Variant report

Variant	nsv1056244
Chromosome Location	chr19:41329218-41397661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:732)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr19:41370633-41370945	K562	blood:	n/a	n/a
3	ARID3A	chr19:41337675-41338160	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:41332662-41332725	K562	blood:	n/a	n/a
5	ARID3A	chr19:41329339-41329381	HepG2	liver:	n/a	n/a
6	ARID3A	chr19:41378197-41378436	K562	blood:	n/a	n/a
7	ATF1	chr19:41378237-41378485	K562	blood:	n/a	n/a
8	ATF1	chr19:41331479-41331663	K562	blood:	n/a	n/a
9	ATF1	chr19:41328759-41329240	K562	blood:	n/a	n/a
10	ATF1	chr19:41370536-41370948	K562	blood:	n/a	n/a
11	ATF1	chr19:41339642-41339915	K562	blood:	n/a	n/a
12	ATF3	chr19:41337642-41338304	A549	lung:	n/a	n/a
13	ATF3	chr19:41339265-41339474	K562	blood:	n/a	n/a
14	ATF3	chr19:41339727-41339986	K562	blood:	n/a	n/a
15	ATF3	chr19:41378141-41378430	K562	blood:	n/a	n/a
16	ATF3	chr19:41370620-41370877	K562	blood:	n/a	n/a
17	BCL3	chr19:41337271-41338291	A549	lung:	n/a	n/a
18	BCL3	chr19:41337399-41338400	A549	lung:	n/a	n/a
19	BHLHE40	chr19:41339813-41339844	K562	blood:	n/a	n/a
20	BHLHE40	chr19:41337782-41338177	HepG2	liver:	n/a	chr19:41337896-41337917
21	BHLHE40	chr19:41337763-41338048	HepG2	liver:	n/a	chr19:41337896-41337917
22	BHLHE40	chr19:41337595-41338254	HepG2	liver:	n/a	chr19:41337896-41337917
23	BHLHE40	chr19:41339267-41339464	K562	blood:	n/a	n/a
24	BHLHE40	chr19:41337704-41338087	A549	lung:	n/a	chr19:41337896-41337917
25	BHLHE40	chr19:41337685-41338115	K562	blood:	n/a	chr19:41337896-41337917
26	BHLHE40	chr19:41332617-41332833	K562	blood:	n/a	n/a
27	BRCA1	chr19:41329863-41330001	HepG2	liver:	n/a	n/a
28	BRCA1	chr19:41337806-41338121	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr19:41328493-41329264	K562	blood:	n/a	n/a
30	CBX3	chr19:41332491-41333023	K562	blood:	n/a	n/a
31	CBX3	chr19:41381255-41381833	K562	blood:	n/a	n/a
32	CBX3	chr19:41339143-41339980	K562	blood:	n/a	n/a
33	CBX3	chr19:41347915-41348277	K562	blood:	n/a	n/a
34	CBX3	chr19:41379821-41380148	K562	blood:	n/a	n/a
35	CBX3	chr19:41333737-41334193	K562	blood:	n/a	n/a
36	CBX3	chr19:41347938-41348304	K562	blood:	n/a	n/a
37	CBX3	chr19:41333751-41334179	K562	blood:	n/a	n/a
38	CBX3	chr19:41379769-41380227	K562	blood:	n/a	n/a
39	CBX3	chr19:41349182-41350047	K562	blood:	n/a	n/a
40	CBX3	chr19:41337733-41338384	K562	blood:	n/a	n/a
41	CBX3	chr19:41370123-41371107	K562	blood:	n/a	n/a
42	CCNT2	chr19:41339675-41339875	K562	blood:	n/a	n/a
43	CCNT2	chr19:41370582-41370786	K562	blood:	n/a	n/a
44	CEBPB	chr19:41373920-41374208	K562	blood:	n/a	n/a
45	CEBPB	chr19:41362024-41362201	K562	blood:	n/a	n/a
46	CEBPB	chr19:41337619-41338177	A549	lung:	n/a	n/a
47	CEBPB	chr19:41337713-41338232	IMR90	lung:	n/a	n/a
48	CEBPB	chr19:41342862-41343338	A549	lung:	n/a	chr19:41343121-41343132
49	CEBPB	chr19:41368761-41369068	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr19:41337643-41338329	HCT-116	colon:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41354142-41354192	GM12878	blood:	n/a
2	chr19:41386507-41386557	AG09319	gingival:	n/a
3	chr19:41389684-41389734	A549	lung:	n/a
4	chr19:41389684-41389734	AG10803	skin:	n/a
5	chr19:41386441-41386491	HRCEpiC	kidney:	n/a
6	chr19:41386441-41386491	HEEpiC	esophagus:	n/a
7	chr19:41386507-41386557	BE2_C	brain:	n/a
8	chr19:41354142-41354192	HL-60	blood:	n/a
9	chr19:41354682-41354732	PANC-1	pancreas:	n/a
10	chr19:41388384-41388434	HRCEpiC	kidney:	n/a
11	chr19:41351924-41351974	HPAEpiC	pulmonary alveolar:	n/a
12	chr19:41355973-41356023	BE2_C	brain:	n/a
13	chr19:41354682-41354732	U87	brain:	n/a
14	chr19:41354682-41354732	K562	blood:	n/a
15	chr19:41354142-41354192	HCM	heart:	n/a
16	chr19:41383654-41383704	Hela-S3	cervix:	n/a
17	chr19:41355973-41356023	GM06990	blood:	n/a
18	chr19:41354553-41354603	ovcar-3	ovarian:	n/a
19	chr19:41355973-41356023	ECC-1	luminal epithelium:	n/a
20	chr19:41354682-41354732	A549	lung:	n/a
21	chr19:41386441-41386491	BJ	skin:	n/a
22	chr19:41385865-41385915	Hepatocyte	liver:	n/a
23	chr19:41354553-41354603	NH-A	brain:	n/a
24	chr19:41354142-41354192	GM06990	blood:	n/a
25	chr19:41354553-41354603	MCF-7	breast:	n/a
26	chr19:41388232-41388282	HEK293	kidney:	embryo
27	chr19:41355973-41356023	NT2-D1	testis:	n/a
28	chr19:41354142-41354192	H1-hESC	embryonic stem cell:	embryo
29	chr19:41386441-41386491	HCM	heart:	n/a
30	chr19:41351924-41351974	LNCaP	prostate:	n/a
31	chr19:41354682-41354732	HRE	kidney:	n/a
32	chr19:41388232-41388282	H1-hESC	embryonic stem cell:	embryo
33	chr19:41354553-41354603	HL-60	blood:	n/a
34	chr19:41354553-41354603	AoSMC	blood vessel:	n/a
35	chr19:41354142-41354192	HEEpiC	esophagus:	n/a
36	chr19:41355973-41356023	AG09309	skin:	n/a
37	chr19:41354682-41354732	HCM	heart:	n/a
38	chr19:41354553-41354603	GM12878	blood:	n/a
39	chr19:41386507-41386557	SK-N-MC	brain:	n/a
40	chr19:41351924-41351974	U87	brain:	n/a
