Variant report

Variant	nsv1008318
Chromosome Location	chr4:77042356-77095658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:862)
CpG islands
(count:794)
Chromatin interactive
region (count:56)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:862 , 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	chr4:77069028-77069034	K562	blood:	n/a	n/a
2	ARID3A	chr4:77069450-77069768	K562	blood:	n/a	n/a
3	ARID3A	chr4:77069430-77069797	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:77068478-77068665	K562	blood:	n/a	n/a
5	ATF1	chr4:77069431-77069856	K562	blood:	n/a	n/a
6	ATF2	chr4:77068637-77069112	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:77069344-77069833	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:77068660-77069202	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:77069361-77069972	GM12878	blood:	n/a	n/a
10	ATF2	chr4:77069361-77069931	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:77069305-77069941	GM12878	blood:	n/a	n/a
12	ATF3	chr4:77069420-77069698	K562	blood:	n/a	n/a
13	ATF3	chr4:77069306-77069911	A549	lung:	n/a	n/a
14	ATF3	chr4:77069433-77069872	K562	blood:	n/a	n/a
15	ATF3	chr4:77069348-77069849	A549	lung:	n/a	n/a
16	BACH1	chr4:77068641-77068982	K562	blood:	n/a	n/a
17	BACH1	chr4:77068703-77069963	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:77069202-77069449	K562	blood:	n/a	n/a
19	BATF	chr4:77069478-77069766	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:77068834-77068981	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr4:77069307-77069882	A549	lung:	n/a	chr4:77069713-77069722
22	BCL3	chr4:77069356-77069851	A549	lung:	n/a	chr4:77069713-77069722
23	BCLAF1	chr4:77069018-77069913	GM12878	blood:	n/a	chr4:77069196-77069209 chr4:77069713-77069722
24	BCLAF1	chr4:77069305-77069906	K562	blood:	n/a	chr4:77069713-77069722
25	BCLAF1	chr4:77069138-77069924	K562	blood:	n/a	chr4:77069196-77069209 chr4:77069713-77069722
26	BCLAF1	chr4:77069305-77070018	GM12878	blood:	n/a	chr4:77069713-77069722
27	BHLHE40	chr4:77077888-77078045	K562	blood:	n/a	n/a
28	BHLHE40	chr4:77069399-77069930	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:77068918-77069948	K562	blood:	n/a	n/a
30	BRCA1	chr4:77069038-77069869	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr4:77069369-77069788	HepG2	liver:	n/a	n/a
32	BRCA1	chr4:77069442-77069955	GM12878	blood:	n/a	n/a
33	BRCA1	chr4:77069412-77069889	H1-hESC	embryonic stem cell:	n/a	n/a
34	CBX3	chr4:77069322-77070029	K562	blood:	n/a	n/a
35	CBX3	chr4:77069415-77069817	K562	blood:	n/a	n/a
36	CBX3	chr4:77068738-77069292	K562	blood:	n/a	n/a
37	CCNT2	chr4:77068908-77069784	K562	blood:	n/a	chr4:77069052-77069061 chr4:77069005-77069014
38	CCNT2	chr4:77070228-77070323	K562	blood:	n/a	n/a
39	CEBPB	chr4:77069301-77070222	GM12878	blood:	n/a	n/a
40	CEBPB	chr4:77045717-77045936	A549	lung:	n/a	chr4:77045842-77045853
41	CEBPB	chr4:77076388-77076448	A549	lung:	n/a	n/a
42	CEBPB	chr4:77068983-77069801	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:77045673-77046011	K562	blood:	n/a	chr4:77045842-77045853
44	CEBPB	chr4:77047392-77047669	IMR90	lung:	n/a	chr4:77047528-77047539 chr4:77047527-77047538
45	CEBPB	chr4:77062401-77062714	K562	blood:	n/a	n/a
46	CEBPB	chr4:77045706-77045952	IMR90	lung:	n/a	chr4:77045842-77045853
47	CEBPB	chr4:77047370-77047671	HepG2	liver:	n/a	chr4:77047528-77047539 chr4:77047527-77047538
48	CEBPB	chr4:77045704-77046000	HepG2	liver:	n/a	chr4:77045842-77045853
49	CEBPB	chr4:77069444-77069842	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr4:77069379-77069795	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:77070069-77070119	H1-hESC	embryonic stem cell:	embryo
2	chr4:77070069-77070119	H1-hESC	embryonic stem cell:	embryo
3	chr4:77067214-77067264	AG04449	skin:	fetal
4	chr4:77069698-77069748	Hela-S3	cervix:	n/a
5	chr4:77070069-77070119	NT2-D1	testis:	n/a
6	chr4:77069145-77069195	NH-A	brain:	n/a
7	chr4:77061304-77061354	AG09319	gingival:	n/a
8	chr4:77069462-77069512	HCM	heart:	n/a
9	chr4:77082402-77082452	SKMC	muscle:	n/a
10	chr4:77069770-77069820	H1-hESC	embryonic stem cell:	embryo
11	chr4:77082402-77082452	PFSK-1	brain:	n/a
12	chr4:77069671-77069721	HEEpiC	esophagus:	n/a
13	chr4:77082402-77082452	Caco-2	colon:	n/a
14	chr4:77069145-77069195	AG09309	skin:	n/a
15	chr4:77067214-77067264	RPTEC	kidney:	n/a
16	chr4:77069770-77069820	HRPEpiC	eye:	n/a
17	chr4:77069145-77069195	AG10803	skin:	n/a
18	chr4:77069462-77069512	HepG2	liver:	n/a
19	chr4:77082402-77082452	SK-N-SH	brain:	n/a
20	chr4:77061304-77061354	AG04450	lung:	fetal
21	chr4:77069145-77069195	T-47D	breast:	n/a
22	chr4:77069462-77069512	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:77069462-77069512	T-47D	breast:	n/a
