Variant report

Variant	nsv911674
Chromosome Location	chr19:39391547-39398631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:305)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:62 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr19:39392305-39392681	K562	blood:	n/a	n/a
2	CEBPB	chr19:39391561-39391868	IMR90	lung:	n/a	chr19:39391678-39391689
3	CEBPB	chr19:39391561-39391867	A549	lung:	n/a	chr19:39391678-39391689
4	CEBPB	chr19:39391532-39391856	K562	blood:	n/a	chr19:39391678-39391689
5	CEBPB	chr19:39391628-39391872	HepG2	liver:	n/a	chr19:39391678-39391689
6	CEBPB	chr19:39395211-39395534	A549	lung:	n/a	n/a
7	CEBPB	chr19:39391727-39391847	HepG2	liver:	n/a	n/a
8	CEBPB	chr19:39391563-39391879	Hela-S3	cervix:	n/a	chr19:39391678-39391689
9	CEBPB	chr19:39395220-39395519	HepG2	liver:	n/a	n/a
10	CEBPB	chr19:39391510-39391882	K562	blood:	n/a	chr19:39391678-39391689
11	CTCF	chr19:39394102-39394145	Kidney_OC	kidney:	n/a	n/a
12	CUX1	chr19:39390999-39391863	K562	blood:	n/a	n/a
13	FOXA1	chr19:39391253-39391870	HepG2	liver:	n/a	n/a
14	FOXA2	chr19:39395276-39395853	A549	lung:	n/a	n/a
15	FOXA2	chr19:39395194-39395795	A549	lung:	n/a	n/a
16	FOXA2	chr19:39395337-39395709	HepG2	liver:	n/a	n/a
17	FOXA2	chr19:39391650-39391843	HepG2	liver:	n/a	n/a
18	GATA1	chr19:39389861-39391860	PBDE	blood:	n/a	chr19:39390295-39390304
19	GATA2	chr19:39391502-39391910	HUVEC	blood vessel:	n/a	n/a
20	GATA2	chr19:39391668-39391857	SH-SY5Y	brain:	n/a	n/a
21	GATA3	chr19:39391205-39391873	SH-SY5Y	brain:	n/a	chr19:39391697-39391705
22	GATA3	chr19:39389595-39391907	A549	lung:	n/a	chr19:39389669-39389679 chr19:39391697-39391705 chr19:39390295-39390304
23	HCFC1	chr19:39389667-39391967	Hela-S3	cervix:	n/a	n/a
24	HDAC2	chr19:39395405-39395635	HepG2	liver:	n/a	n/a
25	HMGN3	chr19:39398139-39398198	K562	blood:	n/a	n/a
26	HNF4G	chr19:39395416-39395770	HepG2	liver:	n/a	chr19:39395619-39395632 chr19:39395509-39395522 chr19:39395614-39395636 chr19:39395510-39395522 chr19:39395619-39395632 chr19:39395507-39395525 chr19:39395510-39395523 chr19:39395619-39395631 chr19:39395618-39395632 chr19:39395510-39395523 chr19:39395617-39395632 chr19:39395509-39395523 chr19:39395617-39395632 chr19:39395618-39395632 chr19:39395619-39395632 chr19:39395510-39395522 chr19:39395619-39395631 chr19:39395625-39395639 chr19:39395617-39395632 chr19:39395618-39395632 chr19:39395619-39395631 chr19:39395618-39395633 chr19:39395510-39395522 chr19:39395616-39395634 chr19:39395510-39395523 chr19:39395618-39395631 chr19:39395510-39395522 chr19:39395619-39395631
27	JUN	chr19:39389766-39391981	K562	blood:	n/a	chr19:39390500-39390509 chr19:39391294-39391306
28	JUND	chr19:39391540-39391734	K562	blood:	n/a	n/a
29	KAP1	chr19:39392310-39392627	K562	blood:	n/a	n/a
30	KAP1	chr19:39389908-39391701	U2OS	brain:	n/a	n/a
31	MAFF	chr19:39395458-39395658	HepG2	liver:	n/a	chr19:39395489-39395507
32	MAFK	chr19:39395510-39395594	HepG2	liver:	n/a	n/a
33	MXI1	chr19:39389394-39391628	SK-N-SH	brain:	n/a	n/a
34	NR2F2	chr19:39395245-39395984	MCF-7	breast:	n/a	n/a
35	NRF1	chr19:39391553-39391712	K562	blood:	n/a	n/a
36	POLR2A	chr19:39398524-39398828	K562	blood:	n/a	n/a
37	POLR2A	chr19:39396209-39396219	A549	lung:	n/a	n/a
38	POLR2A	chr19:39398066-39398222	A549	lung:	n/a	n/a
39	POLR2A	chr19:39398361-39398578	HepG2	liver:	n/a	n/a
40	POLR2A	chr19:39397686-39397741	A549	lung:	n/a	n/a
41	POLR2A	chr19:39398273-39398850	GM12891	blood:	n/a	n/a
42	POLR2A	chr19:39397743-39397917	GM12878	blood:	n/a	n/a
43	POLR2A	chr19:39398297-39398954	GM12878	blood:	n/a	n/a
44	POLR2A	chr19:39397829-39397862	HepG2	liver:	n/a	n/a
45	POLR2A	chr19:39397651-39398078	GM12878	blood:	n/a	n/a
46	POLR2A	chr19:39398051-39398219	A549	lung:	n/a	n/a
47	POLR2A	chr19:39395931-39395956	MCF-7	breast:	n/a	n/a
48	POLR2A	chr19:39398093-39398370	K562	blood:	n/a	n/a
49	POLR2A	chr19:39396556-39396622	A549	lung:	n/a	n/a
50	POLR2A	chr19:39395871-39395928	MCF-7	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39397911-39397961	K562	blood:	n/a
2	chr19:39395717-39395767	NB4	blood:	n/a
3	chr19:39398122-39398172	GM12878	blood:	n/a
4	chr19:39395882-39395932	AoSMC	blood vessel:	n/a
5	chr19:39395882-39395932	PrEC	prostate:	n/a
