Variant report

Variant	nsv471506
Chromosome Location	chr15:56659709-56896385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1482)
CpG islands
(count:919)
Chromatin interactive
region (count:53)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1482 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56788756-56789177	K562	blood:	n/a	chr15:56788814-56788830
2	ARID3A	chr15:56881619-56881703	K562	blood:	n/a	n/a
3	ARID3A	chr15:56757439-56757589	K562	blood:	n/a	n/a
4	ARID3A	chr15:56757183-56757342	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:56788752-56789118	HepG2	liver:	n/a	chr15:56788814-56788830
6	ARID3A	chr15:56721089-56721405	K562	blood:	n/a	n/a
7	ATF1	chr15:56785297-56785306	K562	blood:	n/a	n/a
8	ATF1	chr15:56701414-56701616	K562	blood:	n/a	n/a
9	ATF1	chr15:56761692-56762037	K562	blood:	n/a	n/a
10	ATF2	chr15:56663598-56664493	GM12878	blood:	n/a	n/a
11	ATF2	chr15:56757025-56757555	GM12878	blood:	n/a	n/a
12	ATF2	chr15:56663797-56664492	GM12878	blood:	n/a	n/a
13	ATF3	chr15:56767569-56767875	K562	blood:	n/a	n/a
14	BACH1	chr15:56757137-56757703	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:56757918-56757978	K562	blood:	n/a	n/a
16	BATF	chr15:56663915-56664384	GM12878	blood:	n/a	n/a
17	BATF	chr15:56663904-56664369	GM12878	blood:	n/a	n/a
18	BATF	chr15:56788822-56789212	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:56663906-56664378	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:56663977-56664272	GM12878	blood:	n/a	n/a
21	BCL3	chr15:56757103-56757795	A549	lung:	n/a	n/a
22	BCL3	chr15:56757037-56757647	GM12878	blood:	n/a	n/a
23	BCL3	chr15:56663980-56664306	GM12878	blood:	n/a	n/a
24	BCL3	chr15:56663757-56664346	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:56663809-56664496	GM12878	blood:	n/a	n/a
26	BCLAF1	chr15:56663925-56664375	GM12878	blood:	n/a	n/a
27	BCLAF1	chr15:56757083-56757625	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:56757184-56757611	K562	blood:	n/a	chr15:56757254-56757270
29	BHLHE40	chr15:56830099-56830356	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:56704886-56704981	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:56844843-56845124	K562	blood:	n/a	n/a
32	BHLHE40	chr15:56783358-56783670	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:56757494-56757730	HepG2	liver:	n/a	n/a
34	BHLHE40	chr15:56663829-56664374	GM12878	blood:	n/a	n/a
35	CBX3	chr15:56757309-56757702	K562	blood:	n/a	n/a
36	CBX3	chr15:56878353-56878826	HCT-116	colon:	n/a	n/a
37	CBX3	chr15:56878445-56878784	K562	blood:	n/a	n/a
38	CBX3	chr15:56757101-56757760	K562	blood:	n/a	n/a
39	CBX3	chr15:56878477-56878666	K562	blood:	n/a	n/a
40	CCNT2	chr15:56757151-56757524	K562	blood:	n/a	n/a
41	CEBPB	chr15:56724449-56724866	HepG2	liver:	n/a	chr15:56724724-56724735
42	CEBPB	chr15:56767644-56767889	Hela-S3	cervix:	n/a	chr15:56767741-56767752
43	CEBPB	chr15:56683119-56683285	A549	lung:	n/a	n/a
44	CEBPB	chr15:56752307-56752555	K562	blood:	n/a	n/a
45	CEBPB	chr15:56708065-56708209	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:56748579-56748651	A549	lung:	n/a	n/a
47	CEBPB	chr15:56708105-56708119	IMR90	lung:	n/a	n/a
48	CEBPB	chr15:56854327-56854483	HepG2	liver:	n/a	chr15:56854398-56854409
49	CEBPB	chr15:56848778-56849077	Hela-S3	cervix:	n/a	chr15:56848952-56848963
50	CEBPB	chr15:56701741-56701793	K562	blood:	n/a	n/a

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56757625-56757675	SK-N-SH	brain:	n/a
2	chr15:56757325-56757375	GM19239	blood:	n/a
3	chr15:56757314-56757364	NHBE	bronchial:	n/a
4	chr15:56757499-56757549	HEK293	kidney:	embryo
5	chr15:56757625-56757675	SK-N-SH	brain:	n/a
6	chr15:56757325-56757375	GM19239	blood:	n/a
7	chr15:56757314-56757364	NHBE	bronchial:	n/a
8	chr15:56757499-56757549	HEK293	kidney:	embryo
9	chr15:56757499-56757549	HAEpiC	amniotic membrane:	n/a
10	chr15:56758270-56758320	HepG2	liver:	n/a
11	chr15:56757180-56757230	SK-N-SH	brain:	n/a
12	chr15:56757180-56757230	HEEpiC	esophagus:	n/a
13	chr15:56759655-56759705	AoSMC	blood vessel:	n/a
14	chr15:56757325-56757375	BJ	skin:	n/a
15	chr15:56757180-56757230	HepG2	liver:	n/a
16	chr15:56757325-56757375	HRPEpiC	eye:	n/a
17	chr15:56757499-56757549	AG09309	skin:	n/a
18	chr15:56725876-56725926	GM19239	blood:	n/a
19	chr15:56757382-56757432	IMR90	lung:	fetal
20	chr15:56757382-56757432	AoSMC	blood vessel:	n/a
21	chr15:56757552-56757602	HCM	heart:	n/a
22	chr15:56725876-56725926	A549	lung:	n/a
23	chr15:56757312-56757362	HUVEC	blood vessel:	n/a
24	chr15:56725876-56725926	SK-N-MC	brain:	n/a
25	chr15:56759655-56759705	MCF-7	breast:	n/a
26	chr15:56757625-56757675	HRPEpiC	eye:	n/a