24	chr4:77069770-77069820	U87	brain:	n/a
25	chr4:77070069-77070119	HNPCEpiC	eye:	n/a
26	chr4:77070069-77070119	NHDF-neo	bronchial:	n/a
27	chr4:77069698-77069748	PANC-1	pancreas:	n/a
28	chr4:77069719-77069769	RPTEC	kidney:	n/a
29	chr4:77069462-77069512	SK-N-MC	brain:	n/a
30	chr4:77069563-77069613	MCF10A-Er-Src	breast:	n/a
31	chr4:77069698-77069748	T-47D	breast:	n/a
32	chr4:77069563-77069613	HMEC	breast:	n/a
33	chr4:77070069-77070119	AG10803	skin:	n/a
34	chr4:77067214-77067264	GM19239	blood:	n/a
35	chr4:77069573-77069623	BE2_C	brain:	n/a
36	chr4:77061304-77061354	HCM	heart:	n/a
37	chr4:77070069-77070119	ovcar-3	ovarian:	n/a
38	chr4:77069698-77069748	HNPCEpiC	eye:	n/a
39	chr4:77070069-77070119	PFSK-1	brain:	n/a
40	chr4:77069145-77069195	SK-N-SH	brain:	n/a
41	chr4:77069770-77069820	HAEpiC	amniotic membrane:	n/a
42	chr4:77069671-77069721	GM06990	blood:	n/a
43	chr4:77061304-77061354	PrEC	prostate:	n/a
44	chr4:77069770-77069820	MCF-7	breast:	n/a
45	chr4:77069462-77069512	HCT-116	colon:	n/a
46	chr4:77069462-77069512	AG09319	gingival:	n/a
47	chr4:77069462-77069512	SAEC	small airway:	n/a
48	chr4:77069462-77069512	AoSMC	blood vessel:	n/a
49	chr4:77067214-77067264	AG09319	gingival:	n/a
50	chr4:77069671-77069721	GM12878	blood:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:77062870..77064723-chr4:77131850..77133606,2	K562	blood:
2	chr4:77070668..77073537-chr4:77076068..77077976,2	MCF-7	breast:
3	chr4:77047745..77051558-chr4:77062903..77066801,7	K562	blood:
4	chr4:77061702..77065283-chr4:77067091..77070259,5	MCF-7	breast:
5	chr4:77056276..77058049-chr4:77058093..77060100,3	K562	blood:
6	chr20:52812919..52815134-chr4:77041883..77044239,2	MCF-7	breast:
7	chr4:77054225..77056351-chr4:77067941..77069735,2	MCF-7	breast:
8	chr4:77058580..77061268-chr4:77061902..77064829,3	MCF-7	breast:
9	chr4:77065717..77067394-chr4:77069102..77070883,2	MCF-7	breast:
10	chr4:77068043..77069924-chr4:77085351..77088646,3	K562	blood:
11	chr4:77068833..77070867-chr4:77072557..77075265,2	MCF-7	breast:
12	chr20:30192878..30193473-chr4:77069155..77070047,2	HCT-116	colon:
13	chr4:77058580..77061268-chr4:77061902..77064829,3	MCF-7	breast:
14	chr4:77054225..77056351-chr4:77067941..77069735,2	MCF-7	breast:
15	chr4:76860116..76861672-chr4:77068138..77069757,2	MCF-7	breast:
16	chr4:77067723..77069563-chr4:77082506..77084530,2	K562	blood:
17	chr4:77055702..77058489-chr4:77060298..77061923,3	K562	blood:
18	chr4:77065569..77067596-chr4:77067716..77071190,4	MCF-7	breast:
19	chr15:41624744..41625412-chr4:77069044..77069605,2	Hela-S3	cervix:
20	chr4:77069568..77071228-chr4:77073316..77074829,2	MCF-7	breast:
21	chr4:77068526..77071865-chr4:77074983..77079477,5	MCF-7	breast:
22	chr4:77049049..77051567-chr4:77051782..77053760,2	K562	blood:
23	chr4:77068261..77070256-chr4:77079541..77081890,2	MCF-7	breast:
24	chr18:9474779..9475635-chr4:77069246..77070192,2	Hela-S3	cervix:
25	chr4:77037122..77039449-chr4:77042114..77044067,2	K562	blood:
26	chr4:76910882..76913070-chr4:77069181..77071952,2	MCF-7	breast:
27	chr4:77069994..77072704-chr4:77086339..77088505,2	K562	blood:
28	chr10:65280781..65281512-chr4:77069031..77069623,2	NB4	blood:
29	chr4:77071127..77073816-chr4:77194296..77196061,2	K562	blood:
30	chr4:77067214..77072530-chr4:77074887..77081962,12	K562	blood:
31	chr4:77057316..77058882-chr4:77066248..77068900,2	MCF-7	breast:
32	chr4:77050141..77053778-chr4:77066166..77070004,4	MCF-7	breast:
33	chr4:77058522..77060950-chr4:77099295..77101938,2	MCF-7	breast:
34	chr4:77052258..77055216-chr4:77247896..77249907,2	K562	blood:
35	chr4:77042420..77043971-chr4:77226885..77228605,2	K562	blood:
36	chr4:77069655..77071461-chr4:77869809..77871934,2	K562	blood:
37	chr4:77069302..77071113-chr4:77170408..77173032,2	MCF-7	breast:
38	chr4:77050141..77053778-chr4:77066166..77070004,4	MCF-7	breast:
39	chr10:102756766..102757730-chr4:77069104..77069645,2	Hela-S3	cervix:
40	chr4:77035266..77040414-chr4:77041570..77044067,5	K562	blood:
41	chr4:77067778..77069460-chr4:77134577..77136401,2	K562	blood:
42	chr4:77031133..77035310-chr4:77057270..77059295,3	K562	blood:
43	chr4:77055702..77058489-chr4:77060298..77061923,3	K562	blood:
44	chr4:77069025..77069713-chr8:135725164..135725715,2	Hela-S3	cervix:
45	chr4:76910728..76913331-chr4:77052548..77055482,2	MCF-7	breast:
46	chr4:77047745..77051558-chr4:77062903..77066801,7	K562	blood:
47	chr4:77056276..77058049-chr4:77058093..77060100,3	K562	blood:
48	chr4:77084049..77086922-chr4:77101661..77103722,2	K562	blood:
49	chr4:77065569..77067596-chr4:77067716..77071190,4	MCF-7	breast:
50	chr4:77056272..77058794-chr4:77068022..77070741,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCARB2-2	chr4:77065337-77065445	NONHSAT096987
