Variant report

Variant	nsv569402
Chromosome Location	chr15:51019117-51117524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1133)
CpG islands
(count:1039)
Chromatin interactive
region (count:119)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1133 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:51069432-51069509	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:51059347-51059688	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:51045651-51046001	K562	blood:	n/a	n/a
4	ARID3A	chr15:51110747-51110790	K562	blood:	n/a	n/a
5	ARID3A	chr15:51056430-51057534	K562	blood:	n/a	n/a
6	ARID3A	chr15:51058735-51059038	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:51056462-51056754	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:51057958-51058011	K562	blood:	n/a	n/a
9	ARID3A	chr15:51102246-51102334	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:51057083-51058225	HepG2	liver:	n/a	n/a
11	ATF1	chr15:51045773-51045996	K562	blood:	n/a	n/a
12	ATF1	chr15:51090944-51091269	K562	blood:	n/a	n/a
13	ATF2	chr15:51057209-51058191	GM12878	blood:	n/a	n/a
14	ATF3	chr15:51090913-51091271	K562	blood:	n/a	n/a
15	ATF3	chr15:51057123-51057710	A549	lung:	n/a	n/a
16	ATF3	chr15:51045700-51045997	K562	blood:	n/a	n/a
17	ATF3	chr15:51057183-51057646	K562	blood:	n/a	n/a
18	BCL11A	chr15:51057810-51058299	GM12878	blood:	n/a	chr15:51058009-51058022
19	BCL3	chr15:51090917-51091281	GM12878	blood:	n/a	n/a
20	BCL3	chr15:51057076-51058175	A549	lung:	n/a	chr15:51058009-51058022 chr15:51057801-51057814
21	BCL3	chr15:51057102-51058408	A549	lung:	n/a	chr15:51058009-51058022 chr15:51057801-51057814
22	BCLAF1	chr15:51057573-51058194	GM12878	blood:	n/a	chr15:51058009-51058022 chr15:51057801-51057814
23	BCLAF1	chr15:51056598-51057205	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:51066644-51067308	K562	blood:	n/a	n/a
25	BHLHE40	chr15:51057125-51058312	K562	blood:	n/a	n/a
26	BHLHE40	chr15:51058775-51059006	HepG2	liver:	n/a	n/a
27	BHLHE40	chr15:51056542-51057226	GM12878	blood:	n/a	n/a
28	BRCA1	chr15:51108340-51108820	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr15:51058134-51058305	HepG2	liver:	n/a	n/a
30	BRCA1	chr15:51057677-51057834	HepG2	liver:	n/a	n/a
31	BRCA1	chr15:51045608-51045972	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr15:51057024-51058404	K562	blood:	n/a	n/a
33	CBX3	chr15:51057190-51057517	K562	blood:	n/a	n/a
34	CBX3	chr15:51090131-51090504	HCT-116	colon:	n/a	n/a
35	CCNT2	chr15:51057370-51058205	K562	blood:	n/a	chr15:51057613-51057622
36	CCNT2	chr15:51115557-51115616	K562	blood:	n/a	n/a
37	CCNT2	chr15:51045653-51046083	K562	blood:	n/a	chr15:51045942-51045962
38	CEBPB	chr15:51057829-51058244	A549	lung:	n/a	n/a
39	CEBPB	chr15:51081952-51082181	K562	blood:	n/a	chr15:51082025-51082036
40	CEBPB	chr15:51033262-51033434	A549	lung:	n/a	n/a
41	CEBPB	chr15:51045696-51045964	A549	lung:	n/a	chr15:51045815-51045826 chr15:51045875-51045886 chr15:51045875-51045888
42	CEBPB	chr15:51065374-51065523	Hela-S3	cervix:	n/a	chr15:51065414-51065425
43	CEBPB	chr15:51078632-51079087	MCF-7	breast:	n/a	chr15:51078837-51078848
44	CEBPB	chr15:51056949-51058416	A549	lung:	n/a	n/a
45	CEBPB	chr15:51090092-51090657	MCF-7	breast:	n/a	n/a
46	CEBPB	chr15:51116741-51117067	Hela-S3	cervix:	n/a	chr15:51116903-51116914
47	CEBPB	chr15:51066711-51067002	IMR90	lung:	n/a	n/a
48	CEBPB	chr15:51098898-51099228	A549	lung:	n/a	chr15:51099051-51099062 chr15:51099051-51099064 chr15:51099052-51099063
49	CEBPB	chr15:51057271-51057523	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:51045622-51046046	K562	blood:	n/a	chr15:51045815-51045826 chr15:51045875-51045886 chr15:51045875-51045888

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51057714-51057764	HCPEpiC	choroid plexus:	n/a
2	chr15:51058050-51058100	PANC-1	pancreas:	n/a
3	chr15:51057714-51057764	HCPEpiC	choroid plexus:	n/a
4	chr15:51058050-51058100	PANC-1	pancreas:	n/a
5	chr15:51058050-51058100	AG10803	skin:	n/a
6	chr15:51058100-51058150	PFSK-1	brain:	n/a
7	chr15:51057714-51057764	HCM	heart:	n/a
8	chr15:51115739-51115789	HEEpiC	esophagus:	n/a
9	chr15:51060843-51060893	HEK293	kidney:	embryo
10	chr15:51057417-51057467	Hepatocyte	liver:	n/a
11	chr15:51044672-51044722	GM12891	blood:	n/a
12	chr15:51058035-51058085	NHDF-neo	bronchial:	n/a
13	chr15:51058084-51058134	IMR90	lung:	fetal
14	chr15:51058050-51058100	Caco-2	colon:	n/a
15	chr15:51057417-51057467	K562	blood:	n/a
16	chr15:51044672-51044722	AG09319	gingival:	n/a
17	chr15:51054077-51054127	HCT-116	colon:	n/a
18	chr15:51058035-51058085	AG10803	skin:	n/a
19	chr15:51057859-51057909	AG09319	gingival:	n/a
20	chr15:51058035-51058085	SK-N-SH_RA	brain:	n/a
21	chr15:51057859-51057909	AoSMC	blood vessel:	n/a
22	chr15:51058050-51058100	A549	lung:	n/a
23	chr15:51057714-51057764	IMR90	lung:	fetal
