Variant report

Variant	nsv871352
Chromosome Location	chr1:92761127-92807238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:952)
CpG islands
(count:794)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92766611-92766631	K562	blood:	n/a	n/a
2	ARID3A	chr1:92763503-92763504	K562	blood:	n/a	n/a
3	ARID3A	chr1:92783280-92783972	K562	blood:	n/a	n/a
4	ARID3A	chr1:92764599-92764839	HepG2	liver:	n/a	n/a
5	ATF1	chr1:92783398-92784024	K562	blood:	n/a	n/a
6	ATF2	chr1:92764096-92764644	GM12878	blood:	n/a	n/a
7	BACH1	chr1:92799529-92799536	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:92766645-92766648	K562	blood:	n/a	n/a
9	BACH1	chr1:92764301-92764587	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr1:92764017-92765143	GM12878	blood:	n/a	chr1:92764418-92764427
11	BCLAF1	chr1:92764045-92764833	GM12878	blood:	n/a	chr1:92764418-92764427
12	BHLHE40	chr1:92764027-92764709	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:92764095-92764711	K562	blood:	n/a	n/a
14	BRCA1	chr1:92764324-92764518	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr1:92763513-92764724	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:92793313-92793793	K562	blood:	n/a	n/a
17	CBX3	chr1:92793362-92793654	K562	blood:	n/a	n/a
18	CBX3	chr1:92764060-92764743	K562	blood:	n/a	n/a
19	CCNT2	chr1:92764104-92764787	K562	blood:	n/a	n/a
20	CCNT2	chr1:92783392-92783684	K562	blood:	n/a	n/a
21	CEBPB	chr1:92783037-92783606	K562	blood:	n/a	chr1:92783382-92783395
22	CEBPB	chr1:92771822-92771931	K562	blood:	n/a	n/a
23	CEBPB	chr1:92771826-92771859	A549	lung:	n/a	n/a
24	CEBPB	chr1:92783071-92783306	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:92790412-92790461	A549	lung:	n/a	n/a
26	CEBPB	chr1:92764454-92764538	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:92764006-92764665	Hela-S3	cervix:	n/a	n/a
28	CEBPD	chr1:92764215-92764762	HepG2	liver:	n/a	n/a
29	CEBPD	chr1:92783312-92783988	K562	blood:	n/a	n/a
30	CEBPD	chr1:92783298-92783907	K562	blood:	n/a	n/a
31	CEBPD	chr1:92764083-92764697	K562	blood:	n/a	n/a
32	CEBPD	chr1:92764388-92764748	HepG2	liver:	n/a	n/a
33	CHD1	chr1:92764651-92765033	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr1:92763593-92764440	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr1:92763931-92765499	GM12878	blood:	n/a	n/a
36	CHD2	chr1:92764068-92764890	GM12878	blood:	n/a	n/a
37	CHD2	chr1:92764260-92764530	HepG2	liver:	n/a	n/a
38	CHD2	chr1:92764087-92765032	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:92764188-92764682	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:92764830-92764837	HepG2	liver:	n/a	n/a
41	CREB1	chr1:92764107-92764841	A549	lung:	n/a	n/a
42	CREB1	chr1:92764123-92764757	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr1:92764448-92764690	A549	lung:	n/a	n/a
44	CREB1	chr1:92764014-92764843	K562	blood:	n/a	n/a
45	CREB1	chr1:92764080-92764821	GM12878	blood:	n/a	n/a
46	CREB1	chr1:92764028-92765116	HepG2	liver:	n/a	n/a
47	CTCF	chr1:92775340-92775490	HPF	lung:	n/a	n/a
48	CTCF	chr1:92775740-92775890	HCPEpiC	choroid plexus:	n/a	chr1:92775835-92775851 chr1:92775836-92775857 chr1:92775834-92775852
49	CTCF	chr1:92775680-92775830	HCT-116	colon:	n/a	n/a
50	CTCF	chr1:92764140-92764290	GM12869	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92764431-92764481	AG09319	gingival:	n/a
2	chr1:92764431-92764481	AG09319	gingival:	n/a
3	chr1:92764770-92764820	Hela-S3	cervix:	n/a
4	chr1:92764431-92764481	NT2-D1	testis:	n/a
5	chr1:92764536-92764586	HepG2	liver:	n/a
6	chr1:92764431-92764481	SKMC	muscle:	n/a
7	chr1:92764536-92764586	T-47D	breast:	n/a
8	chr1:92764419-92764469	RPTEC	kidney:	n/a
9	chr1:92764833-92764883	Hepatocyte	liver:	n/a
10	chr1:92764419-92764469	Hepatocyte	liver:	n/a
11	chr1:92764536-92764586	HMEC	breast:	n/a
12	chr1:92764536-92764586	BE2_C	brain:	n/a
13	chr1:92764574-92764624	HCF	heart:	n/a
14	chr1:92764349-92764399	HCPEpiC	choroid plexus:	n/a
15	chr1:92764419-92764469	BE2_C	brain:	n/a
16	chr1:92764188-92764238	U87	brain:	n/a
17	chr1:92764536-92764586	AG04449	skin:	fetal
18	chr1:92764770-92764820	AoSMC	blood vessel:	n/a
19	chr1:92764419-92764469	SK-N-MC	brain:	n/a
20	chr1:92764777-92764827	GM19239	blood:	n/a
21	chr1:92764770-92764820	SK-N-SH_RA	brain:	n/a
