Variant report

Variant	esv3421154
Chromosome Location	chr19:55958040-55962238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:196)
CpG islands
(count:185)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:196 , 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	chr19:55959031-55959773	A549	lung:	n/a	n/a
2	BHLHE40	chr19:55958415-55958511	HepG2	liver:	n/a	n/a
3	BHLHE40	chr19:55958359-55959413	K562	blood:	n/a	n/a
4	BHLHE40	chr19:55958540-55959403	A549	lung:	n/a	n/a
5	BRCA1	chr19:55959029-55959096	HepG2	liver:	n/a	n/a
6	BRCA1	chr19:55959180-55959269	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr19:55959332-55960334	K562	blood:	n/a	n/a
8	CBX3	chr19:55959099-55960452	K562	blood:	n/a	n/a
9	CEBPB	chr19:55958938-55959325	A549	lung:	n/a	chr19:55959106-55959119
10	CEBPB	chr19:55959084-55959150	K562	blood:	n/a	chr19:55959106-55959119
11	CEBPB	chr19:55958956-55959275	Hela-S3	cervix:	n/a	chr19:55959106-55959119
12	CEBPB	chr19:55959055-55959186	HepG2	liver:	n/a	chr19:55959106-55959119
13	CHD2	chr19:55958940-55959070	HepG2	liver:	n/a	n/a
14	CTCF	chr19:55959180-55959330	BE2_C	brain:	n/a	chr19:55959318-55959327
15	CTCF	chr19:55959220-55959370	HRE	kidney:	n/a	chr19:55959318-55959327
16	CTCF	chr19:55959293-55959306	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr19:55959383-55959401	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr19:55959180-55959330	HMF	breast:	n/a	chr19:55959318-55959327
19	CTCF	chr19:55959163-55959363	K562	blood:	n/a	chr19:55959318-55959327
20	CTCF	chr19:55959200-55959350	HEEpiC	esophagus:	n/a	chr19:55959318-55959327
21	CTCF	chr19:55959180-55959330	AG04450	lung:	n/a	chr19:55959318-55959327
22	CTCF	chr19:55959240-55959390	HEK293	kidney:	n/a	chr19:55959318-55959327
23	CTCF	chr19:55959160-55959310	MCF-7	breast:	n/a	n/a
24	CTCF	chr19:55959200-55959350	HMEC	breast:	n/a	chr19:55959318-55959327
25	CTCF	chr19:55959160-55959310	K562	blood:	n/a	n/a
26	CTCF	chr19:55959375-55960379	GM19239	blood:	n/a	n/a
27	CTCF	chr19:55959200-55959350	SAEC	small airway:	n/a	chr19:55959318-55959327
28	CTCF	chr19:55960116-55960175	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr19:55959220-55959370	SK-N-SH_RA	brain:	n/a	chr19:55959318-55959327
30	CTCF	chr19:55959288-55959558	NHEK	skin:	n/a	chr19:55959318-55959327
31	CTCF	chr19:55959240-55959390	HCFaa	heart:	n/a	chr19:55959318-55959327
32	CTCF	chr19:55959140-55959290	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:55959252-55959282	NHEK	skin:	n/a	n/a
34	CTCF	chr19:55959180-55959330	HEEpiC	esophagus:	n/a	chr19:55959318-55959327
35	CTCF	chr19:55959120-55959270	HepG2	liver:	n/a	n/a
36	CTCF	chr19:55959376-55959378	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr19:55959220-55959370	K562	blood:	n/a	chr19:55959318-55959327
38	CTCF	chr19:55959413-55959447	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr19:55959220-55959370	SAEC	small airway:	n/a	chr19:55959318-55959327
40	CTCF	chr19:55959200-55959350	NHEK	skin:	n/a	chr19:55959318-55959327
41	CTCF	chr19:55959200-55959350	NHDF-neo	bronchial:	n/a	chr19:55959318-55959327
42	CTCF	chr19:55959611-55959615	NHEK	skin:	n/a	n/a
43	CTCF	chr19:55959180-55959330	AG09309	skin:	n/a	chr19:55959318-55959327
44	CTCF	chr19:55959200-55959350	BJ	skin:	n/a	chr19:55959318-55959327
45	CTCF	chr19:55959200-55959350	HBMEC	blood vessel:	n/a	chr19:55959318-55959327
46	CTCF	chr19:55959200-55959350	AG04449	skin:	n/a	chr19:55959318-55959327
47	CTCF	chr19:55959260-55959410	HCM	heart:	n/a	chr19:55959318-55959327
48	CTCF	chr19:55959243-55959282	MCF-7	breast:	n/a	n/a
49	CTCF	chr19:55959260-55959410	A549	lung:	n/a	chr19:55959318-55959327
50	CTCF	chr19:55959285-55959306	K562	blood:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:55959105-55959155	U87	brain:	n/a
2	chr19:55960947-55960997	NHDF-neo	bronchial:	n/a
3	chr19:55959105-55959155	U87	brain:	n/a
4	chr19:55960947-55960997	NHDF-neo	bronchial:	n/a
5	chr19:55960947-55960997	HNPCEpiC	eye:	n/a
6	chr19:55960947-55960997	AoSMC	blood vessel:	n/a
7	chr19:55958493-55958543	SK-N-SH	brain:	n/a
8	chr19:55959105-55959155	HUVEC	blood vessel:	n/a
