Variant report

Variant	nsv830448
Chromosome Location	chr1:85294094-85491110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2826)
CpG islands
(count:2380)
Chromatin interactive
region (count:59)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2826 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:85411712-85411930	K562	blood:	n/a	n/a
2	ARID3A	chr1:85410506-85410854	K562	blood:	n/a	n/a
3	ATF1	chr1:85300892-85301171	K562	blood:	n/a	n/a
4	ATF1	chr1:85422386-85422442	K562	blood:	n/a	n/a
5	ATF1	chr1:85320073-85320347	K562	blood:	n/a	n/a
6	ATF2	chr1:85437628-85438125	GM12878	blood:	n/a	n/a
7	ATF2	chr1:85401867-85402274	GM12878	blood:	n/a	n/a
8	ATF2	chr1:85439375-85440116	GM12878	blood:	n/a	n/a
9	ATF2	chr1:85328351-85328788	GM12878	blood:	n/a	n/a
10	ATF2	chr1:85435264-85436184	GM12878	blood:	n/a	n/a
11	ATF2	chr1:85410484-85411367	GM12878	blood:	n/a	n/a
12	ATF2	chr1:85424815-85425551	GM12878	blood:	n/a	n/a
13	ATF2	chr1:85454171-85454687	GM12878	blood:	n/a	n/a
14	ATF2	chr1:85435218-85436219	GM12878	blood:	n/a	n/a
15	ATF2	chr1:85437537-85438676	GM12878	blood:	n/a	n/a
16	ATF2	chr1:85410440-85411346	GM12878	blood:	n/a	n/a
17	ATF2	chr1:85454138-85454764	GM12878	blood:	n/a	n/a
18	ATF2	chr1:85460975-85462328	GM12878	blood:	n/a	n/a
19	ATF2	chr1:85358227-85358549	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr1:85319781-85320448	GM12878	blood:	n/a	n/a
21	ATF2	chr1:85424822-85425594	GM12878	blood:	n/a	n/a
22	ATF2	chr1:85456684-85457419	GM12878	blood:	n/a	n/a
23	ATF2	chr1:85390467-85391015	GM12878	blood:	n/a	n/a
24	ATF2	chr1:85328228-85328916	GM12878	blood:	n/a	n/a
25	ATF2	chr1:85461001-85462170	GM12878	blood:	n/a	n/a
26	ATF2	chr1:85319943-85320470	GM12878	blood:	n/a	n/a
27	ATF2	chr1:85456557-85457627	GM12878	blood:	n/a	n/a
28	ATF2	chr1:85439191-85440151	GM12878	blood:	n/a	n/a
29	BACH1	chr1:85411607-85411959	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr1:85358564-85359295	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr1:85331547-85331582	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr1:85462556-85462963	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr1:85463401-85463435	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr1:85411667-85411935	K562	blood:	n/a	n/a
35	BACH1	chr1:85463795-85463995	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr1:85427121-85427426	GM12878	blood:	n/a	chr1:85427344-85427353
37	BATF	chr1:85461189-85461461	GM12878	blood:	n/a	n/a
38	BATF	chr1:85435229-85436067	GM12878	blood:	n/a	n/a
39	BATF	chr1:85411622-85411924	GM12878	blood:	n/a	chr1:85411784-85411795 chr1:85411772-85411783 chr1:85411785-85411795
40	BATF	chr1:85435396-85436030	GM12878	blood:	n/a	n/a
41	BATF	chr1:85424950-85425433	GM12878	blood:	n/a	chr1:85425158-85425169
42	BATF	chr1:85456748-85457237	GM12878	blood:	n/a	n/a
43	BATF	chr1:85454290-85454675	GM12878	blood:	n/a	n/a
44	BATF	chr1:85424964-85425350	GM12878	blood:	n/a	chr1:85425158-85425169
45	BATF	chr1:85439501-85439958	GM12878	blood:	n/a	n/a
46	BATF	chr1:85461580-85461958	GM12878	blood:	n/a	n/a
47	BATF	chr1:85320007-85320356	GM12878	blood:	n/a	n/a
48	BATF	chr1:85444292-85444525	GM12878	blood:	n/a	n/a
49	BATF	chr1:85461158-85462031	GM12878	blood:	n/a	chr1:85461561-85461572
50	BATF	chr1:85456799-85457126	GM12878	blood:	n/a	n/a

(count:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:85462953-85463003	HCT-116	colon:	n/a
2	chr1:85462953-85463003	HCT-116	colon:	n/a
3	chr1:85331084-85331134	HCF	heart:	n/a
4	chr1:85373213-85373263	GM12891	blood:	n/a
5	chr1:85355904-85355954	HAEpiC	amniotic membrane:	n/a
6	chr1:85313514-85313564	HAEpiC	amniotic membrane:	n/a
7	chr1:85463364-85463414	PANC-1	pancreas:	n/a
8	chr1:85464110-85464160	MCF10A-Er-Src	breast:	n/a
9	chr1:85458682-85458732	CMK	blood:	n/a
10	chr1:85359106-85359156	Jurkat	blood:	n/a
11	chr1:85313514-85313564	Hepatocyte	liver:	n/a
12	chr1:85331899-85331949	AG04449	skin:	fetal
13	chr1:85357136-85357186	HMEC	breast:	n/a
14	chr1:85411171-85411221	BE2_C	brain:	n/a
15	chr1:85359334-85359384	NB4	blood:	n/a
16	chr1:85359119-85359169	Hepatocyte	liver:	n/a
17	chr1:85331899-85331949	HUVEC	blood vessel:	n/a
18	chr1:85462483-85462533	BE2_C	brain:	n/a
19	chr1:85359334-85359384	GM12891	blood:	n/a
20	chr1:85458682-85458732	NB4	blood:	n/a
21	chr1:85462812-85462862	GM12891	blood:	n/a
22	chr1:85313514-85313564	GM12891	blood:	n/a
23	chr1:85359912-85359962	SK-N-SH	brain:	n/a
24	chr1:85461303-85461353	HRPEpiC	eye:	n/a
