Variant report

Variant	nsv569299
Chromosome Location	chr15:44598642-44776075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1730)
CpG islands
(count:917)
Chromatin interactive
region (count:66)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1730 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:44718966-44719733	K562	blood:	n/a	n/a
2	ARID3A	chr15:44677230-44677411	K562	blood:	n/a	n/a
3	ARID3A	chr15:44718966-44720044	HepG2	liver:	n/a	chr15:44719841-44719849
4	ARID3A	chr15:44720644-44720707	K562	blood:	n/a	n/a
5	ARID3A	chr15:44732846-44733620	K562	blood:	n/a	n/a
6	ATF1	chr15:44719111-44720014	K562	blood:	n/a	n/a
7	ATF2	chr15:44718891-44720017	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:44603317-44603674	GM12878	blood:	n/a	n/a
9	ATF2	chr15:44601703-44602208	GM12878	blood:	n/a	n/a
10	ATF2	chr15:44719011-44719953	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr15:44600451-44601424	GM12878	blood:	n/a	n/a
12	ATF2	chr15:44677030-44677438	GM12878	blood:	n/a	n/a
13	ATF2	chr15:44600385-44601563	GM12878	blood:	n/a	n/a
14	ATF2	chr15:44677174-44677854	GM12878	blood:	n/a	n/a
15	ATF2	chr15:44719105-44720020	GM12878	blood:	n/a	n/a
16	ATF2	chr15:44719025-44720207	GM12878	blood:	n/a	n/a
17	ATF2	chr15:44611541-44611946	GM12878	blood:	n/a	n/a
18	BACH1	chr15:44677390-44677496	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:44719386-44719911	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:44753198-44753225	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:44600194-44600250	K562	blood:	n/a	n/a
22	BACH1	chr15:44677223-44677573	K562	blood:	n/a	n/a
23	BACH1	chr15:44718032-44718323	K562	blood:	n/a	n/a
24	BATF	chr15:44677259-44677509	GM12878	blood:	n/a	chr15:44677404-44677415
25	BATF	chr15:44677285-44677584	GM12878	blood:	n/a	chr15:44677404-44677415
26	BATF	chr15:44601086-44601635	GM12878	blood:	n/a	n/a
27	BATF	chr15:44706288-44706574	GM12878	blood:	n/a	n/a
28	BATF	chr15:44600545-44600974	GM12878	blood:	n/a	n/a
29	BATF	chr15:44611620-44611972	GM12878	blood:	n/a	n/a
30	BATF	chr15:44601085-44601411	GM12878	blood:	n/a	n/a
31	BATF	chr15:44600509-44601056	GM12878	blood:	n/a	n/a
32	BATF	chr15:44706233-44706588	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:44601085-44601422	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:44706292-44706510	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:44600611-44600896	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:44600601-44601015	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:44677234-44677511	GM12878	blood:	n/a	n/a
38	BCL3	chr15:44719019-44719765	A549	lung:	n/a	n/a
39	BCL3	chr15:44600529-44601008	GM12878	blood:	n/a	n/a
40	BCL3	chr15:44600545-44600963	GM12878	blood:	n/a	n/a
41	BCL3	chr15:44719358-44719949	A549	lung:	n/a	n/a
42	BCLAF1	chr15:44611541-44612118	GM12878	blood:	n/a	n/a
43	BCLAF1	chr15:44718871-44720397	GM12878	blood:	n/a	chr15:44720148-44720157
44	BCLAF1	chr15:44677158-44677627	GM12878	blood:	n/a	n/a
45	BCLAF1	chr15:44718904-44720353	GM12878	blood:	n/a	chr15:44720148-44720157
46	BCLAF1	chr15:44600394-44601426	GM12878	blood:	n/a	n/a
47	BHLHE40	chr15:44600593-44601475	GM12878	blood:	n/a	n/a
48	BHLHE40	chr15:44611640-44611889	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:44733294-44733585	K562	blood:	n/a	n/a
50	BHLHE40	chr15:44685862-44685951	K562	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:44718396-44718446	SK-N-SH_RA	brain:	n/a
2	chr15:44719213-44719263	AG09309	skin:	n/a
3	chr15:44718396-44718446	SK-N-SH_RA	brain:	n/a
4	chr15:44719213-44719263	AG09309	skin:	n/a
5	chr15:44718852-44718902	SKMC	muscle:	n/a
6	chr15:44719516-44719566	Hela-S3	cervix:	n/a
7	chr15:44715351-44715401	ECC-1	luminal epithelium:	n/a
8	chr15:44617767-44617817	NHDF-neo	bronchial:	n/a
9	chr15:44617767-44617817	T-47D	breast:	n/a
10	chr15:44719030-44719080	GM12891	blood:	n/a
11	chr15:44719516-44719566	PFSK-1	brain:	n/a
12	chr15:44729878-44729928	Hela-S3	cervix:	n/a
