Variant report

Variant	nsv872413
Chromosome Location	chr1:149582448-149752366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2312)
CpG islands
(count:1956)
Chromatin interactive
region (count:8)
LncRNA
region (count:80)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:149603124-149603299	K562	blood:	n/a	n/a
2	ARID3A	chr1:149658538-149658730	K562	blood:	n/a	n/a
3	ARID3A	chr1:149684047-149684303	K562	blood:	n/a	n/a
4	ARID3A	chr1:149748718-149748918	K562	blood:	n/a	n/a
5	ARID3A	chr1:149680090-149680394	K562	blood:	n/a	n/a
6	ARID3A	chr1:149747121-149747405	K562	blood:	n/a	n/a
7	ARID3A	chr1:149684007-149684371	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:149605895-149606086	K562	blood:	n/a	n/a
9	ATF1	chr1:149747159-149747411	K562	blood:	n/a	n/a
10	ATF1	chr1:149605569-149605770	K562	blood:	n/a	n/a
11	ATF1	chr1:149658516-149658757	K562	blood:	n/a	n/a
12	ATF2	chr1:149683980-149684475	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:149605943-149606170	GM12878	blood:	n/a	n/a
14	ATF2	chr1:149683987-149684400	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:149605958-149606148	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr1:149605958-149606157	GM12878	blood:	n/a	n/a
17	ATF3	chr1:149664047-149664500	K562	blood:	n/a	n/a
18	ATF3	chr1:149711658-149712146	A549	lung:	n/a	n/a
19	ATF3	chr1:149683968-149684507	A549	lung:	n/a	n/a
20	ATF3	chr1:149679933-149680415	A549	lung:	n/a	n/a
21	ATF3	chr1:149605963-149606153	K562	blood:	n/a	n/a
22	ATF3	chr1:149683987-149684447	K562	blood:	n/a	n/a
23	ATF3	chr1:149683962-149684559	A549	lung:	n/a	n/a
24	ATF3	chr1:149711653-149712227	A549	lung:	n/a	n/a
25	ATF3	chr1:149680115-149680371	HCT-116	colon:	n/a	n/a
26	ATF3	chr1:149684003-149684461	HCT-116	colon:	n/a	n/a
27	ATF3	chr1:149680102-149680402	HCT-116	colon:	n/a	n/a
28	ATF3	chr1:149679965-149680393	A549	lung:	n/a	n/a
29	ATF3	chr1:149679963-149680389	K562	blood:	n/a	n/a
30	BACH1	chr1:149605885-149606093	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr1:149606050-149606083	K562	blood:	n/a	n/a
32	BACH1	chr1:149685097-149685104	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr1:149679774-149680151	GM12878	blood:	n/a	n/a
34	BATF	chr1:149711835-149712141	GM12878	blood:	n/a	chr1:149711949-149711958
35	BATF	chr1:149658464-149658735	GM12878	blood:	n/a	n/a
36	BATF	chr1:149678689-149679023	GM12878	blood:	n/a	chr1:149678898-149678909
37	BATF	chr1:149736086-149736381	GM12878	blood:	n/a	n/a
38	BATF	chr1:149704424-149704722	GM12878	blood:	n/a	n/a
39	BATF	chr1:149711785-149712234	GM12878	blood:	n/a	chr1:149711949-149711958
40	BATF	chr1:149591112-149591491	GM12878	blood:	n/a	chr1:149591277-149591288
41	BATF	chr1:149683235-149683530	GM12878	blood:	n/a	n/a
42	BATF	chr1:149681039-149681280	GM12878	blood:	n/a	n/a
43	BATF	chr1:149589130-149589384	GM12878	blood:	n/a	n/a
44	BATF	chr1:149583778-149584048	GM12878	blood:	n/a	n/a
45	BATF	chr1:149643480-149643688	GM12878	blood:	n/a	n/a
46	BATF	chr1:149604738-149604934	GM12878	blood:	n/a	n/a
47	BATF	chr1:149591520-149591763	GM12878	blood:	n/a	n/a
48	BATF	chr1:149589765-149589994	GM12878	blood:	n/a	n/a
49	BATF	chr1:149676700-149677043	GM12878	blood:	n/a	n/a
50	BATF	chr1:149679795-149680410	GM12878	blood:	n/a	n/a

