Variant report

Variant	nsv546690
Chromosome Location	chr1:84562265-84655238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1042)
CpG islands
(count:61)
Chromatin interactive
region (count:47)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:84568896-84569476	K562	blood:	n/a	n/a
2	ARID3A	chr1:84588503-84588838	HepG2	liver:	n/a	n/a
3	ATF1	chr1:84568983-84569442	K562	blood:	n/a	n/a
4	ATF1	chr1:84625274-84625597	K562	blood:	n/a	n/a
5	ATF2	chr1:84618224-84618863	GM12878	blood:	n/a	n/a
6	ATF2	chr1:84569015-84569438	GM12878	blood:	n/a	n/a
7	ATF3	chr1:84568989-84569425	K562	blood:	n/a	n/a
8	ATF3	chr1:84621649-84622441	HCT-116	colon:	n/a	n/a
9	ATF3	chr1:84639743-84640360	A549	lung:	n/a	n/a
10	ATF3	chr1:84569103-84569374	K562	blood:	n/a	n/a
11	BACH1	chr1:84568927-84569534	K562	blood:	n/a	n/a
12	BACH1	chr1:84568830-84569522	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr1:84622058-84622350	GM12878	blood:	n/a	chr1:84622196-84622207
14	BATF	chr1:84618291-84618802	GM12878	blood:	n/a	n/a
15	BATF	chr1:84618271-84618830	GM12878	blood:	n/a	n/a
16	BATF	chr1:84573215-84573613	GM12878	blood:	n/a	chr1:84573424-84573435
17	BATF	chr1:84573219-84573600	GM12878	blood:	n/a	chr1:84573424-84573435
18	BATF	chr1:84569141-84569355	GM12878	blood:	n/a	n/a
19	BATF	chr1:84632577-84632840	GM12878	blood:	n/a	chr1:84632738-84632749
20	BCL11A	chr1:84618300-84618565	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:84618235-84618750	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:84618223-84618787	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:84569016-84569438	K562	blood:	n/a	n/a
24	BHLHE40	chr1:84622132-84622332	A549	lung:	n/a	n/a
25	BRCA1	chr1:84568769-84569351	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr1:84612020-84612700	HCT-116	colon:	n/a	n/a
27	CBX3	chr1:84573647-84573938	K562	blood:	n/a	n/a
28	CBX3	chr1:84621472-84622485	HCT-116	colon:	n/a	n/a
29	CBX3	chr1:84612000-84612544	HCT-116	colon:	n/a	n/a
30	CBX3	chr1:84639712-84640465	HCT-116	colon:	n/a	n/a
31	CBX3	chr1:84609716-84610267	HCT-116	colon:	n/a	n/a
32	CBX3	chr1:84639583-84640587	HCT-116	colon:	n/a	n/a
33	CBX3	chr1:84568973-84569422	K562	blood:	n/a	n/a
34	CBX3	chr1:84621201-84622949	HCT-116	colon:	n/a	chr1:84621269-84621280
35	CBX3	chr1:84565691-84566150	K562	blood:	n/a	n/a
36	CBX3	chr1:84568901-84569481	K562	blood:	n/a	n/a
37	CBX3	chr1:84583514-84583839	HCT-116	colon:	n/a	n/a
38	CCNT2	chr1:84568900-84569348	K562	blood:	n/a	n/a
39	CEBPB	chr1:84641972-84642221	IMR90	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
40	CEBPB	chr1:84583537-84583893	K562	blood:	n/a	n/a
41	CEBPB	chr1:84639922-84640406	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:84596192-84596483	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:84606771-84607494	HCT-116	colon:	n/a	chr1:84607466-84607479 chr1:84607141-84607153 chr1:84607466-84607477
44	CEBPB	chr1:84583536-84583853	K562	blood:	n/a	n/a
45	CEBPB	chr1:84583517-84583893	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr1:84619289-84619449	HepG2	liver:	n/a	chr1:84619337-84619348
47	CEBPB	chr1:84641972-84642191	A549	lung:	n/a	chr1:84642138-84642149 chr1:84642137-84642150
48	CEBPB	chr1:84568814-84569480	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:84569059-84569423	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:84596178-84596498	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84609007-84609057	LNCaP	prostate:	n/a
2	chr1:84609007-84609057	HAEpiC	amniotic membrane:	n/a
3	chr1:84609007-84609057	K562	blood:	n/a
4	chr1:84609007-84609057	PFSK-1	brain:	n/a
5	chr1:84609007-84609057	GM06990	blood:	n/a
6	chr1:84609007-84609057	HMEC	breast:	n/a
7	chr1:84609007-84609057	Hela-S3	cervix:	n/a
8	chr1:84609007-84609057	HepG2	liver:	n/a
9	chr1:84609007-84609057	Caco-2	colon:	n/a
10	chr1:84609007-84609057	NT2-D1	testis:	n/a
11	chr1:84609007-84609057	HCM	heart:	n/a
12	chr1:84609007-84609057	BE2_C	brain:	n/a
13	chr1:84609007-84609057	SK-N-SH_RA	brain:	n/a
14	chr1:84609007-84609057	HCT-116	colon:	n/a
15	chr1:84609007-84609057	RPTEC	kidney:	n/a
16	chr1:84609007-84609057	NHDF-neo	bronchial:	n/a
17	chr1:84609007-84609057	NB4	blood:	n/a
18	chr1:84609007-84609057	MCF10A-Er-Src	breast:	n/a
19	chr1:84609007-84609057	GM12878	blood:	n/a
20	chr1:84609007-84609057	A549	lung:	n/a
21	chr1:84609007-84609057	GM12891	blood:	n/a
22	chr1:84609007-84609057	HL-60	blood:	n/a
23	chr1:84609007-84609057	GM12892	blood:	n/a
24	chr1:84609007-84609057	AG10803	skin:	n/a
