Variant report

Variant	nsv911729
Chromosome Location	chr19:41321372-41383828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1358)
CpG islands
(count:428)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41329750-41329937	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41328860-41329133	K562	blood:	n/a	n/a
3	ARID3A	chr19:41378197-41378436	K562	blood:	n/a	n/a
4	ARID3A	chr19:41332662-41332725	K562	blood:	n/a	n/a
5	ARID3A	chr19:41325732-41325933	K562	blood:	n/a	n/a
6	ARID3A	chr19:41337675-41338160	HepG2	liver:	n/a	n/a
7	ARID3A	chr19:41329339-41329381	HepG2	liver:	n/a	n/a
8	ARID3A	chr19:41370633-41370945	K562	blood:	n/a	n/a
9	ATF1	chr19:41328759-41329240	K562	blood:	n/a	n/a
10	ATF1	chr19:41378237-41378485	K562	blood:	n/a	n/a
11	ATF1	chr19:41331479-41331663	K562	blood:	n/a	n/a
12	ATF1	chr19:41370536-41370948	K562	blood:	n/a	n/a
13	ATF1	chr19:41339642-41339915	K562	blood:	n/a	n/a
14	ATF2	chr19:41328765-41329159	GM12878	blood:	n/a	n/a
15	ATF3	chr19:41370620-41370877	K562	blood:	n/a	n/a
16	ATF3	chr19:41378141-41378430	K562	blood:	n/a	n/a
17	ATF3	chr19:41328783-41329158	K562	blood:	n/a	n/a
18	ATF3	chr19:41339727-41339986	K562	blood:	n/a	n/a
19	ATF3	chr19:41337642-41338304	A549	lung:	n/a	n/a
20	ATF3	chr19:41339265-41339474	K562	blood:	n/a	n/a
21	BATF	chr19:41328872-41329097	GM12878	blood:	n/a	n/a
22	BATF	chr19:41328854-41329148	GM12878	blood:	n/a	n/a
23	BCL3	chr19:41337399-41338400	A549	lung:	n/a	n/a
24	BCL3	chr19:41324316-41325122	A549	lung:	n/a	n/a
25	BCL3	chr19:41325415-41325988	A549	lung:	n/a	n/a
26	BCL3	chr19:41337271-41338291	A549	lung:	n/a	n/a
27	BHLHE40	chr19:41337595-41338254	HepG2	liver:	n/a	chr19:41337896-41337917
28	BHLHE40	chr19:41328602-41329132	K562	blood:	n/a	n/a
29	BHLHE40	chr19:41328117-41328352	K562	blood:	n/a	n/a
30	BHLHE40	chr19:41332617-41332833	K562	blood:	n/a	n/a
31	BHLHE40	chr19:41339267-41339464	K562	blood:	n/a	n/a
32	BHLHE40	chr19:41337704-41338087	A549	lung:	n/a	chr19:41337896-41337917
33	BHLHE40	chr19:41337782-41338177	HepG2	liver:	n/a	chr19:41337896-41337917
34	BHLHE40	chr19:41337685-41338115	K562	blood:	n/a	chr19:41337896-41337917
35	BHLHE40	chr19:41325720-41325781	GM12878	blood:	n/a	n/a
36	BHLHE40	chr19:41337763-41338048	HepG2	liver:	n/a	chr19:41337896-41337917
37	BHLHE40	chr19:41339813-41339844	K562	blood:	n/a	n/a
38	BRCA1	chr19:41337806-41338121	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr19:41329863-41330001	HepG2	liver:	n/a	n/a
40	BRCA1	chr19:41325734-41325927	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr19:41347938-41348304	K562	blood:	n/a	n/a
42	CBX3	chr19:41337733-41338384	K562	blood:	n/a	n/a
43	CBX3	chr19:41333737-41334193	K562	blood:	n/a	n/a
44	CBX3	chr19:41333751-41334179	K562	blood:	n/a	n/a
45	CBX3	chr19:41349182-41350047	K562	blood:	n/a	n/a
46	CBX3	chr19:41347915-41348277	K562	blood:	n/a	n/a
47	CBX3	chr19:41381255-41381833	K562	blood:	n/a	n/a
48	CBX3	chr19:41379769-41380227	K562	blood:	n/a	n/a
49	CBX3	chr19:41370123-41371107	K562	blood:	n/a	n/a
50	CBX3	chr19:41379821-41380148	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41354682-41354732	HEEpiC	esophagus:	n/a
2	chr19:41354682-41354732	HEEpiC	esophagus:	n/a
3	chr19:41321438-41321488	SK-N-MC	brain:	n/a
