Variant report

Variant	nsv911807
Chromosome Location	chr19:42920555-42929254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:490)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:42927405-42927427	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:42924330-42924562	HepG2	liver:	n/a	n/a
3	ATF1	chr19:42924212-42924515	K562	blood:	n/a	n/a
4	ATF2	chr19:42927036-42927474	GM12878	blood:	n/a	n/a
5	ATF2	chr19:42924079-42924520	GM12878	blood:	n/a	n/a
6	ATF2	chr19:42924128-42924576	GM12878	blood:	n/a	n/a
7	ATF2	chr19:42924079-42924489	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:42924180-42924506	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr19:42927187-42927770	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr19:42926950-42927301	GM12878	blood:	n/a	n/a
11	BCL3	chr19:42926895-42928320	A549	lung:	n/a	chr19:42927843-42927856 chr19:42927842-42927851 chr19:42927888-42927897 chr19:42927855-42927864
12	BHLHE40	chr19:42927069-42928123	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:42924258-42924559	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:42924241-42924627	K562	blood:	n/a	n/a
15	BHLHE40	chr19:42927250-42927653	HepG2	liver:	n/a	n/a
16	BHLHE40	chr19:42924237-42924629	HepG2	liver:	n/a	n/a
17	BRCA1	chr19:42927281-42927600	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr19:42927869-42928021	GM12878	blood:	n/a	n/a
19	BRCA1	chr19:42927162-42927582	GM12878	blood:	n/a	n/a
20	CBX3	chr19:42924093-42924544	K562	blood:	n/a	n/a
21	CBX3	chr19:42924195-42924446	K562	blood:	n/a	n/a
22	CEBPB	chr19:42927592-42927979	A549	lung:	n/a	n/a
23	CEBPB	chr19:42927467-42928125	A549	lung:	n/a	n/a
24	CEBPB	chr19:42924274-42924832	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:42927405-42927967	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr19:42924172-42924596	A549	lung:	n/a	n/a
27	CEBPB	chr19:42928170-42928496	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr19:42924216-42924428	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:42924097-42924517	MCF-7	breast:	n/a	n/a
30	CEBPB	chr19:42924156-42924559	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr19:42927627-42927885	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:42924184-42924488	K562	blood:	n/a	n/a
33	CEBPB	chr19:42925771-42926067	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr19:42927596-42927980	IMR90	lung:	n/a	n/a
35	CHD1	chr19:42923999-42924906	IMR90	lung:	n/a	n/a
36	CHD1	chr19:42926653-42928296	IMR90	lung:	n/a	n/a
37	CHD1	chr19:42927123-42927699	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr19:42926733-42928070	GM12878	blood:	n/a	n/a
39	CHD1	chr19:42928304-42928485	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr19:42927905-42928084	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr19:42927511-42928641	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr19:42927396-42928056	GM12878	blood:	n/a	n/a
43	CREB1	chr19:42927454-42928227	A549	lung:	n/a	n/a
44	CREB1	chr19:42924229-42924587	A549	lung:	n/a	n/a
45	CTCF	chr19:42924240-42924390	RPTEC	kidney:	n/a	n/a
46	CTCF	chr19:42928944-42929094	MCF-7	breast:	n/a	n/a
47	CTCF	chr19:42927000-42927150	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr19:42924180-42924330	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr19:42924300-42924450	RPTEC	kidney:	n/a	n/a
50	CTCF	chr19:42924280-42924430	BE2_C	brain:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42928015-42928065	NT2-D1	testis:	n/a
2	chr19:42927074-42927124	PrEC	prostate:	n/a
3	chr19:42928015-42928065	NT2-D1	testis:	n/a
4	chr19:42927074-42927124	PrEC	prostate:	n/a
5	chr19:42928015-42928065	GM06990	blood:	n/a
6	chr19:42928597-42928647	PANC-1	pancreas:	n/a
7	chr19:42928195-42928245	ECC-1	luminal epithelium:	n/a
