Variant report

Variant	nsv1015770
Chromosome Location	chr5:91911877-92498264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3524)
CpG islands
(count:795)
Chromatin interactive
region (count:57)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3524 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:92243628-92244260	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:92389338-92389960	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:92334242-92334547	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:92265795-92266142	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:92414075-92415220	HepG2	liver:	n/a	chr5:92415053-92415069
6	ARID3A	chr5:92251711-92252109	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:92125151-92125263	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:92278482-92279031	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:92137670-92137982	HepG2	liver:	n/a	chr5:92137816-92137832 chr5:92137817-92137833
10	ARID3A	chr5:92415566-92415645	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:92222730-92223443	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:92280245-92282170	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:91976876-91977418	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:92031123-92031376	HepG2	liver:	n/a	n/a
15	ARID3A	chr5:92262710-92263751	HepG2	liver:	n/a	n/a
16	ARID3A	chr5:92305019-92306486	HepG2	liver:	n/a	n/a
17	ATF1	chr5:92477071-92477099	K562	blood:	n/a	n/a
18	ATF1	chr5:91922993-91923059	K562	blood:	n/a	n/a
19	ATF2	chr5:92413606-92414879	GM12878	blood:	n/a	n/a
20	ATF2	chr5:92407439-92407899	GM12878	blood:	n/a	n/a
21	ATF2	chr5:92413700-92414458	GM12878	blood:	n/a	n/a
22	ATF3	chr5:92280679-92281275	A549	lung:	n/a	n/a
23	ATF3	chr5:92414022-92414911	A549	lung:	n/a	n/a
24	ATF3	chr5:92280678-92281228	A549	lung:	n/a	n/a
25	ATF3	chr5:92414032-92414885	HCT-116	colon:	n/a	n/a
26	ATF3	chr5:91976762-91977592	A549	lung:	n/a	n/a
27	ATF3	chr5:92414076-92414840	A549	lung:	n/a	n/a
28	BACH1	chr5:92259688-92259979	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr5:92413856-92414859	GM12878	blood:	n/a	chr5:92414829-92414838
30	BATF	chr5:92407499-92407722	GM12878	blood:	n/a	n/a
31	BATF	chr5:92414391-92414753	GM12878	blood:	n/a	n/a
32	BATF	chr5:92001332-92001541	GM12878	blood:	n/a	n/a
33	BCL11A	chr5:92414154-92414729	GM12878	blood:	n/a	chr5:92414576-92414585
34	BCL3	chr5:92280502-92281882	A549	lung:	n/a	n/a
35	BCL3	chr5:92414083-92414913	A549	lung:	n/a	chr5:92414576-92414585
36	BCL3	chr5:92413805-92414097	GM12878	blood:	n/a	chr5:92414056-92414065
37	BCL3	chr5:92414111-92414686	GM12878	blood:	n/a	chr5:92414576-92414585
38	BCL3	chr5:91976547-91977738	A549	lung:	n/a	chr5:91976642-91976651 chr5:91977303-91977312
39	BCL3	chr5:92305386-92305994	A549	lung:	n/a	n/a
40	BCL3	chr5:92011776-92012032	GM12878	blood:	n/a	n/a
41	BCL3	chr5:92413750-92415089	A549	lung:	n/a	chr5:92414576-92414585 chr5:92414056-92414065
42	BCL3	chr5:92280784-92281794	A549	lung:	n/a	n/a
43	BCLAF1	chr5:92413737-92414382	GM12878	blood:	n/a	chr5:92414056-92414065
44	BHLHE40	chr5:91970930-91971299	HepG2	liver:	n/a	n/a
45	BHLHE40	chr5:92223030-92223294	HepG2	liver:	n/a	n/a
46	BHLHE40	chr5:92414175-92414962	HepG2	liver:	n/a	n/a
47	BHLHE40	chr5:92125182-92125242	HepG2	liver:	n/a	n/a
48	BHLHE40	chr5:92262912-92263639	HepG2	liver:	n/a	n/a
49	BHLHE40	chr5:92414397-92414563	GM12878	blood:	n/a	n/a
50	BRCA1	chr5:92414196-92414663	Hela-S3	cervix:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:92179430-92179480	Caco-2	colon:	n/a
2	chr5:91976944-91976994	HUVEC	blood vessel:	n/a
3	chr5:92179430-92179480	Caco-2	colon:	n/a
4	chr5:91976944-91976994	HUVEC	blood vessel:	n/a
5	chr5:92456475-92456525	HRE	kidney:	n/a
6	chr5:92414398-92414448	MCF10A-Er-Src	breast:	n/a
7	chr5:91976944-91976994	K562	blood:	n/a
8	chr5:91970207-91970257	MCF10A-Er-Src	breast:	n/a