27	chr15:56757552-56757602	BJ	skin:	n/a
28	chr15:56757625-56757675	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:56757806-56757856	HL-60	blood:	n/a
30	chr15:56725876-56725926	MCF10A-Er-Src	breast:	n/a
31	chr15:56757382-56757432	HMEC	breast:	n/a
32	chr15:56725876-56725926	GM12878	blood:	n/a
33	chr15:56757625-56757675	GM12892	blood:	n/a
34	chr15:56757499-56757549	HEEpiC	esophagus:	n/a
35	chr15:56757325-56757375	PrEC	prostate:	n/a
36	chr15:56757312-56757362	HCT-116	colon:	n/a
37	chr15:56725876-56725926	HUVEC	blood vessel:	n/a
38	chr15:56757625-56757675	HCM	heart:	n/a
39	chr15:56757806-56757856	GM06990	blood:	n/a
40	chr15:56757180-56757230	AG10803	skin:	n/a
41	chr15:56757312-56757362	MCF10A-Er-Src	breast:	n/a
42	chr15:56757180-56757230	HNPCEpiC	eye:	n/a
43	chr15:56757517-56757567	GM19239	blood:	n/a
44	chr15:56757517-56757567	Jurkat	blood:	n/a
45	chr15:56757312-56757362	HL-60	blood:	n/a
46	chr15:56758270-56758320	HCF	heart:	n/a
47	chr15:56757325-56757375	HCF	heart:	n/a
48	chr15:56757552-56757602	AoSMC	blood vessel:	n/a
49	chr15:56757499-56757549	MCF-7	breast:	n/a
50	chr15:56757552-56757602	HAEpiC	amniotic membrane:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
2	chr15:56537725..56539025-chr15:56720287..56722326,16	MCF-7	breast:
3	chr15:56541018..56541999-chr15:56720733..56721455,3	MCF-7	breast:
4	chr15:56656054..56659160-chr15:56661634..56663822,3	K562	blood:
5	chr15:56540398..56542023-chr15:56720800..56721752,16	MCF-7	breast:
6	chr15:56662948..56665522-chr15:56683951..56686718,2	MCF-7	breast:
7	chr15:56787707..56790107-chr15:57597582..57600140,2	MCF-7	breast:
8	chr15:56756734..56759056-chr15:56761429..56763544,2	K562	blood:
9	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
10	chr15:56696715..56699099-chr15:56700955..56702991,2	MCF-7	breast:
11	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:
12	chr15:56788688..56789403-chr15:57430424..57431057,2	MCF-7	breast:
13	chr15:56657402..56659160-chr15:56661272..56663134,2	K562	blood:
14	chr15:56066629..56067204-chr15:56720771..56721659,2	K562	blood:
15	chr15:56536734..56539507-chr15:56718886..56721172,2	MCF-7	breast:
16	chr15:56540966..56543133-chr15:56718827..56720916,2	MCF-7	breast:
17	chr15:56537986..56539019-chr15:56720847..56721772,4	K562	blood:
18	chr15:55940442..55941185-chr15:56720975..56721740,2	K562	blood:
19	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
20	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
21	chr15:56663360..56664228-chr20:52363663..52364657,2	MCF-7	breast:
22	chr15:56537987..56538847-chr15:56756234..56756979,2	MCF-7	breast:
23	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
24	chr15:56788851..56789408-chr15:57103635..57104349,2	MCF-7	breast:
25	chr15:56817798..56822839-chr15:56825097..56828742,5	K562	blood:
26	chr15:56814069..56816681-chr15:56818491..56820321,2	K562	blood:
27	chr15:56788702..56789394-chr15:57161523..57162414,2	MCF-7	breast:
28	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
29	chr15:56811740..56813746-chr15:56822934..56825907,2	K562	blood:
30	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
31	chr15:56773647..56776313-chr15:57177229..57179430,2	K562	blood:
32	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
33	chr15:56662303..56664925-chr15:56669257..56671232,2	MCF-7	breast:
34	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
35	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
36	chr15:56535922..56537613-chr15:56658440..56660656,2	MCF-7	breast:
37	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
38	chr15:56662303..56664925-chr15:56669257..56671232,2	MCF-7	breast:
39	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
40	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
41	chr15:56817798..56822286-chr15:56825097..56828742,4	K562	blood:
42	chr15:56791160..56793250-chr15:56794933..56796796,2	K562	blood:
43	chr15:56541012..56541917-chr15:56720826..56721341,2	K562	blood:
44	chr15:56788456..56789162-chr15:57113822..57114589,2	MCF-7	breast:
45	chr15:56782685..56785505-chr15:57019755..57021681,2	K562	blood:
46	chr15:56788444..56789415-chr15:57598413..57599206,3	K562	blood:
47	chr15:56788753..56789362-chr15:57161247..57161954,2	K562	blood:
48	chr15:56538080..56538849-chr15:56720711..56721356,4	MCF-7	breast:
49	chr15:56783040..56784156-chr15:57161563..57162645,6	K562	blood:
50	chr15:56587524..56588313-chr15:56720286..56721333,4	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF280D-1	chr15:56840058-56840205	ENSG00000260392.1
2	lnc-MNS1-1	chr15:56701994-56702384	ENSG00000261823.1
3	lnc-ZNF280D-1	chr15:56835757-56836010	ENSG00000260392.1