2	lnc-SCARB2-2	chr4:77069243-77069353	NONHSAT096987
3	lnc-SCARB2-2	chr4:77066708-77066844	NONHSAT096987
4	lnc-SCARB2-2	chr4:77065543-77065626	NONHSAT096987

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SCARB2	hsa-miR-222-3p	chr4:77082379-77082399
2	SCARB2	hsa-miR-365a-3p	chr4:77081525-77081546
3	SCARB2	hsa-miR-7-5p	chr4:77082280-77082303
4	SCARB2	hsa-miR-222-3p	chr4:77079986-77080009

Variant related genes	Relation type
SCARB2	TF binding region
NUP54	TF binding region
SCARB2	CpG island
NUP54	CpG island
ENSG00000198301	chromatin interactions
ENSG00000165476	chromatin interactions
ENSG00000138760	chromatin interactions
ENSG00000189157	chromatin interactions
ENSG00000138758	chromatin interactions
ENSG00000066827	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000138750	chromatin interactions
ENSG00000138744	chromatin interactions
ENSG00000104147	chromatin interactions
ENSG00000107816	chromatin interactions
ENSG00000118804	chromatin interactions
ENSG00000272414	chromatin interactions
ENSG00000248240	chromatin interactions
ENSG00000156219	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000137804	chromatin interactions
ENSG00000172244	chromatin interactions

Extended variants
information (count: 2134 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2134 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370521928	chr4:77042392-77042393	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs578126192	chr4:77042393-77042394	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575378718	chr4:77042394-77042395	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs9307079	chr4:77042443-77042444	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs181963719	chr4:77042541-77042542	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528193264	chr4:77042579-77042580	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs537586730	chr4:77042631-77042632	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs528474435	chr4:77042638-77042639	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs9307080	chr4:77042665-77042666	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs187109331	chr4:77042708-77042709	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532112629	chr4:77042730-77042731	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs557579096	chr4:77042750-77042751	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs551813893	chr4:77042759-77042760	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs62299354	chr4:77042781-77042782	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs62299355	chr4:77042789-77042790	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs549548499	chr4:77042812-77042813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs567473620	chr4:77042907-77042908	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534802315	chr4:77042927-77042928	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553014751	chr4:77042948-77042949	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs577636760	chr4:77043067-77043068	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200471795	chr4:77043092-77043093	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559816268	chr4:77043138-77043139	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539001955	chr4:77043157-77043158	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs148469224	chr4:77043158-77043159	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575485290	chr4:77043174-77043175	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542505034	chr4:77043178-77043179	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs41498548	chr4:77043213-77043214	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs4386628	chr4:77043245-77043246	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544664154	chr4:77043332-77043333	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112073897	chr4:77043352-77043353	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540347691	chr4:77043363-77043364	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564950180	chr4:77043365-77043366	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532044273	chr4:77043370-77043371	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564567524	chr4:77043416-77043417	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs56788469	chr4:77043450-77043451	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs563871012	chr4:77043479-77043480	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs531238197	chr4:77043499-77043500	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs549224399	chr4:77043500-77043501	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs567534716	chr4:77043506-77043507	