Variant report

Variant	esv3430671
Chromosome Location	chr19:45147612-45149810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr19:45146679-45148185	A549	lung:	n/a	chr19:45147570-45147583 chr19:45147200-45147209 chr19:45147572-45147581 chr19:45147569-45147582
2	BCL3	chr19:45146754-45147958	A549	lung:	n/a	chr19:45147570-45147583 chr19:45147200-45147209 chr19:45147572-45147581 chr19:45147569-45147582
3	BRCA1	chr19:45147697-45147861	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr19:45148016-45148023	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr19:45146500-45148251	IMR90	lung:	n/a	n/a
6	CREB1	chr19:45147522-45148029	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr19:45146652-45148107	HepG2	liver:	n/a	n/a
8	CREB1	chr19:45146771-45148000	A549	lung:	n/a	n/a
9	CREB1	chr19:45147641-45147904	A549	lung:	n/a	n/a
10	CTBP2	chr19:45146913-45147958	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr19:45147560-45147710	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr19:45147817-45147911	MCF-7	breast:	n/a	n/a
13	CTCF	chr19:45147843-45147965	MCF-7	breast:	n/a	n/a
14	CTCF	chr19:45147580-45147730	Caco-2	colon:	n/a	n/a
15	E2F6	chr19:45146772-45148055	H1-hESC	embryonic stem cell:	n/a	chr19:45147125-45147134 chr19:45147131-45147140 chr19:45147136-45147151 chr19:45147137-45147149
16	E2F6	chr19:45147538-45148045	H1-hESC	embryonic stem cell:	n/a	n/a
17	E2F6	chr19:45147812-45147925	K562	blood:	n/a	n/a
18	E2F6	chr19:45147536-45147707	K562	blood:	n/a	n/a
19	E2F6	chr19:45146839-45147740	A549	lung:	n/a	chr19:45147125-45147134 chr19:45147131-45147140 chr19:45147136-45147151 chr19:45147137-45147149
20	E2F6	chr19:45146559-45148071	A549	lung:	n/a	chr19:45147125-45147134 chr19:45147131-45147140 chr19:45147136-45147151 chr19:45147137-45147149
21	ELF1	chr19:45146763-45148031	A549	lung:	n/a	n/a
22	EP300	chr19:45146481-45148133	A549	lung:	n/a	chr19:45147338-45147347
23	EP300	chr19:45146707-45148143	A549	lung:	n/a	chr19:45147338-45147347
24	EP300	chr19:45146965-45148202	ECC-1	luminal epithelium:	n/a	chr19:45147338-45147347
25	ETS1	chr19:45146727-45147974	A549	lung:	n/a	n/a
26	FOS	chr19:45147693-45147949	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr19:45147659-45147991	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr19:45147670-45147991	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr19:45147651-45147999	MCF10A-Er-Src	breast:	n/a	n/a
30	FOSL2	chr19:45146616-45148066	A549	lung:	n/a	chr19:45147271-45147280
31	GATA3	chr19:45146580-45148224	A549	lung:	n/a	n/a
32	GTF2F1	chr19:45147741-45147766	H1-hESC	embryonic stem cell:	n/a	n/a
33	HEY1	chr19:45147523-45147982	HepG2	liver:	n/a	chr19:45147568-45147583 chr19:45147569-45147584
34	JUN	chr19:45147770-45147970	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUND	chr19:45146645-45148069	A549	lung:	n/a	chr19:45147271-45147280
36	JUND	chr19:45147645-45147900	H1-hESC	embryonic stem cell:	n/a	n/a
37	JUND	chr19:45147728-45147961	HepG2	liver:	n/a	n/a
38	JUND	chr19:45147643-45147977	H1-hESC	embryonic stem cell:	n/a	n/a