13	chr15:44732685-44732735	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:44729878-44729928	MCF10A-Er-Src	breast:	n/a
15	chr15:44732685-44732735	H1-hESC	embryonic stem cell:	embryo
16	chr15:44719030-44719080	HCPEpiC	choroid plexus:	n/a
17	chr15:44718852-44718902	RPTEC	kidney:	n/a
18	chr15:44715351-44715401	SAEC	small airway:	n/a
19	chr15:44719030-44719080	AG04450	lung:	fetal
20	chr15:44719213-44719263	HIPEpiC	eye:	n/a
21	chr15:44719665-44719715	AG04450	lung:	fetal
22	chr15:44720131-44720181	NHDF-neo	bronchial:	n/a
23	chr15:44715351-44715401	PFSK-1	brain:	n/a
24	chr15:44723502-44723552	U87	brain:	n/a
25	chr15:44719213-44719263	HRE	kidney:	n/a
26	chr15:44719516-44719566	K562	blood:	n/a
27	chr15:44729878-44729928	ECC-1	luminal epithelium:	n/a
28	chr15:44720131-44720181	ProgFib	skin:	n/a
29	chr15:44719510-44719560	ProgFib	skin:	n/a
30	chr15:44723502-44723552	PFSK-1	brain:	n/a
31	chr15:44719030-44719080	GM12892	blood:	n/a
32	chr15:44719510-44719560	NHDF-neo	bronchial:	n/a
33	chr15:44729878-44729928	AG09309	skin:	n/a
34	chr15:44719030-44719080	K562	blood:	n/a
35	chr15:44718852-44718902	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:44723502-44723552	PANC-1	pancreas:	n/a
37	chr15:44719213-44719263	IMR90	lung:	fetal
38	chr15:44718852-44718902	HCPEpiC	choroid plexus:	n/a
39	chr15:44720131-44720181	NH-A	brain:	n/a
40	chr15:44719510-44719560	HCF	heart:	n/a
41	chr15:44719935-44719985	PFSK-1	brain:	n/a
42	chr15:44720131-44720181	RPTEC	kidney:	n/a
43	chr15:44719516-44719566	SK-N-SH	brain:	n/a
44	chr15:44719510-44719560	T-47D	breast:	n/a
45	chr15:44719213-44719263	HPAEpiC	pulmonary alveolar:	n/a
46	chr15:44617767-44617817	GM19239	blood:	n/a
47	chr15:44715351-44715401	Caco-2	colon:	n/a
48	chr15:44718396-44718446	Caco-2	colon:	n/a
49	chr15:44729878-44729928	U87	brain:	n/a
50	chr15:44732685-44732735	HCPEpiC	choroid plexus:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:44587861..44590547-chr15:44741463..44744452,2	K562	blood:
2	chr15:44767423..44770241-chr15:44775945..44778021,2	MCF-7	breast:
3	chr15:44701657..44704527-chr15:44717641..44719842,2	K562	blood:
4	chr15:44768699..44770255-chr15:44803080..44806001,2	K562	blood:
5	chr15:44767423..44770241-chr15:44775945..44778021,2	MCF-7	breast:
6	chr15:44643947..44646779-chr15:44717762..44720215,2	MCF-7	breast:
7	chr15:44738517..44741148-chr15:44741345..44743976,2	K562	blood:
8	chr15:44641156..44643504-chr15:44646406..44648886,2	K562	blood:
9	chr15:44718254..44723247-chr15:44726957..44730809,6	K562	blood:
10	chr15:44719719..44720241-chr16:31470736..31471244,2	Hela-S3	cervix:
11	chr15:44674181..44676932-chr15:44716918..44719048,2	K562	blood:
12	chr15:44718173..44721119-chr15:44770497..44772983,2	MCF-7	breast:
13	chr15:44718811..44719781-chr17:62501482..62502406,2	Hela-S3	cervix:
14	chr15:44718440..44720700-chr15:44829136..44830677,2	K562	blood:
15	chr15:44719522..44720101-chrX:12993258..12994089,2	Hela-S3	cervix:
16	chr10:92980435..92981251-chr15:44719397..44720060,2	Hela-S3	cervix:
17	chr15:44673967..44676346-chr15:44716009..44718980,2	K562	blood:
18	chr15:44719279..44719851-chr16:29802138..29802810,2	Hela-S3	cervix:
19	chr15:44682303..44684802-chr15:44709673..44711281,2	K562	blood:
20	chr15:44598749..44601264-chr15:44602549..44605810,3	K562	blood:
21	chr15:44704582..44707025-chr15:44716948..44718913,2	K562	blood:
22	chr15:44719181..44719868-chr9:95526680..95527658,2	Hela-S3	cervix:
23	chr15:44722842..44724510-chr15:44732921..44735166,2	K562	blood:
24	chr14:103800177..103800718-chr15:44719817..44720485,2	Hela-S3	cervix:
25	chr15:44707778..44710924-chr15:44716587..44719642,3	K562	blood:
26	chr15:44733894..44736774-chr15:44740235..44741858,2	K562	blood:
27	chr15:44586214..44590579-chr15:44718275..44720991,4	K562	blood:
28	chr15:44600099..44602547-chr15:44607758..44609414,2	K562	blood:
29	chr15:44718905..44719745-chr15:91445892..91446538,2	Hela-S3	cervix:
30	chr15:44722842..44724510-chr15:44732921..44735166,2	K562	blood:
31	chr15:44752993..44755599-chr15:44759460..44761272,2	K562	blood:
32	chr15:44728934..44731532-chr15:44731569..44733789,3	K562	blood:
33	chr12:121148004..121148973-chr15:44718306..44718935,2	NB4	blood:
34	chr15:44752993..44755599-chr15:44759460..44761272,2	K562	blood:
35	chr15:44597254..44598879-chr15:44647094..44649629,2	K562	blood:
36	chr15:44598927..44601826-chr15:44602549..44604440,2	K562	blood:
37	chr15:44718817..44719519-chr6:26198901..26199786,2	Hela-S3	cervix:
38	chr1:11968301..11970323-chr15:44722385..44724773,2	K562	blood:
39	chr15:44718835..44721035-chr15:44723501..44725751,3	K562	blood:
40	chr15:44714578..44716892-chr15:44722864..44724371,2	K562	blood:
41	chr15:44719413..44722163-chr15:44807893..44809754,2	K562	blood:
42	chr15:44580352..44582378-chr15:44719445..44721367,2	MCF-7	breast:
43	chr15:44693244..44697152-chr15:44700579..44703781,3	K562	blood:
44	chr15:44600099..44602547-chr15:44607758..44609414,2	K562	blood:
45	chr15:44627409..44629841-chr15:44832460..44835215,2	MCF-7	breast:
46	chr15:44728691..44731050-chr15:44731813..44733565,2	K562	blood:
47	chr15:44707950..44709936-chr15:44718362..44720165,2	K562	blood:
48	chr15:44719732..44721943-chr15:44731703..44735323,3	K562	blood:
49	chr15:44579706..44582433-chr15:44718054..44720169,2	MCF-7	breast:
50	chr15:44719096..44719799-chr16:69458630..69459143,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASC4-1	chr15:44726452-44726705	NONHSAT042155
2	lnc-CTDSPL2-1	chr15:44715559-44715737	XLOC_011235
3	lnc-SPG11-3	chr15:44694883-44695137	ENSG00000259595.1
4	lnc-CTDSPL2-1	chr15:44718492-44718499	XLOC_011235
5	lnc-CTDSPL2-3	chr15:44698528-44699081	NONHSAT042152
6	lnc-SPG11-4	chr15:44679518-44679686	ENSG00000259499.1
7	lnc-CTDSPL2-1	chr15:44717965-44718171	XLOC_011235
8	lnc-SPG11-3	chr15:44697525-44697600	ENSG00000259595.1
9	lnc-SPG11-3	chr15:44706408-44706559	ENSG00000259595.1
10	lnc-SPG11-3	chr15:44719307-44719342	ENSG00000259595.1
11	lnc-CTDSPL2-5	chr15:44673062-44673174	NONHSAT042149
12	lnc-SPG11-3	chr15:44705532-44705637	ENSG00000259595.1
13	lnc-SPG11-4	chr15:44682164-44682649	ENSG00000259499.1
14	lnc-CTDSPL2-3	chr15:44701717-44702045	NONHSAT042152
15	lnc-CTDSPL2-5	chr15:44674277-44674427	NONHSAT042149

No data

Variant related genes	Relation type
ENSG00000203574	TF binding region
ENSG00000259595	TF binding region
ENSG00000203572	TF binding region
RN7SL347P	TF binding region
CTDSPL2	TF binding region
CASC4	TF binding region
ENSG00000259499	TF binding region
HNRNPMP1	TF binding region
ENSG00000196274	TF binding region
ENSG00000203573	TF binding region
ENSG00000250130	TF binding region
ENSG00000203574	CpG island
ENSG00000259595	CpG island
ENSG00000203572	CpG island
RN7SL347P	CpG island
CTDSPL2	CpG island
CASC4	CpG island
ENSG00000259499	CpG island
HNRNPMP1	CpG island
ENSG00000196274	CpG island
ENSG00000203573	CpG island
ENSG00000250130	CpG island
ENSG00000203573	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000259563	chromatin interactions
ENSG00000205542	chromatin interactions
ENSG00000259499	chromatin interactions
ENSG00000166734	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000259335	chromatin interactions
ENSG00000137770	chromatin interactions
ENSG00000203575	chromatin interactions
ENSG00000079616	chromatin interactions
ENSG00000100664	chromatin interactions
ENSG00000185963	chromatin interactions
ENSG00000203574	chromatin interactions
ENSG00000250130	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000203572	chromatin interactions
ENSG00000104131	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000265191	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000175970	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000259595	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000180628	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000103018	chromatin interactions

Extended variants
