Variant report

Variant	nsv904178
Chromosome Location	chr15:44609796-44724287
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1382)
CpG islands
(count:794)
Chromatin interactive
region (count:40)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1382 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:44720644-44720707	K562	blood:	n/a	n/a
2	ARID3A	chr15:44718966-44719733	K562	blood:	n/a	n/a
3	ARID3A	chr15:44677230-44677411	K562	blood:	n/a	n/a
4	ARID3A	chr15:44718966-44720044	HepG2	liver:	n/a	chr15:44719841-44719849
5	ATF1	chr15:44719111-44720014	K562	blood:	n/a	n/a
6	ATF2	chr15:44719105-44720020	GM12878	blood:	n/a	n/a
7	ATF2	chr15:44677030-44677438	GM12878	blood:	n/a	n/a
8	ATF2	chr15:44611541-44611946	GM12878	blood:	n/a	n/a
9	ATF2	chr15:44677174-44677854	GM12878	blood:	n/a	n/a
10	ATF2	chr15:44719011-44719953	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr15:44719025-44720207	GM12878	blood:	n/a	n/a
12	ATF2	chr15:44718891-44720017	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:44718032-44718323	K562	blood:	n/a	n/a
14	BACH1	chr15:44677223-44677573	K562	blood:	n/a	n/a
15	BACH1	chr15:44719386-44719911	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:44677390-44677496	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr15:44706288-44706574	GM12878	blood:	n/a	n/a
18	BATF	chr15:44611620-44611972	GM12878	blood:	n/a	n/a
19	BATF	chr15:44706233-44706588	GM12878	blood:	n/a	n/a
20	BATF	chr15:44677285-44677584	GM12878	blood:	n/a	chr15:44677404-44677415
21	BATF	chr15:44677259-44677509	GM12878	blood:	n/a	chr15:44677404-44677415
22	BCL11A	chr15:44706292-44706510	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:44677234-44677511	GM12878	blood:	n/a	n/a
24	BCL3	chr15:44719019-44719765	A549	lung:	n/a	n/a
25	BCL3	chr15:44719358-44719949	A549	lung:	n/a	n/a
26	BCLAF1	chr15:44677158-44677627	GM12878	blood:	n/a	n/a
27	BCLAF1	chr15:44611541-44612118	GM12878	blood:	n/a	n/a
28	BCLAF1	chr15:44718871-44720397	GM12878	blood:	n/a	chr15:44720148-44720157
29	BCLAF1	chr15:44718904-44720353	GM12878	blood:	n/a	chr15:44720148-44720157
30	BHLHE40	chr15:44719036-44720387	K562	blood:	n/a	n/a
31	BHLHE40	chr15:44611640-44611889	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:44685862-44685951	K562	blood:	n/a	n/a
33	BHLHE40	chr15:44719109-44719966	GM12878	blood:	n/a	n/a
34	BRCA1	chr15:44719092-44720060	HepG2	liver:	n/a	chr15:44719873-44719880
35	BRCA1	chr15:44718912-44721421	Hela-S3	cervix:	n/a	chr15:44719873-44719880
36	BRCA1	chr15:44719876-44719937	H1-hESC	embryonic stem cell:	n/a	n/a
37	CBX3	chr15:44718918-44720110	K562	blood:	n/a	n/a
38	CCNT2	chr15:44718897-44720149	K562	blood:	n/a	n/a
39	CCNT2	chr15:44718453-44718653	K562	blood:	n/a	n/a
40	CEBPB	chr15:44673450-44673771	HepG2	liver:	n/a	chr15:44673592-44673605 chr15:44673592-44673605 chr15:44673592-44673603
41	CEBPB	chr15:44673418-44673770	K562	blood:	n/a	chr15:44673592-44673605 chr15:44673592-44673605 chr15:44673592-44673603
42	CEBPB	chr15:44685723-44686118	K562	blood:	n/a	chr15:44685945-44685956
43	CEBPB	chr15:44614089-44614233	K562	blood:	n/a	chr15:44614208-44614219
44	CEBPB	chr15:44673461-44673774	MCF-7	breast:	n/a	chr15:44673592-44673605 chr15:44673592-44673605 chr15:44673592-44673603
45	CEBPB	chr15:44685892-44686006	IMR90	lung:	n/a	chr15:44685945-44685956
46	CEBPB	chr15:44718924-44720856	Hela-S3	cervix:	n/a	chr15:44720672-44720685 chr15:44720661-44720673 chr15:44720674-44720685
47	CEBPB	chr15:44686352-44686663	HepG2	liver:	n/a	chr15:44686490-44686501
48	CEBPB	chr15:44685860-44685995	H1-hESC	embryonic stem cell:	n/a	chr15:44685945-44685956
49	CEBPB	chr15:44719142-44720091	K562	blood:	n/a	n/a
50	CEBPB	chr15:44685868-44686002	A549	lung:	n/a	chr15:44685945-44685956

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:44720131-44720181	NHBE	bronchial:	n/a
2	chr15:44720131-44720181	NHBE	bronchial:	n/a
3	chr15:44719030-44719080	HIPEpiC	eye:	n/a
4	chr15:44715351-44715401	U87	brain:	n/a
5	chr15:44719510-44719560	ovcar-3	ovarian:	n/a
6	chr15:44723502-44723552	AG04449	skin:	fetal
7	chr15:44719516-44719566	NT2-D1	testis:	n/a
8	chr15:44719213-44719263	PrEC	prostate:	n/a
9	chr15:44719012-44719062	SAEC	small airway:	n/a
10	chr15:44617767-44617817	Hela-S3	cervix:	n/a
11	chr15:44719510-44719560	K562	blood:	n/a
12	chr15:44715351-44715401	K562	blood:	n/a
13	chr15:44718396-44718446	SKMC	muscle:	n/a
14	chr15:44719516-44719566	GM19239	blood:	n/a
15	chr15:44617767-44617817	ProgFib	skin:	n/a
16	chr15:44723502-44723552	A549	lung:	n/a
17	chr15:44719935-44719985	GM12878	blood:	n/a
18	chr15:44720131-44720181	SKMC	muscle:	n/a
19	chr15:44718396-44718446	NHBE	bronchial:	n/a
20	chr15:44719012-44719062	ProgFib	skin:	n/a
21	chr15:44719012-44719062	Jurkat	blood:	n/a
22	chr15:44719665-44719715	SK-N-MC	brain:	n/a
23	chr15:44723502-44723552	GM06990	blood:	n/a