24	chr15:51058100-51058150	BJ	skin:	n/a
25	chr15:51058114-51058164	H1-hESC	embryonic stem cell:	embryo
26	chr15:51054077-51054127	SAEC	small airway:	n/a
27	chr15:51115739-51115789	Hepatocyte	liver:	n/a
28	chr15:51054077-51054127	AG10803	skin:	n/a
29	chr15:51054077-51054127	GM12892	blood:	n/a
30	chr15:51057768-51057818	HCT-116	colon:	n/a
31	chr15:51058014-51058064	HRPEpiC	eye:	n/a
32	chr15:51044672-51044722	NHBE	bronchial:	n/a
33	chr15:51060843-51060893	NHDF-neo	bronchial:	n/a
34	chr15:51057768-51057818	NH-A	brain:	n/a
35	chr15:51056548-51056598	AG09309	skin:	n/a
36	chr15:51056548-51056598	SK-N-MC	brain:	n/a
37	chr15:51058014-51058064	ovcar-3	ovarian:	n/a
38	chr15:51058100-51058150	ProgFib	skin:	n/a
39	chr15:51058100-51058150	HRCEpiC	kidney:	n/a
40	chr15:51044672-51044722	SKMC	muscle:	n/a
41	chr15:51056548-51056598	NB4	blood:	n/a
42	chr15:51057417-51057467	SKMC	muscle:	n/a
43	chr15:51058100-51058150	MCF10A-Er-Src	breast:	n/a
44	chr15:51057417-51057467	HCT-116	colon:	n/a
45	chr15:51058014-51058064	AG04449	skin:	fetal
46	chr15:51057714-51057764	HCF	heart:	n/a
47	chr15:51044672-51044722	GM19239	blood:	n/a
48	chr15:51058035-51058085	Caco-2	colon:	n/a
49	chr15:51060843-51060893	BE2_C	brain:	n/a
50	chr15:51058050-51058100	U87	brain:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:51039062..51042009-chr15:51057876..51060168,3	MCF-7	breast:
2	chr15:51056915..51057558-chr15:51070113..51070977,2	MCF-7	breast:
3	chr15:51059873..51062365-chr15:51065766..51068595,2	K562	blood:
4	chr15:51056364..51059035-chr15:51076545..51079419,2	K562	blood:
5	chr15:50982278..50983197-chr15:51056944..51057802,4	MCF-7	breast:
6	chr15:51096365..51098220-chr15:51106260..51108454,2	MCF-7	breast:
7	chr15:50918354..50921026-chr15:51021586..51024072,2	MCF-7	breast:
8	chr15:51014164..51017311-chr15:51023770..51026173,3	MCF-7	breast:
9	chr15:51037199..51038791-chr15:51054779..51056301,2	K562	blood:
10	chr15:51025715..51027452-chr15:51057581..51060241,2	MCF-7	breast:
11	chr15:50976295..50981465-chr15:51052766..51059546,15	MCF-7	breast:
12	chr15:51056750..51061263-chr15:51087602..51092500,6	MCF-7	breast:
13	chr15:51110106..51113018-chr15:51115605..51118067,2	K562	blood:
14	chr15:50978751..50980715-chr15:51047104..51049659,2	K562	blood:
15	chr15:51059872..51062621-chr15:51075621..51077496,2	MCF-7	breast:
16	chr15:50978732..50980573-chr15:51017236..51021857,4	K562	blood:
17	chr15:51055359..51059302-chr15:51076639..51080808,6	MCF-7	breast:
18	chr15:51090561..51092703-chr15:51108354..51111264,3	MCF-7	breast:
19	chr15:51046404..51048794-chr15:51049414..51052213,2	K562	blood:
20	chr15:51055767..51057855-chr19:39899197..39901640,2	MCF-7	breast:
21	chr15:51056515..51059362-chr15:51088829..51092887,6	MCF-7	breast:
22	chr15:51096365..51098220-chr15:51106260..51108454,2	MCF-7	breast:
23	chr15:51032315..51034610-chr15:51041268..51043342,2	MCF-7	breast:
24	chr15:50978375..50980189-chr15:51105380..51108693,3	K562	blood:
25	chr15:51056319..51059244-chr15:51115290..51117379,3	MCF-7	breast:
26	chr15:51080266..51082238-chr17:56734970..56736664,2	MCF-7	breast:
27	chr15:51054229..51056382-chr15:51058543..51060392,2	K562	blood:
28	chr15:51021620..51024253-chr15:51027951..51030254,2	K562	blood:
29	chr15:51021620..51024253-chr15:51027951..51030254,2	K562	blood:
30	chr15:51057652..51059901-chr15:51083890..51085609,2	K562	blood:
31	chr15:50977075..50980199-chr15:51027449..51029550,3	MCF-7	breast:
32	chr15:50977319..50980700-chr15:51053372..51060901,7	MCF-7	breast:
33	chr15:50987564..50989809-chr15:51045515..51047081,2	MCF-7	breast:
34	chr15:51059872..51062621-chr15:51075621..51077496,2	MCF-7	breast:
35	chr15:51045886..51047999-chr15:51058293..51060374,2	K562	blood:
36	chr15:51039545..51042117-chr15:51054834..51058033,5	MCF-7	breast:
37	chr15:51033137..51038584-chr15:51056604..51059356,6	MCF-7	breast:
38	chr15:51059873..51062365-chr15:51065766..51068595,2	K562	blood:
39	chr15:51101484..51104365-chr15:51107028..51109009,2	K562	blood:
40	chr15:51040134..51042718-chr15:51055883..51057595,3	K562	blood:
41	chr15:51083211..51087261-chr15:51087532..51090501,5	MCF-7	breast:
42	chr15:51057767..51058453-chr5:32174404..32175249,2	Hela-S3	cervix:
43	chr15:51023962..51026987-chr15:51030777..51033771,3	MCF-7	breast:
44	chr15:51039545..51042117-chr15:51054834..51058033,5	MCF-7	breast:
45	chr15:50977419..50980911-chr15:51055926..51058477,4	K562	blood:
46	chr15:51083211..51087261-chr15:51087532..51090501,5	MCF-7	breast:
47	chr15:51056442..51059084-chr15:51199726..51202707,2	MCF-7	breast:
48	chr15:51069319..51071729-chr15:51072874..51075260,2	MCF-7	breast:
49	chr15:51101484..51104365-chr15:51107028..51109009,2	K562	blood:
50	chr15:50977470..50980168-chr15:51041572..51044508,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP4E1-5	chr15:51090867-51091148	NONHSAT042437