9	chr5:92106286-92106336	GM12891	blood:	n/a
10	chr5:92414263-92414313	MCF-7	breast:	n/a
11	chr5:91988522-91988572	ovcar-3	ovarian:	n/a
12	chr5:92353980-92354030	GM12892	blood:	n/a
13	chr5:92359386-92359436	HRPEpiC	eye:	n/a
14	chr5:92359386-92359436	Hela-S3	cervix:	n/a
15	chr5:91970207-91970257	SK-N-MC	brain:	n/a
16	chr5:92246958-92247008	AG04449	skin:	fetal
17	chr5:92179430-92179480	RPTEC	kidney:	n/a
18	chr5:92414263-92414313	NB4	blood:	n/a
19	chr5:92414263-92414313	SK-N-SH_RA	brain:	n/a
20	chr5:92353980-92354030	AG10803	skin:	n/a
21	chr5:92179430-92179480	HAEpiC	amniotic membrane:	n/a
22	chr5:92414263-92414313	RPTEC	kidney:	n/a
23	chr5:92359386-92359436	HCM	heart:	n/a
24	chr5:92179430-92179480	HCT-116	colon:	n/a
25	chr5:91988522-91988572	HUVEC	blood vessel:	n/a
26	chr5:91970207-91970257	HCF	heart:	n/a
27	chr5:91988522-91988572	GM06990	blood:	n/a
28	chr5:92353980-92354030	AG09319	gingival:	n/a
29	chr5:92443321-92443371	HL-60	blood:	n/a
30	chr5:92246958-92247008	HEK293	kidney:	embryo
31	chr5:92359386-92359436	LNCaP	prostate:	n/a
32	chr5:92390297-92390347	ProgFib	skin:	n/a
33	chr5:92179430-92179480	Hela-S3	cervix:	n/a
34	chr5:91976944-91976994	NT2-D1	testis:	n/a
35	chr5:92359386-92359436	HL-60	blood:	n/a
36	chr5:92359386-92359436	MCF10A-Er-Src	breast:	n/a
37	chr5:92456475-92456525	Jurkat	blood:	n/a
38	chr5:91970207-91970257	HNPCEpiC	eye:	n/a
39	chr5:92106286-92106336	HCF	heart:	n/a
40	chr5:91970207-91970257	A549	lung:	n/a
41	chr5:92443321-92443371	GM19239	blood:	n/a
42	chr5:91970207-91970257	RPTEC	kidney:	n/a
43	chr5:92456475-92456525	Caco-2	colon:	n/a
44	chr5:92390297-92390347	HRCEpiC	kidney:	n/a
45	chr5:92179430-92179480	NHDF-neo	bronchial:	n/a
46	chr5:91988522-91988572	IMR90	lung:	fetal
47	chr5:91970207-91970257	PFSK-1	brain:	n/a
48	chr5:92456475-92456525	HL-60	blood:	n/a
49	chr5:91976944-91976994	ProgFib	skin:	n/a
50	chr5:92106286-92106336	HEK293	kidney:	embryo

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:92221557..92222255-chr5:92397971..92398957,3	MCF-7	breast:
2	chr5:92193677..92196199-chr5:92200612..92203294,2	MCF-7	breast:
3	chr5:92251422..92252255-chr5:92398378..92398924,2	MCF-7	breast:
4	chr5:92047627..92050284-chr5:92057636..92060353,2	MCF-7	breast:
5	chr5:92023531..92024476-chr5:92173706..92174359,2	MCF-7	breast:
6	chr5:92449412..92451915-chr5:92457992..92460687,2	K562	blood:
7	chr5:92148259..92150776-chr5:92153209..92155137,2	K562	blood:
8	chr5:91604865..91605951-chr5:92173616..92174632,4	MCF-7	breast:
9	chr5:91971734..91973467-chr5:91976033..91978682,2	MCF-7	breast:
10	chr5:92003404..92005151-chr5:92021003..92023923,2	MCF-7	breast:
11	chr5:92221557..92222255-chr5:92397971..92398957,3	MCF-7	breast:
12	chr5:92140555..92143345-chr5:92152785..92155527,2	K562	blood:
13	chr5:92023157..92023758-chr5:92173968..92174654,2	MCF-7	breast:
14	chr5:92003404..92005151-chr5:92021003..92023923,2	MCF-7	breast:
15	chr5:92318316..92320626-chr5:92328876..92330818,2	K562	blood:
16	chr5:92251422..92252255-chr5:92398378..92398924,2	MCF-7	breast:
17	chr5:91853947..91854674-chr5:92173947..92174546,2	MCF-7	breast:
18	chr5:92140555..92143345-chr5:92152785..92155527,2	K562	blood:
19	chr5:92405044..92407618-chr5:92412622..92415093,2	MCF-7	breast:
20	chr5:92014050..92014925-chr5:92173501..92174178,2	MCF-7	breast:
21	chr5:92047627..92050284-chr5:92057636..92060353,2	MCF-7	breast:
22	chr5:92110796..92112626-chr5:92114304..92117125,2	MCF-7	breast:
23	chr5:91853989..91854741-chr5:92173857..92174425,2	MCF-7	breast:
24	chr5:92459385..92461272-chr5:92463234..92464762,2	K562	blood:
25	chr5:92318316..92320626-chr5:92328876..92330818,2	K562	blood:
26	chr5:92459385..92461272-chr5:92463234..92464762,2	K562	blood:
27	chr5:92110796..92112626-chr5:92114304..92117125,2	MCF-7	breast:
28	chr5:92385196..92386714-chr5:92403830..92406331,2	MCF-7	breast:
29	chr1:17231322..17232130-chr5:92137365..92138365,3	HCT-116	colon:
30	chr5:92148259..92150776-chr5:92153209..92155137,2	K562	blood:
31	chr5:92492798..92494347-chr5:92496334..92499006,2	MCF-7	breast:
32	chr5:92405044..92407618-chr5:92412622..92415093,2	MCF-7	breast:
33	chr5:92341494..92343841-chr5:92349667..92352121,2	MCF-7	breast:
34	chr5:92407114..92407835-chr6:11032821..11033413,2	MCF-7	breast:
35	chr5:91975903..91977517-chr5:91980878..91982915,2	MCF-7	breast:
36	chr5:92492798..92494347-chr5:92496334..92499006,2	MCF-7	breast:
37	chr5:91975903..91977517-chr5:91980878..91982915,2	MCF-7	breast:
38	chr4:90725590..90726217-chr5:92493530..92494422,2	MCF-7	breast:
39	chr5:92259322..92261638-chr5:92261984..92263695,2	MCF-7	breast:
40	chr5:92341478..92344657-chr5:92345293..92348897,3	K562	blood:
41	chr5:92341494..92343841-chr5:92349667..92352121,2	MCF-7	breast:
42	chr5:92490041..92490820-chr6:106582809..106583364,2	MCF-7	breast:
43	chr5:91971734..91973467-chr5:91976033..91978682,2	MCF-7	breast:
44	chr22:43410477..43412444-chr5:92216225..92218325,2	MCF-7	breast:
45	chr5:91605328..91605934-chr5:92396912..92397633,2	MCF-7	breast:
46	chr1:17230499..17232098-chr5:92137865..92139365,2	MCF-7	breast:
47	chr5:92014050..92014925-chr5:92173501..92174178,2	MCF-7	breast:
48	chr5:92341478..92344657-chr5:92345293..92348897,3	K562	blood:
49	chr5:92449412..92451915-chr5:92457992..92460687,2	K562	blood:
50	chr5:92259322..92261638-chr5:92261984..92263695,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NR2F1-3	chr5:92179384-92179711	ENSG00000248588
2	lnc-FAM172A-7	chr5:91975153-91975204	XLOC_004925
3	lnc-FAM172A-5	chr5:92011663-92012257	XLOC_004927
4	lnc-NR2F1-3	chr5:92161962-92162218	ENSG00000248588
5	lnc-FAM172A-3	chr5:92387376-92387482	XLOC_004929
6	lnc-FAM172A-6	chr5:92007191-92007287	XLOC_004926
7	lnc-NR2F1-4	chr5:92005579-92006441	XLOC_004472
8	lnc-FAM172A-4	chr5:92275178-92275298	XLOC_004928
9	lnc-NR2F1-8	chr5:92164187-92164320	NONHSAT102782
10	lnc-FAM172A-4	chr5:92249426-92249592	XLOC_004928
11	lnc-FAM172A-3	chr5:92404332-92404375	XLOC_004929
12	lnc-NR2F1-4	chr5:91990555-91990643	XLOC_004472
13	lnc-NR2F1-4	chr5:92005577-92005737	XLOC_004472
14	lnc-FAM172A-6	chr5:92005457-92005603	XLOC_004926
15	lnc-NR2F1-8	chr5:92163905-92163983	NONHSAT102782
16	lnc-NR2F1-2	chr5:92424509-92424627	XLOC_004474
17	lnc-FAM172A-5	chr5:92023827-92023961	XLOC_004927
18	lnc-FAM172A-3	chr5:92355369-92355842	XLOC_004929
19	lnc-FAM172A-4	chr5:92242887-92243175	XLOC_004928
20	lnc-NR2F1-4	chr5:92014438-92014848	XLOC_004472
21	lnc-NR2F1-2	chr5:92426103-92426530	XLOC_004474
22	lnc-FAM172A-12	chr5:92176514-92177335	NONHSAT102783
23	lnc-FAM172A-4	chr5:92249713-92249842	XLOC_004928
24	lnc-FAM172A-7	chr5:91996437-91996570	XLOC_004925

No data

Variant related genes	Relation type
ENSG00000249169	TF binding region
ENSG00000249984	TF binding region
ENSG00000251361	TF binding region
LDHBP3	TF binding region
ENSG00000248588	TF binding region
CCT7P2	TF binding region
ENSG00000221810	TF binding region
ENSG00000249776	TF binding region
ENSG00000248528	TF binding region
ENSG00000249169	CpG island
ENSG00000249984	CpG island
ENSG00000251361	CpG island
LDHBP3	CpG island
ENSG00000248588	CpG island
CCT7P2	CpG island
ENSG00000221810	CpG island
ENSG00000249776	CpG island
ENSG00000248528	CpG island
ENSG00000251361	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000100266	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000249984	chromatin interactions
C1orf144	miRNA target sites
SYPL1	miRNA target sites
CCNE2	miRNA target sites
ARHGAP12	miRNA target sites
CCNE1	miRNA target sites
WDR60	miRNA target sites

Extended variants
information (count: 14427 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:14427 , 50 per page) page: 1 2 3 4 5 6 7 ... 289

