Variant report

Variant	nsv523355
Chromosome Location	chr1:94351328-94385591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:894)
CpG islands
(count:978)
Chromatin interactive
region (count:42)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94375931-94376232	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94374945-94375386	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94374926-94375295	K562	blood:	n/a	n/a
4	ARID3A	chr1:94371189-94371780	HepG2	liver:	n/a	n/a
5	ATF2	chr1:94374831-94375599	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:94375039-94375433	GM12878	blood:	n/a	n/a
7	ATF3	chr1:94374938-94375358	K562	blood:	n/a	chr1:94375165-94375174 chr1:94375190-94375199
8	ATF3	chr1:94374827-94375256	K562	blood:	n/a	chr1:94375165-94375174 chr1:94375190-94375199
9	BACH1	chr1:94354474-94354816	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:94374230-94375589	K562	blood:	n/a	n/a
11	BACH1	chr1:94374217-94375497	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr1:94382913-94383147	GM12878	blood:	n/a	n/a
13	BCL3	chr1:94374857-94375401	GM12878	blood:	n/a	chr1:94375184-94375197 chr1:94374989-94374997 chr1:94375068-94375081 chr1:94374904-94374913 chr1:94374931-94374944 chr1:94374954-94374967 chr1:94375129-94375142 chr1:94374899-94374912
14	BCLAF1	chr1:94374826-94375435	K562	blood:	n/a	chr1:94375184-94375197 chr1:94374989-94374997 chr1:94375068-94375081 chr1:94374904-94374913 chr1:94374931-94374944 chr1:94374836-94374849 chr1:94374954-94374967 chr1:94375129-94375142 chr1:94374899-94374912 chr1:94374842-94374855
15	BCLAF1	chr1:94374802-94375369	K562	blood:	n/a	chr1:94375184-94375197 chr1:94374989-94374997 chr1:94375068-94375081 chr1:94374904-94374913 chr1:94374931-94374944 chr1:94374836-94374849 chr1:94374954-94374967 chr1:94375129-94375142 chr1:94374899-94374912 chr1:94374842-94374855
16	BCLAF1	chr1:94374936-94375451	GM12878	blood:	n/a	chr1:94375184-94375197 chr1:94374989-94374997 chr1:94375068-94375081 chr1:94374954-94374967 chr1:94375129-94375142
17	BCLAF1	chr1:94375020-94375426	GM12878	blood:	n/a	chr1:94375184-94375197 chr1:94375068-94375081 chr1:94375129-94375142
18	BHLHE40	chr1:94374870-94375633	K562	blood:	n/a	chr1:94375066-94375082 chr1:94375191-94375207
19	BHLHE40	chr1:94375009-94375476	GM12878	blood:	n/a	chr1:94375066-94375082 chr1:94375191-94375207
20	BRCA1	chr1:94375004-94375394	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:94374959-94375041	GM12878	blood:	n/a	n/a
22	CBX3	chr1:94374793-94375777	K562	blood:	n/a	n/a
23	CBX3	chr1:94374903-94375344	K562	blood:	n/a	n/a
24	CCNT2	chr1:94374329-94375458	K562	blood:	n/a	chr1:94375075-94375084
25	CEBPB	chr1:94374994-94375418	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:94370963-94371720	HepG2	liver:	n/a	chr1:94371066-94371083
27	CEBPB	chr1:94371382-94371609	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:94374914-94375185	K562	blood:	n/a	n/a
29	CEBPB	chr1:94371414-94371615	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:94375030-94375154	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:94371392-94371664	A549	lung:	n/a	n/a
32	CEBPB	chr1:94374780-94375254	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr1:94370947-94371710	IMR90	lung:	n/a	chr1:94371066-94371083
34	CEBPB	chr1:94370934-94371724	Hela-S3	cervix:	n/a	chr1:94371066-94371083
35	CEBPB	chr1:94374935-94375379	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:94354584-94354784	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:94370954-94371591	K562	blood:	n/a	chr1:94371066-94371083
38	CHD1	chr1:94374837-94375565	GM12878	blood:	n/a	chr1:94375076-94375086
39	CHD1	chr1:94374187-94374327	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr1:94374804-94375272	H1-hESC	embryonic stem cell:	n/a	chr1:94375076-94375086
41	CHD1	chr1:94373019-94376024	IMR90	lung:	n/a	chr1:94375076-94375086
42	CHD2	chr1:94374236-94375394	Hela-S3	cervix:	n/a	chr1:94375076-94375086
43	CHD2	chr1:94374494-94374588	K562	blood:	n/a	n/a
44	CHD2	chr1:94374987-94375733	GM12878	blood:	n/a	chr1:94375076-94375086
45	CHD2	chr1:94374875-94375421	K562	blood:	n/a	chr1:94375076-94375086
46	CHD2	chr1:94375146-94375346	HepG2	liver:	n/a	n/a
47	CHD2	chr1:94374945-94375489	H1-hESC	embryonic stem cell:	n/a	chr1:94375076-94375086
48	CREB1	chr1:94371280-94371637	HepG2	liver:	n/a	n/a
49	CREB1	chr1:94374750-94375487	A549	lung:	n/a	n/a
50	CREB1	chr1:94374835-94375572	GM12878	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94374370-94374420	GM12891	blood:	n/a
2	chr1:94352637-94352687	AG04449	skin:	fetal
3	chr1:94374370-94374420	GM12891	blood:	n/a
