Variant report

Variant	nsv828582
Chromosome Location	chr19:51140749-51142731
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	ATF3	chr19:51142439-51142693	K562	blood:	n/a	n/a
2	ATF3	chr19:51142322-51142752	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:51142724-51143397	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr19:51142552-51142628	K562	blood:	n/a	chr19:51142582-51142598
5	CBX3	chr19:51142433-51142844	K562	blood:	n/a	n/a
6	CHD2	chr19:51142434-51142958	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr19:51142476-51142891	K562	blood:	n/a	n/a
8	CREB1	chr19:51142375-51142768	A549	lung:	n/a	n/a
9	ELF1	chr19:51142453-51142637	K562	blood:	n/a	n/a
10	ELF1	chr19:51142503-51142757	A549	lung:	n/a	n/a
11	ELF1	chr19:51142392-51142770	GM12878	blood:	n/a	n/a
12	EP300	chr19:51142637-51142759	K562	blood:	n/a	chr19:51142675-51142689 chr19:51142674-51142688
13	EP300	chr19:51142529-51143032	H1-hESC	embryonic stem cell:	n/a	chr19:51142675-51142689 chr19:51142674-51142688
14	ETS1	chr19:51142429-51142709	GM12878	blood:	n/a	chr19:51142629-51142642 chr19:51142558-51142571 chr19:51142530-51142543 chr19:51142557-51142570
15	ETS1	chr19:51142281-51142822	K562	blood:	n/a	chr19:51142317-51142328 chr19:51142629-51142642 chr19:51142558-51142571 chr19:51142530-51142543 chr19:51142557-51142570
16	ETS1	chr19:51142303-51142867	A549	lung:	n/a	chr19:51142317-51142328 chr19:51142629-51142642 chr19:51142558-51142571 chr19:51142530-51142543 chr19:51142557-51142570
17	ETS1	chr19:51142401-51142803	A549	lung:	n/a	chr19:51142629-51142642 chr19:51142558-51142571 chr19:51142530-51142543 chr19:51142557-51142570
18	ETS1	chr19:51142427-51142690	K562	blood:	n/a	chr19:51142629-51142642 chr19:51142558-51142571 chr19:51142530-51142543 chr19:51142557-51142570
19	GTF2F1	chr19:51142112-51142131	H1-hESC	embryonic stem cell:	n/a	n/a
20	HCFC1	chr19:51142327-51143253	K562	blood:	n/a	n/a
21	HMGN3	chr19:51142300-51143360	K562	blood:	n/a	n/a
22	JUND	chr19:51142517-51142714	K562	blood:	n/a	n/a
23	MAFK	chr19:51142530-51142681	K562	blood:	n/a	n/a
24	MAX	chr19:51142559-51143154	A549	lung:	n/a	chr19:51142879-51142889 chr19:51142879-51142888 chr19:51142874-51142893 chr19:51142879-51142888 chr19:51142878-51142889 chr19:51142877-51142890 chr19:51142878-51142889 chr19:51142878-51142888 chr19:51142880-51142887
25	MAX	chr19:51142716-51143328	K562	blood:	n/a	chr19:51142879-51142889 chr19:51142879-51142888 chr19:51142874-51142893 chr19:51142879-51142888 chr19:51142878-51142889 chr19:51142877-51142890 chr19:51142878-51142889 chr19:51142878-51142888 chr19:51142880-51142887
26	MAX	chr19:51142696-51143342	H1-hESC	embryonic stem cell:	n/a	chr19:51142879-51142889 chr19:51142879-51142888 chr19:51142874-51142893 chr19:51142879-51142888 chr19:51142878-51142889 chr19:51142877-51142890 chr19:51142878-51142889 chr19:51142878-51142888 chr19:51142880-51142887
27	MAZ	chr19:51142368-51143377	K562	blood:	n/a	chr19:51142879-51142889 chr19:51142879-51142888 chr19:51142874-51142893 chr19:51142879-51142888 chr19:51142878-51142889 chr19:51142514-51142524 chr19:51142877-51142890 chr19:51142878-51142889 chr19:51142878-51142888 chr19:51142880-51142887
28	MAZ	chr19:51142254-51143649	IMR90	lung:	n/a	chr19:51142879-51142889 chr19:51142879-51142888 chr19:51142874-51142893 chr19:51142879-51142888 chr19:51142878-51142889 chr19:51142514-51142524 chr19:51142877-51142890 chr19:51142878-51142889 chr19:51142878-51142888 chr19:51142880-51142887
29	MYC	chr19:51142474-51143400	K562	blood:	n/a	chr19:51142879-51142889 chr19:51142879-51142888 chr19:51142874-51142893 chr19:51142879-51142888 chr19:51142878-51142889 chr19:51142514-51142524 chr19:51142877-51142890 chr19:51142878-51142889 chr19:51142878-51142888 chr19:51142880-51142887
30	POLR2A	chr19:51142689-51143389	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr19:51142549-51142645	HUVEC	blood vessel:	n/a	n/a
32	RCOR1	chr19:51142599-51142869	K562	blood:	n/a	n/a
33	RCOR1	chr19:51142584-51142742	K562	blood:	n/a	n/a
34	REST	chr19:51142368-51143231	H1-neurons	neurons:	n/a	chr19:51143025-51143038 chr19:51143153-51143166 chr19:51143013-51143026
35	SIN3A	chr19:51142387-51143383	H1-hESC	embryonic stem cell:	n/a	n/a
