Variant report

Variant	nsv819004
Chromosome Location	chr19:51566937-51569403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:51568081-51568174	K562	blood:	n/a	n/a
2	BACH1	chr19:51567961-51568300	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr19:51567711-51568524	K562	blood:	n/a	n/a
4	CCNT2	chr19:51568048-51568353	K562	blood:	n/a	chr19:51568197-51568206
5	CTCF	chr19:51568480-51568630	HEK293	kidney:	n/a	n/a
6	CTCF	chr19:51568533-51568670	H1-hESC	embryonic stem cell:	n/a	n/a
7	E2F6	chr19:51568139-51568427	K562	blood:	n/a	chr19:51568245-51568254 chr19:51568353-51568362
8	EGR1	chr19:51567948-51568390	ECC-1	luminal epithelium:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
9	EGR1	chr19:51568675-51569163	K562	blood:	n/a	n/a
10	EGR1	chr19:51568692-51569179	K562	blood:	n/a	n/a
11	EGR1	chr19:51567915-51568476	K562	blood:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
12	EGR1	chr19:51567715-51568637	HCT-116	colon:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568484-51568494 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
13	EGR1	chr19:51567907-51568513	ECC-1	luminal epithelium:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568484-51568494 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
14	EGR1	chr19:51567906-51568466	MCF-7	breast:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
15	EGR1	chr19:51568007-51568488	MCF-7	breast:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
16	EGR1	chr19:51567905-51568375	H1-hESC	embryonic stem cell:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
17	EGR1	chr19:51568006-51568414	H1-hESC	embryonic stem cell:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
18	EGR1	chr19:51567768-51568644	HCT-116	colon:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568484-51568494 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
19	EGR1	chr19:51567928-51568531	K562	blood:	n/a	chr19:51568348-51568358 chr19:51568192-51568205 chr19:51568253-51568262 chr19:51568484-51568494 chr19:51568246-51568259 chr19:51568252-51568265 chr19:51568191-51568206 chr19:51568252-51568265 chr19:51568352-51568362 chr19:51568166-51568179 chr19:51568252-51568265
20	ELF1	chr19:51568814-51569186	K562	blood:	n/a	chr19:51568996-51569009
21	ELF1	chr19:51567931-51568617	K562	blood:	n/a	chr19:51568168-51568180
22	ELF1	chr19:51567849-51568602	K562	blood:	n/a	chr19:51568168-51568180
23	ELF1	chr19:51568820-51569139	K562	blood:	n/a	chr19:51568996-51569009
24	EP300	chr19:51568997-51569104	K562	blood:	n/a	n/a
25	EP300	chr19:51568021-51568437	K562	blood:	n/a	n/a
26	HCFC1	chr19:51568039-51568400	K562	blood:	n/a	n/a
27	HDAC2	chr19:51568064-51568429	K562	blood:	n/a	n/a
28	HEY1	chr19:51567923-51568188	K562	blood:	n/a	n/a
29	HMGN3	chr19:51568042-51568652	K562	blood:	n/a	n/a
30	IRF1	chr19:51567953-51568617	K562	blood:	n/a	chr19:51568170-51568184
31	JUND	chr19:51568221-51568523	H1-hESC	embryonic stem cell:	n/a	chr19:51568352-51568361
32	JUND	chr19:51567892-51568470	K562	blood:	n/a	chr19:51568352-51568361
33	MAFK	chr19:51568968-51569001	K562	blood:	n/a	chr19:51568988-51568998 chr19:51568985-51568999 chr19:51568984-51569000
34	MAX	chr19:51568125-51568421	K562	blood:	n/a	chr19:51568164-51568174
35	MAX	chr19:51568024-51568726	H1-hESC	embryonic stem cell:	n/a	chr19:51568164-51568174 chr19:51568483-51568493
36	MAX	chr19:51568006-51568542	K562	blood:	n/a	chr19:51568164-51568174 chr19:51568483-51568493
37	MAX	chr19:51568098-51568457	K562	blood:	n/a	chr19:51568164-51568174
38	MAX	chr19:51568074-51568590	H1-hESC	embryonic stem cell:	n/a	chr19:51568164-51568174 chr19:51568483-51568493
39	MAZ	chr19:51568305-51568342	HepG2	liver:	n/a	n/a
40	MAZ	chr19:51567945-51569315	K562	blood:	n/a	chr19:51568164-51568174 chr19:51568483-51568493
41	MXI1	chr19:51568307-51568664	H1-hESC	embryonic stem cell:	n/a	n/a
42	MYC	chr19:51568079-51568611	K562	blood:	n/a	chr19:51568164-51568174 chr19:51568483-51568493
43	MYC	chr19:51568193-51568310	MCF-7	breast:	n/a	n/a
44	MYC	chr19:51567969-51568788	K562	blood:	n/a	chr19:51568164-51568174 chr19:51568483-51568493
45	MYC	chr19:51568132-51568332	H1-hESC	embryonic stem cell:	n/a	chr19:51568164-51568174
46	MYC	chr19:51568180-51568433	K562	blood:	n/a	n/a
47	NR2F2	chr19:51568065-51568627	MCF-7	breast:	n/a	n/a
48	NR2F2	chr19:51567951-51568959	K562	blood:	n/a	n/a
49	NR2F2	chr19:51567887-51568516	MCF-7	breast:	n/a	n/a
50	NR2F2	chr19:51568049-51568451	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51568863-51568913	HIPEpiC	eye:	n/a
2	chr19:51568918-51568968	CMK	blood:	n/a
3	chr19:51568918-51568968	BJ	skin:	n/a
4	chr19:51569106-51569156	HRCEpiC	kidney:	n/a
5	chr19:51568336-51568386	HEK293	kidney:	embryo
6	chr19:51568918-51568968	PANC-1	pancreas:	n/a
7	chr19:51568523-51568573	HCT-116	colon:	n/a
8	chr19:51567972-51568022	MCF10A-Er-Src	breast:	n/a
9	chr19:51569106-51569156	AG04449	skin:	fetal
10	chr19:51568523-51568573	NHDF-neo	bronchial:	n/a
11	chr19:51568330-51568380	AG10803	skin:	n/a
12	chr19:51569106-51569156	HL-60	blood:	n/a
13	chr19:51568918-51568968	HRCEpiC	kidney:	n/a
