Variant report

Variant	nsv1041803
Chromosome Location	chr9:96299639-96342013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1292)
CpG islands
(count:610)
Chromatin interactive
region (count:100)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1292 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:96328679-96329164	K562	blood:	n/a	n/a
2	ARID3A	chr9:96328578-96329163	HepG2	liver:	n/a	n/a
3	ATF2	chr9:96328888-96329208	GM12878	blood:	n/a	n/a
4	ATF2	chr9:96328596-96329271	GM12878	blood:	n/a	n/a
5	ATF2	chr9:96328574-96329477	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr9:96328612-96329080	A549	lung:	n/a	chr9:96328929-96328938
7	ATF3	chr9:96328710-96329245	A549	lung:	n/a	chr9:96328929-96328938
8	BACH1	chr9:96325333-96325483	K562	blood:	n/a	n/a
9	BACH1	chr9:96339995-96340072	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:96338618-96338801	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:96328644-96329436	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr9:96339631-96339675	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr9:96327420-96327728	GM12878	blood:	n/a	n/a
14	BATF	chr9:96327402-96327698	GM12878	blood:	n/a	n/a
15	BCL3	chr9:96328641-96329340	GM12878	blood:	n/a	chr9:96328855-96328868
16	BCL3	chr9:96328573-96329355	A549	lung:	n/a	chr9:96328855-96328868
17	BCL3	chr9:96328563-96329273	A549	lung:	n/a	chr9:96328855-96328868
18	BCL3	chr9:96303201-96303654	GM12878	blood:	n/a	n/a
19	BCL3	chr9:96303280-96303617	GM12878	blood:	n/a	n/a
20	BCL3	chr9:96328552-96329334	K562	blood:	n/a	chr9:96328855-96328868
21	BCLAF1	chr9:96328588-96329323	GM12878	blood:	n/a	chr9:96328855-96328868
22	BCLAF1	chr9:96328590-96329215	GM12878	blood:	n/a	chr9:96328855-96328868
23	BHLHE40	chr9:96328637-96329771	K562	blood:	n/a	chr9:96329521-96329530 chr9:96329521-96329530 chr9:96329522-96329531
24	BHLHE40	chr9:96328663-96329070	HepG2	liver:	n/a	n/a
25	BHLHE40	chr9:96338048-96338301	K562	blood:	n/a	n/a
26	BHLHE40	chr9:96340625-96340638	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:96328647-96329668	GM12878	blood:	n/a	chr9:96329521-96329530 chr9:96329521-96329530 chr9:96329522-96329531
28	BHLHE40	chr9:96338010-96338256	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:96339920-96339967	GM12878	blood:	n/a	n/a
30	BRCA1	chr9:96328547-96329194	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr9:96328664-96328800	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr9:96338141-96338210	HepG2	liver:	n/a	n/a
33	CBX3	chr9:96333073-96333749	K562	blood:	n/a	n/a
34	CBX3	chr9:96328614-96329245	K562	blood:	n/a	n/a
35	CCNT2	chr9:96328669-96329485	K562	blood:	n/a	n/a
36	CCNT2	chr9:96338204-96339839	K562	blood:	n/a	chr9:96339670-96339679
37	CEBPB	chr9:96328201-96328402	H1-hESC	embryonic stem cell:	n/a	chr9:96328270-96328281
38	CEBPB	chr9:96328742-96328942	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:96334254-96334546	HepG2	liver:	n/a	n/a
40	CEBPB	chr9:96334237-96334515	K562	blood:	n/a	n/a
41	CEBPB	chr9:96328738-96329003	K562	blood:	n/a	n/a
42	CEBPB	chr9:96328114-96328447	HepG2	liver:	n/a	chr9:96328270-96328281
43	CEBPB	chr9:96335078-96335270	H1-hESC	embryonic stem cell:	n/a	chr9:96335113-96335124
44	CEBPB	chr9:96334942-96335294	IMR90	lung:	n/a	chr9:96335113-96335124
45	CEBPB	chr9:96334976-96335302	K562	blood:	n/a	chr9:96335113-96335124
46	CEBPB	chr9:96339886-96340346	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr9:96328194-96328400	Hela-S3	cervix:	n/a	chr9:96328270-96328281
48	CEBPB	chr9:96328656-96329185	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr9:96328142-96328440	A549	lung:	n/a	chr9:96328270-96328281
50	CEBPB	chr9:96334957-96335286	A549	lung:	n/a	chr9:96335113-96335124

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96338308-96338358	HCF	heart:	n/a
2	chr9:96339159-96339209	BE2_C	brain:	n/a
3	chr9:96329060-96329110	AG10803	skin:	n/a
4	chr9:96338308-96338358	A549	lung:	n/a
5	chr9:96339738-96339788	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:96328767-96328817	ProgFib	skin:	n/a
7	chr9:96337982-96338032	AG09319	gingival:	n/a
8	chr9:96328529-96328579	NHBE	bronchial:	n/a
9	chr9:96328529-96328579	SK-N-SH	brain:	n/a
10	chr9:96337982-96338032	PrEC	prostate:	n/a
11	chr9:96329060-96329110	A549	lung:	n/a
12	chr9:96330917-96330967	Caco-2	colon:	n/a
13	chr9:96328767-96328817	NHBE	bronchial:	n/a
14	chr9:96328529-96328579	IMR90	lung:	fetal
15	chr9:96339738-96339788	HRCEpiC	kidney:	n/a
16	chr9:96338308-96338358	HEEpiC	esophagus:	n/a
17	chr9:96339159-96339209	SK-N-SH_RA	brain:	n/a
18	chr9:96330917-96330967	ProgFib	skin:	n/a
19	chr9:96329060-96329110	HEEpiC	esophagus:	n/a
20	chr9:96339159-96339209	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:96328529-96328579	AG04449	skin:	fetal