41	chr19:41388232-41388282	Caco-2	colon:	n/a
42	chr19:41385865-41385915	HEEpiC	esophagus:	n/a
43	chr19:41389684-41389734	ovcar-3	ovarian:	n/a
44	chr19:41386507-41386557	AG04449	skin:	fetal
45	chr19:41389684-41389734	HCT-116	colon:	n/a
46	chr19:41385865-41385915	GM12891	blood:	n/a
47	chr19:41355973-41356023	GM12892	blood:	n/a
48	chr19:41389684-41389734	ProgFib	skin:	n/a
49	chr19:41385865-41385915	HRCEpiC	kidney:	n/a
50	chr19:41354142-41354192	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:41168873..41171001-chr19:41337568..41339858,2	MCF-7	breast:
2	chr19:41308981..41310761-chr19:41328950..41331084,2	K562	blood:
3	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
4	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
5	chr19:41309668..41312632-chr19:41335922..41337729,2	MCF-7	breast:
6	chr19:41195484..41197379-chr19:41368669..41371255,2	K562	blood:
7	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
8	chr16:4474827..4477394-chr19:41351022..41353007,2	MCF-7	breast:
9	chr19:41333069..41334753-chr19:41334934..41336779,2	K562	blood:
10	chr19:41167522..41169643-chr19:41327340..41330313,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ENSG00000269843	TF binding region
CYP2G1P	TF binding region
CYP2F2P	TF binding region
CYP2A6	TF binding region
CYP2A7	TF binding region
ENSG00000269843	CpG island
CYP2G1P	CpG island
CYP2F2P	CpG island
CYP2A6	CpG island
CYP2A7	CpG island
ENSG00000105245	chromatin interactions
ENSG00000103423	chromatin interactions
ENSG00000262246	chromatin interactions
ENSG00000269858	chromatin interactions

Extended variants
information (count: 3535 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3535 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111780974	chr19:41329300-41329301	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535236287	chr19:41329327-41329328	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs553565363	chr19:41329381-41329382	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184756703	chr19:41329382-41329383	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541921529	chr19:41329457-41329458	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550223904	chr19:41329459-41329460	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs115104353	chr19:41329506-41329507	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562577977	chr19:41329539-41329540	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149782418	chr19:41329550-41329551	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546118266	chr19:41329557-41329558	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138842270	chr19:41329586-41329587	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528322344	chr19:41329587-41329588	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200041409	chr19:41329676-41329677	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371827759	chr19:41329677-41329678	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540047006	chr19:41329685-41329686	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs561510450	chr19:41329688-41329689	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112393173	chr19:41329731-41329732	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554680896	chr19:41329733-41329734	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs36144641	chr19:41329734-41329735	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376553177	chr19:41329762-41329763	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189089273	chr19:41329767-41329768	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142091297	chr19:41329813-41329814	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563742835	chr19:41329814-41329815	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs68060906	chr19:41329839-41329840	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs59090656	chr19:41329842-41329843	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530809664	chr19:41329889-41329890	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552497894	chr19:41329906-41329907	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2604862	chr19:41329908-41329909	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs535303135	chr19:41329952-41329953	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547240455	chr19:41329961-41329962	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568650499	chr19:41329978-41329979	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs73553012	chr19:41330010-41330011	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556767861	chr19:41330014-41330015	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs575243474	chr19:41330080-41330081	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539063570	chr19:41330104-41330105	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557694979	chr19:41330137-41330138	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs79366653	