8	chr19:42927668-42927718	AG09309	skin:	n/a
9	chr19:42929067-42929117	GM12878	blood:	n/a
10	chr19:42928597-42928647	HRCEpiC	kidney:	n/a
11	chr19:42927668-42927718	CMK	blood:	n/a
12	chr19:42927074-42927124	PANC-1	pancreas:	n/a
13	chr19:42928195-42928245	NHBE	bronchial:	n/a
14	chr19:42927286-42927336	AG04449	skin:	fetal
15	chr19:42928015-42928065	ovcar-3	ovarian:	n/a
16	chr19:42928195-42928245	HCPEpiC	choroid plexus:	n/a
17	chr19:42928597-42928647	Caco-2	colon:	n/a
18	chr19:42927676-42927726	NHDF-neo	bronchial:	n/a
19	chr19:42927286-42927336	LNCaP	prostate:	n/a
20	chr19:42927668-42927718	PANC-1	pancreas:	n/a
21	chr19:42927074-42927124	NHDF-neo	bronchial:	n/a
22	chr19:42927074-42927124	NB4	blood:	n/a
23	chr19:42928195-42928245	HNPCEpiC	eye:	n/a
24	chr19:42927286-42927336	ovcar-3	ovarian:	n/a
25	chr19:42929067-42929117	GM06990	blood:	n/a
26	chr19:42928195-42928245	MCF10A-Er-Src	breast:	n/a
27	chr19:42927074-42927124	GM12891	blood:	n/a
28	chr19:42928015-42928065	HCF	heart:	n/a
29	chr19:42929067-42929117	SK-N-SH_RA	brain:	n/a
30	chr19:42927286-42927336	ECC-1	luminal epithelium:	n/a
31	chr19:42927668-42927718	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:42927668-42927718	HUVEC	blood vessel:	n/a
33	chr19:42927074-42927124	HCF	heart:	n/a
34	chr19:42929067-42929117	SK-N-SH	brain:	n/a
35	chr19:42928597-42928647	MCF10A-Er-Src	breast:	n/a
36	chr19:42928597-42928647	HPAEpiC	pulmonary alveolar:	n/a
37	chr19:42928597-42928647	NHBE	bronchial:	n/a
38	chr19:42927286-42927336	HUVEC	blood vessel:	n/a
39	chr19:42927074-42927124	U87	brain:	n/a
40	chr19:42928195-42928245	SK-N-SH	brain:	n/a
41	chr19:42928597-42928647	Jurkat	blood:	n/a
42	chr19:42928015-42928065	HCPEpiC	choroid plexus:	n/a
43	chr19:42928195-42928245	SK-N-MC	brain:	n/a
44	chr19:42927676-42927726	HNPCEpiC	eye:	n/a
45	chr19:42928015-42928065	BE2_C	brain:	n/a
46	chr19:42927676-42927726	HMEC	breast:	n/a
47	chr19:42927074-42927124	AG09309	skin:	n/a
48	chr19:42927286-42927336	SAEC	small airway:	n/a
49	chr19:42928597-42928647	HCF	heart:	n/a
50	chr19:42928597-42928647	Hepatocyte	liver:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:42905670..42907944-chr19:42921112..42922967,2	K562	blood:
2	chr19:42927142..42929606-chr19:42930289..42932952,2	MCF-7	breast:
3	chr19:42637501..42639898-chr19:42924232..42925782,2	K562	blood:
4	chr19:42923927..42924838-chr19:42937872..42938431,4	MCF-7	breast:
5	chr19:42593805..42596172-chr19:42919024..42921548,2	K562	blood:
6	chr19:42747404..42749057-chr19:42923034..42925507,2	K562	blood:
7	chr19:42682574..42684413-chr19:42921728..42924640,2	K562	blood:
8	chr19:42787574..42789864-chr19:42923760..42926145,2	MCF-7	breast:
9	chr19:42923683..42924698-chr19:42937367..42938479,4	MCF-7	breast:
10	chr19:42923954..42924758-chr2:222313250..222313936,2	MCF-7	breast:
11	chr19:42900219..42901127-chr19:42923966..42924540,2	MCF-7	breast:
12	chr19:42903448..42905839-chr19:42923535..42926055,2	MCF-7	breast:
13	chr19:42923833..42924814-chr19:42944126..42944646,2	K562	blood:
14	chr19:42921780..42924678-chr19:42930501..42932558,2	K562	blood:
15	chr19:42924851..42926943-chr19:42928310..42931390,3	MCF-7	breast:
16	chr19:42925339..42926995-chr19:42928878..42931861,2	K562	blood:
17	chr19:42923925..42924921-chr19:42937449..42938520,3	K562	blood:
18	chr19:42921780..42924507-chr19:42929179..42932042,4	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011497.1-2	chr19:42927907-42929356	ENSG00000213904.4
2	lnc-AC011497.1-2	chr19:42928421-42929356	ENSG00000213904.4
3	lnc-CXCL17-1	chr19:42928816-42929223	ENSG00000268605.1
4	lnc-CXCL17-1	chr19:42928536-42928688	ENSG00000268605.1
5	lnc-AC011497.1-2	chr19:42928465-42929294	ENSG00000213904.4
6	lnc-AC011497.1-2	chr19:42927907-42929356	NONHSAT066551