22	chr9:96328529-96328579	PANC-1	pancreas:	n/a
23	chr9:96328767-96328817	HCM	heart:	n/a
24	chr9:96337681-96337731	NB4	blood:	n/a
25	chr9:96328401-96328451	HUVEC	blood vessel:	n/a
26	chr9:96339738-96339788	SK-N-MC	brain:	n/a
27	chr9:96339159-96339209	NH-A	brain:	n/a
28	chr9:96329060-96329110	IMR90	lung:	fetal
29	chr9:96328767-96328817	GM19239	blood:	n/a
30	chr9:96338308-96338358	Hepatocyte	liver:	n/a
31	chr9:96339738-96339788	H1-hESC	embryonic stem cell:	embryo
32	chr9:96328401-96328451	HepG2	liver:	n/a
33	chr9:96330917-96330967	SKMC	muscle:	n/a
34	chr9:96329060-96329110	HRE	kidney:	n/a
35	chr9:96337982-96338032	NHDF-neo	bronchial:	n/a
36	chr9:96329060-96329110	Hepatocyte	liver:	n/a
37	chr9:96337681-96337731	GM12891	blood:	n/a
38	chr9:96337681-96337731	BJ	skin:	n/a
39	chr9:96337982-96338032	HEK293	kidney:	embryo
40	chr9:96329060-96329110	HL-60	blood:	n/a
41	chr9:96329060-96329110	Caco-2	colon:	n/a
42	chr9:96338308-96338358	HMEC	breast:	n/a
43	chr9:96328529-96328579	HCPEpiC	choroid plexus:	n/a
44	chr9:96338308-96338358	HIPEpiC	eye:	n/a
45	chr9:96329060-96329110	HPAEpiC	pulmonary alveolar:	n/a
46	chr9:96338308-96338358	NT2-D1	testis:	n/a
47	chr9:96329060-96329110	MCF10A-Er-Src	breast:	n/a
48	chr9:96330917-96330967	AG10803	skin:	n/a
49	chr9:96330917-96330967	A549	lung:	n/a
50	chr9:96328529-96328579	NB4	blood:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:96211528..96214948-chr9:96337573..96343441,10	MCF-7	breast:
2	chr9:96213191..96216184-chr9:96305386..96307946,2	MCF-7	breast:
3	chr9:96310257..96312252-chr9:96337769..96339963,2	MCF-7	breast:
4	chr9:96319216..96322786-chr9:96325553..96328069,3	MCF-7	breast:
5	chr9:96316374..96320163-chr9:96337191..96341614,7	MCF-7	breast:
6	chr9:96290421..96292489-chr9:96327392..96330270,2	MCF-7	breast:
7	chr15:64672393..64674955-chr9:96338463..96341441,2	MCF-7	breast:
8	chr9:96333987..96335844-chr9:111755686..111758072,2	MCF-7	breast:
9	chr9:96307326..96310948-chr9:96316247..96319026,3	K562	blood:
10	chr9:96212788..96214389-chr9:96318862..96321524,2	MCF-7	breast:
11	chr9:96258848..96260349-chr9:96307458..96309398,2	K562	blood:
12	chr9:96212024..96217170-chr9:96326121..96330116,7	MCF-7	breast:
13	chr9:96337657..96339290-chr9:96927321..96930180,2	K562	blood:
14	chr9:96213389..96215386-chr9:96309872..96311378,2	MCF-7	breast:
15	chr9:96320066..96322068-chr9:96325915..96330379,3	K562	blood:
16	chr9:96322191..96324124-chr9:96324483..96327194,2	K562	blood:
17	chr17:30993194..30993694-chr9:96329039..96329540,2	HCT-116	colon:
18	chr9:96322191..96324124-chr9:96324483..96327194,2	K562	blood:
19	chr9:96319216..96322786-chr9:96325553..96328069,3	MCF-7	breast:
20	chr5:43121431..43122251-chr9:96338410..96338951,2	Hela-S3	cervix:
21	chr9:96324653..96326761-chr9:96337595..96340198,2	MCF-7	breast:
22	chr9:96328414..96329044-chr9:96339964..96340763,2	MCF-7	breast:
23	chr9:96298295..96300963-chr9:96339660..96341258,2	MCF-7	breast:
24	chr9:96213362..96215557-chr9:96327494..96329016,2	K562	blood:
25	chr9:96299951..96301653-chr9:96312978..96315917,2	MCF-7	breast:
26	chr14:52455551..52457081-chr9:96338294..96340039,2	MCF-7	breast:
27	chr9:96298295..96300963-chr9:96339660..96341258,2	MCF-7	breast:
28	chr9:96308737..96311417-chr9:96314055..96315720,2	MCF-7	breast:
29	chr9:96286264..96288852-chr9:96329560..96332298,3	MCF-7	breast:
30	chr9:96214499..96217099-chr9:96338317..96340265,2	K562	blood:
31	chr9:96299100..96302686-chr9:96306350..96308675,3	K562	blood:
32	chr9:96334438..96336370-chr9:96418829..96421734,2	MCF-7	breast:
33	chr9:96309589..96311843-chr9:96313849..96315976,2	K562	blood:
34	chr9:96323290..96325963-chr9:96339113..96341830,2	MCF-7	breast:
35	chr9:96207292..96208805-chr9:96339241..96341688,2	MCF-7	breast:
36	chr9:95856094..95858375-chr9:96337008..96340445,3	MCF-7	breast:
37	chr9:96305713..96308881-chr9:96337221..96340440,3	MCF-7	breast:
38	chr9:96213112..96215429-chr9:96313984..96316508,2	MCF-7	breast:
39	chr9:96289339..96291734-chr9:96339194..96341014,2	MCF-7	breast:
40	chr9:96295942..96297811-chr9:96304126..96306733,2	K562	blood:
41	chr9:96302294..96305267-chr9:96306337..96308458,2	MCF-7	breast:
42	chr9:95895154..95898000-chr9:96338001..96340609,3	MCF-7	breast:
43	chr9:96324507..96327332-chr9:96327489..96329838,2	K562	blood:
44	chr9:96300899..96303747-chr9:96334511..96337154,2	MCF-7	breast:
45	chr9:96328414..96329044-chr9:96339964..96340763,2	MCF-7	breast:
46	chr9:96327412..96330304-chr9:96331068..96333359,2	K562	blood:
47	chr9:96318350..96320504-chr9:96329383..96332231,2	MCF-7	breast:
48	chr9:95922383..95922884-chr9:96328410..96328999,2	K562	blood:
49	chr20:2853581..2854096-chr9:96328936..96329437,2	Hela-S3	cervix:
50	chr9:96212589..96215619-chr9:96298935..96305511,9	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF2-1	chr9:96322548-96322860	ENSG00000234543.1
2	lnc-PHF2-1	chr9:96301210-96301261	ENSG00000234543.1
3	lnc-FAM120AOS-5	chr9:96336376-96337293	NONHSAT133277

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAM120A	hsa-miR-155-5p	chr9:96327216-96327240
2	FAM120A	hsa-miR-124-3p	chr9:96326689-96326708
3	FAM120A	hsa-miR-124-3p	chr9:96327912-96327931
4	FAM120A	hsa-miR-155-5p	chr9:96327882-96327904

Variant related genes	Relation type
ENSG00000263875	TF binding region
PHF2	TF binding region
ENSG00000263875	CpG island
PHF2	CpG island
ENSG00000188938	chromatin interactions
ENSG00000231990	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000203499	chromatin interactions
ENSG00000263875	chromatin interactions
ENSG00000223446	chromatin interactions
ENSG00000087302	chromatin interactions
ENSG00000131669	chromatin interactions
ENSG00000132670	chromatin interactions
ENSG00000166803	chromatin interactions
ENSG00000197724	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000048828	chromatin interactions
ENSG00000129355	chromatin interactions
ENSG00000172262	chromatin interactions

Extended variants
information (count: 1361 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550478747	chr9:96299658-96299659	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs369250561	chr9:96299659-96299660	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs139366167	chr9:96299684-96299685	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs572074325	chr9:96299775-96299776	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs539065071	chr9:96299809-96299810	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536652425	chr9:96299839-96299840	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs553891111	chr9:96299868-96299869	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs181448680	chr9:96299899-96299900	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs565692637	chr9:96299905-96299906	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs184215006	chr9:96299922-96299923	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564196287	chr9:96299967-96299968	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs554611387	chr9:96299990-96299991	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs573532847	chr9:96299999-96300000	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs370503375	chr9:96300028-96300029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs190012449	chr9:96300119-96300120	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs556466320	chr9:96300151-96300152	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs142682949	chr9:96300194-96300195	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs12551084	chr9:96300295-96300296	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs3841292	chr9:96300322-96300323	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs559310434	chr9:96300333-96300334	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs527250343	chr9:96300354-96300355	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs542759566	chr9:96300363-96300364	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs560944505	chr9:96300396-96300397	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs531980559	chr9:96300404-96300405	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs3841291	chr9:96300495-96300496	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs398011511	chr9:96300498-96300499	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs377579196	chr9:96300557-96300558	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs150944021	chr9:96300563-96300564	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs111985268	chr9:96300580-96300581	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs3813388	chr9:96300597-96300598	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs566413622	chr9:96300620-96300621	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs3813387	chr9:96300682-96300683	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181273382	chr9:96300685-96300686	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139451738	chr9:96300771-96300772	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs186207310	chr9:96300793-96300794	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149702573	chr9:96300804-96300805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147789265	chr9:96300820-96300821	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556092714	chr9:96300829-96300830	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577719505	chr9:96300853-96300854	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35540150	