25	chr1:84609007-84609057	HRE	kidney:	n/a
26	chr1:84609007-84609057	Jurkat	blood:	n/a
27	chr1:84609007-84609057	AG09319	gingival:	n/a
28	chr1:84609007-84609057	IMR90	lung:	fetal
29	chr1:84609007-84609057	NH-A	brain:	n/a
30	chr1:84609007-84609057	BJ	skin:	n/a
31	chr1:84609007-84609057	HRPEpiC	eye:	n/a
32	chr1:84609007-84609057	T-47D	breast:	n/a
33	chr1:84609007-84609057	PrEC	prostate:	n/a
34	chr1:84609007-84609057	GM19239	blood:	n/a
35	chr1:84609007-84609057	AG04449	skin:	fetal
36	chr1:84609007-84609057	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:84609007-84609057	HNPCEpiC	eye:	n/a
38	chr1:84609007-84609057	AoSMC	blood vessel:	n/a
39	chr1:84609007-84609057	MCF-7	breast:	n/a
40	chr1:84609007-84609057	AG09309	skin:	n/a
41	chr1:84609007-84609057	SKMC	muscle:	n/a
42	chr1:84609007-84609057	PANC-1	pancreas:	n/a
43	chr1:84609007-84609057	ECC-1	luminal epithelium:	n/a
44	chr1:84609007-84609057	HUVEC	blood vessel:	n/a
45	chr1:84609007-84609057	U87	brain:	n/a
46	chr1:84609007-84609057	SK-N-SH	brain:	n/a
47	chr1:84609007-84609057	Hepatocyte	liver:	n/a
48	chr1:84609007-84609057	NHBE	bronchial:	n/a
49	chr1:84609007-84609057	HCPEpiC	choroid plexus:	n/a
50	chr1:84609007-84609057	CMK	blood:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84373495..84376180-chr1:84584057..84587374,3	K562	blood:
2	chr1:84596861..84598405-chr1:84603464..84605048,2	K562	blood:
3	chr1:84542019..84545394-chr1:84564150..84567617,5	K562	blood:
4	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
5	chr1:84541330..84545077-chr1:84567686..84570781,4	K562	blood:
6	chr1:84594754..84597545-chr1:84597865..84602064,4	K562	blood:
7	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
8	chr1:84642752..84644786-chr1:84646959..84648659,2	K562	blood:
9	chr1:84536131..84538617-chr1:84567747..84570815,3	K562	blood:
10	chr1:84577775..84580533-chr1:84581972..84584955,2	K562	blood:
11	chr1:84594754..84597545-chr1:84597865..84602064,4	K562	blood:
12	chr1:84577775..84580533-chr1:84581972..84584955,2	K562	blood:
13	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
14	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
15	chr1:84563814..84566575-chr1:84567797..84569864,2	K562	blood:
16	chr1:84463824..84465552-chr1:84584447..84586130,2	MCF-7	breast:
17	chr1:84539350..84542065-chr1:84568304..84570726,2	K562	blood:
18	chr1:84633326..84635826-chr1:84640053..84642677,3	K562	blood:
19	chr1:84370472..84371650-chr1:84588196..84589156,3	K562	blood:
20	chr1:84397009..84398516-chr1:84587647..84589545,7	K562	blood:
21	chr1:84545204..84547427-chr1:84607809..84609728,2	K562	blood:
22	chr1:84546484..84549256-chr1:84565111..84567143,2	K562	blood:
23	chr1:84563814..84566575-chr1:84567797..84569864,2	K562	blood:
24	chr1:84553847..84557736-chr1:84560723..84565476,4	K562	blood:
25	chr1:84606589..84609383-chr1:85086485..85089260,2	MCF-7	breast:
26	chr1:84547756..84549761-chr1:84565111..84567613,2	K562	blood:
27	chr1:84542584..84544583-chr1:84564103..84567078,2	MCF-7	breast:
28	chr1:84628795..84632177-chr1:84635427..84638265,3	K562	blood:
29	chr1:84596861..84598405-chr1:84603464..84605048,2	K562	blood:
30	chr1:84549529..84551692-chr1:84562263..84565321,3	K562	blood:
31	chr1:84587966..84589963-chr1:84603179..84604852,2	K562	blood:
32	chr1:84619466..84621949-chr1:84622598..84626604,3	K562	blood:
33	chr1:84587966..84589963-chr1:84603179..84604852,2	K562	blood:
34	chr1:78469054..78471731-chr1:84565810..84568656,2	K562	blood:
35	chr1:84554743..84559247-chr1:84561300..84565476,7	K562	blood:
36	chr1:84606626..84607485-chr1:85006757..85007586,2	MCF-7	breast:
37	chr1:84633326..84636042-chr1:84640053..84642677,3	K562	blood:
38	chr1:84606627..84607493-chr1:84899132..84900125,4	MCF-7	breast:
39	chr1:84397099..84398235-chr1:84588137..84589156,6	MCF-7	breast:
40	chr1:84547425..84549381-chr1:84569524..84571663,2	K562	blood:
41	chr1:84639501..84640001-chr11:32381239..32382124,2	MCF-7	breast:
42	chr1:84542674..84544962-chr1:84565037..84567617,2	K562	blood:
43	chr1:84559252..84561971-chr1:84565558..84569310,4	K562	blood:
44	chr1:84541371..84543109-chr1:84583953..84586517,2	K562	blood:
45	chr1:84639020..84640539-chr1:84647151..84649519,2	MCF-7	breast:
46	chr1:84397136..84397730-chr1:84588264..84588912,2	MCF-7	breast:
47	chr1:84540791..84543154-chr1:84633401..84635166,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD13-1	chr1:84641482-84641490	NONHSAT004190
2	lnc-SAMD13-1	chr1:84644860-84644903	NONHSAT004190
3	lnc-SAMD13-1	chr1:84639013-84639035	NONHSAT004191