6	chr19:39393347-39393397	SK-N-SH	brain:	n/a
7	chr19:39398122-39398172	BJ	skin:	n/a
8	chr19:39398122-39398172	AoSMC	blood vessel:	n/a
9	chr19:39397911-39397961	ovcar-3	ovarian:	n/a
10	chr19:39395717-39395767	Caco-2	colon:	n/a
11	chr19:39397911-39397961	SKMC	muscle:	n/a
12	chr19:39393347-39393397	GM12891	blood:	n/a
13	chr19:39395717-39395767	NH-A	brain:	n/a
14	chr19:39397911-39397961	HCF	heart:	n/a
15	chr19:39393347-39393397	HNPCEpiC	eye:	n/a
16	chr19:39395882-39395932	CMK	blood:	n/a
17	chr19:39395882-39395932	Jurkat	blood:	n/a
18	chr19:39395717-39395767	SKMC	muscle:	n/a
19	chr19:39395717-39395767	HUVEC	blood vessel:	n/a
20	chr19:39397911-39397961	HL-60	blood:	n/a
21	chr19:39398122-39398172	SK-N-SH	brain:	n/a
22	chr19:39393347-39393397	AG10803	skin:	n/a
23	chr19:39397911-39397961	NHBE	bronchial:	n/a
24	chr19:39395717-39395767	A549	lung:	n/a
25	chr19:39393347-39393397	AG09319	gingival:	n/a
26	chr19:39395882-39395932	GM19239	blood:	n/a
27	chr19:39393347-39393397	AoSMC	blood vessel:	n/a
28	chr19:39398122-39398172	HRE	kidney:	n/a
29	chr19:39395882-39395932	H1-hESC	embryonic stem cell:	embryo
30	chr19:39395717-39395767	AoSMC	blood vessel:	n/a
31	chr19:39398122-39398172	HMEC	breast:	n/a
32	chr19:39393347-39393397	HCF	heart:	n/a
33	chr19:39395882-39395932	SAEC	small airway:	n/a
34	chr19:39393347-39393397	HMEC	breast:	n/a
35	chr19:39398122-39398172	LNCaP	prostate:	n/a
36	chr19:39398122-39398172	ProgFib	skin:	n/a
37	chr19:39397911-39397961	HRPEpiC	eye:	n/a
38	chr19:39393347-39393397	GM12892	blood:	n/a
39	chr19:39395717-39395767	MCF10A-Er-Src	breast:	n/a
40	chr19:39397911-39397961	AoSMC	blood vessel:	n/a
41	chr19:39398122-39398172	PANC-1	pancreas:	n/a
42	chr19:39395717-39395767	HRPEpiC	eye:	n/a
43	chr19:39393347-39393397	HEK293	kidney:	embryo
44	chr19:39395882-39395932	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:39398122-39398172	NT2-D1	testis:	n/a
46	chr19:39398122-39398172	HRCEpiC	kidney:	n/a
47	chr19:39393347-39393397	PANC-1	pancreas:	n/a
48	chr19:39397911-39397961	U87	brain:	n/a
49	chr19:39397911-39397961	A549	lung:	n/a
50	chr19:39397911-39397961	Caco-2	colon:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39338478..39344219-chr19:39387112..39393304,19	K562	blood:
2	chr19:39398169..39400794-chr19:39403289..39404909,2	MCF-7	breast:
3	chr19:39386472..39392494-chr19:39418718..39424791,9	K562	blood:
4	chr19:39388885..39392214-chr19:39419332..39422757,5	MCF-7	breast:
5	chr19:39390700..39392797-chr19:39401919..39404314,3	K562	blood:
6	chr19:39320984..39323718-chr19:39390338..39392657,3	K562	blood:
7	chr19:39394709..39398675-chr19:39410709..39413256,3	K562	blood:
8	chr19:39337064..39339680-chr19:39397865..39400024,2	K562	blood:
9	chr19:39217426..39220275-chr19:39394811..39396577,2	K562	blood:
10	chr19:39395944..39398654-chr19:39409098..39410676,3	K562	blood:
11	chr19:39391259..39393276-chr19:39393440..39395044,2	MCF-7	breast:
12	chr19:39390131..39392480-chr19:39402477..39404053,2	MCF-7	breast:
13	chr19:39391259..39393276-chr19:39393440..39395044,2	MCF-7	breast:
14	chr19:39388836..39392687-chr19:39409083..39412619,5	K562	blood:
15	chr19:39390244..39393015-chr19:39395233..39398542,3	MCF-7	breast:
16	chr19:39337724..39340689-chr19:39393839..39396661,3	K562	blood:
17	chr19:39394465..39398073-chr19:39398218..39402853,5	MCF-7	breast:
18	chr19:39389410..39392783-chr19:39420988..39423307,4	MCF-7	breast:
19	chr19:39394310..39397205-chr19:39405071..39408067,2	K562	blood:
20	chr19:39388731..39393423-chr19:39394024..39400037,10	K562	blood:
21	chr19:39339924..39344199-chr19:39398243..39400684,3	MCF-7	breast:
22	chr19:39390485..39392144-chr19:39409724..39411734,2	MCF-7	breast:
23	chr19:39338023..39344706-chr19:39388476..39392998,12	MCF-7	breast:
24	chr19:39338733..39343337-chr19:39388774..39392675,12	K562	blood:
25	chr19:39395804..39397367-chr19:39401550..39403461,2	MCF-7	breast:

No data

Variant related genes	Relation type
SIRT2	TF binding region
SIRT2	CpG island
ENSG00000262484	chromatin interactions
ENSG00000104824	chromatin interactions
ENSG00000068903	chromatin interactions
ENSG00000128626	chromatin interactions
ENSG00000104825	chromatin interactions
ENSG00000104835	chromatin interactions