chr19:41330162-41330163	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141777035	chr19:41330172-41330173	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561574663	chr19:41330177-41330178	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573492198	chr19:41330178-41330179	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs7507400	chr19:41330179-41330180	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563635372	chr19:41330190-41330191	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142194898	chr19:41330208-41330209	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570111434	chr19:41330216-41330217	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12975933	chr19:41330231-41330232	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546006055	chr19:41330249-41330250	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568197419	chr19:41330267-41330268	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs150579175	chr19:41330282-41330283	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs139624977	chr19:41330331-41330332	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78937168	chr19:41330332-41330333	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 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:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41315000-41332600	Weak transcription	Aorta	Aorta
2	chr19:41320200-41332800	Weak transcription	HSMMtube	muscle
3	chr19:41322600-41330600	Enhancers	Placenta	Placenta
4	chr19:41324600-41332600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr19:41324600-41332600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:41324600-41332600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr19:41324600-41332600	Weak transcription	NHLF	lung
8	chr19:41324800-41332600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr19:41324800-41332600	Weak transcription	Fetal Brain Male	brain
10	chr19:41324800-41332600	Weak transcription	Fetal Brain Female	brain
11	chr19:41324800-41332800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:41324800-41332800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr19:41324800-41332800	Weak transcription	Esophagus	oesophagus
14	chr19:41324800-41337400	Weak transcription	Colonic Mucosa	Colon
15	chr19:41324800-41339200	Weak transcription	Brain Germinal Matrix	brain
16	chr19:41325000-41337400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr19:41325400-41329800	Weak transcription	Fetal Muscle Trunk	muscle
18	chr19:41325600-41337400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr19:41325800-41330200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr19:41325800-41331000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr19:41325800-41331200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr19:41325800-41331200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr19:41325800-41332600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr19:41325800-41332600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr19:41325800-41332600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr19:41325800-41332600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr19:41325800-41332600	Weak transcription	Fetal Stomach	stomach
28	chr19:41325800-41332800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr19:41325800-41332800	Weak transcription	Dnd41	blood
30	chr19:41325800-41332800	Weak transcription	NHDF-Ad	bronchial
31	chr19:41325800-41332800	Weak transcription	Osteobl	bone
32	chr19:41325800-41333000	Weak transcription	Thymus	Thymus
33	chr19:41326000-41331000	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr19:41326000-41332600	Weak transcription	Fetal Thymus	thymus
35	chr19:41326000-41332600	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr19:41326000-41339800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr19:41326200-41329800	Weak transcription	Primary T cells from cord blood	blood
38	chr19:41326200-41329800	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr19:41326200-41329800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr19:41326200-41332800	Weak transcription	Fetal Kidney	kidney
41	chr19:41327600-41330400	Enhancers	Fetal Intestine Small	intestine
42	chr19:41327600-41331400	Enhancers	K562	blood
43	chr19:41327600-41332600	Weak transcription	HSMM	muscle
44	chr19:41327800-41330200	Enhancers	Right Ventricle	heart
45	chr19:41327800-41330600	Enhancers	Fetal Intestine Large	intestine
46	chr19:41327800-41330800	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr19:41327800-41331400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:41327800-41332600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:41328000-41329400	Enhancers	Fetal Heart	heart
50	chr19:41328000-41330000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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