information (count: 6039 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6039 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2412864	chr15:44598642-44598643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559849557	chr15:44598656-44598657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117210992	chr15:44598730-44598731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142941113	chr15:44598734-44598735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147713076	chr15:44598758-44598759	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs185668570	chr15:44598791-44598792	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs375629416	chr15:44598808-44598809	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs548487061	chr15:44598818-44598819	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs534819356	chr15:44598822-44598823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs568341969	chr15:44598878-44598879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555024864	chr15:44598880-44598881	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115829296	chr15:44598892-44598893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs142506570	chr15:44598909-44598910	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs190383614	chr15:44598929-44598930	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs558741888	chr15:44598950-44598951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573723211	chr15:44598964-44598965	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs75113892	chr15:44599004-44599005	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs555270894	chr15:44599102-44599103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs147786021	chr15:44599127-44599128	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540462807	chr15:44599128-44599129	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560307963	chr15:44599160-44599161	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576974385	chr15:44599198-44599199	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs117235694	chr15:44599202-44599203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538968476	chr15:44599252-44599253	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs35842768	chr15:44599283-44599284	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs10152313	chr15:44599284-44599285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs10152314	chr15:44599286-44599287	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547863594	chr15:44599339-44599340	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs370659327	chr15:44599410-44599411	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370148616	chr15:44599411-44599412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs562006770	chr15:44599442-44599443	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527581290	chr15:44599473-44599474	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs554010271	chr15:44599474-44599475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs368116112	chr15:44599495-44599496	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs547666590	chr15:44599504-44599505	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570670019	chr15:44599505-44599506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539224772	chr15:44599534-44599535	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141178522	chr15:44599537-44599538	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569229102	chr15:44599563-44599564	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs150295400	chr15:44599567-44599568	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554533560	chr15:44599600-44599601	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571714399	chr15:44599619-44599620	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534222738	chr15:44599631-44599632	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs138107329	chr15:44599632-44599633	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs552702768	chr15:44599639-44599640	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs554412498	chr15:44599645-44599646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs180788332	chr15:44599650-44599651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs546060265	chr15:44599652-44599653	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572751882	chr15:44599675-44599676	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544676214	chr15:44599680-44599681	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3110 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44582000-44602000	Weak transcription	Gastric	stomach
