Variant report

Variant	nsv1021158
Chromosome Location	chr9:1963930-2040728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1660)
CpG islands
(count:1163)
Chromatin interactive
region (count:49)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2022275-2022865	K562	blood:	n/a	n/a
2	ARID3A	chr9:2015069-2015470	K562	blood:	n/a	n/a
3	ARID3A	chr9:2017419-2017721	K562	blood:	n/a	n/a
4	ARID3A	chr9:2014707-2015574	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:1994315-1994445	HepG2	liver:	n/a	n/a
6	ATF1	chr9:2023624-2023993	K562	blood:	n/a	n/a
7	ATF1	chr9:2014946-2015514	K562	blood:	n/a	n/a
8	ATF2	chr9:2017261-2017815	GM12878	blood:	n/a	n/a
9	ATF2	chr9:2014754-2015575	GM12878	blood:	n/a	n/a
10	ATF2	chr9:2012168-2013278	GM12878	blood:	n/a	n/a
11	ATF2	chr9:2012174-2012977	GM12878	blood:	n/a	n/a
12	ATF2	chr9:2014857-2015545	GM12878	blood:	n/a	n/a
13	ATF3	chr9:1995224-1995511	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr9:2015135-2015500	K562	blood:	n/a	chr9:2015196-2015205
15	ATF3	chr9:2012355-2012584	K562	blood:	n/a	n/a
16	BACH1	chr9:2016857-2018078	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr9:2014722-2015365	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr9:2016045-2016494	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr9:2015202-2015228	K562	blood:	n/a	n/a
20	BATF	chr9:2012130-2012836	GM12878	blood:	n/a	chr9:2012489-2012500 chr9:2012494-2012504
21	BATF	chr9:2015151-2015474	GM12878	blood:	n/a	n/a
22	BATF	chr9:2012231-2012720	GM12878	blood:	n/a	chr9:2012489-2012500 chr9:2012494-2012504
23	BATF	chr9:2015231-2015430	GM12878	blood:	n/a	n/a
24	BATF	chr9:1982196-1982410	GM12878	blood:	n/a	n/a
25	BATF	chr9:2017409-2017661	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:1982176-1982424	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:2018869-2019105	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr9:2017312-2017744	GM12878	blood:	n/a	chr9:2017349-2017358
29	BCL11A	chr9:2012367-2012638	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
30	BCL11A	chr9:1982181-1982398	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:2012252-2012716	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
32	BCL3	chr9:2012231-2012873	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
33	BCLAF1	chr9:2014646-2015806	GM12878	blood:	n/a	chr9:2015637-2015645
34	BCLAF1	chr9:2014700-2015613	GM12878	blood:	n/a	n/a
35	BCLAF1	chr9:2017283-2018180	GM12878	blood:	n/a	chr9:2017349-2017358
36	BCLAF1	chr9:2012177-2012878	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
37	BCLAF1	chr9:2016717-2017208	GM12878	blood:	n/a	chr9:2016939-2016952
38	BCLAF1	chr9:2017258-2017827	GM12878	blood:	n/a	chr9:2017349-2017358
39	BCLAF1	chr9:2012286-2012871	GM12878	blood:	n/a	chr9:2012493-2012502 chr9:2012492-2012501
40	BHLHE40	chr9:2012316-2012820	GM12878	blood:	n/a	n/a
41	BHLHE40	chr9:2014851-2015728	GM12878	blood:	n/a	chr9:2015448-2015464 chr9:2015459-2015475
42	BHLHE40	chr9:2017264-2017750	K562	blood:	n/a	chr9:2017340-2017356 chr9:2017444-2017460
43	BHLHE40	chr9:2017318-2017777	GM12878	blood:	n/a	chr9:2017340-2017356 chr9:2017444-2017460
44	BHLHE40	chr9:2015171-2015516	K562	blood:	n/a	chr9:2015448-2015464 chr9:2015459-2015475
45	BHLHE40	chr9:2016027-2016211	K562	blood:	n/a	n/a
46	BHLHE40	chr9:2014812-2014911	K562	blood:	n/a	n/a
47	BHLHE40	chr9:1979943-1980099	GM12878	blood:	n/a	n/a
48	BHLHE40	chr9:2016473-2017012	GM12878	blood:	n/a	chr9:2016535-2016551 chr9:2016540-2016556
49	BHLHE40	chr9:2025363-2025506	GM12878	blood:	n/a	n/a
50	BHLHE40	chr9:2016705-2016991	K562	blood:	n/a	n/a

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2017576-2017626	SAEC	small airway:	n/a
2	chr9:2016253-2016303	ECC-1	luminal epithelium:	n/a
3	chr9:1979255-1979305	HIPEpiC	eye:	n/a
4	chr9:2015788-2015838	HRCEpiC	kidney:	n/a
5	chr9:2017576-2017626	SAEC	small airway:	n/a
6	chr9:2016253-2016303	ECC-1	luminal epithelium:	n/a
7	chr9:1979255-1979305	HIPEpiC	eye:	n/a
8	chr9:2015788-2015838	HRCEpiC	kidney:	n/a
9	chr9:2015788-2015838	Hepatocyte	liver:	n/a
10	chr9:2017199-2017249	CMK	blood:	n/a
11	chr9:2015635-2015685	MCF10A-Er-Src	breast:	n/a
12	chr9:2018164-2018214	PANC-1	pancreas:	n/a
13	chr9:2018164-2018214	HCT-116	colon:	n/a
14	chr9:2005484-2005534	HRPEpiC	eye:	n/a
15	chr9:2016340-2016390	AG10803	skin:	n/a