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:149719536-149719586	SK-N-MC	brain:	n/a
2	chr1:149672625-149672675	NH-A	brain:	n/a
3	chr1:149684561-149684611	AG10803	skin:	n/a
4	chr1:149717620-149717670	A549	lung:	n/a
5	chr1:149719536-149719586	SK-N-MC	brain:	n/a
6	chr1:149672625-149672675	NH-A	brain:	n/a
7	chr1:149684561-149684611	AG10803	skin:	n/a
8	chr1:149717620-149717670	A549	lung:	n/a
9	chr1:149672849-149672899	RPTEC	kidney:	n/a
10	chr1:149679932-149679982	HCT-116	colon:	n/a
11	chr1:149670057-149670107	GM12891	blood:	n/a
12	chr1:149680232-149680282	Hela-S3	cervix:	n/a
13	chr1:149672149-149672199	ECC-1	luminal epithelium:	n/a
14	chr1:149719536-149719586	IMR90	lung:	fetal
15	chr1:149719536-149719586	ovcar-3	ovarian:	n/a
16	chr1:149719461-149719511	BE2_C	brain:	n/a
17	chr1:149718651-149718701	HL-60	blood:	n/a
18	chr1:149672625-149672675	HCF	heart:	n/a
19	chr1:149719536-149719586	NHDF-neo	bronchial:	n/a
20	chr1:149673328-149673378	HRCEpiC	kidney:	n/a
21	chr1:149711854-149711904	HCF	heart:	n/a
22	chr1:149670340-149670390	HEEpiC	esophagus:	n/a
23	chr1:149606322-149606372	HIPEpiC	eye:	n/a
24	chr1:149712057-149712107	HCM	heart:	n/a
25	chr1:149670340-149670390	AG10803	skin:	n/a
26	chr1:149644934-149644984	HIPEpiC	eye:	n/a
27	chr1:149720577-149720627	PFSK-1	brain:	n/a
28	chr1:149606322-149606372	PANC-1	pancreas:	n/a
29	chr1:149718671-149718721	AG04450	lung:	fetal
30	chr1:149670096-149670146	Hela-S3	cervix:	n/a
31	chr1:149672849-149672899	HCPEpiC	choroid plexus:	n/a
32	chr1:149605515-149605565	MCF-7	breast:	n/a
33	chr1:149606322-149606372	AG09319	gingival:	n/a
34	chr1:149721664-149721714	AoSMC	blood vessel:	n/a
35	chr1:149606322-149606372	SK-N-SH	brain:	n/a
36	chr1:149720577-149720627	IMR90	lung:	fetal
37	chr1:149719243-149719293	Hela-S3	cervix:	n/a
38	chr1:149711854-149711904	SK-N-SH_RA	brain:	n/a
39	chr1:149720577-149720627	Hepatocyte	liver:	n/a
40	chr1:149718651-149718701	HepG2	liver:	n/a
41	chr1:149672151-149672201	AG04449	skin:	fetal
42	chr1:149605515-149605565	NHBE	bronchial:	n/a
43	chr1:149673328-149673378	Hela-S3	cervix:	n/a
44	chr1:149721664-149721714	NH-A	brain:	n/a
45	chr1:149684561-149684611	NHDF-neo	bronchial:	n/a
46	chr1:149711854-149711904	AG04450	lung:	fetal
47	chr1:149673689-149673739	Jurkat	blood:	n/a
48	chr1:149670557-149670607	K562	blood:	n/a
49	chr1:149673328-149673378	BE2_C	brain:	n/a
50	chr1:149605515-149605565	Caco-2	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:149272620..149273452-chr1:149658236..149658977,2	MCF-7	breast:
2	chr1:149299280..149300172-chr1:149684615..149685511,3	MCF-7	breast:
3	chr1:149305186..149307455-chr1:149691743..149693791,2	MCF-7	breast:
4	chr1:149298692..149300746-chr1:149683634..149686545,2	MCF-7	breast:
5	chr1:149304628..149306966-chr1:149690305..149693086,2	MCF-7	breast:
6	chr1:144532673..144535225-chr1:149604575..149607265,3	K562	blood:
7	chr1:144533809..144535358-chr1:149604555..149606316,2	K562	blood:
8	chr1:144532726..144534859-chr1:149656717..149660251,3	K562	blood:

(count:80 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM72C-2	chr1:149590752-149590973	XLOC_001011
2	lnc-AL358813.2-2	chr1:149672301-149672983	NONHSAT006216
3	lnc-AL358813.2-2	chr1:149632456-149632691	NONHSAT006237
4	lnc-AL358813.2-2	chr1:149616549-149616643	XLOC_000398
5	lnc-AL358813.2-2	chr1:149616221-149616230	XLOC_000398
6	lnc-AL358813.2-2	chr1:149615765-149616111	ENSG00000232151.3
7	lnc-FAM72C-2	chr1:149591587-149591762	XLOC_001011
8	lnc-HIST2H2BF-1	chr1:149698419-149698606	ENSG00000234232.2
9	lnc-AL358813.2-2	chr1:149632904-149633021	NONHSAT006236
10	lnc-AL358813.2-4	chr1:149689368-149689854	NONHSAT006243
11	lnc-AL358813.2-2	chr1:149580524-149582604	NONHSAT006226
12	lnc-HIST2H2BF-1	chr1:149694411-149694620	ENSG00000234232.2
13	lnc-AL358813.2-2	chr1:149670209-149670452	NONHSAT006213
14	lnc-HIST2H2BF-1	chr1:149694456-149694633	ENSG00000234232.2
15	lnc-HIST2H2BF-1	chr1:149699768-149699819	ENSG00000234232.2
16	lnc-AL358813.2-2	chr1:149632456-149632691	NONHSAT006236
17	lnc-HIST2H2BF-1	chr1:149691554-149691646	ENSG00000234232.2
18	lnc-AL358813.2-2	chr1:149632904-149633208	ENSG00000232151.3
19	lnc-HIST2H2BF-1	chr1:149692947-149693081	ENSG00000234232.2
20	lnc-AL358813.2-2	chr1:149591078-149591237	NONHSAT006222
21	lnc-AL358813.2-2	chr1:149670209-149670452	NR_046138
22	lnc-AL358813.2-2	chr1:149636123-149636159	NONHSAT006235
23	lnc-AL358813.2-2	chr1:149627007-149627107	ENSG00000232151.3
24	lnc-AL358813.2-2	chr1:149676746-149676815	NONHSAT006223
25	lnc-PPIAL4C-8	chr1:149586058-149586279	expReg_chr1_16557_+
26	lnc-HIST2H2BF-3	chr1:149718450-149720133	NONHSAT006245
27	lnc-AL358813.2-2	chr1:149591179-149591237	XLOC_000397
28	lnc-HIST2H2BF-1	chr1:149694461-149694633	ENSG00000234232.2
29	lnc-AL358813.2-2	chr1:149636684-149636735	NONHSAT006236
30	lnc-AL358813.2-2	chr1:149591589-149592306	XLOC_000397
31	lnc-AL358813.2-2	chr1:149591589-149592306	NONHSAT006222
32	lnc-AL358813.2-2	chr1:149616549-149616885	XLOC_000398
33	lnc-HIST2H2BF-1	chr1:149698419-149698683	ENSG00000234232.2
34	lnc-AL358813.2-2	chr1:149632456-149632691	ENSG00000232151.3
35	lnc-AL358813.2-2	chr1:149646785-149649302	NONHSAT006239
36	lnc-AL358813.2-2	chr1:149671772-149671860	NONHSAT006211
37	lnc-AL358813.2-2	chr1:149664468-149664503	NONHSAT006223
38	lnc-AL358813.2-2	chr1:149627007-149627107	NONHSAT006235
39	lnc-AL358813.2-2	chr1:149629757-149629857	NONHSAT006237
40	lnc-AL358813.2-2	chr1:149672301-149672733	NONHSAT006214
41	lnc-AL358813.2-2	chr1:149672301-149672733	NONHSAT006213
42	lnc-AL358813.2-2	chr1:149637498-149637707	NONHSAT006237
43	lnc-AL358813.2-2	chr1:149636144-149636247	ENSG00000232151.3
44	lnc-AL358813.2-2	chr1:149636123-149636247	NONHSAT006236
45	lnc-AL358813.2-2	chr1:149636445-149636583	ENSG00000232151.3
46	lnc-AL358813.2-2	chr1:149591589-149591710	ENSG00000232151.3
47	lnc-HIST2H2BF-3	chr1:149713129-149713281	NONHSAT006245
48	lnc-AL358813.2-2	chr1:149636684-149636930	ENSG00000232151.3
49	lnc-AL358813.2-2	chr1:149616546-149616657	ENSG00000232151.3
50	lnc-AL358813.2-2	chr1:149616546-149616643	XLOC_000398

No data

Variant related genes	Relation type
ENSG00000232151	TF binding region
FCGR1A	TF binding region
ENSG00000239903	TF binding region
ENSG00000229801	TF binding region
ENSG00000263825	TF binding region
ENSG00000237168	TF binding region
ENSG00000269614	TF binding region
FAM231D	TF binding region
RNU1-68P	TF binding region
ENSG00000226500	TF binding region
ENSG00000234232	TF binding region
ENSG00000268554	TF binding region
RNVU1-20	TF binding region
ENSG00000197844	TF binding region
ENSG00000269501	TF binding region
ENSG00000223759	TF binding region
ENSG00000232151	CpG island
FCGR1A	CpG island
ENSG00000239903	CpG island
ENSG00000229801	CpG island
ENSG00000263825	CpG island
ENSG00000237168	CpG island
ENSG00000269614	CpG island
FAM231D	CpG island
RNU1-68P	CpG island
ENSG00000226500	CpG island
ENSG00000234232	CpG island
ENSG00000268554	CpG island
RNVU1-20	CpG island
ENSG00000197844	CpG island
ENSG00000269501	CpG island
ENSG00000223759	CpG island
ENSG00000201699	chromatin interactions
ABHD5	miRNA target sites
SBNO2	miRNA target sites
FGFR3	miRNA target sites

