Variant report

Variant	nsv458582
Chromosome Location	chr19:41449603-41504077
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	ARID3A	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
2	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
3	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
4	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
6	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
7	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
8	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
9	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
10	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
11	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
12	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
13	CEBPB	chr19:41488440-41489019	H1-hESC	embryonic stem cell:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
14	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
15	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
16	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
17	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
18	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
20	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
22	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
23	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
24	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
25	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
26	CEBPD	chr19:41458422-41458815	K562	blood:	n/a	n/a
27	CHD2	chr19:41465957-41466157	K562	blood:	n/a	n/a
28	CREB1	chr19:41468563-41468752	A549	lung:	n/a	n/a
29	CREB1	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr19:41480528-41480773	Fibrobl	skin:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
31	CTCF	chr19:41480520-41480783	GM19240	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
32	CTCF	chr19:41469412-41469457	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr19:41480560-41480710	HBMEC	blood vessel:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
34	CTCF	chr19:41480600-41480750	GM12873	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
35	CTCF	chr19:41480536-41480813	H1-hESC	embryonic stem cell:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
36	CTCF	chr19:41480522-41480770	MCF-7	breast:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
37	CTCF	chr19:41450720-41450870	A549	lung:	n/a	chr19:41450789-41450799 chr19:41450784-41450802 chr19:41450787-41450800
38	CTCF	chr19:41480580-41480730	SAEC	small airway:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
39	CTCF	chr19:41480491-41480800	SK-N-SH_RA	brain:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
40	CTCF	chr19:41480540-41480690	GM12866	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
41	CTCF	chr19:41450208-41450374	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:41483613-41483711	MCF-7	breast:	n/a	n/a
43	CTCF	chr19:41480580-41480730	GM06990	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
44	CTCF	chr19:41480560-41480710	Caco-2	colon:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
45	CTCF	chr19:41480364-41480865	HCT-116	colon:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
46	CTCF	chr19:41480560-41480710	GM12869	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
47	CTCF	chr19:41480540-41480690	BJ	skin:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
48	CTCF	chr19:41480498-41480792	A549	lung:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
49	CTCF	chr19:41480530-41480777	MCF-7	breast:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
50	CTCF	chr19:41480580-41480730	GM12871	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41495942-41495992	HRPEpiC	eye:	n/a
2	chr19:41496043-41496093	AG04450	lung:	fetal
3	chr19:41497222-41497272	HNPCEpiC	eye:	n/a
4	chr19:41495942-41495992	Caco-2	colon:	n/a
5	chr19:41497222-41497272	HEK293	kidney:	embryo
6	chr19:41495942-41495992	CMK	blood:	n/a
7	chr19:41496749-41496799	GM19239	blood:	n/a
8	chr19:41496749-41496799	HNPCEpiC	eye:	n/a
9	chr19:41497222-41497272	HEEpiC	esophagus:	n/a
10	chr19:41496043-41496093	HepG2	liver:	n/a
11	chr19:41496043-41496093	PANC-1	pancreas:	n/a
12	chr19:41495942-41495992	GM06990	blood:	n/a
13	chr19:41496043-41496093	GM06990	blood:	n/a
14	chr19:41497222-41497272	AG04450	lung:	fetal
15	chr19:41496749-41496799	CMK	blood:	n/a
16	chr19:41497222-41497272	T-47D	breast:	n/a
17	chr19:41495942-41495992	HIPEpiC	eye:	n/a
18	chr19:41496043-41496093	HRE	kidney:	n/a
19	chr19:41495942-41495992	SK-N-SH	brain:	n/a
20	chr19:41495942-41495992	MCF-7	breast:	n/a
21	chr19:41496043-41496093	SK-N-MC	brain:	n/a
22	chr19:41496749-41496799	A549	lung:	n/a
23	chr19:41497222-41497272	RPTEC	kidney:	n/a
24	chr19:41497222-41497272	HIPEpiC	eye:	n/a
25	chr19:41496749-41496799	U87	brain:	n/a
26	chr19:41495942-41495992	SK-N-MC	brain:	n/a
27	chr19:41496043-41496093	AG09319	gingival:	n/a
28	chr19:41497222-41497272	HRPEpiC	eye:	n/a
29	chr19:41497222-41497272	HepG2	liver:	n/a
30	chr19:41495942-41495992	HEK293	kidney:	embryo
31	chr19:41497222-41497272	HRCEpiC	kidney:	n/a
32	chr19:41496043-41496093	A549	lung:	n/a
33	chr19:41497222-41497272	Hepatocyte	liver:	n/a
34	chr19:41495942-41495992	HL-60	blood:	n/a
35	chr19:41496749-41496799	ProgFib	skin:	n/a
36	chr19:41497222-41497272	LNCaP	prostate:	n/a
37	chr19:41496749-41496799	SKMC	muscle:	n/a
38	chr19:41496043-41496093	BJ	skin:	n/a
39	chr19:41497222-41497272	PFSK-1	brain:	n/a
40	chr19:41496749-41496799	BJ	skin:	n/a
41	chr19:41496749-41496799	ovcar-3	ovarian:	n/a
42	chr19:41497222-41497272	NHDF-neo	bronchial:	n/a
43	chr19:41495942-41495992	BJ	skin:	n/a
44	chr19:41497222-41497272	MCF10A-Er-Src	breast:	n/a
45	chr19:41496043-41496093	GM19239	blood:	n/a
46	chr19:41496043-41496093	HRPEpiC	eye:	n/a
47	chr19:41497222-41497272	GM06990	blood:	n/a
48	chr19:41496749-41496799	HMEC	breast:	n/a
49	chr19:41495942-41495992	AoSMC	blood vessel:	n/a
50	chr19:41496749-41496799	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
2	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
3	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
4	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
5	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
6	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
7	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
8	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
9	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
10	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
11	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
12	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
13	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
14	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2B6-1	chr19:41493177-41493736	l_1687_chr19:41492503-41503928_testes
2	lnc-CYP2B6-2	chr19:41452252-41452450	ENSG00000269353.1
3	lnc-CYP2B6-2	chr19:41453006-41453355	ENSG00000269353.1
4	lnc-CYP2B6-1	chr19:41503762-41503928	l_1687_chr19:41492503-41503928_testes
5	lnc-CYP2B6-1	chr19:41493956-41494534	l_1687_chr19:41492503-41503928_testes
6	lnc-CYP2B6-1	chr19:41492504-41492600	l_1687_chr19:41492503-41503928_testes
7	lnc-CYP2B6-1	chr19:41495264-41495408	l_1687_chr19:41492503-41503928_testes