16	chr9:1979255-1979305	HRE	kidney:	n/a
17	chr9:2017576-2017626	PFSK-1	brain:	n/a
18	chr9:2016608-2016658	BE2_C	brain:	n/a
19	chr9:2016253-2016303	T-47D	breast:	n/a
20	chr9:2018164-2018214	AG09319	gingival:	n/a
21	chr9:2005484-2005534	LNCaP	prostate:	n/a
22	chr9:1979255-1979305	H1-hESC	embryonic stem cell:	embryo
23	chr9:2017576-2017626	HNPCEpiC	eye:	n/a
24	chr9:2011564-2011614	NH-A	brain:	n/a
25	chr9:2016253-2016303	HCT-116	colon:	n/a
26	chr9:2015064-2015114	AG09319	gingival:	n/a
27	chr9:2015635-2015685	IMR90	lung:	fetal
28	chr9:2016253-2016303	Caco-2	colon:	n/a
29	chr9:2016253-2016303	GM12892	blood:	n/a
30	chr9:1979255-1979305	ovcar-3	ovarian:	n/a
31	chr9:2016608-2016658	AG04449	skin:	fetal
32	chr9:2016253-2016303	HCF	heart:	n/a
33	chr9:2016253-2016303	NHBE	bronchial:	n/a
34	chr9:2015635-2015685	NHDF-neo	bronchial:	n/a
35	chr9:2024387-2024437	GM06990	blood:	n/a
36	chr9:2016253-2016303	SAEC	small airway:	n/a
37	chr9:2024387-2024437	CMK	blood:	n/a
38	chr9:2005484-2005534	GM12891	blood:	n/a
39	chr9:2015039-2015089	PrEC	prostate:	n/a
40	chr9:2017199-2017249	SAEC	small airway:	n/a
41	chr9:2017199-2017249	U87	brain:	n/a
42	chr9:1995528-1995578	AG09309	skin:	n/a
43	chr9:2015788-2015838	ovcar-3	ovarian:	n/a
44	chr9:2024387-2024437	LNCaP	prostate:	n/a
45	chr9:2015039-2015089	AG04450	lung:	fetal
46	chr9:2013970-2014020	HEEpiC	esophagus:	n/a
47	chr9:2015788-2015838	Caco-2	colon:	n/a
48	chr9:2016608-2016658	ECC-1	luminal epithelium:	n/a
49	chr9:2015064-2015114	A549	lung:	n/a
50	chr9:2016608-2016658	HL-60	blood:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2009046..2010738-chr9:2013715..2015276,2	K562	blood:
2	chr9:2035867..2037863-chr9:2040595..2043579,2	MCF-7	breast:
3	chr9:2006922..2009253-chr9:2013169..2015088,2	MCF-7	breast:
4	chr9:2031596..2033809-chr9:2036447..2038109,2	MCF-7	breast:
5	chr9:1989591..1991606-chr9:2004303..2006836,2	MCF-7	breast:
6	chr9:2006630..2009336-chr9:2010265..2012993,2	K562	blood:
7	chr9:2025445..2029095-chr9:2029321..2031633,5	K562	blood:
8	chr9:1981753..1984012-chr9:2012148..2014267,2	K562	blood:
9	chr9:2005663..2011672-chr9:2014113..2018965,7	MCF-7	breast:
10	chr14:51410677..51411191-chr9:2017301..2017897,2	Hela-S3	cervix:
11	chr9:2012580..2014743-chr9:2038420..2041072,2	K562	blood:
12	chr9:2016568..2019114-chr9:2030660..2033552,2	MCF-7	breast:
13	chr9:2027542..2030484-chr9:2031269..2033941,3	K562	blood:
14	chr9:2015330..2018297-chr9:2035684..2039047,3	MCF-7	breast:
15	chr9:2006630..2009336-chr9:2010265..2012993,2	K562	blood:
16	chr9:2027542..2030484-chr9:2031269..2033941,3	K562	blood:
17	chr9:2005250..2009172-chr9:2015225..2018704,4	K562	blood:
18	chr9:2016219..2019918-chr9:2022215..2026324,5	MCF-7	breast:
19	chr9:2015057..2017007-chr9:2029405..2032085,2	K562	blood:
20	chr9:2027773..2030143-chr9:2034628..2037514,2	K562	blood:
21	chr9:2015281..2016857-chr9:6006319..6008670,2	K562	blood:
22	chr8:56986335..56987104-chr9:2016512..2017193,2	Hela-S3	cervix:
23	chr9:2009885..2011957-chr9:2013522..2016362,3	K562	blood:
24	chr9:2013479..2017608-chr9:2017826..2022083,7	MCF-7	breast:
25	chr9:2018308..2020609-chr9:2085608..2087272,2	K562	blood:
26	chr9:2009046..2010738-chr9:2013715..2015276,2	K562	blood:
27	chr9:2012580..2014743-chr9:2038420..2041072,2	K562	blood:
28	chr9:2035810..2037705-chr9:2044015..2046964,2	K562	blood:
29	chr9:2035867..2037863-chr9:2040595..2043579,2	MCF-7	breast:
30	chr9:2019942..2022254-chr9:2022481..2024574,2	MCF-7	breast:
31	chr9:2014683..2019202-chr9:2026620..2030174,6	MCF-7	breast:
32	chr6:56407223..56407766-chr9:2014757..2015410,2	NB4	blood:
33	chr9:2016568..2019114-chr9:2030660..2033552,2	MCF-7	breast:
34	chr9:2015290..2017230-chr9:2035454..2037354,2	MCF-7	breast:
35	chr9:2004426..2007121-chr9:2015163..2018162,2	MCF-7	breast:
36	chr9:2006922..2009253-chr9:2013169..2015088,2	MCF-7	breast:
37	chr9:2013479..2017608-chr9:2017826..2022083,7	MCF-7	breast:
38	chr9:2000498..2002228-chr9:2014699..2016855,2	K562	blood:
39	chr9:2019923..2022306-chr9:2028801..2031582,2	K562	blood:
40	chr9:1989591..1991606-chr9:2004303..2006836,2	MCF-7	breast:
41	chr17:41465202..41465809-chr9:2016258..2017217,2	NB4	blood:
42	chr9:2017363..2019516-chr9:2029024..2032521,3	K562	blood:
43	chr9:2030993..2033791-chr9:2034490..2037168,2	K562	blood:
44	chr9:2009959..2012169-chr9:2015635..2018101,3	MCF-7	breast:
45	chr9:1981753..1984012-chr9:2012148..2014267,2	K562	blood:
46	chr9:2014683..2019202-chr9:2026620..2030174,6	MCF-7	breast:
47	chr9:2025406..2027101-chr9:2041465..2044182,2	K562	blood:
48	chr9:2038457..2040329-chr9:2040850..2042831,2	K562	blood:
49	chr9:2019923..2022306-chr9:2028801..2031582,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-8	chr9:1977784-1978547	NONHSAT129981
2	lnc-SMARCA2-4	chr9:2001907-2002409	NONHSAT129982
3	lnc-SMARCA2-3	chr9:2007539-2007793	expReg_chr9_128_+
4	lnc-SMARCA2-4	chr9:2001764-2001896	NONHSAT129982

No data

Variant related genes	Relation type
SMARCA2	TF binding region
ENSG00000224092	TF binding region
SMARCA2	CpG island
ENSG00000224092	CpG island
ENSG00000008988	chromatin interactions
ENSG00000151914	chromatin interactions
ENSG00000263575	chromatin interactions
ENSG00000238650	chromatin interactions
ENSG00000100504	chromatin interactions
ENSG00000183354	chromatin interactions
ENSG00000080503	chromatin interactions
ENSG00000236199	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 3512 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3512 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546345685	chr9:1963939-1963940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182022505	chr9:1963955-1963956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140531704	chr9:1964013-1964014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144273355	chr9:1964019-1964020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185052911	chr9:1964072-1964073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541084111	chr9:1964083-1964084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560966819	chr9:1964087-1964088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548303195	chr9:1964096-1964097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529684570	chr9:1964134-1964135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7864747	chr9:1964166-1964167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569583113	chr9:1964181-1964182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532818568	chr9:1964195-1964196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75139446	chr9:1964231-1964232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565925788	chr9:1964272-1964273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367751911	chr9:1964275-1964276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559993892	chr9:1964318-1964319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189221384	chr9:1964338-1964339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554597144	chr9:1964341-1964342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568237724	chr9:1964389-1964390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537017576	chr9:1964408-1964409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557310626	chr9:1964414-1964415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527613331	chr9:1964420-1964421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181107679	chr9:1964468-1964469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545287118	chr9:1964505-1964506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558936413	chr9:1964595-1964596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76000484	chr9:1964600-1964601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377562671	chr9:1964611-1964612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4014083	chr9:1964614-1964615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560928367	chr9:1964628-1964629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139405579	chr9:1964636-1964637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528023422	chr9:1964644-1964645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548061036	chr9:1964680-1964681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186467049	chr9:1964681-1964682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532050256	chr9:1964698-1964699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376502064	chr9:1964703-1964704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113728875	chr9:1964719-1964720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559621846	chr9:1964742-1964743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528634609	