Variant report

Variant	nsv9711
Chromosome Location	chr19:35797190-35805196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:414)
CpG islands
(count:427)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:35797652-35797915	K562	blood:	n/a	n/a
2	ARID3A	chr19:35798744-35798763	K562	blood:	n/a	n/a
3	ARID3A	chr19:35796976-35797365	K562	blood:	n/a	n/a
4	ARID3A	chr19:35800871-35801058	K562	blood:	n/a	n/a
5	ARID3A	chr19:35797054-35797462	HepG2	liver:	n/a	n/a
6	ATF3	chr19:35796689-35797439	K562	blood:	n/a	n/a
7	BACH1	chr19:35797797-35798001	K562	blood:	n/a	n/a
8	BACH1	chr19:35796677-35797295	K562	blood:	n/a	n/a
9	BHLHE40	chr19:35797081-35797422	HepG2	liver:	n/a	chr19:35797257-35797278
10	BHLHE40	chr19:35796796-35797332	K562	blood:	n/a	chr19:35797257-35797278
11	BHLHE40	chr19:35800541-35801165	K562	blood:	n/a	n/a
12	BHLHE40	chr19:35797746-35798081	K562	blood:	n/a	n/a
13	BHLHE40	chr19:35798958-35799074	K562	blood:	n/a	n/a
14	CBX3	chr19:35800783-35801102	K562	blood:	n/a	n/a
15	CBX3	chr19:35800317-35801218	K562	blood:	n/a	n/a
16	CBX3	chr19:35796616-35797462	K562	blood:	n/a	n/a
17	CBX3	chr19:35796457-35798208	K562	blood:	n/a	n/a
18	CCNT2	chr19:35800600-35801108	K562	blood:	n/a	n/a
19	CCNT2	chr19:35796971-35797203	K562	blood:	n/a	n/a
20	CEBPB	chr19:35800464-35800492	IMR90	lung:	n/a	n/a
21	CEBPB	chr19:35800318-35800664	K562	blood:	n/a	n/a
22	CEBPB	chr19:35800410-35800834	K562	blood:	n/a	n/a
23	CEBPB	chr19:35800307-35800639	HepG2	liver:	n/a	n/a
24	CEBPB	chr19:35796896-35797349	K562	blood:	n/a	n/a
25	CEBPB	chr19:35796824-35797218	K562	blood:	n/a	n/a
26	CEBPB	chr19:35797026-35797360	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:35796646-35797378	K562	blood:	n/a	n/a
28	CEBPD	chr19:35796577-35797326	K562	blood:	n/a	n/a
29	CHD2	chr19:35796314-35797335	K562	blood:	n/a	n/a
30	CHD2	chr19:35804517-35804797	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr19:35800447-35801162	K562	blood:	n/a	n/a
32	CTCF	chr19:35797700-35797850	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr19:35797680-35797830	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:35797660-35797810	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr19:35801720-35801870	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr19:35797700-35797850	GM12872	blood:	n/a	n/a
37	CTCF	chr19:35797720-35797870	GM12867	blood:	n/a	n/a
38	CTCF	chr19:35797720-35797870	GM12869	blood:	n/a	n/a
39	CTCF	chr19:35797760-35797910	HVMF	connective:	n/a	n/a
40	CTCF	chr19:35797700-35797850	BJ	skin:	n/a	n/a
41	CTCF	chr19:35797740-35797890	A549	lung:	n/a	n/a
42	CTCF	chr19:35798160-35798310	GM12864	blood:	n/a	n/a
43	CTCF	chr19:35797700-35797850	HL-60	blood:	n/a	n/a
44	CTCF	chr19:35797720-35797870	GM12865	blood:	n/a	n/a
45	CTCF	chr19:35797720-35797870	GM12871	blood:	n/a	n/a
46	CTCF	chr19:35797545-35797947	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr19:35797700-35797850	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:35797654-35797887	GM12891	blood:	n/a	n/a
49	CTCF	chr19:35797706-35797873	GM10248	blood:	n/a	n/a
50	CTCF	chr19:35797672-35797877	GM10266	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35801014-35801064	T-47D	breast:	n/a
2	chr19:35800743-35800793	BJ	skin:	n/a
3	chr19:35801215-35801265	AG04450	lung:	fetal
4	chr19:35800925-35800975	HEEpiC	esophagus:	n/a
5	chr19:35800589-35800639	SAEC	small airway:	n/a
6	chr19:35803340-35803390	Hela-S3	cervix:	n/a
7	chr19:35800743-35800793	PANC-1	pancreas:	n/a
8	chr19:35797954-35798004	K562	blood:	n/a
9	chr19:35801014-35801064	RPTEC	kidney:	n/a
10	chr19:35801014-35801064	SAEC	small airway:	n/a
11	chr19:35801014-35801064	K562	blood:	n/a
12	chr19:35801014-35801064	PANC-1	pancreas:	n/a
13	chr19:35800589-35800639	AG09309	skin:	n/a
14	chr19:35801215-35801265	K562	blood:	n/a
15	chr19:35797954-35798004	HCPEpiC	choroid plexus:	n/a
16	chr19:35801014-35801064	AoSMC	blood vessel:	n/a
17	chr19:35801215-35801265	AG04449	skin:	fetal
18	chr19:35800925-35800975	Hela-S3	cervix:	n/a
19	chr19:35801215-35801265	HRE	kidney:	n/a
20	chr19:35801014-35801064	HepG2	liver:	n/a