24	chr15:44719030-44719080	T-47D	breast:	n/a
25	chr15:44719030-44719080	IMR90	lung:	fetal
26	chr15:44719665-44719715	HEEpiC	esophagus:	n/a
27	chr15:44617767-44617817	HPAEpiC	pulmonary alveolar:	n/a
28	chr15:44719012-44719062	H1-hESC	embryonic stem cell:	embryo
29	chr15:44719516-44719566	HRCEpiC	kidney:	n/a
30	chr15:44719012-44719062	SK-N-MC	brain:	n/a
31	chr15:44719665-44719715	PrEC	prostate:	n/a
32	chr15:44719213-44719263	GM12892	blood:	n/a
33	chr15:44617767-44617817	ECC-1	luminal epithelium:	n/a
34	chr15:44718852-44718902	H1-hESC	embryonic stem cell:	embryo
35	chr15:44719510-44719560	HCF	heart:	n/a
36	chr15:44718396-44718446	GM19239	blood:	n/a
37	chr15:44719213-44719263	HRPEpiC	eye:	n/a
38	chr15:44617767-44617817	HUVEC	blood vessel:	n/a
39	chr15:44719510-44719560	HCPEpiC	choroid plexus:	n/a
40	chr15:44718396-44718446	HIPEpiC	eye:	n/a
41	chr15:44715351-44715401	AG09309	skin:	n/a
42	chr15:44719516-44719566	HAEpiC	amniotic membrane:	n/a
43	chr15:44719665-44719715	AG04450	lung:	fetal
44	chr15:44715351-44715401	RPTEC	kidney:	n/a
45	chr15:44617767-44617817	Jurkat	blood:	n/a
46	chr15:44718852-44718902	Jurkat	blood:	n/a
47	chr15:44719665-44719715	U87	brain:	n/a
48	chr15:44718852-44718902	HRPEpiC	eye:	n/a
49	chr15:44720131-44720181	AG09309	skin:	n/a
50	chr15:44718852-44718902	NH-A	brain:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:44643947..44646779-chr15:44717762..44720215,2	MCF-7	breast:
2	chr15:44718440..44720700-chr15:44829136..44830677,2	K562	blood:
3	chr15:44607871..44610243-chr15:44613499..44616382,2	MCF-7	breast:
4	chr15:44714578..44716892-chr15:44722864..44724371,2	K562	blood:
5	chr15:44693244..44697152-chr15:44700579..44703781,3	K562	blood:
6	chr15:44627409..44629841-chr15:44832460..44835215,2	MCF-7	breast:
7	chr15:44682303..44684802-chr15:44709673..44711281,2	K562	blood:
8	chr15:44673967..44676346-chr15:44716009..44718980,2	K562	blood:
9	chr15:44701657..44704527-chr15:44717641..44719842,2	K562	blood:
10	chr15:44722842..44724510-chr15:44732921..44735166,2	K562	blood:
11	chr15:44719719..44720241-chr16:31470736..31471244,2	Hela-S3	cervix:
12	chr15:44719096..44719799-chr16:69458630..69459143,2	Hela-S3	cervix:
13	chr15:44718811..44719781-chr17:62501482..62502406,2	Hela-S3	cervix:
14	chr12:121148004..121148973-chr15:44718306..44718935,2	NB4	blood:
15	chr1:11968301..11970323-chr15:44722385..44724773,2	K562	blood:
16	chr10:92980435..92981251-chr15:44719397..44720060,2	Hela-S3	cervix:
17	chr15:44580352..44582378-chr15:44719445..44721367,2	MCF-7	breast:
18	chr15:44694836..44697659-chr15:44716673..44718460,2	K562	blood:
19	chr15:44707778..44710924-chr15:44716587..44719642,3	K562	blood:
20	chr15:44718817..44719519-chr6:26198901..26199786,2	Hela-S3	cervix:
21	chr15:44707950..44709936-chr15:44718362..44720165,2	K562	blood:
22	chr15:44704582..44707025-chr15:44716948..44718913,2	K562	blood:
23	chr15:44718905..44719745-chr15:91445892..91446538,2	Hela-S3	cervix:
24	chr15:44719181..44719868-chr9:95526680..95527658,2	Hela-S3	cervix:
25	chr15:44674181..44676932-chr15:44716918..44719048,2	K562	blood:
26	chr15:44586214..44590579-chr15:44718275..44720991,4	K562	blood:
27	chr15:44674181..44676932-chr15:44716918..44719048,2	K562	blood:
28	chr15:44704582..44707025-chr15:44716948..44718913,2	K562	blood:
29	chr15:44714578..44716892-chr15:44722864..44724371,2	K562	blood:
30	chr15:44588053..44590579-chr15:44719354..44720991,3	K562	blood:
31	chr15:44597254..44598879-chr15:44647094..44649629,2	K562	blood:
32	chr15:44719522..44720101-chrX:12993258..12994089,2	Hela-S3	cervix:
33	chr15:44641156..44643504-chr15:44646406..44648886,2	K562	blood:
34	chr15:44579706..44582433-chr15:44718054..44720169,2	MCF-7	breast:
35	chr15:44719279..44719851-chr16:29802138..29802810,2	Hela-S3	cervix:
36	chr14:103800177..103800718-chr15:44719817..44720485,2	Hela-S3	cervix:
37	chr15:44719413..44722163-chr15:44807893..44809754,2	K562	blood:
38	chr15:44718835..44721035-chr15:44723501..44725751,3	K562	blood:
39	chr15:44673967..44676346-chr15:44716009..44718980,2	K562	blood:
40	chr1:28974734..28975648-chr15:44718484..44719281,2	NB4	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPG11-3	chr15:44694883-44695137	ENSG00000259595.1
2	lnc-CTDSPL2-1	chr15:44715559-44715737	XLOC_011235
3	lnc-SPG11-3	chr15:44719307-44719342	ENSG00000259595.1
4	lnc-SPG11-4	chr15:44679518-44679686	ENSG00000259499.1
5	lnc-SPG11-3	chr15:44706408-44706559	ENSG00000259595.1
6	lnc-SPG11-3	chr15:44705532-44705637	ENSG00000259595.1
7	lnc-SPG11-4	chr15:44682164-44682649	ENSG00000259499.1
8	lnc-CTDSPL2-5	chr15:44674277-44674427	NONHSAT042149
9	lnc-CTDSPL2-1	chr15:44717965-44718171	XLOC_011235
10	lnc-CTDSPL2-5	chr15:44673062-44673174	NONHSAT042149
11	lnc-CTDSPL2-3	chr15:44698528-44699081	NONHSAT042152
