Variant report

Variant	nsv961283
Chromosome Location	chr19:19293486-19312277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1132)
CpG islands
(count:1161)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:19303868-19304213	K562	blood:	n/a	n/a
2	ARID3A	chr19:19302849-19303108	K562	blood:	n/a	n/a
3	ARID3A	chr19:19302780-19303453	HepG2	liver:	n/a	n/a
4	ATF2	chr19:19302696-19303204	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:19302777-19303426	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:19302740-19303484	GM12878	blood:	n/a	n/a
7	ATF2	chr19:19302893-19303355	GM12878	blood:	n/a	n/a
8	ATF3	chr19:19302754-19303123	A549	lung:	n/a	n/a
9	ATF3	chr19:19302767-19303216	A549	lung:	n/a	n/a
10	BACH1	chr19:19303017-19303231	K562	blood:	n/a	n/a
11	BACH1	chr19:19302939-19303992	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr19:19302635-19303139	GM12878	blood:	n/a	n/a
13	BCL3	chr19:19302749-19303223	A549	lung:	n/a	chr19:19302871-19302884
14	BCL3	chr19:19302676-19303281	A549	lung:	n/a	chr19:19302871-19302884
15	BCLAF1	chr19:19302594-19303338	GM12878	blood:	n/a	chr19:19302871-19302884
16	BCLAF1	chr19:19302648-19303402	GM12878	blood:	n/a	chr19:19302871-19302884
17	BCLAF1	chr19:19302779-19303301	K562	blood:	n/a	chr19:19302871-19302884
18	BHLHE40	chr19:19296840-19297409	K562	blood:	n/a	n/a
19	BHLHE40	chr19:19302742-19304316	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:19302820-19304300	K562	blood:	n/a	n/a
21	BHLHE40	chr19:19303935-19304221	HepG2	liver:	n/a	n/a
22	BRCA1	chr19:19302740-19303619	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr19:19302865-19303371	GM12878	blood:	n/a	n/a
24	BRCA1	chr19:19302968-19303342	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr19:19296913-19296935	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr19:19302931-19303169	HepG2	liver:	n/a	n/a
27	CBX3	chr19:19302421-19303264	K562	blood:	n/a	n/a
28	CBX3	chr19:19296716-19297723	K562	blood:	n/a	n/a
29	CCNT2	chr19:19302708-19303657	K562	blood:	n/a	n/a
30	CEBPB	chr19:19296911-19297013	IMR90	lung:	n/a	chr19:19296926-19296937
31	CEBPB	chr19:19305312-19305609	MCF-7	breast:	n/a	chr19:19305396-19305407
32	CEBPB	chr19:19305839-19305976	K562	blood:	n/a	n/a
33	CEBPB	chr19:19302730-19303605	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr19:19305320-19305652	ECC-1	luminal epithelium:	n/a	chr19:19305396-19305407
35	CEBPB	chr19:19296800-19297090	MCF-7	breast:	n/a	chr19:19296926-19296937
36	CEBPB	chr19:19305261-19305576	IMR90	lung:	n/a	chr19:19305396-19305407
37	CEBPB	chr19:19305299-19305548	Hela-S3	cervix:	n/a	chr19:19305396-19305407
38	CEBPB	chr19:19296759-19297085	H1-hESC	embryonic stem cell:	n/a	chr19:19296926-19296937
39	CEBPB	chr19:19296833-19297057	Hela-S3	cervix:	n/a	chr19:19296926-19296937
40	CEBPB	chr19:19305236-19305556	K562	blood:	n/a	chr19:19305396-19305407
41	CEBPB	chr19:19296749-19297030	K562	blood:	n/a	chr19:19296926-19296937
42	CEBPB	chr19:19302908-19303122	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr19:19305349-19305553	A549	lung:	n/a	chr19:19305396-19305407
44	CEBPB	chr19:19296811-19297034	HepG2	liver:	n/a	chr19:19296926-19296937
45	CEBPB	chr19:19305172-19306017	ECC-1	luminal epithelium:	n/a	chr19:19305396-19305407
46	CEBPB	chr19:19305260-19305573	K562	blood:	n/a	chr19:19305396-19305407
47	CEBPB	chr19:19305299-19305564	HepG2	liver:	n/a	chr19:19305396-19305407
48	CEBPB	chr19:19305820-19306017	IMR90	lung:	n/a	n/a
49	CEBPD	chr19:19303470-19303949	HepG2	liver:	n/a	n/a
50	CEBPD	chr19:19302748-19303112	HepG2	liver:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19301780-19301830	GM19239	blood:	n/a
2	chr19:19300292-19300342	HEK293	kidney:	embryo
3	chr19:19301780-19301830	GM19239	blood:	n/a
4	chr19:19300292-19300342	HEK293	kidney:	embryo
5	chr19:19303269-19303319	HCT-116	colon:	n/a
6	chr19:19302729-19302779	K562	blood:	n/a
7	chr19:19303979-19304029	HIPEpiC	eye:	n/a
8	chr19:19303504-19303554	IMR90	lung:	fetal
9	chr19:19305340-19305390	HCF	heart:	n/a
10	chr19:19305340-19305390	Jurkat	blood:	n/a
11	chr19:19303504-19303554	HIPEpiC	eye:	n/a
12	chr19:19301711-19301761	ovcar-3	ovarian:	n/a
13	chr19:19303979-19304029	Caco-2	colon:	n/a
14	chr19:19305340-19305390	HPAEpiC	pulmonary alveolar:	n/a
15	chr19:19310798-19310848	AG09309	skin:	n/a
16	chr19:19304836-19304886	HIPEpiC	eye:	n/a
17	chr19:19303500-19303550	AG04449	skin:	fetal
18	chr19:19303735-19303785	HCM	heart:	n/a
19	chr19:19303269-19303319	HEK293	kidney:	embryo
20	chr19:19302803-19302853	HEK293	kidney:	embryo
21	chr19:19302729-19302779	BE2_C	brain:	n/a
22	chr19:19303389-19303439	HCM	heart:	n/a
23	chr19:19303500-19303550	PrEC	prostate:	n/a