21	chr19:35797954-35798004	NT2-D1	testis:	n/a
22	chr19:35800925-35800975	T-47D	breast:	n/a
23	chr19:35800743-35800793	NH-A	brain:	n/a
24	chr19:35803340-35803390	GM19239	blood:	n/a
25	chr19:35800589-35800639	SK-N-SH	brain:	n/a
26	chr19:35800743-35800793	PrEC	prostate:	n/a
27	chr19:35800589-35800639	U87	brain:	n/a
28	chr19:35800589-35800639	HCPEpiC	choroid plexus:	n/a
29	chr19:35801014-35801064	Hela-S3	cervix:	n/a
30	chr19:35801215-35801265	RPTEC	kidney:	n/a
31	chr19:35801014-35801064	NHBE	bronchial:	n/a
32	chr19:35801215-35801265	GM12892	blood:	n/a
33	chr19:35797954-35798004	HEK293	kidney:	embryo
34	chr19:35800925-35800975	MCF-7	breast:	n/a
35	chr19:35800589-35800639	HMEC	breast:	n/a
36	chr19:35801215-35801265	HCT-116	colon:	n/a
37	chr19:35800743-35800793	A549	lung:	n/a
38	chr19:35800743-35800793	HPAEpiC	pulmonary alveolar:	n/a
39	chr19:35801014-35801064	GM06990	blood:	n/a
40	chr19:35801014-35801064	BE2_C	brain:	n/a
41	chr19:35800925-35800975	ECC-1	luminal epithelium:	n/a
42	chr19:35800589-35800639	AG04449	skin:	fetal
43	chr19:35800589-35800639	H1-hESC	embryonic stem cell:	embryo
44	chr19:35803340-35803390	ProgFib	skin:	n/a
45	chr19:35803340-35803390	SAEC	small airway:	n/a
46	chr19:35800743-35800793	HepG2	liver:	n/a
47	chr19:35800589-35800639	SKMC	muscle:	n/a
48	chr19:35800925-35800975	HNPCEpiC	eye:	n/a
49	chr19:35800589-35800639	K562	blood:	n/a
50	chr19:35797954-35798004	Hepatocyte	liver:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35798397..35800415-chr19:35842184..35843828,2	MCF-7	breast:
2	chr19:35646046..35647977-chr19:35796625..35798576,2	K562	blood:
3	chr19:35801054..35803091-chr19:35805182..35806855,2	MCF-7	breast:
4	chr19:35761264..35763399-chr19:35801388..35804082,2	K562	blood:
5	chr19:35778338..35780262-chr19:35804621..35807184,2	MCF-7	breast:
6	chr19:35757193..35760230-chr19:35795583..35800096,4	K562	blood:
7	chr19:35606400..35608352-chr19:35800705..35803047,2	MCF-7	breast:
8	chr19:35796764..35800582-chr19:36132788..36136056,3	K562	blood:
9	chr19:35762096..35762857-chr19:35804524..35805135,2	MCF-7	breast:
10	chr19:35779735..35782128-chr19:35802752..35804567,2	MCF-7	breast:
11	chr19:35797242..35798191-chr19:35843391..35844009,2	MCF-7	breast:
12	chr19:35781735..35783754-chr19:35799663..35801226,2	MCF-7	breast:
13	chr19:35780282..35782569-chr19:35797611..35799728,2	MCF-7	breast:
14	chr19:35794912..35797272-chr19:35941605..35944464,2	MCF-7	breast:
15	chr19:35738491..35740445-chr19:35800431..35803185,3	MCF-7	breast:
16	chr19:35794875..35797641-chr19:35798078..35800124,2	MCF-7	breast:
17	chr19:35794875..35797641-chr19:35798078..35800124,2	MCF-7	breast:
18	chr19:35788326..35791177-chr19:35803354..35807024,3	MCF-7	breast:
19	chr19:35757352..35763490-chr19:35798817..35804347,10	MCF-7	breast:
20	chr19:35760524..35761090-chr19:35804405..35805080,2	MCF-7	breast:
21	chr19:35797829..35800128-chr19:35823862..35825668,2	MCF-7	breast:
22	chr19:35795438..35798240-chr19:35810195..35811788,2	MCF-7	breast:
23	chr19:35759321..35763199-chr19:35795656..35798701,4	MCF-7	breast:
24	chr19:35753841..35756119-chr19:35797821..35799359,2	MCF-7	breast:
25	chr19:35800092..35801659-chr19:35829023..35831587,2	K562	blood:
26	chr19:35757837..35761370-chr19:35793689..35797278,5	MCF-7	breast:
27	chr19:35755149..35764508-chr19:35799437..35813142,44	MCF-7	breast:
28	chr19:35801834..35808584-chr19:35810190..35813576,7	MCF-7	breast:
29	chr19:35738675..35740393-chr19:35799543..35801412,2	MCF-7	breast:
30	chr19:35757351..35762248-chr19:35804679..35808319,5	MCF-7	breast:
31	chr19:35794837..35799903-chr19:35800719..35807404,10	MCF-7	breast:

No data

Variant related genes	Relation type
MAG	TF binding region
CD22	TF binding region
MAG	CpG island
CD22	CpG island
ENSG00000126266	chromatin interactions
ENSG00000105699	chromatin interactions
ENSG00000089356	chromatin interactions
ENSG00000012124	chromatin interactions
ENSG00000105698	chromatin interactions
ENSG00000105672	chromatin interactions
ENSG00000105695	chromatin interactions

Extended variants