39	KAP1	chr19:45147648-45148007	U2OS	brain:	n/a	n/a
40	KAP1	chr19:45146796-45148055	HEK293	kidney:	n/a	n/a
41	MAX	chr19:45146787-45148083	ECC-1	luminal epithelium:	n/a	n/a
42	MAX	chr19:45146951-45148055	NB4	blood:	n/a	n/a
43	MAX	chr19:45146646-45147997	HepG2	liver:	n/a	n/a
44	MAX	chr19:45146853-45148030	SK-N-SH	brain:	n/a	n/a
45	MAX	chr19:45146646-45148171	HCT-116	colon:	n/a	n/a
46	MAX	chr19:45146504-45148200	A549	lung:	n/a	n/a
47	MAX	chr19:45146810-45148120	MCF-7	breast:	n/a	n/a
48	MAX	chr19:45146593-45148159	A549	lung:	n/a	n/a
49	MAX	chr19:45146622-45148176	HepG2	liver:	n/a	n/a
50	MAX	chr19:45146690-45148158	ECC-1	luminal epithelium:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45147715-45147765	GM06990	blood:	n/a
2	chr19:45147715-45147765	HNPCEpiC	eye:	n/a
3	chr19:45147715-45147765	Hepatocyte	liver:	n/a
4	chr19:45147715-45147765	HCT-116	colon:	n/a
5	chr19:45147715-45147765	NT2-D1	testis:	n/a
6	chr19:45147715-45147765	NH-A	brain:	n/a
7	chr19:45147715-45147765	MCF10A-Er-Src	breast:	n/a
8	chr19:45147715-45147765	CMK	blood:	n/a
9	chr19:45147715-45147765	IMR90	lung:	fetal
10	chr19:45147715-45147765	ECC-1	luminal epithelium:	n/a
11	chr19:45147715-45147765	GM19239	blood:	n/a
12	chr19:45147715-45147765	HCPEpiC	choroid plexus:	n/a
13	chr19:45147715-45147765	BE2_C	brain:	n/a
14	chr19:45147715-45147765	NHBE	bronchial:	n/a
15	chr19:45147715-45147765	HMEC	breast:	n/a
16	chr19:45147715-45147765	Jurkat	blood:	n/a
17	chr19:45147715-45147765	PFSK-1	brain:	n/a
18	chr19:45147715-45147765	AG09309	skin:	n/a
19	chr19:45147715-45147765	HepG2	liver:	n/a
20	chr19:45147715-45147765	K562	blood:	n/a
21	chr19:45147715-45147765	AG10803	skin:	n/a
22	chr19:45147715-45147765	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:45147715-45147765	SKMC	muscle:	n/a
24	chr19:45147715-45147765	A549	lung:	n/a
25	chr19:45147715-45147765	LNCaP	prostate:	n/a
26	chr19:45147715-45147765	GM12892	blood:	n/a
27	chr19:45147715-45147765	U87	brain:	n/a
28	chr19:45147715-45147765	AG04449	skin:	fetal
29	chr19:45147715-45147765	PrEC	prostate:	n/a
30	chr19:45147715-45147765	BJ	skin:	n/a
31	chr19:45147715-45147765	RPTEC	kidney:	n/a
32	chr19:45147715-45147765	AG04450	lung:	fetal
33	chr19:45147715-45147765	SAEC	small airway:	n/a
34	chr19:45147715-45147765	GM12878	blood:	n/a
35	chr19:45147715-45147765	HAEpiC	amniotic membrane:	n/a
36	chr19:45147715-45147765	ovcar-3	ovarian:	n/a
37	chr19:45147715-45147765	HRPEpiC	eye:	n/a
38	chr19:45147715-45147765	NHDF-neo	bronchial:	n/a
39	chr19:45147715-45147765	SK-N-SH_RA	brain:	n/a
40	chr19:45147715-45147765	HL-60	blood:	n/a
41	chr19:45147715-45147765	GM12891	blood:	n/a
42	chr19:45147715-45147765	HIPEpiC	eye:	n/a
43	chr19:45147715-45147765	HRCEpiC	kidney:	n/a
44	chr19:45147715-45147765	Hela-S3	cervix:	n/a
45	chr19:45147715-45147765	HCM	heart:	n/a
46	chr19:45147715-45147765	NB4	blood:	n/a
47	chr19:45147715-45147765	HCF	heart:	n/a
48	chr19:45147715-45147765	HUVEC	blood vessel:	n/a
49	chr19:45147715-45147765	Caco-2	colon:	n/a
50	chr19:45147715-45147765	H1-hESC	embryonic stem cell:	embryo