36	SIX5	chr19:51142334-51142765	H1-hESC	embryonic stem cell:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
37	SIX5	chr19:51142320-51142786	H1-hESC	embryonic stem cell:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
38	SIX5	chr19:51142424-51142746	GM12878	blood:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
39	SIX5	chr19:51142181-51142991	A549	lung:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
40	SIX5	chr19:51142401-51142771	K562	blood:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
41	SIX5	chr19:51142406-51142722	GM12878	blood:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
42	SIX5	chr19:51142319-51142832	A549	lung:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
43	SIX5	chr19:51142337-51142847	K562	blood:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
44	SIX5	chr19:51142367-51142798	K562	blood:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
45	SIX5	chr19:51142417-51142806	K562	blood:	n/a	chr19:51142557-51142571 chr19:51142559-51142568 chr19:51142561-51142570
46	TAL1	chr19:51142470-51142646	K562	blood:	n/a	n/a
47	TBL1XR1	chr19:51142470-51142756	K562	blood:	n/a	n/a
48	TBL1XR1	chr19:51142521-51142750	K562	blood:	n/a	n/a
49	TBP	chr19:51142693-51142799	K562	blood:	n/a	n/a
50	TCF12	chr19:51142241-51142926	A549	lung:	n/a	chr19:51142852-51142859 chr19:51142472-51142479

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51142285-51142335	Jurkat	blood:	n/a
2	chr19:51141361-51141411	HCM	heart:	n/a
3	chr19:51141269-51141319	H1-hESC	embryonic stem cell:	embryo
4	chr19:51142008-51142058	HNPCEpiC	eye:	n/a
5	chr19:51142580-51142630	BJ	skin:	n/a
6	chr19:51141361-51141411	ECC-1	luminal epithelium:	n/a
7	chr19:51142285-51142335	SKMC	muscle:	n/a
8	chr19:51142613-51142663	RPTEC	kidney:	n/a
9	chr19:51142580-51142630	Hela-S3	cervix:	n/a
10	chr19:51141227-51141277	SK-N-SH	brain:	n/a
11	chr19:51142008-51142058	LNCaP	prostate:	n/a
12	chr19:51142580-51142630	IMR90	lung:	fetal
13	chr19:51142580-51142630	GM06990	blood:	n/a
14	chr19:51142285-51142335	GM12891	blood:	n/a
15	chr19:51142008-51142058	HCM	heart:	n/a
16	chr19:51142285-51142335	HIPEpiC	eye:	n/a
17	chr19:51142613-51142663	HIPEpiC	eye:	n/a
18	chr19:51142285-51142335	PrEC	prostate:	n/a
19	chr19:51142580-51142630	LNCaP	prostate:	n/a
20	chr19:51141227-51141277	HAEpiC	amniotic membrane:	n/a
21	chr19:51142580-51142630	MCF10A-Er-Src	breast:	n/a
22	chr19:51142285-51142335	SAEC	small airway:	n/a
23	chr19:51141413-51141463	NHBE	bronchial:	n/a
24	chr19:51141361-51141411	Hepatocyte	liver:	n/a
25	chr19:51141413-51141463	SK-N-SH	brain:	n/a
26	chr19:51141361-51141411	HUVEC	blood vessel:	n/a
27	chr19:51142613-51142663	NT2-D1	testis:	n/a
28	chr19:51142285-51142335	PFSK-1	brain:	n/a
29	chr19:51142008-51142058	NHBE	bronchial:	n/a
30	chr19:51142008-51142058	HUVEC	blood vessel:	n/a
31	chr19:51142580-51142630	NHBE	bronchial:	n/a
32	chr19:51142008-51142058	HepG2	liver:	n/a
33	chr19:51142008-51142058	HRE	kidney:	n/a
34	chr19:51142375-51142425	Jurkat	blood:	n/a
35	chr19:51141413-51141463	SK-N-SH_RA	brain:	n/a
36	chr19:51142613-51142663	BJ	skin:	n/a
37	chr19:51142613-51142663	HEEpiC	esophagus:	n/a
38	chr19:51142285-51142335	HCM	heart:	n/a
39	chr19:51141361-51141411	H1-hESC	embryonic stem cell:	embryo
40	chr19:51142580-51142630	HepG2	liver:	n/a
41	chr19:51142285-51142335	ovcar-3	ovarian:	n/a
42	chr19:51142008-51142058	NHDF-neo	bronchial:	n/a
43	chr19:51141361-51141411	PrEC	prostate:	n/a
44	chr19:51142580-51142630	ECC-1	luminal epithelium:	n/a
45	chr19:51142375-51142425	U87	brain:	n/a
46	chr19:51141413-51141463	A549	lung:	n/a
47	chr19:51141227-51141277	NT2-D1	testis:	n/a
48	chr19:51141227-51141277	GM06990	blood:	n/a
49	chr19:51141269-51141319	HepG2	liver:	n/a
50	chr19:51142375-51142425	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:51141748..51145368-chr19:51159075..51162375,5	MCF-7	breast:
2	chr19:51140689..51143199-chr19:51151505..51153507,2	K562	blood:
3	chr19:51141693..51144819-chr19:51159818..51163424,3	K562	blood:

Variant related genes	Relation type
SYT3	TF binding region
SYT3	CpG island
ENSG00000235034	chromatin interactions

Extended variants