information (count: 395 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:395 , 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	rs544015642	chr19:35797273-35797274	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs9304870	chr19:35797281-35797282	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs541966585	chr19:35797337-35797338	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs148925051	chr19:35797407-35797408	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs559833455	chr19:35797414-35797415	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs183317040	chr19:35797429-35797430	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs572511100	chr19:35797545-35797546	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs539814608	chr19:35797550-35797551	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs11879566	chr19:35797588-35797589	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571570969	chr19:35797604-35797605	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs536818400	chr19:35797612-35797613	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs550769882	chr19:35797627-35797628	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs567225778	chr19:35797669-35797670	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs12974702	chr19:35797671-35797672	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs552538922	chr19:35797688-35797689	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs572462557	chr19:35797690-35797691	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs538249249	chr19:35797811-35797812	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs550531117	chr19:35797842-35797843	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs720309	chr19:35797916-35797917	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs578207391	chr19:35797933-35797934	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs77047755	chr19:35797943-35797944	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs720307	chr19:35797951-35797952	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs371395540	chr19:35797959-35797960	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs74842767	chr19:35797966-35797967	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs77076215	chr19:35797973-35797974	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs12185506	chr19:35797980-35797981	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs528450623	chr19:35798027-35798028	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs720308	chr19:35798060-35798061	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs565144944	chr19:35798061-35798062	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs16970204	chr19:35798073-35798074	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs550498001	chr19:35798089-35798090	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs146576632	chr19:35798137-35798138	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs138539777	chr19:35798189-35798190	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs529856174	chr19:35798191-35798192	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs187055187	chr19:35798193-35798194	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs566251334	chr19:35798203-35798204	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs375217812	chr19:35798218-35798219	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs190643790	chr19:35798223-35798224	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs369461003	chr19:35798420-35798421	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs41407744	chr19:35798422-35798423	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs141301170	chr19:35798454-35798455	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs59516638	chr19:35798464-35798465	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs537796787	chr19:35798465-35798466	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs557263721	chr19:35798504-35798505	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs574137222	chr19:35798513-35798514	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs543249117	chr19:35798514-35798515	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs553479241	chr19:35798554-35798555	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs573392867	chr19:35798568-35798569	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs138684764	chr19:35798583-35798584	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs141316819	chr19:35798584-35798585	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 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