chr9:96300854-96300855	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs141778411	chr9:96300859-96300860	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs572098899	chr9:96300881-96300882	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs10821153	chr9:96300885-96300886	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs190731412	chr9:96300886-96300887	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576067487	chr9:96300938-96300939	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543459787	chr9:96300979-96300980	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565361761	chr9:96301013-96301014	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532707437	chr9:96301121-96301122	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs547721830	chr9:96301155-96301156	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs56333792	chr9:96301160-96301161	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2342 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96276000-96300000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr9:96278400-96310800	Strong transcription	Rectal Mucosa Donor 31	rectum
3	chr9:96278400-96327000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr9:96278400-96327200	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr9:96278400-96328200	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr9:96278600-96311200	Strong transcription	Rectal Mucosa Donor 29	rectum
7	chr9:96279000-96310400	Strong transcription	Primary B cells from peripheral blood	blood
8	chr9:96279000-96327400	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr9:96282200-96323400	Strong transcription	Primary B cells from cord blood	blood
10	chr9:96284600-96327200	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr9:96284600-96328200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:96284800-96309800	Strong transcription	Duodenum Mucosa	Duodenum
13	chr9:96284800-96327200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr9:96285000-96301400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr9:96285000-96304000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr9:96285000-96327000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr9:96285000-96327000	Strong transcription	Dnd41	blood
18	chr9:96285200-96327800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr9:96285400-96299800	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr9:96285400-96304200	Strong transcription	HSMM	muscle
21	chr9:96285400-96327800	Strong transcription	Liver	Liver
22	chr9:96285600-96301000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr9:96285600-96310000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr9:96285800-96303400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr9:96286000-96301200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:96286000-96302800	Strong transcription	Osteobl	bone
27	chr9:96286000-96304000	Strong transcription	Adipose Nuclei	Adipose
28	chr9:96287200-96303800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr9:96288600-96304200	Strong transcription	K562	blood
30	chr9:96289200-96316000	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr9:96291600-96305400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:96291800-96303800	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr9:96291800-96317000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr9:96291800-96317000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr9:96292000-96316600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr9:96292800-96310000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr9:96293000-96299800	Strong transcription	Primary T cells from cord blood	blood
38	chr9:96293000-96310400	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr9:96293200-96309600	Strong transcription	Primary hematopoietic stem cells	blood
40	chr9:96293600-96302800	Strong transcription	Fetal Muscle Leg	muscle
41	chr9:96293600-96303800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr9:96293800-96301200	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr9:96294200-96303600	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr9:96295000-96305200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr9:96295200-96306200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr9:96295200-96308600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:96295600-96305600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr9:96295800-96307600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr9:96295800-96315600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr9:96296000-96305600	Weak transcription	Fetal Kidney	kidney

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