2	lnc-AP4E1-1	chr15:51038906-51039027	ENSG00000259773.1
3	lnc-AP4E1-1	chr15:51041845-51042026	ENSG00000259773.1
4	lnc-TRPM7-3	chr15:51034900-51035473	NONHSAT042435
5	lnc-TRPM7-1	chr15:51025117-51025495	ENSG00000250395

No data

Variant related genes	Relation type
ENSG00000241130	TF binding region
SPPL2A	TF binding region
ENSG00000259773	TF binding region
ENSG00000241130	CpG island
SPPL2A	CpG island
ENSG00000259773	CpG island
ENSG00000119541	chromatin interactions
ENSG00000163874	chromatin interactions
ENSG00000259773	chromatin interactions
ENSG00000243027	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000113384	chromatin interactions
ENSG00000266559	chromatin interactions
ENSG00000272086	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000154429	chromatin interactions
ENSG00000092439	chromatin interactions
ENSG00000167987	chromatin interactions
ENSG00000198366	chromatin interactions
ENSG00000081014	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000077150	chromatin interactions
ENSG00000241130	chromatin interactions
ENSG00000179818	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000196176	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000201699	chromatin interactions
PITPNA	miRNA target sites

Extended variants
information (count: 3690 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3690 , 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	rs11855605	chr15:51019117-51019118	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62018799	chr15:51019165-51019166	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs535413848	chr15:51019180-51019181	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557105154	chr15:51019207-51019208	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72742308	chr15:51019259-51019260	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546003939	chr15:51019311-51019312	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs181465698	chr15:51019331-51019332	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576962021	chr15:51019357-51019358	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543741747	chr15:51019397-51019398	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187566683	chr15:51019455-51019456	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559348228	chr15:51019479-51019480	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375374559	chr15:51019543-51019544	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191847405	chr15:51019560-51019561	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs542122556	chr15:51019623-51019624	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116804294	chr15:51019730-51019731	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs17646025	chr15:51019812-51019813	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs552747090	chr15:51019813-51019814	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150873021	chr15:51019862-51019863	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs114788110	chr15:51019867-51019868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138279520	chr15:51019913-51019914	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs62018800	chr15:51019964-51019965	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs114026860	chr15:51019976-51019977	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542727985	chr15:51020000-51020001	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372849232	chr15:51020008-51020009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs550575921	chr15:51020064-51020065	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569138146	chr15:51020084-51020085	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560930162	chr15:51020089-51020090	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114579547	chr15:51020103-51020104	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182887832	chr15:51020164-51020165	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115146721	chr15:51020165-51020166	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531418979	chr15:51020188-51020189	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs376298864	chr15:51020194-51020195	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs62018801	chr15:51020195-51020196	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs577253642	chr15:51020221-51020222	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs75964827	chr15:51020264-51020265	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112081590	chr15:51020265-51020266	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542209355	chr15:51020272-51020273	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112800672	chr15:51020278-51020279	