9	chr19:55960947-55960997	U87	brain:	n/a
10	chr19:55960947-55960997	NT2-D1	testis:	n/a
11	chr19:55958493-55958543	HEK293	kidney:	embryo
12	chr19:55959105-55959155	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:55958493-55958543	NHDF-neo	bronchial:	n/a
14	chr19:55960947-55960997	HCPEpiC	choroid plexus:	n/a
15	chr19:55958493-55958543	IMR90	lung:	fetal
16	chr19:55958493-55958543	GM12892	blood:	n/a
17	chr19:55959105-55959155	NHBE	bronchial:	n/a
18	chr19:55960947-55960997	HCM	heart:	n/a
19	chr19:55960947-55960997	ECC-1	luminal epithelium:	n/a
20	chr19:55960947-55960997	CMK	blood:	n/a
21	chr19:55960947-55960997	HepG2	liver:	n/a
22	chr19:55959105-55959155	HEEpiC	esophagus:	n/a
23	chr19:55958493-55958543	MCF10A-Er-Src	breast:	n/a
24	chr19:55958493-55958543	GM19239	blood:	n/a
25	chr19:55958493-55958543	RPTEC	kidney:	n/a
26	chr19:55959105-55959155	AG09319	gingival:	n/a
27	chr19:55960947-55960997	HRE	kidney:	n/a
28	chr19:55960947-55960997	NH-A	brain:	n/a
29	chr19:55959105-55959155	HCF	heart:	n/a
30	chr19:55958493-55958543	AG04450	lung:	fetal
31	chr19:55959105-55959155	NT2-D1	testis:	n/a
32	chr19:55960947-55960997	NHBE	bronchial:	n/a
33	chr19:55960947-55960997	HRPEpiC	eye:	n/a
34	chr19:55960947-55960997	K562	blood:	n/a
35	chr19:55958493-55958543	SKMC	muscle:	n/a
36	chr19:55958493-55958543	CMK	blood:	n/a
37	chr19:55960947-55960997	GM12892	blood:	n/a
38	chr19:55959105-55959155	MCF-7	breast:	n/a
39	chr19:55960947-55960997	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:55958493-55958543	NT2-D1	testis:	n/a
41	chr19:55959105-55959155	HIPEpiC	eye:	n/a
42	chr19:55959105-55959155	RPTEC	kidney:	n/a
43	chr19:55960947-55960997	T-47D	breast:	n/a
44	chr19:55958493-55958543	HCF	heart:	n/a
45	chr19:55958493-55958543	HCPEpiC	choroid plexus:	n/a
46	chr19:55959105-55959155	T-47D	breast:	n/a
47	chr19:55958493-55958543	NH-A	brain:	n/a
48	chr19:55958493-55958543	H1-hESC	embryonic stem cell:	embryo
49	chr19:55960947-55960997	HEEpiC	esophagus:	n/a
50	chr19:55960947-55960997	HEK293	kidney:	embryo

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:55812869..55814451-chr19:55956440..55958345,2	K562	blood:
2	chr19:55915948..55921315-chr19:55958410..55968133,14	K562	blood:
3	chr19:55954834..55957911-chr19:55959708..55962559,3	K562	blood:
4	chr19:55956258..55958945-chr19:55964103..55966551,2	K562	blood:
5	chr19:55720436..55722894-chr19:55958561..55960707,2	K562	blood:
6	chr19:55897394..55899897-chr19:55955952..55958626,2	K562	blood:
7	chr19:55959145..55962445-chr19:55970867..55973246,4	MCF-7	breast:
8	chr19:55951993..55955744-chr19:55955995..55960866,9	K562	blood:
9	chr19:55917160..55921382-chr19:55952217..55958073,12	K562	blood:
10	chr19:55960899..55962877-chr19:55970190..55972301,2	MCF-7	breast:
11	chr19:55962141..55964199-chr19:55986076..55988718,2	K562	blood:
12	chr19:55961478..55964648-chr19:56109524..56113001,4	K562	blood:
13	chr19:55917232..55920888-chr19:55959942..55966428,7	K562	blood:
14	chr19:55953882..55955402-chr19:55958561..55961003,2	MCF-7	breast:
15	chr19:55961478..55964648-chr19:56109795..56113001,3	K562	blood:
16	chr19:55951334..55954027-chr19:55956073..55960032,6	K562	blood:
17	chr19:55917660..55921323-chr19:55957478..55961144,4	MCF-7	breast:
18	chr19:55895254..55899821-chr19:55961359..55968155,8	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF628-1	chr19:55959772-55960406	NONHSAT068039
2	lnc-ZNF628-1	chr19:55959329-55959496	NONHSAT068038
3	lnc-ZNF628-1	chr19:55959329-55959496	NONHSAT068039
4	lnc-ZNF628-1	chr19:55959755-55960406	NONHSAT068038

No data

Variant related genes	Relation type
SHISA7	TF binding region
SHISA7	CpG island
ENSG00000080031	chromatin interactions
ENSG00000171443	chromatin interactions
ENSG00000197483	chromatin interactions
ENSG00000187902	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000063241	chromatin interactions
ENSG00000233493	chromatin interactions
ENSG00000269859	chromatin interactions
ENSG00000160469	chromatin interactions
ENSG00000108107	chromatin interactions
ENSG00000179943	chromatin interactions

