Variant report

Variant	nsv911803
Chromosome Location	chr19:42916841-42926406
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:42924330-42924562	HepG2	liver:	n/a	n/a
2	ATF1	chr19:42924212-42924515	K562	blood:	n/a	n/a
3	ATF2	chr19:42924079-42924489	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:42924079-42924520	GM12878	blood:	n/a	n/a
5	ATF2	chr19:42924128-42924576	GM12878	blood:	n/a	n/a
6	ATF3	chr19:42924180-42924506	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr19:42924241-42924627	K562	blood:	n/a	n/a
8	BHLHE40	chr19:42924237-42924629	HepG2	liver:	n/a	n/a
9	BHLHE40	chr19:42924258-42924559	GM12878	blood:	n/a	n/a
10	CBX3	chr19:42924195-42924446	K562	blood:	n/a	n/a
11	CBX3	chr19:42924093-42924544	K562	blood:	n/a	n/a
12	CEBPB	chr19:42924216-42924428	HepG2	liver:	n/a	n/a
13	CEBPB	chr19:42924172-42924596	A549	lung:	n/a	n/a
14	CEBPB	chr19:42924184-42924488	K562	blood:	n/a	n/a
15	CEBPB	chr19:42924274-42924832	IMR90	lung:	n/a	n/a
16	CEBPB	chr19:42925771-42926067	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:42924156-42924559	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:42924097-42924517	MCF-7	breast:	n/a	n/a
19	CHD1	chr19:42923999-42924906	IMR90	lung:	n/a	n/a
20	CREB1	chr19:42924229-42924587	A549	lung:	n/a	n/a
21	CTCF	chr19:42924202-42924598	GM19239	blood:	n/a	n/a
22	CTCF	chr19:42924205-42924500	T-47D	breast:	n/a	n/a
23	CTCF	chr19:42924280-42924430	AG09319	gingival:	n/a	n/a
24	CTCF	chr19:42923940-42924090	GM12875	blood:	n/a	n/a
25	CTCF	chr19:42924185-42924557	K562	blood:	n/a	n/a
26	CTCF	chr19:42924300-42924450	GM06990	blood:	n/a	n/a
27	CTCF	chr19:42924204-42924489	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr19:42924300-42924450	HCT-116	colon:	n/a	n/a
29	CTCF	chr19:42924320-42924470	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr19:42924280-42924430	BE2_C	brain:	n/a	n/a
31	CTCF	chr19:42924217-42924521	MCF-7	breast:	n/a	n/a
32	CTCF	chr19:42923968-42924074	K562	blood:	n/a	n/a
33	CTCF	chr19:42924059-42924659	K562	blood:	n/a	n/a
34	CTCF	chr19:42924280-42924430	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr19:42924280-42924430	HPF	lung:	n/a	n/a
36	CTCF	chr19:42924280-42924430	GM12872	blood:	n/a	n/a
37	CTCF	chr19:42924217-42924500	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr19:42924260-42924410	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr19:42924280-42924430	HMF	breast:	n/a	n/a
40	CTCF	chr19:42923940-42924090	GM12872	blood:	n/a	n/a
41	CTCF	chr19:42924126-42924586	IMR90	lung:	n/a	n/a
42	CTCF	chr19:42924005-42924067	GM13977	blood:	n/a	n/a
43	CTCF	chr19:42924280-42924430	HVMF	connective:	n/a	n/a
44	CTCF	chr19:42924280-42924430	AG10803	skin:	n/a	n/a
45	CTCF	chr19:42924119-42924681	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:42924218-42924502	GM13977	blood:	n/a	n/a
47	CTCF	chr19:42924260-42924410	AG04450	lung:	n/a	n/a
48	CTCF	chr19:42924193-42924571	GM19238	blood:	n/a	n/a
49	CTCF	chr19:42924280-42924430	GM06990	blood:	n/a	n/a
50	CTCF	chr19:42924667-42924737	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42916966-42917016	SAEC	small airway:	n/a
2	chr19:42916966-42917016	HEK293	kidney:	embryo
3	chr19:42916966-42917016	HNPCEpiC	eye:	n/a
4	chr19:42916966-42917016	AG04450	lung:	fetal
5	chr19:42916966-42917016	BE2_C	brain:	n/a
6	chr19:42916966-42917016	CMK	blood:	n/a
7	chr19:42916966-42917016	NHBE	bronchial:	n/a