4	chr1:94352637-94352687	AG04449	skin:	fetal
5	chr1:94375392-94375442	HL-60	blood:	n/a
6	chr1:94374268-94374318	MCF10A-Er-Src	breast:	n/a
7	chr1:94375159-94375209	HRE	kidney:	n/a
8	chr1:94375517-94375567	HAEpiC	amniotic membrane:	n/a
9	chr1:94375598-94375648	GM12878	blood:	n/a
10	chr1:94385022-94385072	MCF10A-Er-Src	breast:	n/a
11	chr1:94374612-94374662	HCM	heart:	n/a
12	chr1:94385022-94385072	AoSMC	blood vessel:	n/a
13	chr1:94374268-94374318	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:94374268-94374318	GM12892	blood:	n/a
15	chr1:94375027-94375077	NHDF-neo	bronchial:	n/a
16	chr1:94375598-94375648	AG04449	skin:	fetal
17	chr1:94375328-94375378	HCM	heart:	n/a
18	chr1:94374370-94374420	Jurkat	blood:	n/a
19	chr1:94375598-94375648	PANC-1	pancreas:	n/a
20	chr1:94375598-94375648	ECC-1	luminal epithelium:	n/a
21	chr1:94374612-94374662	GM12892	blood:	n/a
22	chr1:94352637-94352687	ProgFib	skin:	n/a
23	chr1:94373434-94373484	HRCEpiC	kidney:	n/a
24	chr1:94375598-94375648	GM06990	blood:	n/a
25	chr1:94375598-94375648	K562	blood:	n/a
26	chr1:94374966-94375016	HCM	heart:	n/a
27	chr1:94374370-94374420	AG09319	gingival:	n/a
28	chr1:94374612-94374662	T-47D	breast:	n/a
29	chr1:94374966-94375016	HRPEpiC	eye:	n/a
30	chr1:94374966-94375016	GM12891	blood:	n/a
31	chr1:94375027-94375077	AG04450	lung:	fetal
32	chr1:94375159-94375209	A549	lung:	n/a
33	chr1:94374966-94375016	HUVEC	blood vessel:	n/a
34	chr1:94375392-94375442	AG04450	lung:	fetal
35	chr1:94375392-94375442	SAEC	small airway:	n/a
36	chr1:94375027-94375077	MCF10A-Er-Src	breast:	n/a
37	chr1:94375246-94375296	NT2-D1	testis:	n/a
38	chr1:94374966-94375016	AG04449	skin:	fetal
39	chr1:94375246-94375296	RPTEC	kidney:	n/a
40	chr1:94352637-94352687	Caco-2	colon:	n/a
41	chr1:94375064-94375114	PrEC	prostate:	n/a
42	chr1:94352637-94352687	NHBE	bronchial:	n/a
43	chr1:94375392-94375442	ECC-1	luminal epithelium:	n/a
44	chr1:94375064-94375114	HepG2	liver:	n/a
45	chr1:94385022-94385072	BJ	skin:	n/a
46	chr1:94375027-94375077	PANC-1	pancreas:	n/a
47	chr1:94375517-94375567	HIPEpiC	eye:	n/a
48	chr1:94375598-94375648	HCT-116	colon:	n/a
49	chr1:94375328-94375378	SKMC	muscle:	n/a
50	chr1:94354654-94354704	GM12878	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:94350854..94353775-chr1:94372233..94374131,2	K562	blood:
2	chr1:94310847..94313357-chr1:94374431..94376609,2	K562	blood:
3	chr1:94343732..94346422-chr1:94366022..94369432,3	MCF-7	breast:
4	chr1:94343582..94346281-chr1:94346551..94353410,8	MCF-7	breast:
5	chr1:94344707..94346290-chr1:94353302..94354969,2	MCF-7	breast:
6	chr1:94349522..94351991-chr1:94354138..94356917,3	K562	blood:
7	chr1:94340990..94343514-chr1:94369991..94373741,3	K562	blood:
8	chr1:94343019..94346037-chr1:94356947..94359226,3	K562	blood:
9	chr1:94375220..94377246-chr1:94405325..94407050,2	MCF-7	breast:
10	chr1:94343372..94347640-chr1:94364498..94367458,3	K562	blood:
11	chr1:94332093..94333597-chr1:94363497..94365167,2	K562	blood:
12	chr1:94346434..94348935-chr1:94356766..94358812,2	K562	blood:
13	chr1:94372270..94376088-chr1:94480112..94484516,4	K562	blood:
14	chr1:94310017..94313015-chr1:94371318..94373997,3	K562	blood:
15	chr1:94350854..94353775-chr1:94372233..94374131,2	K562	blood:
16	chr1:94349796..94351991-chr1:94353690..94356917,3	K562	blood:
17	chr1:94344004..94346272-chr1:94357080..94360433,6	K562	blood:
18	chr1:94349796..94351991-chr1:94353690..94356917,3	K562	blood:
19	chr1:93811453..93814121-chr1:94372637..94375148,3	K562	blood:
20	chr1:94343831..94347542-chr1:94348227..94351449,4	MCF-7	breast:
21	chr1:94310017..94311987-chr1:94371318..94373172,2	K562	blood:
22	chr1:93811453..93813762-chr1:94372603..94376116,3	K562	blood:
23	chr1:94366538..94368489-chr1:94369960..94371845,2	MCF-7	breast:
24	chr1:94342433..94344872-chr1:94364498..94367701,3	K562	blood:
25	chr1:94374517..94375294-chr5:612302..612832,2	Hela-S3	cervix:
26	chr1:94343199..94347658-chr1:94372955..94376562,9	MCF-7	breast:
27	chr1:94344173..94346291-chr1:94372636..94375124,3	K562	blood:
28	chr1:94360896..94362879-chr1:94374618..94376301,2	MCF-7	breast:
29	chr1:94337226..94339966-chr1:94373816..94376815,2	K562	blood:
30	chr1:94349522..94351991-chr1:94354138..94356917,3	K562	blood:
31	chr1:94368166..94370770-chr1:94373424..94375142,2	MCF-7	breast:
32	chr1:94370087..94372566-chr1:94373448..94376204,3	MCF-7	breast:
33	chr1:94343706..94346474-chr1:94354724..94357887,3	MCF-7	breast:
34	chr1:94363097..94365555-chr1:94372047..94374626,2	MCF-7	breast:
35	chr1:94344690..94346304-chr1:94373768..94376372,3	MCF-7	breast:
36	chr1:94336863..94338499-chr1:94348884..94351600,2	K562	blood:
37	chr1:94312303..94314752-chr1:94373572..94376301,2	MCF-7	breast:
38	chr1:94342014..94348814-chr1:94369991..94376733,14	K562	blood:
39	chr1:94338439..94340228-chr1:94354900..94357420,2	K562	blood:
40	chr1:94335805..94338499-chr1:94348129..94351600,3	K562	blood:
41	chr1:94366538..94368489-chr1:94369960..94371845,2	MCF-7	breast:
42	chr1:94353990..94356297-chr1:94372035..94374503,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNTTIP2-2	chr1:94374221-94374480	NONHSAT004556
2	lnc-FNBP1L-5	chr1:94383515-94383763	NONHSAT004557
3	lnc-FNBP1L-5	chr1:94383255-94383357	NONHSAT004557
4	lnc-DNTTIP2-2	chr1:94369822-94370144	NONHSAT004556

No data

Variant related genes	Relation type
GCLM	TF binding region
GCLM	CpG island
ENSG00000260464	chromatin interactions
ENSG00000137936	chromatin interactions
ENSG00000211575	chromatin interactions
ENSG00000112877	chromatin interactions
ENSG00000249650	chromatin interactions
ENSG00000117505	chromatin interactions
ENSG00000223745	chromatin interactions
ENSG00000198691	chromatin interactions
ENSG00000067334	chromatin interactions
ENSG00000023909	chromatin interactions

Extended variants
information (count: 1194 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3170633	chr1:94351328-94351329	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150214178	chr1:94351386-94351387	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550784448	chr1:94351456-94351457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191236117	chr1:94351618-94351619	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs539217874	chr1:94351677-94351678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs34212520	chr1:94351681-94351682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs35508812	chr1:94351696-94351697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549830062	chr1:94351749-94351750	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs116246085	chr1:94351752-94351753	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201978082	chr1:94351769-94351770	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs398103031	chr1:94351777-94351778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200861898	chr1:94351789-94351790	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139164563	chr1:94351800-94351801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs569602270	chr1:94351862-94351863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538265939	chr1:94351942-94351943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34049489	chr1:94352017-94352018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575113853	chr1:94352151-94352152	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34571118	chr1:94352237-94352238	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs397819233	chr1:94352245-94352246	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs398103032	chr1:94352246-94352247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112686711	chr1:94352247-94352248	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111614613	chr1:94352249-94352250	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558026009	chr1:94352278-94352279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs183871755	chr1:94352323-94352324	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs141508435	chr1:94352359-94352360	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10489605	chr1:94352381-94352382	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs546378666	chr1:94352423-94352424	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114561680	chr1:94352474-94352475	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573372199	chr1:94352512-94352513	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540664553	chr1:94352526-94352527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs189329140	chr1:94352535-94352536	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377362793	chr1:94352553-94352554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371279218	chr1:94352554-94352555	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577905684	chr1:94352556-94352557	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs71652546	chr1:94352558-94352559	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs147039062	chr1:94352562-94352563	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369598352	chr1:94352563-94352564	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs60252290	chr1:94352569-94352570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562408964	