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81686687..81687304-chr19:45147100..45147918,2	Hela-S3	cervix:
2	chr19:44258125..44259814-chr19:45145810..45147652,2	MCF-7	breast:
3	chr19:45149403..45152148-chr19:45154474..45156366,2	K562	blood:
4	chr19:45147274..45147946-chr3:101568067..101568848,2	Hela-S3	cervix:
5	chr19:45146195..45148606-chr19:45175248..45176784,2	MCF-7	breast:
6	chr19:45147094..45148808-chr19:45149467..45152344,2	MCF-7	breast:
7	chr19:45149710..45152694-chr19:45240654..45242344,2	MCF-7	breast:
8	chr19:45148126..45150959-chr19:45153045..45156023,2	K562	blood:

No data

Variant related genes	Relation type
PVR	TF binding region
PVR	CpG island
ENSG00000105771	chromatin interactions
ENSG00000186567	chromatin interactions
ENSG00000073008	chromatin interactions
ENSG00000144802	chromatin interactions
ENSG00000165417	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573497914	chr19:45147616-45147617	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs377093980	chr19:45147686-45147687	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs562146780	chr19:45147705-45147706	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs10426401	chr19:45147719-45147720	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs544311749	chr19:45147720-45147721	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs536823151	chr19:45147745-45147746	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs139223077	chr19:45147768-45147769	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs533132038	chr19:45147784-45147785	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs546631637	chr19:45147791-45147792	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs559597721	chr19:45147836-45147837	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs556747279	chr19:45147838-45147839	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs528381229	chr19:45147855-45147856	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548328813	chr19:45147864-45147865	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs568177534	chr19:45147872-45147873	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs116753796	chr19:45147912-45147913	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs144071531	chr19:45147976-45147977	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150985779	chr19:45147992-45147993	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11362724	chr19:45148020-45148021	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs574192982	chr19:45148021-45148022	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs398034756	chr19:45148036-45148037	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112403827	chr19:45148039-45148040	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539429175	chr19:45148046-45148047	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs11360299	chr19:45148054-45148055	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190775300	chr19:45148089-45148090	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567106634	chr19:45148110-45148111	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547819052	chr19:45148118-45148119	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555892628	chr19:45148120-45148121	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575768284	chr19:45148121-45148122	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533976680	chr19:45148138-45148139	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs373060085	chr19:45148152-45148153	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs557812755	chr19:45148180-45148181	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs577764197	chr19:45148181-45148182	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140877007	chr19:45148227-45148228	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181878326	chr19:45148235-45148236	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201537825	chr19:45148306-45148307	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs367653685	chr19:45148351-45148352	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs372903613	chr19:45148352-45148353	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375843957	chr19:45148356-45148357	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs200193491	chr19:45148359-45148360	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs199959385	chr19:45148365-45148366	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs61145656	chr19:45148370-45148371	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs203705	chr19:45148405-45148406	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs139484678	chr19:45148417-45148418	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs144207587	chr19:45148418-45148419	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs12976059	chr19:45148428-45148429	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs368486294	chr19:45148432-45148433	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368011348	chr19:45148433-45148434	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs371873500	chr19:45148437-45148438	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs12976066	chr19:45148438-45148439	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs77915132	chr19:45148442-45148443	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Adrenocortical carcinoma	18281524	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45146600-45147800	Active TSS	Brain Hippocampus Middle	brain
2	chr19:45146600-45148200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr19:45146600-45148200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr19:45146600-45148200	Active TSS	Liver	Liver
5	chr19:45146600-45148200	Active TSS	Brain Cingulate Gyrus	brain
6	chr19:45146600-45148200	Active TSS	Rectal Smooth Muscle	rectum
7	chr19:45146600-45148400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr19:45146600-45148800	Active TSS	Psoas Muscle	Psoas
9	chr19:45146600-45148800	Active TSS	NH-A	brain
10	chr19:45146600-45149200	Active TSS	Osteobl	bone
11	chr19:45146800-45147800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
12	chr19:45146800-45147800	Active TSS	Thymus	Thymus
13	chr19:45146800-45148000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:45146800-45148000	Active TSS	Fetal Heart	heart
15	chr19:45146800-45148000	Active TSS	Gastric	stomach
16	chr19:45146800-45148200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr19:45146800-45148200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr19:45146800-45148200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr19:45146800-45148200	Active TSS	H9 Cell Line	embryonic stem cell
20	chr19:45146800-45148200	Active TSS	Primary T cells from cord blood	blood
21	chr19:45146800-45148200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:45146800-45148200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr19:45146800-45148200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
24	chr19:45146800-45148200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr19:45146800-45148200	Active TSS	Brain Angular Gyrus	brain
26	chr19:45146800-45148200	Active TSS	Brain Anterior Caudate	brain
27	chr19:45146800-45148200	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr19:45146800-45148200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr19:45146800-45148200	Active TSS	Fetal Brain Female	brain
30	chr19:45146800-45148200	Active TSS	Fetal Kidney	kidney
31	chr19:45146800-45148200	Active TSS	Fetal Lung	lung
32	chr19:45146800-45148200	Active TSS	Left Ventricle	heart
33	chr19:45146800-45148200	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr19:45146800-45148200	Active TSS	HSMM	muscle
35	chr19:45146800-45149200	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr19:45146800-45149200	Active TSS	A549	lung
37	chr19:45146800-45149200	Active TSS	Hela-S3	cervix
38	chr19:45147000-45147800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr19:45147000-45147800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr19:45147000-45147800	Bivalent/Poised TSS	Fetal Thymus	thymus
41	chr19:45147000-45147800	Active TSS	Lung	lung
42	chr19:45147000-45147800	Active TSS	K562	blood
43	chr19:45147000-45148000	Active TSS	Aorta	Aorta
44	chr19:45147000-45148000	Active TSS	Placenta Amnion	Placenta Amnion
45	chr19:45147000-45148000	Active TSS	Sigmoid Colon	Sigmoid Colon
46	chr19:45147000-45148000	Bivalent/Poised TSS	Small Intestine	intestine
47	chr19:45147000-45148000	Active TSS	GM12878-XiMat	blood
48	chr19:45147000-45148200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr19:45147000-45148200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr19:45147000-45148200	Active TSS	HUES48 Cell Line	embryonic stem cell

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