No data

Variant related genes	Relation type
LIPE	TF binding region
LIPE-AS1	TF binding region
ENSG00000268605	TF binding region
LIPE	CpG island
LIPE-AS1	CpG island
ENSG00000268605	CpG island
ENSG00000268605	chromatin interactions
ENSG00000254887	chromatin interactions
ENSG00000266226	chromatin interactions
ENSG00000213904	chromatin interactions
ENSG00000079432	chromatin interactions
ENSG00000079435	chromatin interactions

Extended variants
information (count: 307 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:307 , 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	rs35241185	chr19:42920555-42920556	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541123719	chr19:42920626-42920627	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559029405	chr19:42920644-42920645	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572411396	chr19:42920690-42920691	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548530454	chr19:42920759-42920760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149338480	chr19:42920760-42920761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530767242	chr19:42920787-42920788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552346251	chr19:42920804-42920805	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570514360	chr19:42920850-42920851	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534730997	chr19:42920853-42920854	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552766178	chr19:42920863-42920864	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567747451	chr19:42920919-42920920	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541830343	chr19:42920933-42920934	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77711132	chr19:42920940-42920941	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191456838	chr19:42920969-42920970	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576329067	chr19:42920971-42920972	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76760779	chr19:42920973-42920974	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559112373	chr19:42921001-42921002	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577329391	chr19:42921111-42921112	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541535093	chr19:42921165-42921166	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs559569348	chr19:42921166-42921167	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs530151027	chr19:42921167-42921168	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542233777	chr19:42921173-42921174	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563621473	chr19:42921174-42921175	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs556463766	chr19:42921217-42921218	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs552154629	chr19:42921261-42921262	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570647137	chr19:42921262-42921263	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528252551	chr19:42921274-42921275	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546710603	chr19:42921282-42921283	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567809111	chr19:42921307-42921308	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535126467	chr19:42921308-42921309	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10414969	chr19:42921335-42921336	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs575003434	chr19:42921367-42921368	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537762044	chr19:42921368-42921369	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114386930	chr19:42921375-42921376	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577394639	chr19:42921403-42921404	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114953493	chr19:42921435-42921436	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs182947326	chr19:42921531-42921532	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs77213871	chr19:42921565-42921566	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542296943	chr19:42921566-42921567	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs568678648	chr19:42921579-42921580	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs7254956	chr19:42921721-42921722	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs75445139	chr19:42921763-42921764	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541930329	chr19:42921767-42921768	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546108213	chr19:42921803-42921804	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs143717665	chr19:42921928-42921929	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs369744984	chr19:42921951-42921952	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs147200763	chr19:42921995-42921996	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs188048119	chr19:42921998-42921999	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs11670831	chr19:42922034-42922035	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 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
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
Multiple myeloma	17550852	CNVD

Chromatin state (count:772 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42906200-42926200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr19:42906400-42924400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr19:42906400-42926400	Weak transcription	Colonic Mucosa	Colon
4	chr19:42906600-42926400	Weak transcription	Fetal Lung	lung
5	chr19:42906800-42923200	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr19:42906800-42924000	Weak transcription	A549	lung
7	chr19:42906800-42924400	Weak transcription	Osteobl	bone
8	chr19:42906800-42925200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr19:42907000-42924200	Strong transcription	Fetal Stomach	stomach
10	chr19:42907000-42924400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr19:42907400-42926600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:42909000-42925800	Weak transcription	Dnd41	blood
13	chr19:42910400-42924200	Weak transcription	GM12878-XiMat	blood
14	chr19:42911000-42924000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr19:42911000-42924400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr19:42911200-42923800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr19:42911600-42923600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr19:42912200-42925000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr19:42912600-42924000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr19:42912600-42924200	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr19:42912600-42925600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:42912800-42926200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr19:42913800-42925800	Weak transcription	NHDF-Ad	bronchial
24	chr19:42914000-42923600	Weak transcription	Lung	lung
25	chr19:42914000-42924200	Weak transcription	Pancreas	Pancrea
26	chr19:42914000-42924400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:42914000-42926400	Weak transcription	Ovary	ovary
28	chr19:42914200-42924400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr19:42914400-42926000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr19:42915000-42925600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr19:42915200-42924400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr19:42915200-42925400	Weak transcription	Stomach Smooth Muscle	stomach
33	chr19:42915200-42925800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr19:42915400-42924000	Weak transcription	Brain Germinal Matrix	brain
35	chr19:42915400-42924200	Weak transcription	NHLF	lung
36	chr19:42915800-42920600	Weak transcription	Fetal Brain Female	brain
37	chr19:42917000-42920600	Strong transcription	Fetal Intestine Small	intestine
38	chr19:42917000-42923200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr19:42917000-42924000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr19:42917000-42926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr19:42917200-42922600	Weak transcription	Esophagus	oesophagus
42	chr19:42917200-42923000	Weak transcription	Left Ventricle	heart
43	chr19:42917200-42923400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr19:42917200-42923400	Weak transcription	Right Ventricle	heart
45	chr19:42917200-42923600	Weak transcription	Gastric	stomach
46	chr19:42917200-42923600	Weak transcription	Right Atrium	heart
47	chr19:42917200-42924200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr19:42917200-42924400	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr19:42917400-42923600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr19:42917400-42924200	Weak transcription	Brain Angular Gyrus	brain

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