8	chr19:42916966-42917016	RPTEC	kidney:	n/a
9	chr19:42916966-42917016	HL-60	blood:	n/a
10	chr19:42916966-42917016	A549	lung:	n/a
11	chr19:42916966-42917016	HCM	heart:	n/a
12	chr19:42916966-42917016	NH-A	brain:	n/a
13	chr19:42916966-42917016	HCT-116	colon:	n/a
14	chr19:42916966-42917016	HIPEpiC	eye:	n/a
15	chr19:42916966-42917016	AG09309	skin:	n/a
16	chr19:42916966-42917016	Caco-2	colon:	n/a
17	chr19:42916966-42917016	HPAEpiC	pulmonary alveolar:	n/a
18	chr19:42916966-42917016	ProgFib	skin:	n/a
19	chr19:42916966-42917016	NT2-D1	testis:	n/a
20	chr19:42916966-42917016	U87	brain:	n/a
21	chr19:42916966-42917016	LNCaP	prostate:	n/a
22	chr19:42916966-42917016	SK-N-SH_RA	brain:	n/a
23	chr19:42916966-42917016	ECC-1	luminal epithelium:	n/a
24	chr19:42916966-42917016	Jurkat	blood:	n/a
25	chr19:42916966-42917016	PANC-1	pancreas:	n/a
26	chr19:42916966-42917016	GM12891	blood:	n/a
27	chr19:42916966-42917016	HMEC	breast:	n/a
28	chr19:42916966-42917016	IMR90	lung:	fetal
29	chr19:42916966-42917016	GM12892	blood:	n/a
30	chr19:42916966-42917016	HRCEpiC	kidney:	n/a
31	chr19:42916966-42917016	GM12878	blood:	n/a
32	chr19:42916966-42917016	Hela-S3	cervix:	n/a
33	chr19:42916966-42917016	PrEC	prostate:	n/a
34	chr19:42916966-42917016	SK-N-SH	brain:	n/a
35	chr19:42916966-42917016	NHDF-neo	bronchial:	n/a
36	chr19:42916966-42917016	AG09319	gingival:	n/a
37	chr19:42916966-42917016	AG10803	skin:	n/a
38	chr19:42916966-42917016	MCF-7	breast:	n/a
39	chr19:42916966-42917016	HepG2	liver:	n/a
40	chr19:42916966-42917016	HRE	kidney:	n/a
41	chr19:42916966-42917016	PFSK-1	brain:	n/a
42	chr19:42916966-42917016	HRPEpiC	eye:	n/a
43	chr19:42916966-42917016	AoSMC	blood vessel:	n/a
44	chr19:42916966-42917016	H1-hESC	embryonic stem cell:	embryo
45	chr19:42916966-42917016	GM19239	blood:	n/a
46	chr19:42916966-42917016	MCF10A-Er-Src	breast:	n/a
47	chr19:42916966-42917016	HEEpiC	esophagus:	n/a
48	chr19:42916966-42917016	SK-N-MC	brain:	n/a
49	chr19:42916966-42917016	HCPEpiC	choroid plexus:	n/a
50	chr19:42916966-42917016	T-47D	breast:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:42787574..42789864-chr19:42923760..42926145,2	MCF-7	breast:
2	chr19:42787351..42790273-chr19:42916971..42918941,2	MCF-7	breast:
3	chr19:42925339..42926995-chr19:42928878..42931861,2	K562	blood:
4	chr19:42903448..42905839-chr19:42923535..42926055,2	MCF-7	breast:
5	chr19:42593805..42596172-chr19:42919024..42921548,2	K562	blood:
6	chr19:42921780..42924678-chr19:42930501..42932558,2	K562	blood:
7	chr19:42900219..42901127-chr19:42923966..42924540,2	MCF-7	breast:
8	chr19:42905458..42907156-chr19:42917466..42920003,2	K562	blood:
9	chr19:42923833..42924814-chr19:42944126..42944646,2	K562	blood:
10	chr19:42637501..42639898-chr19:42924232..42925782,2	K562	blood:
11	chr19:42923925..42924921-chr19:42937449..42938520,3	K562	blood:
12	chr19:42923954..42924758-chr2:222313250..222313936,2	MCF-7	breast:
13	chr19:42923927..42924838-chr19:42937872..42938431,4	MCF-7	breast:
14	chr19:42924851..42926943-chr19:42928310..42931390,3	MCF-7	breast:
15	chr19:42923683..42924698-chr19:42937367..42938479,4	MCF-7	breast:
16	chr19:42682574..42684413-chr19:42921728..42924640,2	K562	blood:
17	chr19:42747404..42749057-chr19:42923034..42925507,2	K562	blood:
18	chr19:42921780..42924507-chr19:42929179..42932042,4	K562	blood:
19	chr19:42905670..42907944-chr19:42921112..42922967,2	K562	blood:

No data

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

Extended variants
information (count: 338 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:338 , 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	rs35544765	chr19:42916841-42916842	Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550217269	chr19:42916847-42916848	Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs540018363	chr19:42916967-42916968	Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs558263876	chr19:42916975-42916976	Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs573245712	chr19:42916983-42916984	Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534242383	chr19:42916996-42916997	Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555478345	chr19:42917004-42917005	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573657369	chr19:42917031-42917032	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544115359	chr19:42917048-42917049	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs142242005	chr19:42917062-42917063	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs35917849	chr19:42917102-42917103	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs372659922	chr19:42917111-42917112	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs544867594	chr19:42917147-42917148	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs376332678	chr19:42917182-42917183	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs560242287	chr19:42917252-42917253	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568861377	chr19:42917262-42917263	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs567659570	chr19:42917272-42917273	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549022608	chr19:42917285-42917286	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs560885401	chr19:42917339-42917340	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558842622	chr19:42917341-42917342	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531308483	chr19:42917346-42917347	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551326428	chr19:42917410-42917411	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs374370796	chr19:42917477-42917478	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs112180266	chr19:42917479-42917480	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs536390227	chr19:42917544-42917545	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs386809420	chr19:42917545-42917546	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs34637823	chr19:42917546-42917547	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs111641711	chr19:42917598-42917599	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs567004975	chr19:42917633-42917634	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs192654578	chr19:42917649-42917650	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555796184	chr19:42917675-42917676	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs536543822	chr19:42917677-42917678	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs372128430	chr19:42917718-42917719	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs537825909	chr19:42917734-42917735	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs35067200	chr19:42917747-42917748	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs35266309	chr19:42917773-42917774	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs189174852	chr19:42917815-42917816	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs566499058	chr19:42917837-42917838	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs376783523	chr19:42917850-42917851	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs572172257	chr19:42917851-42917852	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs28474957	chr19:42917873-42917874	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs34147230	chr19:42917909-42917910	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192083666	chr19:42917920-42917921	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs145208021	chr19:42917992-42917993	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs35822438	chr19:42918024-42918025	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs559316636	chr19:42918052-42918053	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376723064	chr19:42918059-42918060	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs140796756	chr19:42918079-42918080	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs566967583	chr19:42918093-42918094	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs149687600	chr19:42918099-42918100	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region 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:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr19:42906600-42918600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr19:42906600-42926400	Weak transcription	Fetal Lung	lung
6	chr19:42906800-42923200	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr19:42906800-42924000	Weak transcription	A549	lung
8	chr19:42906800-42924400	Weak transcription	Osteobl	bone
9	chr19:42906800-42925200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr19:42907000-42924200	Strong transcription	Fetal Stomach	stomach
11	chr19:42907000-42924400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr19:42907400-42926600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr19:42909000-42925800	Weak transcription	Dnd41	blood
14	chr19:42910400-42924200	Weak transcription	GM12878-XiMat	blood
15	chr19:42911000-42924000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr19:42911000-42924400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr19:42911200-42923800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr19:42911600-42923600	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr19:42911800-42918200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr19:42912200-42925000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr19:42912400-42917800	Weak transcription	Primary B cells from peripheral blood	blood
22	chr19:42912600-42924000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr19:42912600-42924200	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr19:42912600-42925600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr19:42912800-42926200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr19:42913800-42925800	Weak transcription	NHDF-Ad	bronchial
27	chr19:42914000-42923600	Weak transcription	Lung	lung
28	chr19:42914000-42924200	Weak transcription	Pancreas	Pancrea
29	chr19:42914000-42924400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr19:42914000-42926400	Weak transcription	Ovary	ovary
31	chr19:42914200-42924400	Weak transcription	Duodenum Mucosa	Duodenum
32	chr19:42914400-42917200	Weak transcription	Fetal Heart	heart
33	chr19:42914400-42926000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr19:42914600-42918000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr19:42914600-42918400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr19:42914600-42918600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr19:42915000-42917200	Weak transcription	Primary T cells from cord blood	blood
38	chr19:42915000-42919000	Strong transcription	Primary B cells from cord blood	blood
39	chr19:42915000-42925600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr19:42915200-42917400	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr19:42915200-42918000	Weak transcription	Fetal Thymus	thymus
42	chr19:42915200-42918400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr19:42915200-42918600	Weak transcription	Thymus	Thymus
44	chr19:42915200-42924400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr19:42915200-42925400	Weak transcription	Stomach Smooth Muscle	stomach
46	chr19:42915200-42925800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr19:42915400-42924000	Weak transcription	Brain Germinal Matrix	brain
48	chr19:42915400-42924200	Weak transcription	NHLF	lung
49	chr19:42915600-42918000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr19:42915600-42918000	Enhancers	Fetal Muscle Leg	muscle

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