Variant report

Variant	nsv911675
Chromosome Location	chr19:39394271-39398631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:244)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr19:39395211-39395534	A549	lung:	n/a	n/a
2	CEBPB	chr19:39395220-39395519	HepG2	liver:	n/a	n/a
3	FOXA2	chr19:39395276-39395853	A549	lung:	n/a	n/a
4	FOXA2	chr19:39395194-39395795	A549	lung:	n/a	n/a
5	FOXA2	chr19:39395337-39395709	HepG2	liver:	n/a	n/a
6	HDAC2	chr19:39395405-39395635	HepG2	liver:	n/a	n/a
7	HMGN3	chr19:39398139-39398198	K562	blood:	n/a	n/a
8	HNF4G	chr19:39395416-39395770	HepG2	liver:	n/a	chr19:39395619-39395632 chr19:39395509-39395522 chr19:39395614-39395636 chr19:39395510-39395522 chr19:39395619-39395632 chr19:39395507-39395525 chr19:39395510-39395523 chr19:39395619-39395631 chr19:39395618-39395632 chr19:39395510-39395523 chr19:39395617-39395632 chr19:39395509-39395523 chr19:39395617-39395632 chr19:39395618-39395632 chr19:39395619-39395632 chr19:39395510-39395522 chr19:39395619-39395631 chr19:39395625-39395639 chr19:39395617-39395632 chr19:39395618-39395632 chr19:39395619-39395631 chr19:39395618-39395633 chr19:39395510-39395522 chr19:39395616-39395634 chr19:39395510-39395523 chr19:39395618-39395631 chr19:39395510-39395522 chr19:39395619-39395631
9	MAFF	chr19:39395458-39395658	HepG2	liver:	n/a	chr19:39395489-39395507
10	MAFK	chr19:39395510-39395594	HepG2	liver:	n/a	n/a
11	NR2F2	chr19:39395245-39395984	MCF-7	breast:	n/a	n/a
12	POLR2A	chr19:39398066-39398222	A549	lung:	n/a	n/a
13	POLR2A	chr19:39398602-39398926	K562	blood:	n/a	n/a
14	POLR2A	chr19:39398051-39398219	A549	lung:	n/a	n/a
15	POLR2A	chr19:39398361-39398578	HepG2	liver:	n/a	n/a
16	POLR2A	chr19:39397287-39398991	PANC-1	pancreas:	n/a	n/a
17	POLR2A	chr19:39396209-39396219	A549	lung:	n/a	n/a
18	POLR2A	chr19:39398093-39398370	K562	blood:	n/a	n/a
19	POLR2A	chr19:39395931-39395956	MCF-7	breast:	n/a	n/a
20	POLR2A	chr19:39396372-39396721	GM12891	blood:	n/a	n/a
21	POLR2A	chr19:39397829-39397862	HepG2	liver:	n/a	n/a
22	POLR2A	chr19:39396016-39396027	MCF-7	breast:	n/a	n/a
23	POLR2A	chr19:39398273-39398850	GM12891	blood:	n/a	n/a
24	POLR2A	chr19:39396556-39396622	A549	lung:	n/a	n/a
25	POLR2A	chr19:39397743-39397917	GM12878	blood:	n/a	n/a
26	POLR2A	chr19:39397686-39397741	A549	lung:	n/a	n/a
27	POLR2A	chr19:39398524-39398828	K562	blood:	n/a	n/a
28	POLR2A	chr19:39395871-39395928	MCF-7	breast:	n/a	n/a
29	POLR2A	chr19:39398297-39398954	GM12878	blood:	n/a	n/a
30	POLR2A	chr19:39397651-39398078	GM12878	blood:	n/a	n/a
31	SETDB1	chr19:39398367-39398599	U2OS	brain:	n/a	n/a
32	ZNF274	chr19:39398051-39398821	K562	blood:	n/a	n/a
33	ZNF274	chr19:39398226-39398815	GM08714	blood:	n/a	n/a
34	ZNF274	chr19:39398380-39398837	NT2-D1	testis:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39395882-39395932	GM12878	blood:	n/a
2	chr19:39395882-39395932	AG09319	gingival:	n/a
3	chr19:39395882-39395932	SK-N-MC	brain:	n/a
4	chr19:39397911-39397961	SK-N-SH	brain:	n/a
5	chr19:39395717-39395767	AG09319	gingival:	n/a