chr9:1964780-1964781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548390834	chr9:1964823-1964824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191698379	chr9:1964830-1964831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144915038	chr9:1964838-1964839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149214616	chr9:1964843-1964844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570818281	chr9:1964858-1964859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182983445	chr9:1964945-1964946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7865747	chr9:1964966-1964967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186203707	chr9:1964971-1964972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534948705	chr9:1964974-1964975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554782208	chr9:1964992-1964993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76164300	chr9:1965002-1965003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543494038	chr9:1965016-1965017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Peripheral t-cell lymphoma	19118030	CNVD

Chromatin state (count:1866 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1960200-1964000	Enhancers	Fetal Lung	lung
2	chr9:1961000-1967400	Weak transcription	Psoas Muscle	Psoas
3	chr9:1963400-1964800	Enhancers	Fetal Stomach	stomach
4	chr9:1966400-1966800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr9:1967800-1968000	Enhancers	Liver	Liver
6	chr9:1968000-1968800	Enhancers	Fetal Muscle Leg	muscle
7	chr9:1968400-1970200	Weak transcription	Liver	Liver
8	chr9:1970200-1970600	Enhancers	Liver	Liver
9	chr9:1970600-1978200	Weak transcription	Liver	Liver
10	chr9:1976800-1977400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr9:1976800-1981400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr9:1977200-1977400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr9:1977200-1977600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:1977200-1979400	Enhancers	Esophagus	oesophagus
15	chr9:1977400-1978000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr9:1977400-1979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr9:1977600-1979000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr9:1977600-1980600	Enhancers	Fetal Stomach	stomach
19	chr9:1977800-1978000	Enhancers	Placenta	Placenta
20	chr9:1977800-1978000	Enhancers	GM12878-XiMat	blood
21	chr9:1978000-1979200	Enhancers	NHDF-Ad	bronchial
22	chr9:1978000-1980200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:1978200-1978400	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr9:1978200-1978800	Enhancers	Fetal Lung	lung
25	chr9:1978200-1979000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:1978200-1979200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:1978200-1979200	Weak transcription	Placenta	Placenta
28	chr9:1978200-1979400	Enhancers	Liver	Liver
29	chr9:1978200-1979600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr9:1978200-1981600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:1978400-1979200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:1978400-1979400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr9:1978400-1979800	Enhancers	Pancreas	Pancrea
34	chr9:1978400-1980000	Enhancers	Ovary	ovary
35	chr9:1978400-1980200	Enhancers	Fetal Muscle Leg	muscle
36	chr9:1978600-1979400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr9:1978600-1980800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr9:1978800-1980000	Enhancers	HepG2	liver
39	chr9:1978800-1980600	Flanking Active TSS	Fetal Lung	lung
40	chr9:1978800-1980600	Enhancers	HMEC	breast
41	chr9:1979000-1979200	Enhancers	Aorta	Aorta
42	chr9:1979000-1979200	Enhancers	Brain Anterior Caudate	brain
43	chr9:1979000-1979600	Enhancers	Fetal Muscle Trunk	muscle
44	chr9:1979000-1980000	Enhancers	Adipose Nuclei	Adipose
45	chr9:1979000-1980200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr9:1979000-1980200	Enhancers	Brain Germinal Matrix	brain
47	chr9:1979000-1980400	Enhancers	Fetal Heart	heart
48	chr9:1979000-1980400	Enhancers	Stomach Smooth Muscle	stomach
49	chr9:1979000-1980400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr9:1979000-1980600	Enhancers	Primary neutrophils fromperipheralblood	blood

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