Variant report

Variant	nsv963047
Chromosome Location	chr19:40151942-40168890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:432)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:40166454-40167085	GM12878	blood:	n/a	n/a
2	ATF2	chr19:40166517-40167044	GM12878	blood:	n/a	n/a
3	BATF	chr19:40166440-40167020	GM12878	blood:	n/a	n/a
4	BATF	chr19:40164543-40164840	GM12878	blood:	n/a	n/a
5	BATF	chr19:40166542-40166952	GM12878	blood:	n/a	n/a
6	BCL11A	chr19:40166534-40167022	GM12878	blood:	n/a	chr19:40166845-40166854
7	BCL3	chr19:40166584-40167009	GM12878	blood:	n/a	chr19:40166845-40166854
8	BCL3	chr19:40166516-40167084	GM12878	blood:	n/a	chr19:40166845-40166854
9	BCLAF1	chr19:40166547-40167019	GM12878	blood:	n/a	chr19:40166845-40166854
10	CHD1	chr19:40162625-40162903	GM12878	blood:	n/a	n/a
11	CTCF	chr19:40162720-40162870	AG04450	lung:	n/a	n/a
12	CTCF	chr19:40162720-40162870	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr19:40162205-40163888	A549	lung:	n/a	n/a
14	CTCF	chr19:40162720-40162870	HEK293	kidney:	n/a	n/a
15	CTCF	chr19:40162740-40162890	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr19:40162820-40162970	HAc	cerebellar:	n/a	n/a
17	CTCF	chr19:40164585-40164769	MCF-7	breast:	n/a	n/a
18	CTCF	chr19:40162740-40162890	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr19:40162740-40162890	HMEC	breast:	n/a	n/a
20	CTCF	chr19:40162740-40162890	NHEK	skin:	n/a	n/a
21	CTCF	chr19:40162740-40162890	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr19:40163340-40163490	GM12864	blood:	n/a	n/a
23	CTCF	chr19:40162551-40163057	HepG2	liver:	n/a	n/a
24	CTCF	chr19:40163120-40163270	HVMF	connective:	n/a	n/a
25	CTCF	chr19:40163240-40163390	HEK293	kidney:	n/a	n/a
26	CTCF	chr19:40162740-40162890	A549	lung:	n/a	n/a
27	CTCF	chr19:40162605-40162896	T-47D	breast:	n/a	n/a
28	CTCF	chr19:40162760-40162910	GM12875	blood:	n/a	n/a
29	CTCF	chr19:40164420-40164570	HFF	foreskin:	n/a	n/a
30	CTCF	chr19:40163040-40163190	BJ	skin:	n/a	n/a
31	CTCF	chr19:40163276-40163330	GM19239	blood:	n/a	n/a
32	CTCF	chr19:40162700-40162850	GM12874	blood:	n/a	n/a
33	CTCF	chr19:40162760-40162910	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:40164640-40164790	GM12878	blood:	n/a	n/a
35	CTCF	chr19:40162800-40162950	HAc	cerebellar:	n/a	n/a
36	CTCF	chr19:40162760-40162910	SAEC	small airway:	n/a	n/a
37	CTCF	chr19:40162617-40163014	IMR90	lung:	n/a	n/a
38	CTCF	chr19:40164558-40164779	GM10248	blood:	n/a	n/a
39	CTCF	chr19:40162760-40162910	HPF	lung:	n/a	n/a
40	CTCF	chr19:40164641-40164761	GM19240	blood:	n/a	n/a
41	CTCF	chr19:40162685-40162963	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr19:40162506-40163073	A549	lung:	n/a	n/a
43	CTCF	chr19:40162582-40163014	A549	lung:	n/a	n/a
44	CTCF	chr19:40162723-40162904	Fibrobl	skin:	n/a	n/a
45	CTCF	chr19:40162713-40162922	K562	blood:	n/a	n/a
46	CTCF	chr19:40162722-40162925	GM10266	blood:	n/a	n/a
47	CTCF	chr19:40162720-40162870	GM12874	blood:	n/a	n/a
48	CTCF	chr19:40162780-40162930	GM12867	blood:	n/a	n/a
49	CTCF	chr19:40162700-40162850	GM12870	blood:	n/a	n/a
50	CTCF	chr19:40162678-40162956	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40168558-40168608	HepG2	liver:	n/a
2	chr19:40168558-40168608	GM12892	blood:	n/a
3	chr19:40168876-40168926	NH-A	brain:	n/a
4	chr19:40168558-40168608	NH-A	brain:	n/a
5	chr19:40168876-40168926	HUVEC	blood vessel:	n/a
6	chr19:40168876-40168926	RPTEC	kidney:	n/a
7	chr19:40168876-40168926	SAEC	small airway:	n/a
8	chr19:40168558-40168608	NT2-D1	testis:	n/a
9	chr19:40168558-40168608	GM12891	blood:	n/a
10	chr19:40168876-40168926	HRPEpiC	eye:	n/a
11	chr19:40168558-40168608	HMEC	breast:	n/a
12	chr19:40168558-40168608	HEK293	kidney:	embryo
13	chr19:40168876-40168926	Hepatocyte	liver:	n/a
14	chr19:40168876-40168926	MCF10A-Er-Src	breast:	n/a
15	chr19:40168876-40168926	AG04450	lung:	fetal
16	chr19:40168876-40168926	HCPEpiC	choroid plexus:	n/a
17	chr19:40168558-40168608	HEEpiC	esophagus:	n/a
18	chr19:40168876-40168926	PrEC	prostate:	n/a
19	chr19:40168876-40168926	NB4	blood:	n/a
20	chr19:40168558-40168608	SK-N-SH	brain:	n/a
21	chr19:40168558-40168608	HCM	heart:	n/a
22	chr19:40168558-40168608	NHBE	bronchial:	n/a
23	chr19:40168558-40168608	HRE	kidney:	n/a
24	chr19:40168558-40168608	HRCEpiC	kidney:	n/a
25	chr19:40168558-40168608	AoSMC	blood vessel:	n/a
26	chr19:40168558-40168608	SKMC	muscle:	n/a
27	chr19:40168876-40168926	A549	lung:	n/a
28	chr19:40168558-40168608	BE2_C	brain:	n/a
29	chr19:40168558-40168608	BJ	skin:	n/a
30	chr19:40168876-40168926	Caco-2	colon:	n/a
31	chr19:40168876-40168926	AG10803	skin:	n/a
32	chr19:40168558-40168608	HCPEpiC	choroid plexus:	n/a
33	chr19:40168558-40168608	NB4	blood:	n/a
34	chr19:40168558-40168608	U87	brain:	n/a
35	chr19:40168558-40168608	SK-N-MC	brain:	n/a
36	chr19:40168876-40168926	Hela-S3	cervix:	n/a
37	chr19:40168876-40168926	H1-hESC	embryonic stem cell:	embryo
38	chr19:40168558-40168608	AG09309	skin:	n/a
39	chr19:40168558-40168608	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:40168876-40168926	NHBE	bronchial:	n/a