Variant related genes	Relation type
CYP2B6	TF binding region
ENSG00000269353	TF binding region
CYP2B7P	TF binding region
CYP2B6	CpG island
ENSG00000269353	CpG island
CYP2B7P	CpG island

Extended variants
information (count: 1985 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1985 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4124633	chr19:41449603-41449604	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141208568	chr19:41449627-41449628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565647874	chr19:41449631-41449632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369907109	chr19:41449657-41449658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527593504	chr19:41449727-41449728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190605846	chr19:41449745-41449746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560742286	chr19:41449769-41449770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181713892	chr19:41449820-41449821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112735272	chr19:41449824-41449825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372217638	chr19:41449841-41449842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571368494	chr19:41449857-41449858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533341261	chr19:41449889-41449890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185974238	chr19:41449913-41449914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs3852875	chr19:41449922-41449923	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566780502	chr19:41449928-41449929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188731302	chr19:41449962-41449963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568672068	chr19:41449979-41449980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555309317	chr19:41449990-41449991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569883348	chr19:41449993-41449994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561947664	chr19:41450016-41450017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567535837	chr19:41450079-41450080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538264288	chr19:41450088-41450089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148893750	chr19:41450096-41450097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555817104	chr19:41450108-41450109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181108879	chr19:41450121-41450122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531082032	chr19:41450172-41450173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554011946	chr19:41450179-41450180	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs572342246	chr19:41450211-41450212	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs542957879	chr19:41450218-41450219	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs541163241	chr19:41450219-41450220	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs561265893	chr19:41450263-41450264	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs114966387	chr19:41450272-41450273	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs543447254	chr19:41450275-41450276	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567948411	chr19:41450278-41450279	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186096524	chr19:41450287-41450288	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs190966934	chr19:41450288-41450289	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs375806976	chr19:41450292-41450293	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs182789621	chr19:41450300-41450301	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs534746119	chr19:41450332-41450333	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs143613710	chr19:41450351-41450352	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs549388317	chr19:41450364-41450365	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs567993541	chr19:41450379-41450380	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs73557121	chr19:41450403-41450404	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs148021275	chr19:41450434-41450435	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs571721690	chr19:41450439-41450440	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs34102690	chr19:41450523-41450524	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs539157850	chr19:41450554-41450555	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs553974834	chr19:41450555-41450556	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs112899021	chr19:41450573-41450574	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs572252204	chr19:41450577-41450578	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41442400-41451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:41442600-41450200	Weak transcription	Lung	lung
3	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
4	chr19:41445400-41450200	Weak transcription	Fetal Intestine Small	intestine
5	chr19:41449600-41451800	Strong transcription	Liver	Liver
6	chr19:41450200-41450400	Bivalent Enhancer	Esophagus	oesophagus
7	chr19:41450200-41450600	ZNF genes & repeats	Lung	lung
8	chr19:41450200-41450800	Strong transcription	Fetal Intestine Small	intestine
9	chr19:41450800-41451800	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr19:41451400-41451800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:41451400-41452200	Flanking Active TSS	K562	blood
12	chr19:41451800-41452200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr19:41451800-41455200	Weak transcription	Liver	Liver
14	chr19:41451800-41456200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr19:41451800-41456200	Weak transcription	Fetal Intestine Small	intestine
16	chr19:41452200-41452400	Enhancers	K562	blood
17	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
18	chr19:41456200-41456400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
20	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
21	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
23	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
24	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
25	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
26	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
27	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:41465400-41465800	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr19:41465400-41466000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr19:41465800-41466000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:41465800-41466000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
32	chr19:41465800-41466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
34	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
35	chr19:41466000-41466200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr19:41466000-41466200	Bivalent Enhancer	Adipose Nuclei	Adipose
37	chr19:41466000-41466200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:41466200-41466600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
39	chr19:41466200-41466600	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr19:41466200-41466800	Enhancers	Adipose Nuclei	Adipose
41	chr19:41466200-41469800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr19:41466200-41469800	Enhancers	Ovary	ovary
43	chr19:41466400-41466600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr19:41466400-41466800	Enhancers	Fetal Intestine Large	intestine
45	chr19:41466400-41466800	Enhancers	Fetal Intestine Small	intestine
46	chr19:41466600-41468000	Weak transcription	Esophagus	oesophagus
47	chr19:41466800-41467000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr19:41466800-41467000	Bivalent Enhancer	A549	lung
49	chr19:41466800-41467200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
50	chr19:41466800-41468000	Weak transcription	Adipose Nuclei	Adipose

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