12	lnc-CTDSPL2-3	chr15:44701717-44702045	NONHSAT042152
13	lnc-CTDSPL2-1	chr15:44718492-44718499	XLOC_011235
14	lnc-SPG11-3	chr15:44697525-44697600	ENSG00000259595.1

No data

Variant related genes	Relation type
ENSG00000203572	TF binding region
CASC4	TF binding region
ENSG00000259499	TF binding region
ENSG00000250130	TF binding region
ENSG00000259595	TF binding region
RN7SL347P	TF binding region
CTDSPL2	TF binding region
ENSG00000203572	CpG island
CASC4	CpG island
ENSG00000259499	CpG island
ENSG00000250130	CpG island
ENSG00000259595	CpG island
RN7SL347P	CpG island
CTDSPL2	CpG island
ENSG00000175970	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000079616	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000259499	chromatin interactions
ENSG00000137770	chromatin interactions
ENSG00000250130	chromatin interactions
ENSG00000205542	chromatin interactions
ENSG00000180628	chromatin interactions
ENSG00000100664	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000185963	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000103018	chromatin interactions
ENSG00000104131	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000259595	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000203572	chromatin interactions
ENSG00000259563	chromatin interactions
ENSG00000166734	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000203575	chromatin interactions

Extended variants
information (count: 3686 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3686 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1021800	chr15:44609796-44609797	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558505626	chr15:44609803-44609804	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs571964987	chr15:44609813-44609814	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188208952	chr15:44609878-44609879	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557799554	chr15:44609879-44609880	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577857228	chr15:44609883-44609884	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543258939	chr15:44609921-44609922	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181743111	chr15:44609988-44609989	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186262750	chr15:44610045-44610046	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573460173	chr15:44610047-44610048	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541934937	chr15:44610066-44610067	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561122459	chr15:44610103-44610104	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs143160731	chr15:44610111-44610112	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs367654503	chr15:44610258-44610259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576799848	chr15:44610259-44610260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547761483	chr15:44610327-44610328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564675902	chr15:44610341-44610342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533682841	chr15:44610358-44610359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201124163	chr15:44610394-44610395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146768267	chr15:44610414-44610415	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs202141257	chr15:44610423-44610424	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190483098	chr15:44610449-44610450	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544608153	chr15:44610451-44610452	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114551997	chr15:44610459-44610460	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140386821	chr15:44610482-44610483	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561402724	chr15:44610500-44610501	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145484389	chr15:44610569-44610570	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530117280	chr15:44610571-44610572	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148039131	chr15:44610628-44610629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140810106	chr15:44610634-44610635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75056084	chr15:44610636-44610637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556802893	chr15:44610640-44610641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4924746	chr15:44610642-44610643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs150431126	chr15:44610687-44610688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138181441	chr15:44610736-44610737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149573628	chr15:44610787-44610788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147241948	chr15:44610811-44610812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564516076	