Variant report

Variant	nsv931600
Chromosome Location	chr1:103548397-104161031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2200)
CpG islands
(count:2017)
Chromatin interactive
region (count:22)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
3	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
4	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
6	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
7	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
8	ATF2	chr1:103715902-103716238	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
10	ATF2	chr1:103715934-103716328	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
12	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
13	BACH1	chr1:103574145-103574516	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
15	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
16	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
17	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
18	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
26	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
27	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
28	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
29	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
30	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
31	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
32	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
33	CEBPB	chr1:104109287-104109643	HepG2	liver:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
34	CEBPB	chr1:103916506-103916758	A549	lung:	n/a	chr1:103916605-103916616
35	CEBPB	chr1:104033510-104033840	IMR90	lung:	n/a	chr1:104033682-104033693
36	CEBPB	chr1:103588958-103589267	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:103695681-103695931	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:104032481-104033124	IMR90	lung:	n/a	chr1:104032645-104032656
39	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
40	CEBPB	chr1:104059336-104059587	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:103569154-103569455	IMR90	lung:	n/a	chr1:103569302-103569311 chr1:103569300-103569311 chr1:103569300-103569313
42	CEBPB	chr1:103749780-103749805	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr1:103660413-103660527	A549	lung:	n/a	n/a
44	CEBPB	chr1:103913925-103914207	A549	lung:	n/a	n/a
45	CEBPB	chr1:103621055-103621263	HepG2	liver:	n/a	chr1:103621118-103621129
46	CEBPB	chr1:104109313-104109613	A549	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
47	CEBPB	chr1:103583757-103584128	A549	lung:	n/a	chr1:103583818-103583829
48	CEBPB	chr1:103662890-103663267	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:103636149-103636512	HepG2	liver:	n/a	chr1:103636327-103636340 chr1:103636329-103636338 chr1:103636329-103636338 chr1:103636329-103636338 chr1:103636378-103636391 chr1:103636328-103636339
50	CEBPB	chr1:104031127-104031327	K562	blood:	n/a	n/a