24	chr19:19310798-19310848	NB4	blood:	n/a
25	chr19:19303269-19303319	HepG2	liver:	n/a
26	chr19:19303389-19303439	AG04449	skin:	fetal
27	chr19:19303541-19303591	GM06990	blood:	n/a
28	chr19:19303735-19303785	SK-N-MC	brain:	n/a
29	chr19:19303541-19303591	SKMC	muscle:	n/a
30	chr19:19305340-19305390	SK-N-SH_RA	brain:	n/a
31	chr19:19302803-19302853	HCT-116	colon:	n/a
32	chr19:19303389-19303439	HEK293	kidney:	embryo
33	chr19:19300292-19300342	GM12878	blood:	n/a
34	chr19:19310798-19310848	AG10803	skin:	n/a
35	chr19:19303979-19304029	HNPCEpiC	eye:	n/a
36	chr19:19310798-19310848	NT2-D1	testis:	n/a
37	chr19:19301711-19301761	HRE	kidney:	n/a
38	chr19:19303500-19303550	AG09319	gingival:	n/a
39	chr19:19303443-19303493	Hela-S3	cervix:	n/a
40	chr19:19303389-19303439	HAEpiC	amniotic membrane:	n/a
41	chr19:19302985-19303035	NB4	blood:	n/a
42	chr19:19310798-19310848	MCF-7	breast:	n/a
43	chr19:19310798-19310848	SK-N-SH_RA	brain:	n/a
44	chr19:19301711-19301761	HMEC	breast:	n/a
45	chr19:19299305-19299355	Caco-2	colon:	n/a
46	chr19:19305340-19305390	CMK	blood:	n/a
47	chr19:19303979-19304029	MCF10A-Er-Src	breast:	n/a
48	chr19:19301780-19301830	GM12878	blood:	n/a
49	chr19:19306927-19306977	AG09319	gingival:	n/a
50	chr19:19301711-19301761	NHBE	bronchial:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19301845..19303815-chr19:19429491..19431433,2	K562	blood:
2	chr19:19296559..19297342-chr19:19453264..19453811,2	MCF-7	breast:
3	chr19:19291680..19293828-chr19:19294510..19298396,4	K562	blood:
4	chr19:19296821..19298878-chr19:19300164..19303100,3	MCF-7	breast:
5	chr19:19302224..19305333-chr19:19312708..19315616,6	MCF-7	breast:
6	chr19:19279506..19282646-chr19:19302669..19304636,3	MCF-7	breast:
7	chr19:18682067..18684109-chr19:19302288..19304450,2	K562	blood:
8	chr17:7475687..7476521-chr19:19303646..19304240,2	NB4	blood:
9	chr19:19295305..19299616-chr19:19301493..19303729,7	K562	blood:
10	chr19:19302763..19305800-chr19:19307599..19310833,3	MCF-7	breast:
11	chr19:19301203..19304689-chr19:19429627..19432561,5	MCF-7	breast:
12	chr19:19142422..19145596-chr19:19300959..19304249,3	K562	blood:
13	chr19:19289333..19292263-chr19:19310891..19313561,2	K562	blood:
14	chr19:19305757..19307573-chr19:19308012..19310576,2	K562	blood:
15	chr19:19308004..19310412-chr19:19430243..19432746,2	K562	blood:
16	chr19:19300955..19305521-chr19:19311679..19315747,10	MCF-7	breast:
17	chr19:19291680..19293828-chr19:19294510..19298396,4	K562	blood:
18	chr19:19296821..19298878-chr19:19300164..19303100,3	MCF-7	breast:
19	chr19:19307070..19310712-chr19:19311051..19314432,7	MCF-7	breast:
20	chr19:19307535..19311874-chr19:19311949..19315894,9	MCF-7	breast:
21	chr19:19299448..19305567-chr19:19306959..19319217,21	K562	blood:
22	chr19:19143660..19145632-chr19:19301840..19304072,2	MCF-7	breast:
23	chr19:19302936..19305152-chr19:19382979..19386540,3	MCF-7	breast:
24	chr19:19304004..19306841-chr19:19429725..19433437,3	MCF-7	breast:
25	chr19:19300955..19305521-chr19:19311679..19315747,10	MCF-7	breast:
26	chr19:19300744..19305499-chr19:19311426..19319217,10	K562	blood:
27	chr19:19291324..19295055-chr19:19301522..19304242,3	MCF-7	breast:
28	chr19:19294693..19300778-chr19:19301483..19306941,9	K562	blood:
29	chr19:19295305..19299616-chr19:19301493..19303729,7	K562	blood:
30	chr19:19291324..19295055-chr19:19301522..19304242,3	MCF-7	breast:
31	chr19:19286456..19293705-chr19:19298673..19304955,13	K562	blood:
32	chr19:19301788..19305469-chr19:19308325..19310505,4	K562	blood:
33	chr19:19302763..19305800-chr19:19307599..19310833,3	MCF-7	breast:
34	chr19:19307535..19311874-chr19:19311949..19315894,9	MCF-7	breast:
35	chr19:19301698..19303429-chr19:19429828..19432129,2	MCF-7	breast:
36	chr19:19291248..19293065-chr19:19301550..19303514,2	K562	blood:
37	chr19:19301631..19304213-chr19:19625502..19628076,2	MCF-7	breast:
38	chr19:19307070..19310712-chr19:19311051..19314432,7	MCF-7	breast:
39	chr19:19303122..19305309-chr19:19496096..19498095,2	K562	blood:
40	chr19:19303809..19306527-chr19:19495529..19497596,2	K562	blood:
41	chr19:19299448..19305567-chr19:19306959..19319217,21	K562	blood:
42	chr19:19300744..19305499-chr19:19311426..19319217,10	K562	blood:
43	chr19:19294693..19300778-chr19:19301483..19306941,9	K562	blood:
44	chr19:19286456..19293705-chr19:19298673..19304955,13	K562	blood:
45	chr19:19301788..19305469-chr19:19308325..19310505,4	K562	blood:
46	chr19:19305583..19307573-chr19:19309076..19310790,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM161A-1	chr19:19303008-19303400	NONHSAT063026

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	NR2C2AP	hsa-miR-221-3p	chr19:19312257-19312279