6	chr19:39398122-39398172	PFSK-1	brain:	n/a
7	chr19:39397911-39397961	NHDF-neo	bronchial:	n/a
8	chr19:39395882-39395932	NB4	blood:	n/a
9	chr19:39398122-39398172	NH-A	brain:	n/a
10	chr19:39395717-39395767	HRE	kidney:	n/a
11	chr19:39397911-39397961	MCF10A-Er-Src	breast:	n/a
12	chr19:39395717-39395767	SAEC	small airway:	n/a
13	chr19:39398122-39398172	HMEC	breast:	n/a
14	chr19:39395717-39395767	ProgFib	skin:	n/a
15	chr19:39398122-39398172	HEK293	kidney:	embryo
16	chr19:39395717-39395767	BJ	skin:	n/a
17	chr19:39395717-39395767	HAEpiC	amniotic membrane:	n/a
18	chr19:39395882-39395932	GM19239	blood:	n/a
19	chr19:39395717-39395767	Hela-S3	cervix:	n/a
20	chr19:39395717-39395767	AG04450	lung:	fetal
21	chr19:39398122-39398172	RPTEC	kidney:	n/a
22	chr19:39395882-39395932	NHBE	bronchial:	n/a
23	chr19:39395882-39395932	SK-N-SH	brain:	n/a
24	chr19:39395882-39395932	SAEC	small airway:	n/a
25	chr19:39395882-39395932	T-47D	breast:	n/a
26	chr19:39397911-39397961	A549	lung:	n/a
27	chr19:39395882-39395932	NHDF-neo	bronchial:	n/a
28	chr19:39397911-39397961	Hepatocyte	liver:	n/a
29	chr19:39398122-39398172	NT2-D1	testis:	n/a
30	chr19:39395717-39395767	GM12878	blood:	n/a
31	chr19:39397911-39397961	HUVEC	blood vessel:	n/a
32	chr19:39395717-39395767	HPAEpiC	pulmonary alveolar:	n/a
33	chr19:39398122-39398172	HL-60	blood:	n/a
34	chr19:39395717-39395767	HEEpiC	esophagus:	n/a
35	chr19:39395717-39395767	PrEC	prostate:	n/a
36	chr19:39395882-39395932	MCF-7	breast:	n/a
37	chr19:39395882-39395932	H1-hESC	embryonic stem cell:	embryo
38	chr19:39395717-39395767	ovcar-3	ovarian:	n/a
39	chr19:39398122-39398172	NB4	blood:	n/a
40	chr19:39398122-39398172	PANC-1	pancreas:	n/a
41	chr19:39395882-39395932	AG09309	skin:	n/a
42	chr19:39397911-39397961	SKMC	muscle:	n/a
43	chr19:39395882-39395932	A549	lung:	n/a
44	chr19:39395882-39395932	PFSK-1	brain:	n/a
45	chr19:39398122-39398172	HepG2	liver:	n/a
46	chr19:39397911-39397961	BJ	skin:	n/a
47	chr19:39398122-39398172	U87	brain:	n/a
48	chr19:39397911-39397961	HEEpiC	esophagus:	n/a
49	chr19:39395882-39395932	Jurkat	blood:	n/a
50	chr19:39397911-39397961	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:39217426..39220275-chr19:39394811..39396577,2	K562	blood:
2	chr19:39394465..39398073-chr19:39398218..39402853,5	MCF-7	breast:
3	chr19:39394310..39397205-chr19:39405071..39408067,2	K562	blood:
4	chr19:39394709..39398675-chr19:39410709..39413256,3	K562	blood:
5	chr19:39398169..39400794-chr19:39403289..39404909,2	MCF-7	breast:
6	chr19:39337724..39340689-chr19:39393839..39396661,3	K562	blood:
7	chr19:39391259..39393276-chr19:39393440..39395044,2	MCF-7	breast:
8	chr19:39395944..39398654-chr19:39409098..39410676,3	K562	blood:
9	chr19:39337064..39339680-chr19:39397865..39400024,2	K562	blood:
10	chr19:39395804..39397367-chr19:39401550..39403461,2	MCF-7	breast:
11	chr19:39339924..39344199-chr19:39398243..39400684,3	MCF-7	breast:
12	chr19:39390244..39393015-chr19:39395233..39398542,3	MCF-7	breast:
13	chr19:39388731..39393423-chr19:39394024..39400037,10	K562	blood:

No data

Variant related genes	Relation type
SIRT2	TF binding region
SIRT2	CpG island
ENSG00000104835	chromatin interactions
ENSG00000068903	chromatin interactions
ENSG00000104824	chromatin interactions
ENSG00000262484	chromatin interactions
ENSG00000130402	chromatin interactions
ENSG00000104825	chromatin interactions

Extended variants
information (count: 259 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12610409	chr19:39394271-39394272	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537681320	chr19:39394387-39394388	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs201606607	chr19:39394433-39394434	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs182448351	chr19:39394440-39394441	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs17886254	chr19:39394481-39394482	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs538300200	chr19:39394528-39394529	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs551129642	chr19:39394594-39394595	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs187771978	chr19:39394597-39394598	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs571308291	chr19:39394603-39394604	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs571749718	chr19:39394624-39394625	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs8104984	chr19:39394640-39394641	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs533001010	chr19:39394652-39394653	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs370722187	chr19:39394674-39394675	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs140531875	chr19:39394725-39394726	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs201933689	chr19:39394735-39394736	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs200023511	chr19:39394736-39394737	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs58249749	chr19:39394746-39394747	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs563037687	chr19:39394767-39394768	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs376505529	chr19:39394775-39394776	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs373967675	chr19:39394776-39394777	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs566891232	chr19:39394780-39394781	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs539869771	chr19:39394795-39394796	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs565449793	chr19:39394844-39394845	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs150397032	chr19:39394887-39394888	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs8108039	chr19:39394915-39394916	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs559875158	chr19:39394917-39394918	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs530147125	chr19:39394919-39394920	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs548549404	chr19:39394923-39394924	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs191551379	chr19:39394928-39394929	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs55984328	chr19:39394958-39394959	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs12610805	chr19:39394962-39394963	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs17884772	chr19:39394989-39394990	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs17880968	chr19:39395056-39395057	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs17880526	chr19:39395072-39395073	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs538438950	chr19:39395091-39395092	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs17881574	chr19:39395097-39395098	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs199968993	chr19:39395116-39395117	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs142380386	chr19:39395117-39395118	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs35131017	chr19:39395119-39395120	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs17880452	chr19:39395120-39395121	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs77974825	chr19:39395121-39395122	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs571784584	chr19:39395145-39395146	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs117682758	chr19:39395156-39395157	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs567163016	chr19:39395209-39395210	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs554515514	chr19:39395210-39395211	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs17878402	chr19:39395226-39395227	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs544044006	chr19:39395236-39395237	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs17878267	chr19:39395296-39395297	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs11879872	chr19:39395331-39395332	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs373869376	chr19:39395339-39395340	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Lung cancer	18438408	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
Breast cancer	21509527	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39391000-39394800	Weak transcription	Spleen	Spleen
2	chr19:39391000-39395000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr19:39391000-39395800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:39391200-39394800	Weak transcription	Gastric	stomach
5	chr19:39391200-39395000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr19:39391200-39395200	Weak transcription	Pancreas	Pancrea
7	chr19:39391200-39395400	Weak transcription	Aorta	Aorta
8	chr19:39391200-39395400	Weak transcription	Esophagus	oesophagus
9	chr19:39391200-39395600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr19:39391200-39420800	Weak transcription	Small Intestine	intestine
11	chr19:39391400-39395200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr19:39391400-39395600	Weak transcription	Brain Germinal Matrix	brain
13	chr19:39391400-39397400	Weak transcription	Fetal Brain Female	brain
14	chr19:39391400-39397600	Weak transcription	Psoas Muscle	Psoas
15	chr19:39391400-39402200	Weak transcription	Fetal Brain Male	brain
16	chr19:39391600-39394800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr19:39391600-39395000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr19:39391600-39395000	Weak transcription	NHDF-Ad	bronchial
19	chr19:39391600-39395200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr19:39391600-39395200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr19:39391600-39395200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:39391600-39395200	Weak transcription	Colonic Mucosa	Colon
23	chr19:39391600-39395200	Weak transcription	Ovary	ovary
24	chr19:39391600-39395200	Weak transcription	Right Ventricle	heart
25	chr19:39391600-39397800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr19:39391600-39414800	Weak transcription	HMEC	breast
27	chr19:39391600-39420600	Weak transcription	Right Atrium	heart
28	chr19:39391800-39394800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr19:39391800-39395000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr19:39391800-39395000	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr19:39391800-39395000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr19:39391800-39395000	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr19:39391800-39395000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr19:39391800-39395000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr19:39391800-39395000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr19:39391800-39395000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr19:39391800-39395000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr19:39391800-39395000	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr19:39391800-39395200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr19:39391800-39395200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr19:39391800-39395200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr19:39391800-39395200	Weak transcription	Brain Substantia Nigra	brain
43	chr19:39391800-39395200	Weak transcription	Colon Smooth Muscle	Colon
44	chr19:39391800-39395200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr19:39391800-39395200	Weak transcription	Thymus	Thymus
46	chr19:39391800-39395400	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr19:39391800-39395400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr19:39391800-39395400	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr19:39391800-39395600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr19:39391800-39395600	Weak transcription	NHLF	lung

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