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs181325480	chr4:77043514-77043515	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs35838174	chr4:77043516-77043517	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs185513645	chr4:77043537-77043538	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs571392226	chr4:77043542-77043543	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs113980442	chr4:77043554-77043555	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs182945703	chr4:77043557-77043558	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs60885790	chr4:77043603-77043604	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550304856	chr4:77043614-77043615	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs368320074	chr4:77043632-77043633	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs536559347	chr4:77043701-77043702	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs560712025	chr4:77043731-77043732	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1988 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:77028000-77068600	Weak transcription	Gastric	stomach
2	chr4:77032200-77049200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:77032600-77067600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:77033000-77044800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:77033000-77046800	Strong transcription	Primary B cells from peripheral blood	blood
6	chr4:77033000-77046800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:77033000-77052000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:77033200-77044400	Weak transcription	Spleen	Spleen
9	chr4:77033200-77045200	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr4:77033200-77045600	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr4:77033200-77046200	Strong transcription	Liver	Liver
12	chr4:77033200-77046600	Strong transcription	Fetal Lung	lung
13	chr4:77033200-77058200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:77033200-77066000	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr4:77033200-77068400	Weak transcription	Small Intestine	intestine
16	chr4:77033400-77043400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:77033400-77045600	Strong transcription	Adipose Nuclei	Adipose
18	chr4:77033400-77046000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:77033400-77046000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:77033400-77046200	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr4:77033400-77046400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr4:77033400-77046600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:77033400-77047800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:77033400-77048200	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr4:77033400-77052000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:77033400-77052200	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr4:77033400-77065600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:77033400-77066000	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr4:77033400-77066600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr4:77033600-77047600	Strong transcription	Duodenum Mucosa	Duodenum
31	chr4:77033600-77065600	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr4:77033800-77066200	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr4:77034000-77045600	Strong transcription	Fetal Intestine Large	intestine
34	chr4:77034000-77046200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr4:77034000-77054000	Strong transcription	Dnd41	blood
36	chr4:77034000-77066000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr4:77034200-77045400	Strong transcription	Placenta	Placenta
38	chr4:77034200-77045600	Strong transcription	Fetal Thymus	thymus
39	chr4:77034200-77046600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:77034400-77045600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:77034400-77046000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr4:77034400-77067200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:77034600-77043200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:77035000-77068400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:77035200-77062000	Weak transcription	Esophagus	oesophagus
46	chr4:77035200-77068600	Weak transcription	Pancreas	Pancrea
47	chr4:77035400-77066000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
48	chr4:77035600-77068400	Weak transcription	Right Ventricle	heart
49	chr4:77036400-77043400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:77036400-77054600	Strong transcription	H1 Cell Line	embryonic stem cell

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