information (count: 75 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:75 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2287819	chr19:51140752-51140753	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558722980	chr19:51140774-51140775	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs17849192	chr19:51140778-51140779	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532190505	chr19:51140842-51140843	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550819352	chr19:51140889-51140890	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562538795	chr19:51140924-51140925	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs529833697	chr19:51140984-51140985	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548170957	chr19:51141018-51141019	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73592647	chr19:51141175-51141176	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs17849191	chr19:51141202-51141203	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552586708	chr19:51141224-51141225	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571158766	chr19:51141228-51141229	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs114802973	chr19:51141245-51141246	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556354693	chr19:51141259-51141260	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150403351	chr19:51141270-51141271	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535556878	chr19:51141297-51141298	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553893819	chr19:51141323-51141324	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs138126200	chr19:51141326-51141327	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149222566	chr19:51141334-51141335	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145180531	chr19:51141341-51141342	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577086190	chr19:51141361-51141362	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372177543	chr19:51141367-51141368	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs139003155	chr19:51141383-51141384	Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs889135	chr19:51141486-51141487	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs142191616	chr19:51141513-51141514	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116028317	chr19:51141530-51141531	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs146360775	chr19:51141553-51141554	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114483993	chr19:51141578-51141579	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372999523	chr19:51141590-51141591	Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs189046822	chr19:51141602-51141603	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs10414900	chr19:51141603-51141604	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs77100496	chr19:51141604-51141605	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs889134	chr19:51141622-51141623	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs141189481	chr19:51141647-51141648	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370090070	chr19:51141681-51141682	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568433875	chr19:51141724-51141725	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150723734	chr19:51141737-51141738	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536148574	chr19:51141766-51141767	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs139059221	chr19:51141773-51141774	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553832758	chr19:51141807-51141808	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566190978	chr19:51141853-51141854	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs552580349	chr19:51141870-51141871	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs116189824	chr19:51141902-51141903	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577025824	chr19:51141961-51141962	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544524010	chr19:51141964-51141965	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556546858	chr19:51142020-51142021	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs3840925	chr19:51142030-51142031	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs397841638	chr19:51142031-51142032	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199676756	chr19:51142032-51142033	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542081008	chr19:51142048-51142049	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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	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