Extended variants
information (count: 3911 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:3911 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2935837	chr1:149582448-149582449	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs2814294	chr1:149582449-149582450	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs61806908	chr1:149582477-149582478	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs376389008	chr1:149582532-149582533	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs12217133	chr1:149582558-149582559	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs587609270	chr1:149582561-149582562	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs7415078	chr1:149582567-149582568	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs527679	chr1:149582647-149582648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200156412	chr1:149582669-149582670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587665238	chr1:149582713-149582714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587744798	chr1:149582756-149582757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77907269	chr1:149582806-149582807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199898331	chr1:149582838-149582839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371131250	chr1:149582839-149582840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373642842	chr1:149582840-149582841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367815180	chr1:149582842-149582843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs608133	chr1:149582860-149582861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201821397	chr1:149582883-149582884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587703159	chr1:149582902-149582903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587618213	chr1:149582903-149582904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587774102	chr1:149582915-149582916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200371262	chr1:149582977-149582978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs587697783	chr1:149583015-149583016	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587729198	chr1:149583072-149583073	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200933796	chr1:149583078-149583079	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587618983	chr1:149583084-149583085	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587682078	chr1:149583135-149583136	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587756610	chr1:149583161-149583162	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587656021	chr1:149583178-149583179	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61806909	chr1:149583269-149583270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs368214219	chr1:149583286-149583287	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs587713115	chr1:149583327-149583328	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs587775979	chr1:149583331-149583332	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs587664490	chr1:149583364-149583365	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs199782730	chr1:149583402-149583403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77301208	chr1:149583472-149583473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146611195	chr1:149583499-149583500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79702593	chr1:149583516-149583517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377407263	chr1:149583519-149583520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587745825	chr1:149583534-149583535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201509229	chr1:149583596-149583597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs199645433	chr1:149583604-149583605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587602249	chr1:149583608-149583609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587647564	chr1:149583623-149583624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587710619	chr1:149583650-149583651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587604083	chr1:149583745-149583746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs61806911	chr1:149583837-149583838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113236658	chr1:149583883-149583884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587665101	chr1:149583897-149583898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112360532	chr1:149583907-149583908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Congenital heart defect	20186050	CNVD
Trilogy of Fallot	22199024	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	23975201	CNVD

Chromatin state (count:1219 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:149577000-149582800	Weak transcription	Osteobl	bone
2	chr1:149577000-149584800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr1:149577000-149584800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:149577000-149584800	Weak transcription	Right Ventricle	heart
5	chr1:149577000-149585000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:149577000-149586600	Weak transcription	Fetal Muscle Leg	muscle
7	chr1:149577000-149586800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr1:149577400-149586400	Weak transcription	Primary T cells from cord blood	blood
9	chr1:149578200-149584800	Weak transcription	Fetal Intestine Small	intestine
10	chr1:149578200-149586800	Weak transcription	Fetal Intestine Large	intestine
11	chr1:149581200-149584600	Weak transcription	Primary B cells from cord blood	blood
12	chr1:149582400-149583200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:149582400-149583400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr1:149582800-149583000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:149582800-149583000	Enhancers	Osteobl	bone
16	chr1:149583000-149583200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:149583000-149583200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:149583000-149583400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr1:149583000-149583400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr1:149583000-149583400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:149583000-149583400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:149583000-149583400	Enhancers	Colon Smooth Muscle	Colon
23	chr1:149583000-149583400	Enhancers	Fetal Heart	heart
24	chr1:149583000-149583400	Enhancers	Stomach Smooth Muscle	stomach
25	chr1:149583000-149583400	Flanking Active TSS	Osteobl	bone
26	chr1:149583200-149583400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr1:149583200-149583400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:149583200-149583400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:149583200-149583400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr1:149583200-149583400	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr1:149583200-149583400	Enhancers	Pancreas	Pancrea
32	chr1:149583200-149583800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr1:149583200-149584800	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:149583200-149586400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:149583200-149586400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr1:149583400-149584800	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr1:149583400-149584800	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr1:149583400-149585000	Weak transcription	Colon Smooth Muscle	Colon
39	chr1:149583400-149585200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:149583400-149585400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:149583600-149584800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:149583600-149584800	Weak transcription	Pancreas	Pancrea
43	chr1:149584800-149585000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:149584800-149585000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr1:149584800-149585000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr1:149584800-149585000	Genic enhancers	Right Ventricle	heart
47	chr1:149584800-149585200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr1:149584800-149585200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr1:149584800-149585200	Genic enhancers	Primary T cells fromperipheralblood	blood
50	chr1:149584800-149585200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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