4	lnc-ZNF280D-1	chr15:56884918-56885050	ENSG00000260392.1
5	lnc-ZNF280D-1	chr15:56896038-56896069	ENSG00000260392.1
6	lnc-TCF12-5	chr15:56665636-56665702	NONHSAT044018
7	lnc-MNS1-1	chr15:56700681-56701128	ENSG00000261823.1
8	lnc-TCF12-5	chr15:56666352-56666821	NONHSAT044018
9	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
10	lnc-ZNF280D-1	chr15:56840645-56840799	ENSG00000260392.1
11	lnc-ZNF280D-2	chr15:56755978-56756445	NONHSAT044023
12	lnc-ZNF280D-2	chr15:56757168-56757283	NONHSAT044023
13	lnc-ZNF280D-1	chr15:56841355-56841708	ENSG00000260392.1
14	lnc-ZNF280D-1	chr15:56840136-56840205	ENSG00000260392.1
15	lnc-ZNF280D-1	chr15:56835150-56835294	ENSG00000260392.1

No data

Variant related genes	Relation type
ENSG00000259941	TF binding region
MNS1	TF binding region
TEX9	TF binding region
ENSG00000261823	TF binding region
ENSG00000259941	CpG island
MNS1	CpG island
TEX9	CpG island
ENSG00000261823	CpG island
ENSG00000261823	chromatin interactions
ENSG00000151575	chromatin interactions
ENSG00000138587	chromatin interactions

Extended variants
information (count: 7843 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7843 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74015413	chr15:56659787-56659788	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183317979	chr15:56659791-56659792	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs188319574	chr15:56659818-56659819	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1426070	chr15:56659828-56659829	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs141080147	chr15:56659840-56659841	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192771057	chr15:56659871-56659872	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550149245	chr15:56659901-56659902	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570193091	chr15:56659930-56659931	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538967460	chr15:56659948-56659949	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112487845	chr15:56659952-56659953	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552808429	chr15:56659991-56659992	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs369549996	chr15:56660067-56660068	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565694021	chr15:56660082-56660083	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534638028	chr15:56660104-56660105	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184076484	chr15:56660191-56660192	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540069388	chr15:56660201-56660202	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574630433	chr15:56660224-56660225	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562578584	chr15:56660243-56660244	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs114634739	chr15:56660282-56660283	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529701288	chr15:56660298-56660299	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188455088	chr15:56660301-56660302	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576920600	chr15:56660317-56660318	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373464541	chr15:56660343-56660344	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545798530	chr15:56660371-56660372	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191381216	chr15:56660383-56660384	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184935872	chr15:56660404-56660405	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs541075373	chr15:56660438-56660439	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560939485	chr15:56660465-56660466	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs116566068	chr15:56660466-56660467	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560347840	chr15:56660496-56660497	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190285411	chr15:56660509-56660510	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150307250	chr15:56660588-56660589	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532705424	chr15:56660593-56660594	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552480145	chr15:56660597-56660598	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531573532	chr15:56660598-56660599	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4774854	chr15:56660617-56660618	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs535331643	chr15:56660641-56660642	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548247601	chr15:56660644-56660645	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs552346113	chr15:56660645-56660646	