4	chr19:41354142-41354192	HMEC	breast:	n/a
5	chr19:41354142-41354192	H1-hESC	embryonic stem cell:	embryo
6	chr19:41354142-41354192	GM12892	blood:	n/a
7	chr19:41321438-41321488	LNCaP	prostate:	n/a
8	chr19:41351924-41351974	HNPCEpiC	eye:	n/a
9	chr19:41355973-41356023	NHBE	bronchial:	n/a
10	chr19:41351924-41351974	BE2_C	brain:	n/a
11	chr19:41351924-41351974	PFSK-1	brain:	n/a
12	chr19:41354682-41354732	ovcar-3	ovarian:	n/a
13	chr19:41351924-41351974	AoSMC	blood vessel:	n/a
14	chr19:41383654-41383704	U87	brain:	n/a
15	chr19:41351924-41351974	BJ	skin:	n/a
16	chr19:41354553-41354603	MCF10A-Er-Src	breast:	n/a
17	chr19:41383654-41383704	GM12892	blood:	n/a
18	chr19:41354553-41354603	HEK293	kidney:	embryo
19	chr19:41355973-41356023	MCF-7	breast:	n/a
20	chr19:41383654-41383704	ovcar-3	ovarian:	n/a
21	chr19:41321438-41321488	SAEC	small airway:	n/a
22	chr19:41354142-41354192	AG04449	skin:	fetal
23	chr19:41354142-41354192	NHBE	bronchial:	n/a
24	chr19:41383654-41383704	HCT-116	colon:	n/a
25	chr19:41383654-41383704	K562	blood:	n/a
26	chr19:41354142-41354192	AG04450	lung:	fetal
27	chr19:41383654-41383704	Hepatocyte	liver:	n/a
28	chr19:41351924-41351974	A549	lung:	n/a
29	chr19:41354142-41354192	HCPEpiC	choroid plexus:	n/a
30	chr19:41355973-41356023	SK-N-SH	brain:	n/a
31	chr19:41354682-41354732	NT2-D1	testis:	n/a
32	chr19:41383654-41383704	PANC-1	pancreas:	n/a
33	chr19:41355973-41356023	HL-60	blood:	n/a
34	chr19:41383654-41383704	NHBE	bronchial:	n/a
35	chr19:41354553-41354603	AG09309	skin:	n/a
36	chr19:41354553-41354603	ECC-1	luminal epithelium:	n/a
37	chr19:41354553-41354603	HepG2	liver:	n/a
38	chr19:41321438-41321488	NH-A	brain:	n/a
39	chr19:41321438-41321488	HRPEpiC	eye:	n/a
40	chr19:41355973-41356023	AG04450	lung:	fetal
41	chr19:41354553-41354603	AG04450	lung:	fetal
42	chr19:41354142-41354192	HCT-116	colon:	n/a
43	chr19:41355973-41356023	HCT-116	colon:	n/a
44	chr19:41355973-41356023	LNCaP	prostate:	n/a
45	chr19:41354553-41354603	GM12878	blood:	n/a
46	chr19:41354682-41354732	HL-60	blood:	n/a
47	chr19:41354142-41354192	GM12891	blood:	n/a
48	chr19:41354682-41354732	GM12892	blood:	n/a
49	chr19:41351924-41351974	PrEC	prostate:	n/a
50	chr19:41351924-41351974	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
2	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
3	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
4	chr19:41323756..41325875-chr19:41632979..41635488,2	MCF-7	breast:
5	chr16:4474827..4477394-chr19:41351022..41353007,2	MCF-7	breast:
6	chr19:41256025..41258219-chr19:41326526..41328364,2	K562	blood:
7	chr19:41252878..41254657-chr19:41324128..41326565,2	K562	blood:
8	chr19:41305847..41307435-chr19:41322147..41325035,2	K562	blood:
9	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
10	chr19:41167522..41169643-chr19:41327340..41330313,2	K562	blood:
11	chr19:41195484..41197379-chr19:41368669..41371255,2	K562	blood:
12	chr19:41308981..41310761-chr19:41328950..41331084,2	K562	blood:
13	chr19:41309668..41312632-chr19:41335922..41337729,2	MCF-7	breast:
14	chr19:41168873..41171001-chr19:41337568..41339858,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2A6-1	chr19:41337126-41337482	ENSG00000269843.1
2	lnc-CYP2A6-1	chr19:41342991-41343115	ENSG00000269843.1