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144292323	chr15:51020285-51020286	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs62018802	chr15:51020318-51020319	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143588983	chr15:51020371-51020372	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146311631	chr15:51020395-51020396	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528180749	chr15:51020415-51020416	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187439226	chr15:51020416-51020417	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs4511475	chr15:51020463-51020464	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs4641679	chr15:51020600-51020601	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189830610	chr15:51020629-51020630	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182813166	chr15:51020639-51020640	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs539745489	chr15:51020662-51020663	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs551143551	chr15:51020689-51020690	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1817 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50988000-51056800	Weak transcription	Esophagus	oesophagus
2	chr15:50988200-51021600	Weak transcription	Pancreas	Pancrea
3	chr15:50990000-51038800	Weak transcription	NHLF	lung
4	chr15:50990200-51021600	Weak transcription	Psoas Muscle	Psoas
5	chr15:50991600-51033600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr15:50995000-51026400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr15:50995600-51046000	Weak transcription	Small Intestine	intestine
8	chr15:50997000-51044800	Weak transcription	K562	blood
9	chr15:50997400-51025000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr15:50997600-51033600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr15:50998200-51026800	Weak transcription	HMEC	breast
12	chr15:50998800-51043200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr15:50999000-51021600	Weak transcription	Dnd41	blood
14	chr15:50999200-51027400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr15:50999200-51041600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr15:50999600-51021600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr15:50999800-51043400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr15:51000000-51045000	Weak transcription	NHEK	skin
19	chr15:51000600-51039200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr15:51004000-51056200	Weak transcription	Brain Angular Gyrus	brain
21	chr15:51004800-51028800	Weak transcription	Gastric	stomach
22	chr15:51005400-51026200	Weak transcription	Fetal Brain Male	brain
23	chr15:51005800-51020600	Strong transcription	Placenta	Placenta
24	chr15:51006800-51020600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:51007400-51026600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:51008800-51033000	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr15:51009000-51019600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:51009200-51019400	Strong transcription	Duodenum Smooth Muscle	Duodenum
29	chr15:51009200-51019600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr15:51009200-51020200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr15:51009200-51022800	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr15:51009200-51041400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr15:51009200-51041400	Strong transcription	Skeletal Muscle Female	skeletal muscle
34	chr15:51009400-51019600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr15:51009400-51020400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr15:51009600-51033400	Strong transcription	Primary B cells from peripheral blood	blood
37	chr15:51009800-51020600	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr15:51009800-51036600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr15:51009800-51042600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr15:51010000-51035400	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr15:51010400-51020200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr15:51010800-51022800	Strong transcription	Adipose Nuclei	Adipose
43	chr15:51011400-51040000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr15:51011400-51045000	Weak transcription	Fetal Heart	heart
45	chr15:51011600-51030800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr15:51012400-51021600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr15:51012400-51021600	Weak transcription	NHDF-Ad	bronchial
48	chr15:51012400-51026200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr15:51012400-51026200	Weak transcription	Fetal Kidney	kidney
50	chr15:51012400-51027200	Weak transcription	Brain Substantia Nigra	brain

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