2	NR2C2AP	hsa-miR-93-5p	chr19:19312263-19312284
3	NR2C2AP	hsa-miR-33a-5p	chr19:19312267-19312287

Variant related genes	Relation type
RFXANK	TF binding region
MEF2BNB-MEF2B	TF binding region
MEF2BNB	TF binding region
MEF2B	TF binding region
RFXANK	CpG island
MEF2BNB-MEF2B	CpG island
MEF2BNB	CpG island
MEF2B	CpG island
ENSG00000267629	chromatin interactions
ENSG00000167491	chromatin interactions
ENSG00000213999	chromatin interactions
ENSG00000064607	chromatin interactions
ENSG00000161960	chromatin interactions
ENSG00000186010	chromatin interactions
ENSG00000105705	chromatin interactions
ENSG00000213996	chromatin interactions
ENSG00000129933	chromatin interactions
ENSG00000258674	chromatin interactions
ENSG00000184162	chromatin interactions
ENSG00000178093	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000064490	chromatin interactions
ENSG00000254901	chromatin interactions
ENSG00000064489	chromatin interactions
ENSG00000105676	chromatin interactions

Extended variants
information (count: 817 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369618700	chr19:19293488-19293489	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs45560433	chr19:19293507-19293508	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs4584957	chr19:19293515-19293516	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs45455303	chr19:19293520-19293521	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs368142902	chr19:19293526-19293527	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs537190424	chr19:19293542-19293543	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs556935745	chr19:19293580-19293581	Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs576834975	chr19:19293611-19293612	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs546051719	chr19:19293612-19293613	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs559638671	chr19:19293643-19293644	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs76682873	chr19:19293661-19293662	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs542042466	chr19:19293735-19293736	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs562348159	chr19:19293755-19293756	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs530517441	chr19:19293773-19293774	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs550697603	chr19:19293878-19293879	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs554553480	chr19:19293888-19293889	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs183437856	chr19:19293906-19293907	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs8101388	chr19:19293938-19293939	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs552258552	chr19:19293943-19293944	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs546888968	chr19:19293951-19293952	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs566633040	chr19:19293989-19293990	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs71332145	chr19:19294011-19294012	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs144209252	chr19:19294053-19294054	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs187978413	chr19:19294080-19294081	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs68147405	chr19:19294091-19294092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs557050034	chr19:19294110-19294111	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs576795689	chr19:19294149-19294150	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs539423770	chr19:19294173-19294174	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs553365916	chr19:19294174-19294175	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs370172544	chr19:19294176-19294177	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs367903162	chr19:19294219-19294220	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs573449148	chr19:19294224-19294225	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs542555670	chr19:19294231-19294232	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs202116068	chr19:19294233-19294234	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs62135499	chr19:19294237-19294238	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192825413	chr19:19294249-19294250	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs544290815	chr19:19294262-19294263	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs113649173	chr19:19294273-19294274	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs368945366	chr19:19294324-19294325	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs184392045	chr19:19294330-19294331	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs188021083	chr19:19294366-19294367	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs72997174	chr19:19294389-19294390	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs113954889	chr19:19294392-19294393	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