14	chr19:51567972-51568022	ECC-1	luminal epithelium:	n/a
15	chr19:51568918-51568968	PrEC	prostate:	n/a
16	chr19:51568330-51568380	AG09309	skin:	n/a
17	chr19:51568330-51568380	HCT-116	colon:	n/a
18	chr19:51568336-51568386	Hela-S3	cervix:	n/a
19	chr19:51569106-51569156	HEK293	kidney:	embryo
20	chr19:51568918-51568968	ovcar-3	ovarian:	n/a
21	chr19:51567972-51568022	GM12892	blood:	n/a
22	chr19:51568260-51568310	ProgFib	skin:	n/a
23	chr19:51569106-51569156	HUVEC	blood vessel:	n/a
24	chr19:51569106-51569156	BJ	skin:	n/a
25	chr19:51568523-51568573	PANC-1	pancreas:	n/a
26	chr19:51568260-51568310	U87	brain:	n/a
27	chr19:51568336-51568386	AG04449	skin:	fetal
28	chr19:51569106-51569156	Caco-2	colon:	n/a
29	chr19:51569106-51569156	NT2-D1	testis:	n/a
30	chr19:51568918-51568968	HRPEpiC	eye:	n/a
31	chr19:51568330-51568380	Hela-S3	cervix:	n/a
32	chr19:51568260-51568310	HRPEpiC	eye:	n/a
33	chr19:51567972-51568022	GM12891	blood:	n/a
34	chr19:51569106-51569156	AG09319	gingival:	n/a
35	chr19:51568523-51568573	IMR90	lung:	fetal
36	chr19:51567972-51568022	GM06990	blood:	n/a
37	chr19:51567972-51568022	Jurkat	blood:	n/a
38	chr19:51568336-51568386	ProgFib	skin:	n/a
39	chr19:51568336-51568386	HepG2	liver:	n/a
40	chr19:51568918-51568968	GM12891	blood:	n/a
41	chr19:51568260-51568310	PrEC	prostate:	n/a
42	chr19:51568260-51568310	HCM	heart:	n/a
43	chr19:51568918-51568968	HRE	kidney:	n/a
44	chr19:51567972-51568022	SK-N-SH_RA	brain:	n/a
45	chr19:51568918-51568968	T-47D	breast:	n/a
46	chr19:51568336-51568386	BJ	skin:	n/a
47	chr19:51568863-51568913	BE2_C	brain:	n/a
48	chr19:51568260-51568310	HEEpiC	esophagus:	n/a
49	chr19:51568863-51568913	HRPEpiC	eye:	n/a
50	chr19:51568336-51568386	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:51553971..51555617-chr19:51568674..51571621,2	MCF-7	breast:
2	chr19:51529957..51532626-chr19:51566053..51568758,2	MCF-7	breast:
3	chr19:51568453..51570056-chr19:51570442..51573390,2	K562	blood:
4	chr19:51569083..51571145-chr19:51594086..51595810,2	K562	blood:
5	chr19:51557988..51559800-chr19:51569078..51571394,2	MCF-7	breast:
6	chr19:51569153..51571193-chr19:51574240..51576462,2	MCF-7	breast:

Variant related genes	Relation type
KLK13	TF binding region
KLK13	CpG island
ENSG00000167757	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2736433	chr19:51566943-51566944	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541477184	chr19:51566972-51566973	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560128724	chr19:51566981-51566982	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571923963	chr19:51566997-51566998	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371627258	chr19:51567018-51567019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375749944	chr19:51567065-51567066	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2736432	chr19:51567089-51567090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2736431	chr19:51567176-51567177	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs141447115	chr19:51567185-51567186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs186456497	chr19:51567186-51567187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562060173	chr19:51567209-51567210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs28714490	chr19:51567220-51567221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs111248011	chr19:51567250-51567251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145176427	chr19:51567274-51567275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566115164	chr19:51567297-51567298	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11665682	chr19:51567310-51567311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs574151560	chr19:51567385-51567386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73049032	chr19:51567393-51567394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs570369404	chr19:51567428-51567429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112725668	chr19:51567429-51567430	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs139007947	chr19:51567442-51567443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140686732	chr19:51567471-51567472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs568140521	chr19:51567518-51567519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186459651	chr19:51567520-51567521	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150455827	chr19:51567542-51567543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572111207	chr19:51567569-51567570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs71358808	chr19:51567576-51567577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs545775057	chr19:51567617-51567618	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558490326	chr19:51567637-51567638	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2691259	chr19:51567650-51567651	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs548681290	chr19:51567667-51567668	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149260623	chr19:51567714-51567715	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs562339970	