(count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:103574958-103575008	NHDF-neo	bronchial:	n/a
2	chr1:103572615-103572665	HAEpiC	amniotic membrane:	n/a
3	chr1:104068301-104068351	GM12891	blood:	n/a
4	chr1:104096621-104096671	HCF	heart:	n/a
5	chr1:103574958-103575008	NHDF-neo	bronchial:	n/a
6	chr1:103572615-103572665	HAEpiC	amniotic membrane:	n/a
7	chr1:104068301-104068351	GM12891	blood:	n/a
8	chr1:104096621-104096671	HCF	heart:	n/a
9	chr1:104068118-104068168	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:104065263-104065313	HEK293	kidney:	embryo
11	chr1:104068490-104068540	HEK293	kidney:	embryo
12	chr1:104068490-104068540	NB4	blood:	n/a
13	chr1:104065263-104065313	AG09319	gingival:	n/a
14	chr1:104112143-104112193	PFSK-1	brain:	n/a
15	chr1:104097670-104097720	LNCaP	prostate:	n/a
16	chr1:104068567-104068617	MCF-7	breast:	n/a
17	chr1:103574532-103574582	IMR90	lung:	fetal
18	chr1:104068490-104068540	SK-N-SH	brain:	n/a
19	chr1:103574532-103574582	SK-N-SH_RA	brain:	n/a
20	chr1:104068419-104068469	HCM	heart:	n/a
21	chr1:104113061-104113111	AG09309	skin:	n/a
22	chr1:104113061-104113111	PrEC	prostate:	n/a
23	chr1:104068121-104068171	SK-N-SH_RA	brain:	n/a
24	chr1:104068704-104068754	NT2-D1	testis:	n/a
25	chr1:104068664-104068714	SK-N-SH_RA	brain:	n/a
26	chr1:103574619-103574669	SKMC	muscle:	n/a
27	chr1:104112143-104112193	HEK293	kidney:	embryo
28	chr1:103572723-103572773	AG10803	skin:	n/a
29	chr1:104096621-104096671	HMEC	breast:	n/a
30	chr1:103572723-103572773	SK-N-MC	brain:	n/a
31	chr1:104068704-104068754	A549	lung:	n/a
32	chr1:104068704-104068754	IMR90	lung:	fetal
33	chr1:103574523-103574573	GM12892	blood:	n/a
34	chr1:104068603-104068653	LNCaP	prostate:	n/a
35	chr1:104068419-104068469	AG04450	lung:	fetal
36	chr1:104068490-104068540	HCPEpiC	choroid plexus:	n/a
37	chr1:103572723-103572773	RPTEC	kidney:	n/a
38	chr1:104068488-104068538	CMK	blood:	n/a
39	chr1:104111877-104111927	HCM	heart:	n/a
40	chr1:104113061-104113111	K562	blood:	n/a
41	chr1:104112143-104112193	MCF-7	breast:	n/a
42	chr1:103573989-103574039	NT2-D1	testis:	n/a
43	chr1:104068490-104068540	HNPCEpiC	eye:	n/a
44	chr1:103573772-103573822	PANC-1	pancreas:	n/a
45	chr1:104096621-104096671	H1-hESC	embryonic stem cell:	embryo
46	chr1:103574619-103574669	LNCaP	prostate:	n/a
47	chr1:104068121-104068171	NH-A	brain:	n/a
48	chr1:104112143-104112193	HL-60	blood:	n/a
49	chr1:104068490-104068540	HepG2	liver:	n/a
50	chr1:104065263-104065313	GM19239	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
2	chr1:103571462..103572103-chr1:104003560..104004261,2	MCF-7	breast:
3	chr1:103571876..103572435-chr1:104003675..104004308,2	MCF-7	breast:
4	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
5	chr1:104067350..104071361-chr1:104071688..104074634,4	K562	blood:
6	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:
7	chr1:103571876..103572435-chr1:104003675..104004308,2	MCF-7	breast:
8	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
9	chr1:103782068..103783588-chr9:68418092..68420757,2	K562	blood:
10	chr1:104067752..104069863-chr1:104085885..104087467,2	MCF-7	breast:
11	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
12	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
13	chr1:103571462..103572103-chr1:104003560..104004261,2	MCF-7	breast:
14	chr1:103546900..103548973-chr1:103549511..103551130,2	K562	blood:
15	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
16	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
17	chr1:104067221..104069850-chr1:104074751..104077723,3	MCF-7	breast:
18	chr1:104084688..104087612-chr1:104092885..104095420,2	K562	blood:
19	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
20	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
21	chr1:104067350..104070075-chr1:104070516..104073483,5	K562	blood:
22	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNPC3-8	chr1:103600583-103600943	NONHSAT004882
2	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
3	lnc-AMY1B-1	chr1:103971909-103971995	ENSG00000224613.2
4	lnc-AMY1B-1	chr1:104011964-104012014	XLOC_000945
5	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
6	lnc-AMY1B-1	chr1:103961376-103961437	ENSG00000224613.2
7	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
8	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
9	lnc-COL11A1-2	chr1:103608369-103608574	NONHSAT004884
10	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
11	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
12	lnc-RNPC3-1	chr1:103957501-103957557	XLOC_000325
13	lnc-RNPC3-8	chr1:103590357-103590413	NONHSAT004882
14	lnc-COL11A1-2	chr1:103604765-103604851	NONHSAT004884
15	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
16	lnc-RNPC3-7	chr1:103740315-103740675	NONHSAT004885
17	lnc-RNPC3-2	chr1:103817769-103817825	XLOC_000324
18	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
19	lnc-AMY1B-1	chr1:103832177-103832263	XLOC_000945
20	lnc-AMY1B-1	chr1:103835781-103835986	XLOC_000945
21	lnc-AMY1B-1	chr1:103961376-103961437	XLOC_000945
22	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
23	lnc-AMY1B-1	chr1:103961391-103961437	XLOC_000945
24	lnc-AMY1B-1	chr1:103975513-103975718	ENSG00000224613.2
25	lnc-COL11A1-2	chr1:103594232-103594293	NONHSAT004884
26	lnc-AMY1B-1	chr1:103820969-103821114	XLOC_000945
27	lnc-AMY1B-1	chr1:104011964-104012012	ENSG00000224613.2
28	lnc-AMY1B-1	chr1:103821659-103821705	XLOC_000945
29	lnc-AMY1B-1	chr1:103832177-103832263	XLOC_000945
30	lnc-AMY1B-1	chr1:103835781-103835986	XLOC_000945
31	lnc-RNPC3-7	chr1:103730089-103730145	NONHSAT004885
32	lnc-AMY1B-1	chr1:103971909-103971995	XLOC_000945
33	lnc-AMY1B-4	chr1:103565699-103566260	NONHSAT004881
34	lnc-AMY1B-1	chr1:103960701-103960846	XLOC_000945
35	lnc-RNPC3-2	chr1:103827995-103828355	XLOC_000324
36	lnc-AMY1B-1	chr1:103821644-103821705	XLOC_000945
37	lnc-AMY1B-1	chr1:103975600-103975718	XLOC_000945
38	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
39	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893
40	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945
41	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
42	lnc-RNPC3-1	chr1:103967727-103968087	XLOC_000325
43	lnc-AMY1B-1	chr1:103975513-103975718	XLOC_000945

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNPC3	hsa-miR-192-5p	chr1:104096163-104096184