Extended variants
information (count: 185 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:185 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188265381	chr19:55958119-55958120	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs115504640	chr19:55958158-55958159	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs73606269	chr19:55958173-55958174	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs530920081	chr19:55958223-55958224	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs550727966	chr19:55958226-55958227	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs567396238	chr19:55958261-55958262	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs113642419	chr19:55958285-55958286	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs146377815	chr19:55958327-55958328	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs80224344	chr19:55958334-55958335	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs372703334	chr19:55958388-55958389	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs73057115	chr19:55958470-55958471	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs117834182	chr19:55958483-55958484	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs181190502	chr19:55958497-55958498	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs370379970	chr19:55958507-55958508	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs534556426	chr19:55958513-55958514	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs558026629	chr19:55958540-55958541	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs572517484	chr19:55958766-55958767	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs537025362	chr19:55958822-55958823	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs74891708	chr19:55958845-55958846	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs573741693	chr19:55958884-55958885	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs112943886	chr19:55958905-55958906	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs184137082	chr19:55958943-55958944	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs553556827	chr19:55959080-55959081	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs573472600	chr19:55959105-55959106	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs114801355	chr19:55959106-55959107	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs565551262	chr19:55959120-55959121	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs531133252	chr19:55959124-55959125	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs544562191	chr19:55959144-55959145	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs560957987	chr19:55959158-55959159	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs562099095	chr19:55959202-55959203	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs146894008	chr19:55959228-55959229	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs138739621	chr19:55959248-55959249	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs189612461	chr19:55959267-55959268	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs79291072	chr19:55959305-55959306	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs528271676	chr19:55959328-55959329	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs118102359	chr19:55959364-55959365	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs201460822	chr19:55959399-55959400	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs62128229	chr19:55959402-55959403	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs200079383	chr19:55959410-55959411	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs140334853	chr19:55959411-55959412	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs62128230	chr19:55959415-55959416	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs200900603	chr19:55959427-55959428	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs202115974	chr19:55959436-55959437	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs144230263	chr19:55959438-55959439	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs373294436	chr19:55959440-55959441	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs151313202	chr19:55959443-55959444	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs62128231	chr19:55959498-55959499	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs113346318	chr19:55959509-55959510	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs571488702	chr19:55959523-55959524	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs529956824	chr19:55959530-55959531	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55954200-55962800	Weak transcription	Right Atrium	heart