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568016500	chr15:56660692-56660693	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs536748350	chr15:56660776-56660777	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs562556738	chr15:56660797-56660798	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs182048656	chr15:56660813-56660814	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs1520531	chr15:56660845-56660846	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs186925287	chr15:56660874-56660875	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs190159398	chr15:56660881-56660882	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs565190234	chr15:56660901-56660902	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs373069868	chr15:56660905-56660906	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs74015414	chr15:56660909-56660910	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs560951704	chr15:56660935-56660936	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56657200-56663200	Active TSS	GM12878-XiMat	blood
2	chr15:56657400-56659800	Active TSS	Duodenum Mucosa	Duodenum
3	chr15:56658000-56662800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:56658200-56659800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr15:56658200-56661400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:56658200-56661400	Weak transcription	Small Intestine	intestine
7	chr15:56658200-56675400	Weak transcription	Pancreas	Pancrea
8	chr15:56658400-56659800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr15:56658400-56660000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr15:56658600-56660400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:56658800-56659800	Active TSS	Brain Anterior Caudate	brain
12	chr15:56658800-56659800	Enhancers	Hela-S3	cervix
13	chr15:56658800-56660000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr15:56658800-56661200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr15:56658800-56661200	Weak transcription	HMEC	breast
16	chr15:56658800-56661400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr15:56658800-56661400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr15:56658800-56661400	Weak transcription	Primary B cells from peripheral blood	blood
19	chr15:56658800-56669600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr15:56659000-56659800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:56659000-56659800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:56659000-56661400	Weak transcription	NHEK	skin
23	chr15:56659200-56659800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr15:56659400-56659800	Active TSS	Brain Germinal Matrix	brain
25	chr15:56659400-56666800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr15:56659600-56659800	Enhancers	Fetal Brain Female	brain
27	chr15:56659600-56659800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr15:56659600-56661400	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr15:56659600-56661400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr15:56659600-56661400	Weak transcription	Fetal Brain Male	brain
31	chr15:56659600-56664000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr15:56659600-56675400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr15:56659800-56660200	Weak transcription	Hela-S3	cervix
34	chr15:56659800-56661400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr15:56659800-56661400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr15:56659800-56662000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr15:56659800-56662200	Enhancers	Brain Germinal Matrix	brain
38	chr15:56659800-56662400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr15:56659800-56663000	Weak transcription	Fetal Brain Female	brain
40	chr15:56659800-56664200	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr15:56660000-56661400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr15:56660200-56660400	Enhancers	Hela-S3	cervix
43	chr15:56660400-56660600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr15:56660400-56674400	Weak transcription	Hela-S3	cervix
45	chr15:56660600-56661000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr15:56661000-56671000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:56661200-56661800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr15:56661200-56662000	Enhancers	HMEC	breast
49	chr15:56661400-56661600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr15:56661400-56661600	Enhancers	Primary B cells from peripheral blood	blood

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