25	chr1:85359119-85359169	K562	blood:	n/a
26	chr1:85462892-85462942	K562	blood:	n/a
27	chr1:85359119-85359169	BE2_C	brain:	n/a
28	chr1:85462700-85462750	SK-N-SH	brain:	n/a
29	chr1:85462939-85462989	AG04449	skin:	fetal
30	chr1:85359334-85359384	HRPEpiC	eye:	n/a
31	chr1:85464261-85464311	PFSK-1	brain:	n/a
32	chr1:85405081-85405131	NB4	blood:	n/a
33	chr1:85391429-85391479	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:85462857-85462907	ovcar-3	ovarian:	n/a
35	chr1:85355904-85355954	K562	blood:	n/a
36	chr1:85463364-85463414	Hepatocyte	liver:	n/a
37	chr1:85362120-85362170	ProgFib	skin:	n/a
38	chr1:85362120-85362170	SK-N-MC	brain:	n/a
39	chr1:85462812-85462862	MCF10A-Er-Src	breast:	n/a
40	chr1:85411171-85411221	NT2-D1	testis:	n/a
41	chr1:85462700-85462750	Hepatocyte	liver:	n/a
42	chr1:85426586-85426636	Hela-S3	cervix:	n/a
43	chr1:85362120-85362170	IMR90	lung:	fetal
44	chr1:85464000-85464050	Hela-S3	cervix:	n/a
45	chr1:85391429-85391479	HL-60	blood:	n/a
46	chr1:85462812-85462862	BJ	skin:	n/a
47	chr1:85313514-85313564	AG04449	skin:	fetal
48	chr1:85462953-85463003	GM12878	blood:	n/a
49	chr1:85358327-85358377	MCF10A-Er-Src	breast:	n/a
50	chr1:85359334-85359384	LNCaP	prostate:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:85403163..85404849-chr1:85410695..85412428,2	K562	blood:
2	chr1:85392212..85394634-chr1:85398558..85401457,2	K562	blood:
3	chr1:85405603..85407474-chr1:85407528..85409146,2	K562	blood:
4	chr1:85247930..85248856-chr1:85350085..85350918,2	MCF-7	breast:
5	chr1:85457596..85460591-chr1:85461678..85464189,2	MCF-7	breast:
6	chr1:85299331..85301423-chr1:85313986..85316140,2	MCF-7	breast:
7	chr1:85410011..85410751-chr1:85491092..85491875,2	MCF-7	breast:
8	chr1:85342133..85343941-chr1:85345825..85348008,2	K562	blood:
9	chr1:85342133..85343941-chr1:85345825..85348008,2	K562	blood:
10	chr1:85410128..85411315-chr1:85490122..85491874,8	MCF-7	breast:
11	chr1:85410326..85411124-chr1:85544047..85544918,2	MCF-7	breast:
12	chr1:85410006..85410936-chr1:85495368..85495874,2	MCF-7	breast:
13	chr1:85400043..85402617-chr1:85426319..85428955,2	MCF-7	breast:
14	chr1:85392212..85394634-chr1:85398558..85401457,2	K562	blood:
15	chr1:85405603..85407474-chr1:85407528..85409146,2	K562	blood:
16	chr1:85350699..85352618-chr1:85361197..85363939,2	K562	blood:
17	chr1:85410258..85411298-chr1:85720149..85720894,4	MCF-7	breast:
18	chr1:85455345..85457020-chr1:85460582..85462706,2	K562	blood:
19	chr1:85411165..85413303-chr1:85416818..85418943,2	K562	blood:
20	chr1:85400043..85402617-chr1:85426319..85428955,2	MCF-7	breast:
21	chr1:85410009..85411013-chr1:85724647..85725830,3	MCF-7	breast:
22	chr1:85301031..85302950-chr1:85309878..85312454,2	MCF-7	breast:
23	chr1:85420041..85422749-chr1:85426305..85427905,2	K562	blood:
24	chr1:85409879..85410688-chr1:85705752..85706654,2	K562	blood:
25	chr1:85410308..85411228-chr1:85705720..85706844,7	MCF-7	breast:
26	chr1:85295614..85297447-chr1:85297666..85299937,3	MCF-7	breast:
27	chr1:85301031..85302950-chr1:85309878..85312454,2	MCF-7	breast:
28	chr1:85403163..85404849-chr1:85410695..85412428,2	K562	blood:
29	chr1:85409622..85411011-chr1:85492995..85494617,8	MCF-7	breast:
30	chr1:85434009..85435841-chr1:85437123..85439359,2	K562	blood:
31	chr1:85300807..85303047-chr1:85305018..85306765,2	K562	blood:
32	chr1:85411165..85413303-chr1:85416818..85418943,2	K562	blood:
33	chr1:85405508..85407651-chr1:85733535..85736514,2	K562	blood:
34	chr1:85410065..85411348-chr1:85724616..85726527,9	K562	blood:
35	chr1:85420041..85422749-chr1:85426305..85427905,2	K562	blood:
36	chr1:85326387..85327891-chr1:85331697..85333643,2	K562	blood:
37	chr1:85410128..85411315-chr1:85490122..85491874,8	MCF-7	breast:
38	chr1:85424847..85426779-chr1:85430134..85432715,2	K562	blood:
39	chr1:85410118..85411009-chr1:85725007..85725639,2	MCF-7	breast:
40	chr1:85410011..85410751-chr1:85491092..85491875,2	MCF-7	breast:
41	chr1:85434009..85435841-chr1:85437123..85439359,2	K562	blood:
42	chr1:85412729..85414874-chr1:85716251..85718921,2	MCF-7	breast:
43	chr1:85324162..85326847-chr1:85346184..85349176,2	K562	blood:
44	chr1:85424847..85426779-chr1:85430134..85432715,2	K562	blood:
45	chr1:85410252..85411181-chr1:85719873..85720677,4	K562	blood:
46	chr1:85371748..85373502-chr1:85374924..85376676,2	K562	blood:
47	chr1:85350699..85352618-chr1:85361197..85363939,2	K562	blood:
48	chr1:85295614..85297447-chr1:85297666..85299937,3	MCF-7	breast:
