Variant report

Variant	nsv832952
Chromosome Location	chr15:31204426-31333998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1835)
CpG islands
(count:1712)
Chromatin interactive
region (count:103)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:1835 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31283051-31284551	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:31306594-31306875	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:31270433-31270976	K562	blood:	n/a	n/a
4	ARID3A	chr15:31316664-31316907	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:31246394-31246733	K562	blood:	n/a	n/a
6	ARID3A	chr15:31281162-31281623	HepG2	liver:	n/a	n/a
7	ATF1	chr15:31327681-31327955	K562	blood:	n/a	n/a
8	ATF1	chr15:31270562-31270957	K562	blood:	n/a	n/a
9	ATF1	chr15:31291330-31291417	K562	blood:	n/a	n/a
10	ATF2	chr15:31296322-31297047	GM12878	blood:	n/a	n/a
11	ATF2	chr15:31296404-31296950	GM12878	blood:	n/a	n/a
12	ATF2	chr15:31214380-31215021	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr15:31283560-31284329	A549	lung:	n/a	chr15:31284198-31284207 chr15:31283948-31283957 chr15:31283933-31283942
14	ATF3	chr15:31248502-31248688	K562	blood:	n/a	n/a
15	BACH1	chr15:31220800-31220801	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:31246250-31246578	K562	blood:	n/a	chr15:31246505-31246519
17	BACH1	chr15:31269254-31269618	K562	blood:	n/a	n/a
18	BACH1	chr15:31214151-31215187	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:31216251-31216362	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:31283405-31283771	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr15:31296361-31296911	GM12878	blood:	n/a	n/a
22	BATF	chr15:31297967-31298281	GM12878	blood:	n/a	n/a
23	BATF	chr15:31297974-31298244	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:31214549-31214960	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr15:31296412-31296960	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:31296458-31296865	GM12878	blood:	n/a	n/a
27	BCL3	chr15:31283816-31284514	A549	lung:	n/a	chr15:31284048-31284061 chr15:31284192-31284205 chr15:31283960-31283973 chr15:31284026-31284039
28	BCL3	chr15:31281244-31281561	GM12878	blood:	n/a	n/a
29	BCL3	chr15:31296357-31296905	GM12878	blood:	n/a	n/a
30	BCL3	chr15:31296443-31296833	GM12878	blood:	n/a	n/a
31	BCLAF1	chr15:31283474-31284450	GM12878	blood:	n/a	chr15:31284048-31284061 chr15:31284192-31284205 chr15:31283960-31283973 chr15:31284026-31284039
32	BCLAF1	chr15:31283564-31284294	GM12878	blood:	n/a	chr15:31284048-31284061 chr15:31284192-31284205 chr15:31283960-31283973 chr15:31284026-31284039
33	BCLAF1	chr15:31296284-31297068	GM12878	blood:	n/a	n/a
34	BCLAF1	chr15:31296435-31296923	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:31283655-31284335	HepG2	liver:	n/a	chr15:31284050-31284066 chr15:31283961-31283977 chr15:31283851-31283867
36	BHLHE40	chr15:31246170-31246599	K562	blood:	n/a	n/a
37	BHLHE40	chr15:31308929-31309114	GM12878	blood:	n/a	n/a
38	BHLHE40	chr15:31270517-31270851	K562	blood:	n/a	n/a
39	BHLHE40	chr15:31283708-31284521	GM12878	blood:	n/a	chr15:31284050-31284066 chr15:31283961-31283977 chr15:31283851-31283867
40	BHLHE40	chr15:31283642-31284380	K562	blood:	n/a	chr15:31284050-31284066 chr15:31283961-31283977 chr15:31283851-31283867
41	BHLHE40	chr15:31296427-31296917	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:31307082-31307280	GM12878	blood:	n/a	n/a
43	BHLHE40	chr15:31283275-31283428	K562	blood:	n/a	n/a
44	BHLHE40	chr15:31282824-31283272	GM12878	blood:	n/a	n/a
45	BRCA1	chr15:31283969-31284155	HepG2	liver:	n/a	n/a
46	BRCA1	chr15:31282527-31282601	HepG2	liver:	n/a	n/a
47	BRCA1	chr15:31283560-31283635	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:31283511-31283693	HepG2	liver:	n/a	n/a
49	BRCA1	chr15:31284130-31284175	H1-hESC	embryonic stem cell:	n/a	n/a
50	CBX3	chr15:31318334-31318611	K562	blood:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31287286-31287336	K562	blood:	n/a
2	chr15:31283468-31283518	PFSK-1	brain:	n/a
3	chr15:31294401-31294451	Jurkat	blood:	n/a
4	chr15:31217417-31217467	SK-N-MC	brain:	n/a
5	chr15:31287286-31287336	K562	blood:	n/a
6	chr15:31283468-31283518	PFSK-1	brain:	n/a
7	chr15:31294401-31294451	Jurkat	blood:	n/a
8	chr15:31217417-31217467	SK-N-MC	brain:	n/a
9	chr15:31316860-31316910	HepG2	liver:	n/a
10	chr15:31294401-31294451	AG09319	gingival:	n/a
11	chr15:31215822-31215872	MCF-7	breast:	n/a
12	chr15:31316195-31316245	GM06990	blood:	n/a
13	chr15:31214501-31214551	BE2_C	brain:	n/a
14	chr15:31215822-31215872	HCPEpiC	choroid plexus:	n/a
15	chr15:31318495-31318545	HepG2	liver:	n/a
16	chr15:31280513-31280563	HAEpiC	amniotic membrane:	n/a
17	chr15:31284413-31284463	GM12891	blood:	n/a
18	chr15:31318495-31318545	AG04449	skin:	fetal
19	chr15:31284284-31284334	SK-N-SH_RA	brain:	n/a
20	chr15:31283468-31283518	AoSMC	blood vessel:	n/a
21	chr15:31316195-31316245	HUVEC	blood vessel:	n/a
22	chr15:31214501-31214551	HCM	heart:	n/a
23	chr15:31287286-31287336	IMR90	lung:	fetal