41	chr19:40168876-40168926	U87	brain:	n/a
42	chr19:40168876-40168926	BE2_C	brain:	n/a
43	chr19:40168558-40168608	PANC-1	pancreas:	n/a
44	chr19:40168876-40168926	GM06990	blood:	n/a
45	chr19:40168876-40168926	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:40168876-40168926	HMEC	breast:	n/a
47	chr19:40168876-40168926	GM12892	blood:	n/a
48	chr19:40168876-40168926	HNPCEpiC	eye:	n/a
49	chr19:40168558-40168608	NHDF-neo	bronchial:	n/a
50	chr19:40168876-40168926	K562	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39988438..39989161-chr19:40162366..40162932,2	K562	blood:
2	chr19:39925057..39927468-chr19:40150682..40153479,2	K562	blood:
3	chr19:40163210..40165073-chr19:40333318..40334922,2	MCF-7	breast:
4	chr19:40166260..40168931-chr19:40253973..40255544,2	MCF-7	breast:
5	chr19:40041871..40042653-chr19:40162390..40162892,2	MCF-7	breast:
6	chr19:39988198..39988763-chr19:40162454..40163227,2	MCF-7	breast:
7	chr19:40164310..40165291-chr19:40476366..40477083,2	MCF-7	breast:
8	chr19:40163659..40164641-chr19:40256992..40257878,2	MCF-7	breast:
9	chr19:40164964..40166897-chr19:40168193..40170501,2	K562	blood:
10	chr19:40168776..40170659-chr19:40171070..40173926,2	MCF-7	breast:
11	chr19:40166471..40169299-chr19:40170755..40172585,2	K562	blood:
12	chr19:40041783..40042891-chr19:40162333..40163330,4	K562	blood:
13	chr19:40041798..40042719-chr19:40162291..40163385,9	MCF-7	breast:
14	chr19:40164188..40165085-chr19:40256246..40256847,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000226025	TF binding region
ENSG00000226025	CpG island
ENSG00000013275	chromatin interactions
ENSG00000105193	chromatin interactions
ENSG00000226025	chromatin interactions
ENSG00000196235	chromatin interactions

Extended variants
information (count: 322 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147507648	chr19:40151948-40151949	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs559054133	chr19:40151957-40151958	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs138508228	chr19:40151973-40151974	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs143902017	chr19:40152015-40152016	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs117626780	chr19:40152024-40152025	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs75746321	chr19:40152099-40152100	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147281483	chr19:40152113-40152114	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs8109558	chr19:40152114-40152115	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530383711	chr19:40152119-40152120	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs139673073	chr19:40152136-40152137	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs116937925	chr19:40152154-40152155	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs149776958	chr19:40152211-40152212	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570544826	chr19:40152267-40152268	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546511980	chr19:40152312-40152313	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs568224013	chr19:40152321-40152322	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs529227267	chr19:40152342-40152343	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550860249	chr19:40152345-40152346	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs570076277	chr19:40152371-40152372	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553691744	chr19:40152436-40152437	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs6508898	chr19:40152481-40152482	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs80033991	chr19:40152527-40152528	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535093912	chr19:40152528-40152529	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369791950	chr19:40152540-40152541	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs553309850	chr19:40152550-40152551	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs574939840	chr19:40152557-40152558	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542122789	chr19:40152569-40152570	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373846261	chr19:40152596-40152597	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs113951874	chr19:40152611-40152612	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs6508899	chr19:40152622-40152623	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs545440292	chr19:40152637-40152638	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs564087819	chr19:40152646-40152647	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs528208421	chr19:40152701-40152702	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540287619	chr19:40152731-40152732	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561754515	chr19:40152732-40152733	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs529050175	chr19:40152750-40152751	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550901082	chr19:40152772-40152773	