49	chr1:85410353..85411305-chr1:85719958..85721105,6	MCF-7	breast:
50	chr1:85238005..85238693-chr1:85400870..85401458,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPAR3-1	chr1:85395241-85395527	NONHSAT004231
2	lnc-WDR63-1	chr1:85463022-85463042	XLOC_000274
3	lnc-MCOLN3-1	chr1:85483656-85483882	NONHSAT004234
4	lnc-WDR63-1	chr1:85463140-85463597	XLOC_000274
5	lnc-LPAR3-1	chr1:85392109-85392404	NONHSAT004231

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	MCOLN2	hsa-miR-32-5p	chr1:85392145-85392138
2	MCOLN2	hsa-miR-92a-3p	chr1:85392139-85392161
3	MCOLN2	hsa-miR-32-5p	chr1:85392139-85392161
4	MCOLN2	hsa-miR-92a-3p	chr1:85392145-85392138

Variant related genes	Relation type
LPAR3	TF binding region
MCOLN2	TF binding region
WDR63	TF binding region
MCOLN3	TF binding region
LPAR3	CpG island
MCOLN2	CpG island
WDR63	CpG island
MCOLN3	CpG island
ENSG00000153898	chromatin interactions
ENSG00000171517	chromatin interactions
ENSG00000055732	chromatin interactions
ENSG00000162642	chromatin interactions

Extended variants
information (count: 7264 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:7264 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559289872	chr1:85294176-85294177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528472429	chr1:85294213-85294214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541506087	chr1:85294217-85294218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112210968	chr1:85294236-85294237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551815996	chr1:85294292-85294293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559489118	chr1:85294293-85294294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537285962	chr1:85294341-85294342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150931337	chr1:85294347-85294348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1359607	chr1:85294434-85294435	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs536323543	chr1:85294477-85294478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553018015	chr1:85294499-85294500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191906114	chr1:85294503-85294504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538604570	chr1:85294525-85294526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111662628	chr1:85294554-85294555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183769442	chr1:85294601-85294602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544007775	chr1:85294638-85294639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563284295	chr1:85294640-85294641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573813980	chr1:85294663-85294664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141082752	chr1:85294700-85294701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559777324	chr1:85294705-85294706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528523776	chr1:85294782-85294783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186618064	chr1:85294818-85294819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574984866	chr1:85294836-85294837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs66609763	chr1:85294861-85294862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77852458	chr1:85294863-85294864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370651449	chr1:85294864-85294865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565448481	chr1:85294892-85294893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191468001	chr1:85294977-85294978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145109661	chr1:85294986-85294987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182381034	chr1:85295112-85295113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567823215	chr1:85295132-85295133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187013481	chr1:85295167-85295168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12407505	chr1:85295202-85295203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs566556297	chr1:85295274-85295275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538267798	chr1:85295287-85295288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76632792	chr1:85295291-85295292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191446048	chr1:85295321-85295322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78418539	chr1:85295389-85295390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528951505	