ENSG00000104823	chromatin interactions
ENSG00000130402	chromatin interactions

Extended variants
information (count: 369 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4803006	chr19:39391547-39391548	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370717780	chr19:39391597-39391598	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs367550422	chr19:39391638-39391639	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs200078435	chr19:39391645-39391646	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs201823900	chr19:39391646-39391647	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs10713585	chr19:39391647-39391648	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs113055550	chr19:39391667-39391668	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs17880730	chr19:39391709-39391710	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs17881351	chr19:39391710-39391711	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs570852882	chr19:39391753-39391754	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs539435483	chr19:39391769-39391770	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs566674953	chr19:39391771-39391772	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs12979755	chr19:39391817-39391818	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs17886984	chr19:39391867-39391868	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs371141274	chr19:39391876-39391877	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs35456924	chr19:39391889-39391890	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs189826170	chr19:39391926-39391927	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs574031843	chr19:39391932-39391933	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs148530152	chr19:39391952-39391953	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs57842338	chr19:39391974-39391975	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs557686799	chr19:39391992-39391993	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs575517636	chr19:39392000-39392001	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs545733361	chr19:39392067-39392068	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs564284282	chr19:39392102-39392103	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs73539687	chr19:39392107-39392108	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs572932760	chr19:39392138-39392139	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs115443618	chr19:39392143-39392144	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs79290677	chr19:39392150-39392151	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs371594219	chr19:39392163-39392164	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs183183812	chr19:39392193-39392194	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs536101200	chr19:39392198-39392199	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs555551688	chr19:39392207-39392208	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs561794645	chr19:39392218-39392219	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs528963000	chr19:39392256-39392257	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs550562760	chr19:39392279-39392280	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs562314762	chr19:39392390-39392391	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs576264888	chr19:39392435-39392436	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs533678761	chr19:39392469-39392470	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs17883664	chr19:39392485-39392486	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs566821803	chr19:39392506-39392507	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs534155225	chr19:39392569-39392570	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs549152742	chr19:39392598-39392599	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs146741297	chr19:39392639-39392640	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs555163877	chr19:39392677-39392678	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs139050682	chr19:39392682-39392683	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs17883178	chr19:39392721-39392722	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs74176475	chr19:39392725-39392726	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs56689256	chr19:39392738-39392739	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs577919425	chr19:39392752-39392753	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs539025092	chr19:39392813-39392814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Pleomorphic liposarcoma	18784837	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