2	chr15:44582000-44639400	Weak transcription	Lung	lung
3	chr15:44582800-44672200	Weak transcription	HSMM	muscle
4	chr15:44583000-44639400	Weak transcription	Fetal Lung	lung
5	chr15:44583200-44600800	Weak transcription	Fetal Thymus	thymus
6	chr15:44583200-44639200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr15:44583600-44602000	Weak transcription	Pancreas	Pancrea
8	chr15:44583800-44639200	Weak transcription	Brain Germinal Matrix	brain
9	chr15:44584200-44625600	Weak transcription	Fetal Brain Female	brain
10	chr15:44585400-44628200	Weak transcription	Thymus	Thymus
11	chr15:44586200-44600800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr15:44588000-44600800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:44589000-44601200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr15:44589000-44619000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:44589000-44631600	Weak transcription	Left Ventricle	heart
16	chr15:44589200-44599200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr15:44589200-44600000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr15:44589200-44626400	Weak transcription	Fetal Muscle Leg	muscle
19	chr15:44589400-44600200	Weak transcription	Adipose Nuclei	Adipose
20	chr15:44589400-44607000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr15:44589400-44607600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr15:44589600-44599600	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr15:44589600-44600200	Weak transcription	Fetal Kidney	kidney
24	chr15:44589600-44602200	Weak transcription	Psoas Muscle	Psoas
25	chr15:44589600-44605600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr15:44589600-44617400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr15:44589800-44599800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr15:44589800-44600600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:44589800-44600600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr15:44589800-44601800	Weak transcription	Osteobl	bone
31	chr15:44589800-44602000	Weak transcription	Right Atrium	heart
32	chr15:44589800-44625200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr15:44589800-44632000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:44589800-44632400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:44589800-44632400	Weak transcription	NHLF	lung
36	chr15:44591400-44632800	Weak transcription	Hela-S3	cervix
37	chr15:44592200-44603000	Weak transcription	Esophagus	oesophagus
38	chr15:44592800-44600400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr15:44592800-44617600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr15:44592800-44639800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr15:44593000-44605800	Weak transcription	Colon Smooth Muscle	Colon
42	chr15:44593200-44602800	Weak transcription	Duodenum Mucosa	Duodenum
43	chr15:44593200-44621200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr15:44593200-44625600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:44593200-44639200	Weak transcription	K562	blood
46	chr15:44593200-44639400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr15:44593600-44599400	Weak transcription	Primary B cells from cord blood	blood
48	chr15:44593600-44603000	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr15:44593600-44621200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr15:44593800-44599600	Weak transcription	Primary B cells from peripheral blood	blood

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