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
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	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
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51137800-51141200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr19:51138000-51140800	Weak transcription	Brain Angular Gyrus	brain
3	chr19:51138000-51141400	Weak transcription	Brain Hippocampus Middle	brain
4	chr19:51139200-51141400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:51140000-51142200	Weak transcription	Pancreas	Pancrea
6	chr19:51140600-51140800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr19:51140600-51141000	Bivalent Enhancer	Fetal Brain Male	brain
8	chr19:51140600-51141400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr19:51140800-51141000	Enhancers	Brain Angular Gyrus	brain
10	chr19:51140800-51141400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr19:51141000-51141200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
12	chr19:51141000-51141600	Bivalent/Poised TSS	Fetal Brain Female	brain
13	chr19:51141000-51143600	Active TSS	Brain Angular Gyrus	brain
14	chr19:51141200-51141600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
15	chr19:51141200-51141600	Bivalent Enhancer	Fetal Brain Male	brain
16	chr19:51141200-51142000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:51141200-51143600	Active TSS	Brain Cingulate Gyrus	brain
18	chr19:51141400-51142000	Active TSS	Brain Hippocampus Middle	brain
19	chr19:51141400-51142200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr19:51141400-51142200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr19:51141400-51142200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr19:51141400-51143600	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr19:51141600-51141800	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
24	chr19:51141600-51141800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
25	chr19:51141600-51143600	Active TSS	Brain Anterior Caudate	brain
26	chr19:51141600-51143800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr19:51141800-51142000	Bivalent/Poised TSS	Fetal Brain Female	brain
28	chr19:51141800-51142200	Bivalent/Poised TSS	Fetal Brain Male	brain
29	chr19:51141800-51142600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr19:51141800-51142600	Bivalent Enhancer	K562	blood
31	chr19:51141800-51143000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
32	chr19:51141800-51143000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
33	chr19:51142000-51142200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
34	chr19:51142000-51142200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr19:51142000-51142200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
36	chr19:51142000-51142200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr19:51142000-51142200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
38	chr19:51142000-51142200	Bivalent/Poised TSS	Brain Substantia Nigra	brain
39	chr19:51142000-51142400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr19:51142000-51142400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
41	chr19:51142000-51142400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:51142000-51142400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr19:51142000-51142400	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
44	chr19:51142000-51142400	Bivalent Enhancer	A549	lung
45	chr19:51142000-51142600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr19:51142000-51142600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
47	chr19:51142000-51142600	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr19:51142000-51143400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr19:51142200-51142400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
50	chr19:51142200-51142400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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