4	lnc-SAMD13-1	chr1:84630580-84630696	NONHSAT004190
5	lnc-SAMD13-1	chr1:84644860-84644921	NONHSAT004188
6	lnc-SAMD13-1	chr1:84640717-84640739	NONHSAT004191
7	lnc-SAMD13-1	chr1:84644861-84644903	NONHSAT004191
8	lnc-SAMD13-1	chr1:84630581-84630696	NONHSAT004191
9	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004188
10	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004188
11	lnc-SAMD13-1	chr1:84640716-84640739	NONHSAT004190
12	lnc-SAMD13-1	chr1:84630387-84630696	NONHSAT004188
13	lnc-SAMD13-1	chr1:84639012-84639035	NONHSAT004190

No data

Variant related genes	Relation type
PRKACB	TF binding region
PRKACB	CpG island
ENSG00000273338	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000271576	chromatin interactions
ENSG00000137941	chromatin interactions
ENSG00000142875	chromatin interactions
ENSG00000213540	chromatin interactions
GCH1	miRNA target sites
GCFC1	miRNA target sites
GCNT2	miRNA target sites

Extended variants
information (count: 3012 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3012 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10493750	chr1:84562265-84562266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549469035	chr1:84562277-84562278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147643036	chr1:84562316-84562317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17130873	chr1:84562324-84562325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs2812454	chr1:84562341-84562342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs373316658	chr1:84562361-84562362	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530399790	chr1:84562371-84562372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534897812	chr1:84562424-84562425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs28369405	chr1:84562567-84562568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs577328814	chr1:84562578-84562579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550204854	chr1:84562584-84562585	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs539806372	chr1:84562589-84562590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556660531	chr1:84562612-84562613	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs28699348	chr1:84562615-84562616	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114226077	chr1:84562645-84562646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181251077	chr1:84562646-84562647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572271994	chr1:84562738-84562739	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs72711192	chr1:84562805-84562806	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs564392289	chr1:84562820-84562821	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34907024	chr1:84562836-84562837	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532774133	chr1:84562868-84562869	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74685488	chr1:84562900-84562901	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142118999	chr1:84562912-84562913	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370174844	chr1:84562919-84562920	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs186763546	chr1:84562941-84562942	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs35951221	chr1:84562942-84562943	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190705980	chr1:84562972-84562973	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs143316321	chr1:84562992-84562993	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs565750915	chr1:84562997-84562998	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs180725043	chr1:84563009-84563010	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12128677	chr1:84563015-84563016	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535704801	chr1:84563020-84563021	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575637848	chr1:84563022-84563023	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555808690	chr1:84563032-84563033	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571559075	chr1:84563055-84563056	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575854613	chr1:84563080-84563081	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186031958	chr1:84563083-84563084	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs544607854	chr1:84563148-84563149	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs190701431	chr1:84563167-84563168	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570168651	