chr19:51567738-51567739	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564449057	chr19:51567745-51567746	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574397281	chr19:51567766-51567767	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370002183	chr19:51567771-51567772	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542819243	chr19:51567789-51567790	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375790299	chr19:51567795-51567796	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201534765	chr19:51567832-51567833	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191259649	chr19:51567847-51567848	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs183416626	chr19:51567852-51567853	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs73049036	chr19:51567897-51567898	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551334281	chr19:51567947-51567948	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570429341	chr19:51567948-51567949	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531536837	chr19:51567953-51567954	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2736435	chr19:51567975-51567976	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs10500306	chr19:51567990-51567991	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs192951548	chr19:51568021-51568022	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2736434	chr19:51568029-51568030	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs377086447	chr19:51568033-51568034	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51555800-51567800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:51559800-51567800	Weak transcription	HMEC	breast
3	chr19:51565800-51568800	Enhancers	Pancreas	Pancrea
4	chr19:51566800-51567000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr19:51566800-51567200	Enhancers	Esophagus	oesophagus
6	chr19:51566800-51567400	Enhancers	Gastric	stomach
7	chr19:51566800-51567400	Enhancers	Right Ventricle	heart
8	chr19:51567000-51567600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr19:51567000-51568000	Enhancers	Stomach Mucosa	stomach
10	chr19:51567200-51567600	Weak transcription	Esophagus	oesophagus
11	chr19:51567200-51568600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr19:51567400-51567800	Weak transcription	Gastric	stomach
13	chr19:51567400-51567800	Weak transcription	Right Ventricle	heart
14	chr19:51567600-51567800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr19:51567600-51567800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr19:51567600-51567800	Enhancers	Esophagus	oesophagus
17	chr19:51567800-51568000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr19:51567800-51568000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
19	chr19:51567800-51568000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:51567800-51568000	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
21	chr19:51567800-51568000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:51567800-51568000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr19:51567800-51568000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr19:51567800-51568000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr19:51567800-51568000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:51567800-51568000	Flanking Active TSS	Esophagus	oesophagus
27	chr19:51567800-51568000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr19:51567800-51568000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr19:51567800-51568000	Enhancers	Ovary	ovary
30	chr19:51567800-51568000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
31	chr19:51567800-51568000	Enhancers	HMEC	breast
32	chr19:51567800-51568000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
33	chr19:51567800-51568200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:51567800-51568200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr19:51567800-51568200	Flanking Active TSS	K562	blood
36	chr19:51567800-51568400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:51567800-51568400	Active TSS	Right Atrium	heart
38	chr19:51567800-51568400	Bivalent/Poised TSS	NHEK	skin
39	chr19:51567800-51568600	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr19:51567800-51568600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
41	chr19:51567800-51568800	Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr19:51567800-51568800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
43	chr19:51567800-51568800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:51567800-51568800	Active TSS	A549	lung
45	chr19:51567800-51569000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
46	chr19:51567800-51569000	Active TSS	H9 Cell Line	embryonic stem cell
47	chr19:51567800-51569000	Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr19:51567800-51569000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr19:51567800-51569000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr19:51567800-51569000	Enhancers	Gastric	stomach

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