22	chr1:92764770-92764820	IMR90	lung:	fetal
23	chr1:92764574-92764624	A549	lung:	n/a
24	chr1:92764775-92764825	HIPEpiC	eye:	n/a
25	chr1:92764422-92764472	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:92764833-92764883	HepG2	liver:	n/a
27	chr1:92762956-92763006	ProgFib	skin:	n/a
28	chr1:92764349-92764399	SKMC	muscle:	n/a
29	chr1:92764431-92764481	GM12892	blood:	n/a
30	chr1:92764777-92764827	SK-N-SH	brain:	n/a
31	chr1:92764188-92764238	ovcar-3	ovarian:	n/a
32	chr1:92762956-92763006	RPTEC	kidney:	n/a
33	chr1:92764770-92764820	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:92764574-92764624	ovcar-3	ovarian:	n/a
35	chr1:92762956-92763006	AG09319	gingival:	n/a
36	chr1:92764188-92764238	HNPCEpiC	eye:	n/a
37	chr1:92764431-92764481	RPTEC	kidney:	n/a
38	chr1:92764419-92764469	PANC-1	pancreas:	n/a
39	chr1:92764536-92764586	BJ	skin:	n/a
40	chr1:92764349-92764399	AG09319	gingival:	n/a
41	chr1:92762956-92763006	A549	lung:	n/a
42	chr1:92764833-92764883	PANC-1	pancreas:	n/a
43	chr1:92764349-92764399	A549	lung:	n/a
44	chr1:92762956-92763006	AG09309	skin:	n/a
45	chr1:92764574-92764624	RPTEC	kidney:	n/a
46	chr1:92764833-92764883	BE2_C	brain:	n/a
47	chr1:92764777-92764827	HAEpiC	amniotic membrane:	n/a
48	chr1:92764833-92764883	SK-N-SH_RA	brain:	n/a
49	chr1:92764188-92764238	Hepatocyte	liver:	n/a
50	chr1:92764422-92764472	HAEpiC	amniotic membrane:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:92763984..92764912-chr17:17184143..17184722,2	Hela-S3	cervix:
2	chr1:92762166..92764342-chr1:93135404..93137126,2	K562	blood:
3	chr1:92763878..92764562-chr7:107220034..107220754,2	Hela-S3	cervix:
4	chr1:92790206..92790996-chr2:74694205..74695187,2	NB4	blood:
5	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:
6	chr1:92756651..92759126-chr1:92759145..92761543,4	K562	blood:
7	chr1:92764055..92764636-chr11:62608722..62609700,2	HCT-116	colon:
8	chr1:92762794..92765730-chr1:93295925..93298205,3	K562	blood:
9	chr1:92764606..92767220-chr1:92781297..92784112,2	K562	blood:
10	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
11	chr1:92751144..92752872-chr1:92762540..92765121,2	K562	blood:
12	chr1:92751701..92754444-chr1:92763776..92766491,2	MCF-7	breast:
13	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
14	chr1:92764062..92764602-chr19:36390162..36391104,2	Hela-S3	cervix:
15	chr1:92775543..92777429-chr1:92779885..92782284,2	K562	blood:
16	chr1:92770418..92773011-chr1:92773916..92776545,2	K562	blood:
17	chr1:92770418..92773011-chr1:92773916..92776545,2	K562	blood:
18	chr1:92775543..92777429-chr1:92779885..92782284,2	K562	blood:
19	chr1:92775257..92776314-chr1:93064696..93065442,3	MCF-7	breast:
20	chr1:92774363..92776060-chr1:92906114..92908200,2	MCF-7	breast:
21	chr1:92763773..92764454-chr6:30711937..30712495,2	Hela-S3	cervix:
22	chr1:92781038..92783482-chr1:92784277..92786700,2	K562	blood:
23	chr1:92494741..92496705-chr1:92764193..92766152,2	MCF-7	breast:
24	chr1:92764662..92766279-chr1:92768201..92769903,2	MCF-7	breast:
25	chr1:92763470..92767298-chr1:92785657..92788225,3	K562	blood:
26	chr1:92798322..92801081-chr1:92801191..92803127,2	K562	blood:
27	chr1:92801067..92802871-chr1:92812427..92814790,2	MCF-7	breast:
28	chr1:92763702..92766598-chr1:92771008..92773495,2	MCF-7	breast:
29	chr1:92763308..92766374-chr1:92766490..92770872,7	K562	blood:
30	chr1:92764332..92765052-chr7:105924734..105925596,2	Hela-S3	cervix:
31	chr1:92763867..92766149-chr1:92769063..92771043,2	K562	blood:
32	chr1:92763854..92764472-chr6:86388159..86388864,2	Hela-S3	cervix:
33	chr1:92764074..92765656-chr1:93296705..93299037,2	K562	blood:
34	chr1:92768070..92770349-chr1:92773069..92775193,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLMN-1	chr1:92764482-92764544	NONHSAT004453
2	lnc-GLMN-1	chr1:92763078-92763586	NONHSAT004453

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RPAP2	hsa-miR-192-5p	chr1:92789423-92789444
2	RPAP2	hsa-miR-215-5p	chr1:92789423-92789444
3	RPAP2	hsa-miR-215-5p	chr1:92789508-92789528
4	RPAP2	hsa-miR-192-5p	chr1:92789508-92789528

Variant related genes	Relation type
RPAP2	TF binding region
GLMN	TF binding region
RPAP2	CpG island
GLMN	CpG island
ENSG00000141030	chromatin interactions