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150039674	chr5:91916652-91916653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557625547	chr5:91916665-91916666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147712514	chr5:91916673-91916674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577513870	chr5:91916699-91916700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545736852	chr5:91916708-91916709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559095749	chr5:91916712-91916713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528140836	chr5:91916760-91916761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114618088	chr5:91916779-91916780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561473839	chr5:91916825-91916826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530601149	chr5:91916846-91916847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs55683670	chr5:91916901-91916902	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs368880025	chr5:91916907-91916908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572203445	chr5:91916966-91916967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142644029	chr5:91916984-91916985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372692774	chr5:91916986-91916987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533076710	chr5:91917037-91917038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78832629	chr5:91917087-91917088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116180645	chr5:91917097-91917098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563895764	chr5:91917146-91917147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535049047	chr5:91917201-91917202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146893253	chr5:91917211-91917212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568612202	chr5:91917219-91917220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs137949967	chr5:91917220-91917221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372154888	chr5:91917228-91917229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187773538	chr5:91917266-91917267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs193116107	chr5:91917348-91917349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7711987	chr5:91917358-91917359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141959466	chr5:91917390-91917391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76438747	chr5:91917392-91917393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188814398	chr5:91918408-91918409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73137061	chr5:91918451-91918452	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531006947	chr5:91918498-91918499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550775102	chr5:91918551-91918552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79040934	chr5:91918557-91918558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571095372	chr5:91918570-91918571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539634002	chr5:91918598-91918599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150350226	chr5:91918641-91918642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566774713	chr5:91918655-91918656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535752234	chr5:91918669-91918670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181188533	chr5:91918700-91918701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577810142	chr5:91918730-91918731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184440550	chr5:91918731-91918732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557561522	chr5:91918734-91918735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115833242	chr5:91918754-91918755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540008439	chr5:91918774-91918775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184533360	