Variant related genes	Relation type
COL11A1	TF binding region
ACTG1P4	TF binding region
SOD2P1	TF binding region
ENSG00000224613	TF binding region
RNPC3	TF binding region
ENSG00000230759	TF binding region
ENSG00000234037	TF binding region
AMY2A	TF binding region
RN7SKP285	TF binding region
ENSG00000232753	TF binding region
AMY2B	TF binding region
COL11A1	CpG island
ACTG1P4	CpG island
SOD2P1	CpG island
ENSG00000224613	CpG island
RNPC3	CpG island
ENSG00000230759	CpG island
ENSG00000234037	CpG island
AMY2A	CpG island
RN7SKP285	CpG island
ENSG00000232753	CpG island
AMY2B	CpG island
ENSG00000224613	chromatin interactions
ENSG00000060718	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000185946	chromatin interactions
ENSG00000240038	chromatin interactions
DYRK2	miRNA target sites
EGLN3	miRNA target sites
EGR2	miRNA target sites
TOMM34	miRNA target sites
EGR1	miRNA target sites
TOM1L2	miRNA target sites
TOMM20	miRNA target sites

Extended variants
information (count: 12209 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:12209 , 50 per page) page: 1 2 3 4 5 6 7 ... 245

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368465064	chr1:103548413-103548414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs56230601	chr1:103548420-103548421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200396868	chr1:103548441-103548442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530441485	chr1:103548461-103548462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139542185	chr1:103548477-103548478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145159429	chr1:103548489-103548490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143159512	chr1:103548496-103548497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11164663	chr1:103548497-103548498	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150090939	chr1:103548505-103548506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369749483	chr1:103548525-103548526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200564243	chr1:103548540-103548541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116458923	chr1:103548555-103548556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369280508	chr1:103548560-103548561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372446406	chr1:103548569-103548570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61817086	chr1:103548677-103548678	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs114694485	chr1:103548734-103548735	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569984314	chr1:103548763-103548764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537431028	chr1:103548774-103548775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138799203	chr1:103548778-103548779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11164664	chr1:103548782-103548783	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574471942	chr1:103548792-103548793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377408824	chr1:103548793-103548794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199745809	chr1:103548798-103548799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200214762	chr1:103548804-103548805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111506935	chr1:103548805-103548806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567408896	chr1:103548819-103548820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541987965	chr1:103548822-103548823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1337183	chr1:103548823-103548824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs3058875	chr1:103548833-103548834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77587366	chr1:103548845-103548846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192830502	chr1:103548862-103548863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185229748	chr1:103548869-103548870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558014287	chr1:103548884-103548885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576003419	chr1:103548922-103548923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75350215	chr1:103548996-103548997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35510340	chr1:103548997-103548998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs3058876	chr1:103548998-103548999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370218895	chr1:103548999-103549000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372223357	chr1:103549000-103549001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369863460	chr1:103549013-103549014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190127466	chr1:103549075-103549076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374050662	chr1:103549086-103549087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372542074	chr1:103549087-103549088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193127529	chr1:103549112-103549113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141196231	chr1:103549182-103549183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573733789	chr1:103549206-103549207	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541668221	chr1:103549235-103549236	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559950882	chr1:103549244-103549245	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4908285	chr1:103549250-103549251	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs575167620	chr1:103549257-103549258	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Multiple myeloma	17550852	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:2464 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103517400-103557200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:103517600-103550800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:103522400-103559000	Weak transcription	HSMM	muscle
4	chr1:103538400-103548600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:103539600-103556600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:103542400-103549600	Weak transcription	Fetal Heart	heart
7	chr1:103544000-103570400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:103544200-103551800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:103545000-103566800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr1:103546200-103556000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:103546600-103549200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:103548000-103564400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:103549200-103550600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:103549600-103550400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:103549800-103550000	Enhancers	Fetal Heart	heart
16	chr1:103549800-103550200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:103549800-103550600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:103550600-103551400	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:103550800-103551000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:103551400-103552000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:103552000-103553000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:103552800-103555600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:103553000-103555200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:103555200-103556400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:103556000-103558000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:103556400-103559200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:103558000-103558400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:103558400-103560200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr1:103559200-103560400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:103560200-103560600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:103560400-103562400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:103560600-103565400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:103562400-103568800	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:103563800-103571400	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr1:103564400-103564800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:103564800-103566000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:103565400-103567200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:103566000-103567400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:103566600-103567200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:103566600-103567200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr1:103566800-103567600	Enhancers	Dnd41	blood
42	chr1:103566800-103571200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr1:103567200-103567400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr1:103567400-103567800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:103567400-103575000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:103567800-103568000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:103568000-103569600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:103568800-103569400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:103569400-103572600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:103569600-103570600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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