ENSG00000167604	chromatin interactions
ENSG00000272854	chromatin interactions
ENSG00000105835	chromatin interactions
ENSG00000172031	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000075790	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000122484	chromatin interactions

Extended variants
information (count: 1507 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1507 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7412559	chr1:92761127-92761128	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116087373	chr1:92761135-92761136	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191545212	chr1:92761197-92761198	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370040022	chr1:92761452-92761453	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114137534	chr1:92761486-92761487	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183498209	chr1:92761494-92761495	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576679622	chr1:92761506-92761507	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113609995	chr1:92761549-92761550	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188792224	chr1:92761574-92761575	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568333771	chr1:92761614-92761615	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373171299	chr1:92761648-92761649	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2391140	chr1:92761654-92761655	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs559619231	chr1:92761664-92761665	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529883395	chr1:92761702-92761703	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs548103949	chr1:92761754-92761755	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563573565	chr1:92761759-92761760	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs369239850	chr1:92761771-92761772	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551716943	chr1:92761773-92761774	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs570102995	chr1:92761790-92761791	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs534360893	chr1:92761868-92761869	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs546651248	chr1:92761902-92761903	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs568093692	chr1:92761948-92761949	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs536821109	chr1:92761953-92761954	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs192421531	chr1:92761969-92761970	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs576762044	chr1:92762001-92762002	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs183849681	chr1:92762010-92762011	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs111754402	chr1:92762020-92762021	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577288100	chr1:92762039-92762040	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs541471485	chr1:92762041-92762042	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs553003639	chr1:92762064-92762065	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs574859823	chr1:92762083-92762084	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs541963835	chr1:92762157-92762158	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs573004675	chr1:92762194-92762195	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563348807	chr1:92762209-92762210	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs530656610	chr1:92762223-92762224	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs186731213	chr1:92762245-92762246	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs564065635	chr1:92762256-92762257	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs375032347	chr1:92762268-92762269	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs114874270	chr1:92762336-92762337	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs562528571	chr1:92762352-92762353	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs546293394	chr1:92762359-92762360	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs144782865	chr1:92762372-92762373	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs535201330	chr1:92762434-92762435	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs548721524	