chr5:91924803-91924804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200299543	chr5:91924849-91924850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115845318	chr5:91924907-91924908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558643760	chr5:91924915-91924916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557950424	chr5:91924930-91924931	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2230 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91916600-91917000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:91916600-91917000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:91916600-91917400	Enhancers	Fetal Heart	heart
4	chr5:91917000-91917200	Enhancers	Left Ventricle	heart
5	chr5:91918400-91918800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:91924800-91925000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:91925000-91927600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:91927600-91928600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:91928800-91930000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:91929200-91930000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr5:91929200-91930200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr5:91929200-91930600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:91929200-91930600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:91929400-91930200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr5:91929400-91930400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr5:91929600-91930200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:91929800-91930200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr5:91929800-91930200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr5:91931200-91931400	Enhancers	Gastric	stomach
20	chr5:91931200-91931600	Enhancers	Ovary	ovary
21	chr5:91935000-91935400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:91941200-91941400	Enhancers	NHDF-Ad	bronchial
23	chr5:91941400-91941600	Enhancers	Fetal Lung	lung
24	chr5:91941400-91941800	Flanking Active TSS	NHDF-Ad	bronchial
25	chr5:91941400-91942000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:91948800-91949000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:91948800-91949600	Enhancers	NH-A	brain
28	chr5:91949000-91963200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:91949200-91949600	Enhancers	HMEC	breast
30	chr5:91949200-91949800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr5:91954000-91968000	Weak transcription	Fetal Lung	lung
32	chr5:91963200-91963400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:91967200-91973000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:91968000-91971200	Enhancers	Fetal Lung	lung
35	chr5:91968800-91969000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:91968800-91970000	Enhancers	Fetal Stomach	stomach
37	chr5:91968800-91970200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr5:91968800-91971200	Enhancers	Fetal Kidney	kidney
39	chr5:91969000-91974000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:91970000-91970800	Weak transcription	Fetal Stomach	stomach
41	chr5:91970200-91971400	Enhancers	Fetal Intestine Small	intestine
42	chr5:91970400-91971200	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr5:91970600-91971200	Enhancers	Fetal Intestine Large	intestine
44	chr5:91970800-91971000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr5:91970800-91971000	Enhancers	Fetal Stomach	stomach
46	chr5:91970800-91971200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:91971000-91971200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr5:91971000-91971200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:91971000-91971200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr5:91971000-91976800	Weak transcription	Fetal Stomach	stomach

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