2	chr19:55955400-55958400	Weak transcription	Brain Anterior Caudate	brain
3	chr19:55955400-55958600	Weak transcription	Brain Substantia Nigra	brain
4	chr19:55956000-55958400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr19:55956600-55958200	Weak transcription	K562	blood
6	chr19:55957000-55958400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr19:55957400-55959600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr19:55957400-55959800	Enhancers	NHEK	skin
9	chr19:55957400-55960200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr19:55957400-55960400	Enhancers	HMEC	breast
11	chr19:55957600-55959600	Enhancers	Esophagus	oesophagus
12	chr19:55957800-55959400	Weak transcription	Pancreas	Pancrea
13	chr19:55957800-55959600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr19:55958200-55960600	Enhancers	K562	blood
15	chr19:55958400-55958600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:55958400-55958800	Enhancers	Brain Cingulate Gyrus	brain
17	chr19:55958400-55959000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr19:55958400-55959200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
19	chr19:55958400-55959200	Enhancers	Brain Anterior Caudate	brain
20	chr19:55958400-55959800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
21	chr19:55958400-55960600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr19:55958400-55960600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr19:55958400-55961000	Enhancers	Brain Hippocampus Middle	brain
24	chr19:55958600-55958800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr19:55958600-55958800	Bivalent Enhancer	Placenta	Placenta
26	chr19:55958600-55958800	Bivalent Enhancer	A549	lung
27	chr19:55958600-55959200	Enhancers	Brain Angular Gyrus	brain
28	chr19:55958600-55959400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr19:55958600-55959400	Enhancers	Right Ventricle	heart
30	chr19:55958600-55959800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr19:55958600-55961400	Enhancers	Brain Substantia Nigra	brain
32	chr19:55958800-55959000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr19:55958800-55959000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr19:55958800-55959000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
35	chr19:55958800-55959400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr19:55958800-55959400	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr19:55958800-55959800	Enhancers	A549	lung
38	chr19:55958800-55961200	Enhancers	Gastric	stomach
39	chr19:55959000-55959200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr19:55959000-55959200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr19:55959000-55959600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr19:55959000-55959600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr19:55959000-55959600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
44	chr19:55959000-55959800	Bivalent Enhancer	Brain Germinal Matrix	brain
45	chr19:55959000-55960200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr19:55959200-55959400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
47	chr19:55959200-55959400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr19:55959200-55959400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr19:55959200-55959400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr19:55959200-55959400	Bivalent Enhancer	Fetal Muscle Leg	muscle

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