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569212567	chr19:40152791-40152792	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs59933428	chr19:40152804-40152805	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs552314241	chr19:40152826-40152827	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570793614	chr19:40152857-40152858	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs368774018	chr19:40152860-40152861	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs534832243	chr19:40152904-40152905	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547027279	chr19:40152912-40152913	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs34077988	chr19:40152937-40152938	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs144575393	chr19:40152949-40152950	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs535693795	chr19:40152954-40152955	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs557130104	chr19:40152970-40152971	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188529545	chr19:40152971-40152972	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540110513	chr19:40153029-40153030	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs567217941	chr19:40153072-40153073	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40152200-40153000	Enhancers	Primary T cells from cord blood	blood
2	chr19:40161200-40162600	Enhancers	H9 Cell Line	embryonic stem cell
3	chr19:40161200-40162600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr19:40161200-40162600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr19:40161200-40162600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr19:40161200-40162800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr19:40161200-40162800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr19:40161200-40162800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr19:40161200-40162800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr19:40161400-40162600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr19:40161400-40162800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr19:40161800-40162000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr19:40162400-40162600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr19:40162400-40162600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
15	chr19:40162400-40162600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr19:40162400-40162600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr19:40162400-40162600	Enhancers	Brain Hippocampus Middle	brain
18	chr19:40162400-40162800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr19:40162400-40163200	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr19:40162400-40163200	Enhancers	GM12878-XiMat	blood
21	chr19:40162400-40164600	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr19:40162400-40164600	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr19:40162600-40162800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr19:40162600-40162800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr19:40162600-40163600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr19:40162600-40164200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr19:40162600-40164600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr19:40162600-40164600	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr19:40162600-40169600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr19:40162800-40163000	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr19:40162800-40163000	Bivalent Enhancer	A549	lung
32	chr19:40162800-40163800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr19:40162800-40164200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:40162800-40164400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr19:40162800-40164600	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr19:40162800-40166800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr19:40163000-40164200	Enhancers	Primary T cells fromperipheralblood	blood
38	chr19:40163200-40163400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr19:40163200-40164200	Weak transcription	GM12878-XiMat	blood
40	chr19:40163200-40168200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr19:40163400-40164200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:40163800-40164400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr19:40164200-40164400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr19:40164200-40164400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr19:40164200-40166200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:40164200-40168600	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr19:40164200-40168600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr19:40164200-40168600	Enhancers	GM12878-XiMat	blood
49	chr19:40164400-40166400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr19:40164400-40168600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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