chr15:44610821-44610822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116217709	chr15:44610840-44610841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115589394	chr15:44610850-44610851	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377246872	chr15:44610893-44610894	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563947641	chr15:44610922-44610923	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115543160	chr15:44610947-44610948	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549588416	chr15:44611072-44611073	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs565682144	chr15:44611075-44611076	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs528191964	chr15:44611086-44611087	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs148309101	chr15:44611126-44611127	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs12591581	chr15:44611221-44611222	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs571237926	chr15:44611262-44611263	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs374984686	chr15:44611271-44611272	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Melanoma	17363583	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44582000-44639400	Weak transcription	Lung	lung
2	chr15:44582800-44672200	Weak transcription	HSMM	muscle
3	chr15:44583000-44639400	Weak transcription	Fetal Lung	lung
4	chr15:44583200-44639200	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr15:44583800-44639200	Weak transcription	Brain Germinal Matrix	brain
6	chr15:44584200-44625600	Weak transcription	Fetal Brain Female	brain
7	chr15:44585400-44628200	Weak transcription	Thymus	Thymus
8	chr15:44589000-44619000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:44589000-44631600	Weak transcription	Left Ventricle	heart
10	chr15:44589200-44626400	Weak transcription	Fetal Muscle Leg	muscle
11	chr15:44589600-44617400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr15:44589800-44625200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:44589800-44632000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:44589800-44632400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr15:44589800-44632400	Weak transcription	NHLF	lung
16	chr15:44591400-44632800	Weak transcription	Hela-S3	cervix
17	chr15:44592800-44617600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr15:44592800-44639800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr15:44593200-44621200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr15:44593200-44625600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr15:44593200-44639200	Weak transcription	K562	blood
22	chr15:44593200-44639400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr15:44593600-44621200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:44593800-44613200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr15:44593800-44639400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr15:44595200-44631600	Weak transcription	Fetal Muscle Trunk	muscle
27	chr15:44597200-44610800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr15:44597800-44613200	Weak transcription	Fetal Stomach	stomach
29	chr15:44597800-44623200	Weak transcription	Fetal Intestine Small	intestine
30	chr15:44598400-44628600	Weak transcription	Primary T cells from cord blood	blood
31	chr15:44598600-44646800	Weak transcription	Right Ventricle	heart
32	chr15:44599600-44632600	Weak transcription	HSMMtube	muscle
33	chr15:44600800-44632400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr15:44601000-44620800	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr15:44601000-44624800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:44601200-44621200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr15:44601600-44617400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:44601600-44638600	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr15:44602200-44614000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr15:44602200-44629200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr15:44602200-44638400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr15:44602400-44621000	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr15:44602400-44639400	Weak transcription	Gastric	stomach
44	chr15:44602400-44639600	Weak transcription	Pancreas	Pancrea
45	chr15:44603200-44629200	Weak transcription	Primary B cells from cord blood	blood
46	chr15:44603600-44624800	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr15:44605800-44632800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr15:44607200-44617400	Weak transcription	HepG2	liver
49	chr15:44607600-44613400	Weak transcription	Small Intestine	intestine
50	chr15:44607800-44609800	Weak transcription	Brain Substantia Nigra	brain

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