No data

Variant related genes	Relation type
ENSG00000269843	TF binding region
CYP2T2P	TF binding region
CYP2F2P	TF binding region
CYP2A6	TF binding region
CYP2A7	TF binding region
ENSG00000269843	CpG island
CYP2T2P	CpG island
CYP2F2P	CpG island
CYP2A6	CpG island
CYP2A7	CpG island
ENSG00000105245	chromatin interactions
ENSG00000262246	chromatin interactions
ENSG00000188493	chromatin interactions
ENSG00000077312	chromatin interactions
ENSG00000103423	chromatin interactions
ENSG00000269858	chromatin interactions
ENSG00000268797	chromatin interactions

Extended variants
information (count: 3059 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3059 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4803372	chr19:41321372-41321373	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554890700	chr19:41321383-41321384	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs373885696	chr19:41321420-41321421	Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs115963203	chr19:41321502-41321503	Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs113717492	chr19:41321524-41321525	Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs188717786	chr19:41321535-41321536	Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs537242506	chr19:41321536-41321537	Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs181148006	chr19:41321559-41321560	Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs578041040	chr19:41321663-41321664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372968738	chr19:41321699-41321700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186073901	chr19:41321748-41321749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189337268	chr19:41321753-41321754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182177628	chr19:41321759-41321760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35718949	chr19:41321765-41321766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542947990	chr19:41321769-41321770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2545766	chr19:41321806-41321807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531832337	chr19:41321808-41321809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2644888	chr19:41321823-41321824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs187212196	chr19:41321825-41321826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371786573	chr19:41321870-41321871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190639872	chr19:41321875-41321876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140878064	chr19:41321954-41321955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569604368	chr19:41321958-41321959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11304786	chr19:41321973-41321974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78287804	chr19:41321975-41321976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144917441	chr19:41321999-41322000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529707062	chr19:41322008-41322009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548552805	chr19:41322084-41322085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7258880	chr19:41322099-41322100	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs56041558	chr19:41322112-41322113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs537301332	chr19:41322134-41322135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7259121	chr19:41322135-41322136	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570599675	chr19:41322174-41322175	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs183196283	chr19:41322223-41322224	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554223154	chr19:41322237-41322238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs572388481	chr19:41322326-41322327	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs542608818	chr19:41322344-41322345	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs186051399	chr19:41322379-41322380	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs576335326	chr19:41322384-41322385	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs146719640	chr19:41322415-41322416	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs371327317	chr19:41322484-41322485	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs71334940	chr19:41322492-41322493	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs565357676	chr19:41322505-41322506	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577354378	chr19:41322510-41322511	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542721836	chr19:41322516-41322517	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559397980	chr19:41322571-41322572	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375959672	chr19:41322572-41322573	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs8113056	chr19:41322583-41322584	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs563241849	chr19:41322655-41322656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530848951	chr19:41322758-41322759	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
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
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	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
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1261 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41315000-41324400	Weak transcription	HepG2	liver
2	chr19:41315000-41332600	Weak transcription	Aorta	Aorta
3	chr19:41316200-41324400	Weak transcription	Gastric	stomach
4	chr19:41316400-41325400	Weak transcription	Dnd41	blood
5	chr19:41317600-41324000	Weak transcription	Hela-S3	cervix
6	chr19:41317600-41324400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr19:41317800-41324200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr19:41317800-41324400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr19:41317800-41324400	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr19:41318000-41324400	Weak transcription	Pancreas	Pancrea
11	chr19:41318000-41324400	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr19:41318000-41324400	Weak transcription	Right Atrium	heart
13	chr19:41318200-41323600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr19:41318200-41323800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr19:41318200-41324400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr19:41318400-41322800	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr19:41318400-41323200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr19:41318400-41323800	Weak transcription	Primary B cells from cord blood	blood
19	chr19:41318400-41323800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr19:41318400-41323800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr19:41318600-41323000	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr19:41318600-41323800	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr19:41318800-41322600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr19:41318800-41323800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr19:41318800-41324200	Weak transcription	Fetal Intestine Large	intestine
26	chr19:41318800-41324400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr19:41319000-41323800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr19:41319000-41324400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr19:41319200-41323800	Weak transcription	Fetal Intestine Small	intestine
30	chr19:41319200-41324000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr19:41319200-41324000	Weak transcription	Lung	lung
32	chr19:41319200-41324200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr19:41319200-41324200	Weak transcription	Adipose Nuclei	Adipose
34	chr19:41319200-41324200	Weak transcription	Brain Anterior Caudate	brain
35	chr19:41319200-41324400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr19:41319200-41324400	Weak transcription	Duodenum Mucosa	Duodenum
37	chr19:41319200-41324400	Weak transcription	NHLF	lung
38	chr19:41319400-41321400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr19:41319400-41324200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:41319400-41324200	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr19:41319400-41324200	Weak transcription	Stomach Smooth Muscle	stomach
42	chr19:41319400-41324400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:41319400-41324400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr19:41319400-41324400	Weak transcription	Colonic Mucosa	Colon
45	chr19:41319400-41324400	Weak transcription	Spleen	Spleen
46	chr19:41319800-41323800	Weak transcription	Brain Cingulate Gyrus	brain
47	chr19:41319800-41323800	Weak transcription	Colon Smooth Muscle	Colon
48	chr19:41319800-41324000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr19:41319800-41324200	Weak transcription	Left Ventricle	heart
50	chr19:41319800-41324400	Weak transcription	Fetal Lung	lung

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