chr1:94352582-94352583	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs138340857	chr1:94352583-94352584	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs536713549	chr1:94352595-94352596	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs367910543	chr1:94352603-94352604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551112725	chr1:94352640-94352641	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566276157	chr1:94352649-94352650	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187575986	chr1:94352655-94352656	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs548993608	chr1:94352661-94352662	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149637681	chr1:94352668-94352669	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs56163360	chr1:94352708-94352709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs557699672	chr1:94352764-94352765	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569526076	chr1:94352805-94352806	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94345000-94357000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:94345000-94374200	Weak transcription	Gastric	stomach
3	chr1:94345000-94374200	Weak transcription	Spleen	Spleen
4	chr1:94345200-94358800	Weak transcription	Left Ventricle	heart
5	chr1:94345200-94374000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:94345200-94374200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:94345400-94353600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:94345400-94353600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr1:94345400-94353600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr1:94345400-94354400	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr1:94345400-94356600	Weak transcription	Aorta	Aorta
12	chr1:94345400-94356800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr1:94345400-94357000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr1:94345400-94357200	Weak transcription	NHLF	lung
15	chr1:94345400-94358800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr1:94345400-94359200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr1:94345400-94361000	Weak transcription	Fetal Thymus	thymus
18	chr1:94345400-94362000	Weak transcription	Fetal Muscle Leg	muscle
19	chr1:94345400-94364000	Weak transcription	Fetal Intestine Small	intestine
20	chr1:94345400-94369400	Weak transcription	Colonic Mucosa	Colon
21	chr1:94345400-94373200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:94345400-94373200	Weak transcription	Brain Substantia Nigra	brain
23	chr1:94345400-94373800	Weak transcription	Fetal Stomach	stomach
24	chr1:94345400-94374000	Weak transcription	Right Ventricle	heart
25	chr1:94345600-94353600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:94345600-94353600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr1:94345600-94353600	Weak transcription	HepG2	liver
28	chr1:94345600-94353600	Weak transcription	NHDF-Ad	bronchial
29	chr1:94345600-94353800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:94345600-94354000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:94345600-94354200	Weak transcription	Adipose Nuclei	Adipose
32	chr1:94345600-94354400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:94345600-94354400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:94345600-94354400	Weak transcription	K562	blood
35	chr1:94345600-94356200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:94345600-94356200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:94345600-94356200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:94345600-94356200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:94345600-94356200	Weak transcription	Duodenum Mucosa	Duodenum
40	chr1:94345600-94356200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr1:94345600-94357600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr1:94345600-94357800	Weak transcription	Hela-S3	cervix
43	chr1:94345600-94358400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr1:94345600-94358400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr1:94345600-94358600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:94345600-94358600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr1:94345600-94358600	Weak transcription	Fetal Intestine Large	intestine
48	chr1:94345600-94358600	Weak transcription	NHEK	skin
49	chr1:94345600-94358800	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr1:94345600-94359400	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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