24	chr15:31284617-31284667	NB4	blood:	n/a
25	chr15:31287286-31287336	U87	brain:	n/a
26	chr15:31284262-31284312	AG10803	skin:	n/a
27	chr15:31318286-31318336	ProgFib	skin:	n/a
28	chr15:31284262-31284312	BE2_C	brain:	n/a
29	chr15:31277661-31277711	NHBE	bronchial:	n/a
30	chr15:31283468-31283518	SKMC	muscle:	n/a
31	chr15:31316195-31316245	HRCEpiC	kidney:	n/a
32	chr15:31318286-31318336	GM12878	blood:	n/a
33	chr15:31233439-31233489	SKMC	muscle:	n/a
34	chr15:31280513-31280563	HPAEpiC	pulmonary alveolar:	n/a
35	chr15:31316195-31316245	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:31318286-31318336	BJ	skin:	n/a
37	chr15:31294401-31294451	HEEpiC	esophagus:	n/a
38	chr15:31319218-31319268	MCF10A-Er-Src	breast:	n/a
39	chr15:31217407-31217457	GM19239	blood:	n/a
40	chr15:31220356-31220406	SAEC	small airway:	n/a
41	chr15:31215822-31215872	HCT-116	colon:	n/a
42	chr15:31295058-31295108	SAEC	small airway:	n/a
43	chr15:31283468-31283518	HCT-116	colon:	n/a
44	chr15:31284262-31284312	MCF-7	breast:	n/a
45	chr15:31318495-31318545	LNCaP	prostate:	n/a
46	chr15:31295094-31295144	HRPEpiC	eye:	n/a
47	chr15:31287286-31287336	CMK	blood:	n/a
48	chr15:31234080-31234130	HEEpiC	esophagus:	n/a
49	chr15:31318286-31318336	Hela-S3	cervix:	n/a
50	chr15:31294401-31294451	U87	brain:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:31282443..31284483-chr15:31294719..31297603,2	K562	blood:
2	chr15:31279758..31282361-chr15:31424414..31426615,2	K562	blood:
3	chr15:31284003..31286017-chr15:31288749..31290296,2	MCF-7	breast:
4	chr15:31253352..31256135-chr15:31282312..31285268,3	K562	blood:
5	chr15:31289018..31291728-chr15:31293591..31295658,2	K562	blood:
6	chr15:31281475..31285433-chr15:31293926..31297603,3	K562	blood:
7	chr15:31218794..31220951-chr15:31282389..31284227,2	K562	blood:
8	chr15:31281226..31284928-chr15:31292691..31294333,3	MCF-7	breast:
9	chr15:31283072..31283773-chr17:29151257..29151810,2	Hela-S3	cervix:
10	chr15:31252830..31256274-chr15:31263661..31267030,3	K562	blood:
11	chr15:31200708..31203485-chr15:31204124..31206171,2	MCF-7	breast:
12	chr15:22892404..22893156-chr15:31283981..31284893,2	Hela-S3	cervix:
13	chr15:31194787..31196462-chr15:31220956..31222742,2	K562	blood:
14	chr15:31282940..31285359-chr15:31285450..31288448,5	K562	blood:
15	chr15:31251466..31253013-chr15:31256953..31259100,2	K562	blood:
16	chr15:31194465..31197297-chr15:31282167..31285499,3	K562	blood:
17	chr15:31271252..31273468-chr15:31279975..31283092,3	K562	blood:
18	chr15:31229079..31231720-chr15:31282287..31284074,2	MCF-7	breast:
19	chr15:31284003..31286017-chr15:31288749..31290296,2	MCF-7	breast:
20	chr15:31194527..31196163-chr15:31206198..31208102,2	K562	blood:
21	chr15:31223541..31225627-chr15:31225836..31228644,2	K562	blood:
22	chr15:31272157..31276720-chr15:31281759..31286309,6	MCF-7	breast:
23	chr15:31283135..31283746-chr6:134495837..134496431,2	Hela-S3	cervix:
24	chr15:31231346..31233400-chr15:31236448..31238686,2	K562	blood:
25	chr15:31284705..31286715-chr15:31291770..31293301,2	K562	blood:
26	chr15:31264761..31266293-chr15:31269997..31271907,2	K562	blood:
27	chr15:31316162..31318225-chr15:31318873..31321784,2	K562	blood:
28	chr15:31271252..31273468-chr15:31279975..31283092,3	K562	blood:
29	chr15:31234145..31235781-chr15:31240039..31242317,2	MCF-7	breast:
30	chr15:31269600..31272390-chr15:31276376..31278340,2	K562	blood:
31	chr15:31269911..31273536-chr15:31281736..31285109,4	MCF-7	breast:
32	chr15:31261989..31264595-chr15:31267773..31270653,3	K562	blood:
33	chr15:31282581..31285579-chr15:31286466..31289868,3	MCF-7	breast:
34	chr15:31322324..31324539-chr15:31326738..31328309,2	K562	blood:
35	chr15:31283952..31284557-chr9:80912141..80912750,2	Hela-S3	cervix:
36	chr15:31281186..31283904-chr15:31357047..31359370,2	MCF-7	breast:
37	chr15:31253352..31256135-chr15:31282609..31285268,3	K562	blood:
38	chr15:31194962..31197804-chr15:31219595..31222456,2	K562	blood:
39	chr15:31264761..31266293-chr15:31269997..31271907,2	K562	blood:
40	chr15:31283320..31285509-chr15:31302776..31304793,2	MCF-7	breast:
41	chr15:31270091..31272253-chr15:31273667..31275260,2	K562	blood:
42	chr15:31194754..31196555-chr15:31204358..31205993,2	K562	blood:
43	chr15:31276854..31278863-chr15:31283840..31285876,2	MCF-7	breast:
44	chr15:31237800..31239595-chr15:31245013..31246822,2	K562	blood:
45	chr15:31228102..31230249-chr15:31285467..31288466,2	K562	blood:
46	chr15:31283675..31284503-chr15:65588312..65589255,3	Hela-S3	cervix:
47	chr15:31258278..31261400-chr15:31264720..31267542,4	K562	blood:
48	chr15:31281475..31285433-chr15:31293926..31297603,3	K562	blood:
49	chr15:31267165..31269336-chr15:31272115..31274886,2	K562	blood:
50	chr15:31244834..31247822-chr15:31248238..31251103,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAN1-1	chr15:31327956-31328125	ENSG00000259720.1
2	lnc-FAN1-1	chr15:31327981-31328125	NONHSAT041422
3	lnc-FAN1-1	chr15:31294216-31294233	ENSG00000259720.1
4	lnc-ARHGAP11B-8	chr15:31218717-31220610	ENSG00000270015.1