44	rs529172717	chr19:19294424-19294425	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs111482653	chr19:19294428-19294429	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs549264397	chr19:19294462-19294463	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs568922354	chr19:19294472-19294473	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs75382602	chr19:19294498-19294499	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs531422635	chr19:19294511-19294512	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs113654890	chr19:19294517-19294518	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1389 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19277400-19300600	Weak transcription	Small Intestine	intestine
2	chr19:19280800-19301600	Weak transcription	NHEK	skin
3	chr19:19281400-19300800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr19:19281600-19297200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr19:19281600-19299400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr19:19281600-19300600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr19:19281600-19302000	Weak transcription	NH-A	brain
8	chr19:19281600-19302200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:19281800-19300000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr19:19281800-19301200	Weak transcription	Stomach Mucosa	stomach
11	chr19:19282000-19301600	Weak transcription	Fetal Heart	heart
12	chr19:19283400-19300600	Weak transcription	Psoas Muscle	Psoas
13	chr19:19283400-19301600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr19:19283400-19302000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr19:19283400-19302200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr19:19283600-19301800	Weak transcription	HSMMtube	muscle
17	chr19:19284200-19302000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr19:19285600-19301800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr19:19286000-19301000	Weak transcription	HepG2	liver
20	chr19:19286000-19302000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr19:19286400-19294000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:19286600-19293600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr19:19286600-19293600	Strong transcription	Ovary	ovary
24	chr19:19286600-19293800	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr19:19286600-19298200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr19:19286800-19293800	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr19:19286800-19293800	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr19:19286800-19293800	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr19:19286800-19294000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr19:19286800-19294000	Strong transcription	Stomach Smooth Muscle	stomach
31	chr19:19286800-19296600	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr19:19287000-19293600	Strong transcription	Gastric	stomach
33	chr19:19287000-19293800	Strong transcription	Pancreas	Pancrea
34	chr19:19287000-19293800	Strong transcription	Thymus	Thymus
35	chr19:19287000-19294000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr19:19287000-19294400	Strong transcription	Primary T cells from cord blood	blood
37	chr19:19287200-19293800	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr19:19287200-19293800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr19:19287200-19293800	Strong transcription	Dnd41	blood
40	chr19:19287200-19294000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr19:19287200-19294000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr19:19287200-19294000	Strong transcription	Skeletal Muscle Female	skeletal muscle
43	chr19:19287400-19293600	Strong transcription	Colonic Mucosa	Colon
44	chr19:19287400-19293800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr19:19287400-19293800	Strong transcription	Brain Anterior Caudate	brain
46	chr19:19287400-19293800	Strong transcription	Duodenum Mucosa	Duodenum
47	chr19:19287600-19293800	Strong transcription	Rectal Mucosa Donor 29	rectum
48	chr19:19287600-19297200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr19:19287800-19293800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr19:19288200-19294000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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