Disorders of sex development	21048976	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
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39389200-39391600	Active TSS	NHDF-Ad	bronchial
2	chr19:39389400-39391600	Active TSS	Right Atrium	heart
3	chr19:39389400-39391800	Active TSS	NHLF	lung
4	chr19:39389600-39391600	Active TSS	H9 Cell Line	embryonic stem cell
5	chr19:39389600-39391600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr19:39389600-39391600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr19:39389600-39391600	Active TSS	Ovary	ovary
8	chr19:39389600-39391800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr19:39389600-39391800	Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr19:39389600-39391800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr19:39389600-39391800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr19:39389800-39391600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr19:39389800-39391600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr19:39389800-39391600	Active TSS	Right Ventricle	heart
15	chr19:39389800-39392000	Active TSS	NHEK	skin
16	chr19:39390000-39391600	Active TSS	H1 Cell Line	embryonic stem cell
17	chr19:39390000-39391600	Active TSS	Colonic Mucosa	Colon
18	chr19:39390000-39391600	Active TSS	Fetal Thymus	thymus
19	chr19:39390000-39391600	Active TSS	GM12878-XiMat	blood
20	chr19:39390000-39391800	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr19:39390000-39391800	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr19:39390000-39391800	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr19:39390200-39391600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr19:39390800-39391600	Flanking Active TSS	Primary B cells from cord blood	blood
25	chr19:39390800-39391600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
26	chr19:39390800-39391600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr19:39390800-39391600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr19:39390800-39391800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr19:39390800-39391800	Flanking Active TSS	NH-A	brain
30	chr19:39390800-39391800	Flanking Active TSS	Osteobl	bone
31	chr19:39391000-39391600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr19:39391000-39391600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr19:39391000-39391600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr19:39391000-39391600	Flanking Active TSS	Fetal Lung	lung
35	chr19:39391000-39391600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
36	chr19:39391000-39391800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr19:39391000-39391800	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr19:39391000-39391800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
39	chr19:39391000-39391800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr19:39391000-39391800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr19:39391000-39391800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr19:39391000-39391800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr19:39391000-39391800	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr19:39391000-39391800	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr19:39391000-39391800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr19:39391000-39391800	Enhancers	Placenta Amnion	Placenta Amnion
47	chr19:39391000-39391800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
48	chr19:39391000-39391800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr19:39391000-39392000	Flanking Active TSS	HUVEC	blood vessel
50	chr19:39391000-39394800	Weak transcription	Spleen	Spleen

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