5	lnc-FAN1-1	chr15:31328656-31329566	NONHSAT041422

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TRPM1	hsa-miR-26b-5p	chr15:31293898-31293918
2	MTMR10	hsa-miR-148b-3p	chr15:31233073-31233067
3	MTMR10	hsa-miR-132-3p	chr15:31232337-31232358
4	MTMR10	hsa-miR-148b-3p	chr15:31233545-31233566
5	MTMR10	hsa-miR-132-3p	chr15:31233070-31233064
6	MTMR10	hsa-miR-132-3p	chr15:31231144-31231164
7	MTMR10	hsa-miR-148b-3p	chr15:31233067-31233088

Variant related genes	Relation type
RNU6-466P	TF binding region
MTMR10	TF binding region
TRPM1	TF binding region
ENSG00000259720	TF binding region
FAN1	TF binding region
ENSG00000270015	TF binding region
RNU6-466P	CpG island
MTMR10	CpG island
TRPM1	CpG island
ENSG00000259720	CpG island
FAN1	CpG island
ENSG00000270015	CpG island
ENSG00000118515	chromatin interactions
ENSG00000168143	chromatin interactions
ENSG00000177674	chromatin interactions
ENSG00000259720	chromatin interactions
ENSG00000163694	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000134160	chromatin interactions
ENSG00000207702	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000068793	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000212526	chromatin interactions
ENSG00000239039	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000198901	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000166912	chromatin interactions
ENSG00000197299	chromatin interactions
ENSG00000198690	chromatin interactions
ENSG00000261423	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000176390	chromatin interactions

Extended variants
information (count: 5047 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:5047 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11631543	chr15:31204426-31204427	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569251193	chr15:31204453-31204454	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190331265	chr15:31204475-31204476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551895966	chr15:31204479-31204480	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370696729	chr15:31204487-31204488	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs367879351	chr15:31204492-31204493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552895311	chr15:31204496-31204497	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs113482660	chr15:31204506-31204507	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533771660	chr15:31204516-31204517	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553626486	chr15:31204532-31204533	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs118089305	chr15:31204637-31204638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536561283	chr15:31204676-31204677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555843315	chr15:31204686-31204687	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575994355	chr15:31204715-31204716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544776062	chr15:31204765-31204766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558728596	chr15:31204769-31204770	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs11854560	chr15:31204772-31204773	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181654824	chr15:31204781-31204782	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs142546301	chr15:31204838-31204839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs115232781	chr15:31204864-31204865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs187610767	chr15:31204875-31204876	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543316153	chr15:31204880-31204881	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144070993	chr15:31204882-31204883	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531770976	chr15:31204975-31204976	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2955796	chr15:31205041-31205042	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs375097064	chr15:31205089-31205090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545335598	chr15:31205195-31205196	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550674650	chr15:31205240-31205241	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190992619	chr15:31205276-31205277	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148213306	chr15:31205278-31205279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs141213848	chr15:31205304-31205305	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs570961211	chr15:31205350-31205351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2949566	chr15:31205400-31205401	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs181065265	chr15:31205413-31205414	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs150708488	chr15:31205418-31205419	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569544090	chr15:31205430-31205431	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538665971	chr15:31205431-31205432	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs59646973	chr15:31205487-31205488	