chr1:84563170-84563171	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535592545	chr1:84563199-84563200	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555804349	chr1:84563212-84563213	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574100552	chr1:84563269-84563270	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541187722	chr1:84563283-84563284	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373421316	chr1:84563308-84563309	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183271127	chr1:84563425-84563426	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370966782	chr1:84563452-84563453	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187334342	chr1:84563490-84563491	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543432987	chr1:84563498-84563499	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558191042	chr1:84563509-84563510	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1603 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84545000-84566800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:84545000-84570000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:84545200-84568600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr1:84545800-84568600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr1:84552200-84569000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:84555400-84568400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:84556400-84568400	Weak transcription	Brain Angular Gyrus	brain
8	chr1:84556400-84568400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr1:84556400-84568400	Weak transcription	A549	lung
10	chr1:84556400-84568400	Weak transcription	HSMM	muscle
11	chr1:84556400-84569000	Weak transcription	Left Ventricle	heart
12	chr1:84556600-84566400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:84556600-84566600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr1:84556600-84568600	Weak transcription	Brain Substantia Nigra	brain
15	chr1:84561000-84568600	Weak transcription	Fetal Lung	lung
16	chr1:84562000-84562600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:84562200-84568800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:84562400-84568400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:84562800-84563800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:84563000-84563600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr1:84563600-84563800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:84563600-84565400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:84563800-84564600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:84563800-84569000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:84565400-84567400	Enhancers	Placenta Amnion	Placenta Amnion
26	chr1:84565800-84567000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:84565800-84568000	Enhancers	Fetal Intestine Large	intestine
28	chr1:84566400-84567200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:84566400-84567400	Enhancers	NHEK	skin
30	chr1:84566600-84567200	Enhancers	HMEC	breast
31	chr1:84566600-84567400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:84566600-84567800	Enhancers	Fetal Intestine Small	intestine
33	chr1:84566600-84568600	Enhancers	K562	blood
34	chr1:84566800-84567000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr1:84566800-84567400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:84567000-84567200	Enhancers	Hela-S3	cervix
37	chr1:84567000-84568600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:84567000-84568800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:84567200-84567400	Enhancers	Stomach Mucosa	stomach
40	chr1:84567200-84568400	Weak transcription	Hela-S3	cervix
41	chr1:84567200-84568600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:84567200-84568600	Weak transcription	HMEC	breast
43	chr1:84567400-84567800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:84567400-84568400	Weak transcription	NHEK	skin
45	chr1:84567400-84568600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:84567400-84568600	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr1:84567400-84568600	Weak transcription	Stomach Mucosa	stomach
48	chr1:84567800-84568200	Weak transcription	Fetal Intestine Small	intestine
49	chr1:84567800-84569000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:84568000-84568200	Weak transcription	Fetal Intestine Large	intestine

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