chr1:92762438-92762439	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs570261987	chr1:92762542-92762543	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34647863	chr1:92762665-92762666	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs78059788	chr1:92762674-92762675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs191871768	chr1:92762676-92762677	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559278415	chr1:92762677-92762678	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78582665	chr1:92762689-92762690	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1997 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92707200-92764000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:92709000-92762800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr1:92710600-92762000	Weak transcription	Fetal Brain Male	brain
4	chr1:92710600-92763400	Weak transcription	Brain Angular Gyrus	brain
5	chr1:92710600-92764000	Weak transcription	Gastric	stomach
6	chr1:92711000-92763600	Weak transcription	HSMMtube	muscle
7	chr1:92711200-92761600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr1:92711200-92764000	Weak transcription	Spleen	Spleen
9	chr1:92719400-92764000	Weak transcription	Pancreas	Pancrea
10	chr1:92720000-92763800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr1:92722400-92763400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:92723000-92763800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:92724600-92763800	Weak transcription	Brain Substantia Nigra	brain
14	chr1:92725800-92764000	Weak transcription	Colonic Mucosa	Colon
15	chr1:92727000-92763800	Weak transcription	Right Ventricle	heart
16	chr1:92727200-92763800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr1:92729800-92763800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr1:92732000-92763600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr1:92736000-92763600	Weak transcription	Liver	Liver
20	chr1:92736800-92763800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr1:92738000-92763800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr1:92738400-92763800	Weak transcription	Brain Anterior Caudate	brain
23	chr1:92738800-92763400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr1:92743200-92763600	Weak transcription	NHDF-Ad	bronchial
25	chr1:92744000-92764000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr1:92745600-92764000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:92745800-92763800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:92745800-92763800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr1:92745800-92764000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:92745800-92764000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr1:92746000-92761800	Weak transcription	Esophagus	oesophagus
32	chr1:92746000-92763600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:92746000-92763800	Weak transcription	Aorta	Aorta
34	chr1:92746000-92763800	Weak transcription	Fetal Intestine Small	intestine
35	chr1:92746000-92764000	Weak transcription	Lung	lung
36	chr1:92746400-92762400	Weak transcription	Fetal Brain Female	brain
37	chr1:92751600-92763400	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr1:92751600-92763800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:92752400-92763600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:92752800-92763800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr1:92753200-92763400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr1:92754200-92761800	Weak transcription	Fetal Muscle Leg	muscle
43	chr1:92755000-92763200	Weak transcription	Brain Germinal Matrix	brain
44	chr1:92755000-92763600	Weak transcription	Stomach Smooth Muscle	stomach
45	chr1:92755400-92761800	Weak transcription	HUVEC	blood vessel
46	chr1:92755400-92763400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr1:92755400-92763400	Weak transcription	Brain Hippocampus Middle	brain
48	chr1:92755400-92763600	Weak transcription	Adipose Nuclei	Adipose
49	chr1:92755400-92763600	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr1:92755400-92763800	Weak transcription	Rectal Mucosa Donor 31	rectum

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