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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35774800-35809600	Weak transcription	Right Atrium	heart
2	chr19:35790000-35797800	Weak transcription	Fetal Kidney	kidney
3	chr19:35791400-35798800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr19:35792800-35801400	Genic enhancers	Brain Hippocampus Middle	brain
5	chr19:35794400-35810000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:35794600-35799400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr19:35795000-35797800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr19:35795000-35800400	Enhancers	HepG2	liver
9	chr19:35795200-35798800	Weak transcription	Spleen	Spleen
10	chr19:35796000-35798000	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr19:35796200-35798000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr19:35796200-35799200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:35796200-35799600	Enhancers	Primary B cells from peripheral blood	blood
14	chr19:35796400-35797800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr19:35796400-35798200	Enhancers	Liver	Liver
16	chr19:35796600-35797600	Weak transcription	Brain Angular Gyrus	brain
17	chr19:35796600-35797800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr19:35796800-35797200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr19:35796800-35797200	Enhancers	K562	blood
20	chr19:35796800-35797800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr19:35796800-35797800	Weak transcription	Brain Substantia Nigra	brain
22	chr19:35796800-35800600	Enhancers	Ovary	ovary
23	chr19:35796800-35801000	Weak transcription	Fetal Thymus	thymus
24	chr19:35797000-35797200	Enhancers	Brain Anterior Caudate	brain
25	chr19:35797000-35799000	Enhancers	GM12878-XiMat	blood
26	chr19:35797000-35800800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:35797200-35798400	Flanking Active TSS	K562	blood
28	chr19:35797200-35799400	Enhancers	Primary hematopoietic stem cells	blood
29	chr19:35797200-35800000	Enhancers	Primary B cells from cord blood	blood
30	chr19:35797200-35802200	Weak transcription	Brain Anterior Caudate	brain
31	chr19:35797400-35797600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr19:35797600-35797800	Enhancers	Brain Angular Gyrus	brain
33	chr19:35797600-35804000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr19:35797800-35798000	Genic enhancers	Brain Cingulate Gyrus	brain
35	chr19:35797800-35798200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr19:35797800-35798800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr19:35797800-35799000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr19:35797800-35800000	Enhancers	Fetal Lung	lung
39	chr19:35797800-35800200	Enhancers	Fetal Kidney	kidney
40	chr19:35797800-35800800	Genic enhancers	Brain Substantia Nigra	brain
41	chr19:35797800-35809600	Weak transcription	Brain Angular Gyrus	brain
42	chr19:35798000-35798200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr19:35798000-35798200	Strong transcription	Brain Cingulate Gyrus	brain
44	chr19:35798000-35801400	Enhancers	Fetal Muscle Trunk	muscle
45	chr19:35798000-35801800	Enhancers	Fetal Stomach	stomach
46	chr19:35798000-35802600	Enhancers	Placenta	Placenta
47	chr19:35798200-35799000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr19:35798200-35799200	Weak transcription	Brain Cingulate Gyrus	brain
49	chr19:35798200-35801400	Enhancers	Fetal Muscle Leg	muscle
50	chr19:35798200-35802800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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