chr1:85295417-85295418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377518308	chr1:85295506-85295507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554429228	chr1:85295532-85295533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146841883	chr1:85295539-85295540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115387254	chr1:85295596-85295597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140678411	chr1:85295625-85295626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76004172	chr1:85295690-85295691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145690745	chr1:85295732-85295733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565253011	chr1:85295764-85295765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531245797	chr1:85295833-85295834	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182153532	chr1:85295864-85295865	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571097215	chr1:85295889-85295890	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
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
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2673 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85264000-85295600	Weak transcription	NHEK	skin
2	chr1:85282400-85295800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:85287600-85295800	Weak transcription	Right Atrium	heart
4	chr1:85288800-85296800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr1:85289400-85330800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr1:85290200-85294200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:85291000-85296000	Weak transcription	Right Ventricle	heart
8	chr1:85291000-85300000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:85291200-85301000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:85291600-85296000	Weak transcription	Left Ventricle	heart
11	chr1:85292600-85294600	Enhancers	Fetal Heart	heart
12	chr1:85293800-85294400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr1:85294200-85294600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:85294200-85294600	Enhancers	HMEC	breast
15	chr1:85294400-85299400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:85294600-85296200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:85294600-85299200	Weak transcription	HMEC	breast
18	chr1:85294600-85300400	Weak transcription	Fetal Heart	heart
19	chr1:85295600-85296800	Strong transcription	NHEK	skin
20	chr1:85295800-85296400	Enhancers	Right Atrium	heart
21	chr1:85295800-85297000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:85296000-85296200	Enhancers	Left Ventricle	heart
23	chr1:85296000-85296400	Enhancers	Pancreas	Pancrea
24	chr1:85296000-85296400	Enhancers	Right Ventricle	heart
25	chr1:85296000-85296600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr1:85296000-85300200	Weak transcription	NHLF	lung
27	chr1:85296200-85296600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:85296400-85297800	Weak transcription	Right Atrium	heart
29	chr1:85296400-85299200	Weak transcription	Pancreas	Pancrea
30	chr1:85296600-85299200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:85296600-85312800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:85296800-85297000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:85296800-85299000	Weak transcription	NHEK	skin
34	chr1:85297000-85299400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr1:85297800-85298000	Enhancers	Right Atrium	heart
36	chr1:85298400-85300600	Enhancers	HUVEC	blood vessel
37	chr1:85298800-85301200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:85298800-85301400	Enhancers	Stomach Mucosa	stomach
39	chr1:85298800-85301600	Enhancers	Hela-S3	cervix
40	chr1:85299000-85299600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr1:85299000-85300400	Enhancers	NHEK	skin
42	chr1:85299000-85300600	Enhancers	A549	lung
43	chr1:85299200-85299600	Enhancers	Esophagus	oesophagus
44	chr1:85299200-85299600	Enhancers	Pancreas	Pancrea
45	chr1:85299200-85299800	Enhancers	Gastric	stomach
46	chr1:85299200-85301600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:85299200-85301600	Enhancers	HMEC	breast
48	chr1:85299400-85300800	Enhancers	NHDF-Ad	bronchial
49	chr1:85299400-85301000	Enhancers	Muscle Satellite Cultured Cells	--
50	chr1:85299400-85301200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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