryonic stem cell:	embryo
44	chr10:99240234-99240284	RPTEC	kidney:	n/a
45	chr10:99240234-99240284	AG09319	gingival:	n/a
46	chr10:99240234-99240284	AG04449	skin:	fetal
47	chr10:99240234-99240284	A549	lung:	n/a
48	chr10:99240234-99240284	SAEC	small airway:	n/a
49	chr10:99240234-99240284	ovcar-3	ovarian:	n/a
50	chr10:99240234-99240284	NT2-D1	testis:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:99235824..99238488-chr10:99250423..99252230,2	MCF-7	breast:
2	chr10:99236922..99238932-chr10:99241740..99243324,2	K562	blood:
3	chr10:99224078..99227999-chr10:99236379..99238987,3	K562	blood:
4	chr10:99212693..99215031-chr10:99236502..99238177,2	MCF-7	breast:
5	chr10:99238086..99241009-chr10:99257354..99259371,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000264677	TF binding region
ENSG00000264677	CpG island
ENSG00000165886	chromatin interactions
ENSG00000171307	chromatin interactions
ENSG00000264677	chromatin interactions
ENSG00000155229	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184467216	chr10:99238070-99238071	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs572827758	chr10:99238091-99238092	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs566453457	chr10:99238116-99238117	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs29001280	chr10:99238117-99238118	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs372934465	chr10:99238125-99238126	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs375836742	chr10:99238179-99238180	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs371742625	chr10:99238186-99238187	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs558315796	chr10:99238197-99238198	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs570356995	chr10:99238223-99238224	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs538336117	chr10:99238322-99238323	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs142480743	chr10:99238345-99238346	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs574737093	chr10:99238354-99238355	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs188475702	chr10:99238415-99238416	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs191791505	chr10:99238496-99238497	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs564795214	chr10:99238507-99238508	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs572758382	chr10:99238548-99238549	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs576839012	chr10:99238581-99238582	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs530615442	chr10:99238597-99238598	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs546558378	chr10:99238599-99238600	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs564666522	chr10:99238682-99238683	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs531814776	chr10:99238727-99238728	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs75768137	chr10:99238740-99238741	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs144695974	chr10:99238744-99238745	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs553482223	chr10:99238746-99238747	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs559082057	chr10:99238761-99238762	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs529665566	chr10:99238765-99238766	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs547762656	chr10:99238766-99238767	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs559751984	chr10:99238767-99238768	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527572292	chr10:99238772-99238773	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs552102191	chr10:99238788-99238789	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs570581913	chr10:99238796-99238797	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs147832686	chr10:99238823-99238824	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs550217455	chr10:99238830-99238831	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs7067759	chr10:99238843-99238844	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs563537846	chr10:99238867-99238868	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs184314053	chr10:99238891-99238892	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs140311427	chr10:99238895-99238896	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs189263457	chr10:99238939-99238940	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs540090280	chr10:99238946-99238947	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs558496712	chr10:99238953-99238954	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs576544635	chr10:99238959-99238960	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs117058638	chr10:99238960-99238961	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562335976	chr10:99238966-99238967	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs138090682	chr10:99239002-99239003	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs182210804	chr10:99239018-99239019	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs538750018	chr10:99239104-99239105	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs527294976	chr10:99239108-99239109	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs552015037	chr10:99239126-99239127	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs564241212	chr10:99239132-99239133	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs549226390	chr10:99239172-99239173	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99210000-99243800	Strong transcription	Primary T cells from cord blood	blood
2	chr10:99210000-99243800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:99210000-99244000	Strong transcription	Fetal Stomach	stomach
4	chr10:99210000-99244200	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr10:99210200-99243800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:99210400-99243600	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr10:99210400-99244800	Strong transcription	Fetal Thymus	thymus
8	chr10:99210600-99238800	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr10:99210600-99239000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:99210600-99241800	Strong transcription	Thymus	Thymus
11	chr10:99210600-99243800	Strong transcription	Duodenum Mucosa	Duodenum
12	chr10:99210600-99244200	Strong transcription	Placenta	Placenta
13	chr10:99210800-99239000	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr10:99210800-99243800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr10:99210800-99244000	Strong transcription	Sigmoid Colon	Sigmoid Colon
16	chr10:99210800-99246000	Strong transcription	Primary B cells from peripheral blood	blood
17	chr10:99211000-99238800	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr10:99211000-99243800	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr10:99211000-99246400	Strong transcription	Dnd41	blood
20	chr10:99211200-99244800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr10:99211200-99246200	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr10:99211200-99246600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:99211400-99239000	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr10:99211400-99241600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr10:99211600-99239000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr10:99211800-99241200	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr10:99214400-99242000	Strong transcription	Fetal Muscle Trunk	muscle
28	chr10:99214400-99246400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr10:99214600-99242800	Strong transcription	Fetal Muscle Leg	muscle
30	chr10:99214600-99243800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr10:99214600-99243800	Strong transcription	Stomach Smooth Muscle	stomach
32	chr10:99214800-99243800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr10:99215200-99242400	Strong transcription	Left Ventricle	heart
34	chr10:99215200-99243800	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr10:99215400-99243800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr10:99215400-99254600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr10:99216800-99243800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr10:99217800-99242000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
39	chr10:99218200-99244000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr10:99224200-99245000	Strong transcription	Fetal Intestine Small	intestine
41	chr10:99224400-99244800	Strong transcription	Fetal Intestine Large	intestine
42	chr10:99225000-99240400	Strong transcription	A549	lung
43	chr10:99225400-99242000	Strong transcription	Brain Substantia Nigra	brain
44	chr10:99225600-99238800	Strong transcription	HepG2	liver
45	chr10:99227600-99246600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr10:99228200-99240400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr10:99229200-99238800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr10:99229600-99242200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr10:99229800-99238800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr10:99230800-99250400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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