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572143365	chr15:31205492-31205493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs541143589	chr15:31205518-31205519	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554368789	chr15:31205540-31205541	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185323384	chr15:31205541-31205542	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542941167	chr15:31205546-31205547	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563230702	chr15:31205574-31205575	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189678317	chr15:31205587-31205588	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183316584	chr15:31205618-31205619	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372724816	chr15:31205759-31205760	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139461076	chr15:31205774-31205775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs527736878	chr15:31205882-31205883	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552507456	chr15:31205909-31205910	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:156)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Intellectual disability	21811512	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19521722	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4045 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31196600-31210800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr15:31196800-31210400	Weak transcription	HSMMtube	muscle
3	chr15:31196800-31213000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:31196800-31215000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:31197000-31206200	Weak transcription	NH-A	brain
6	chr15:31197000-31210600	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr15:31197000-31213400	Weak transcription	Stomach Mucosa	stomach
8	chr15:31197000-31216400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr15:31197200-31204600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr15:31197200-31214000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:31197400-31207200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr15:31197400-31207400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr15:31197400-31208400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr15:31197400-31210600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr15:31197400-31211200	Strong transcription	A549	lung
16	chr15:31197400-31215000	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr15:31198200-31210400	Weak transcription	K562	blood
18	chr15:31198200-31224000	Strong transcription	Dnd41	blood
19	chr15:31198400-31204600	Weak transcription	Fetal Brain Male	brain
20	chr15:31198400-31213000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr15:31198800-31205400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr15:31199200-31208600	Weak transcription	Fetal Heart	heart
23	chr15:31199800-31213400	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr15:31200000-31211600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr15:31200000-31213200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr15:31200200-31211800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr15:31200200-31213400	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr15:31200200-31214400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr15:31200200-31224000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:31200400-31213000	Strong transcription	Fetal Muscle Trunk	muscle
31	chr15:31200400-31213400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr15:31200400-31213800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:31200400-31216200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr15:31200400-31221200	Strong transcription	Placenta	Placenta
35	chr15:31200400-31223200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:31200400-31242200	Strong transcription	Primary T cells from cord blood	blood
37	chr15:31200600-31211400	Strong transcription	Fetal Muscle Leg	muscle
38	chr15:31200600-31254800	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr15:31200800-31213400	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr15:31200800-31213600	Strong transcription	Liver	Liver
41	chr15:31201000-31207600	Strong transcription	NHEK	skin
42	chr15:31201000-31211200	Strong transcription	Brain Hippocampus Middle	brain
43	chr15:31201200-31207600	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr15:31201200-31211200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr15:31201200-31211200	Strong transcription	Fetal Brain Female	brain
46	chr15:31201200-31211400	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr15:31201200-31224000	Strong transcription	Rectal Mucosa Donor 29	rectum
48	chr15:31201200-31241400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr15:31201400-31206200	Strong transcription	Colonic Mucosa	Colon
50	chr15:31201600-31207600	Strong transcription	Brain Cingulate Gyrus	brain

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