Variant report

Variant	esv3362439
Chromosome Location	chr1:113376621-113450321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1108)
CpG islands
(count:795)
Chromatin interactive
region (count:82)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1108 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:113423665-113423907	K562	blood:	n/a	n/a
2	ARID3A	chr1:113412037-113412274	K562	blood:	n/a	n/a
3	ARID3A	chr1:113446409-113446995	K562	blood:	n/a	n/a
4	ATF1	chr1:113446644-113447073	K562	blood:	n/a	n/a
5	ATF1	chr1:113432160-113432197	K562	blood:	n/a	n/a
6	ATF1	chr1:113415318-113415731	K562	blood:	n/a	n/a
7	ATF1	chr1:113420915-113421274	K562	blood:	n/a	n/a
8	ATF1	chr1:113431369-113431645	K562	blood:	n/a	n/a
9	ATF1	chr1:113412031-113412267	K562	blood:	n/a	n/a
10	ATF3	chr1:113406594-113406740	K562	blood:	n/a	n/a
11	ATF3	chr1:113446575-113446961	K562	blood:	n/a	n/a
12	BACH1	chr1:113391962-113392548	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:113430716-113430722	K562	blood:	n/a	n/a
14	BATF	chr1:113387894-113388170	GM12878	blood:	n/a	chr1:113388042-113388053
15	BATF	chr1:113446481-113446839	GM12878	blood:	n/a	n/a
16	BCL3	chr1:113448098-113448370	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:113423639-113423881	K562	blood:	n/a	n/a
18	BHLHE40	chr1:113420905-113421278	K562	blood:	n/a	n/a
19	BHLHE40	chr1:113383269-113383658	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:113424441-113424609	K562	blood:	n/a	n/a
21	BHLHE40	chr1:113446845-113446978	K562	blood:	n/a	n/a
22	BHLHE40	chr1:113431202-113431700	K562	blood:	n/a	n/a
23	BHLHE40	chr1:113415376-113415652	K562	blood:	n/a	n/a
24	BRCA1	chr1:113423607-113423885	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr1:113448712-113449164	K562	blood:	n/a	n/a
26	CBX3	chr1:113425899-113426286	K562	blood:	n/a	n/a
27	CBX3	chr1:113431039-113431607	K562	blood:	n/a	n/a
28	CBX3	chr1:113436070-113436699	K562	blood:	n/a	n/a
29	CBX3	chr1:113420876-113421355	K562	blood:	n/a	n/a
30	CBX3	chr1:113436046-113436428	K562	blood:	n/a	n/a
31	CCNT2	chr1:113420936-113421303	K562	blood:	n/a	n/a
32	CCNT2	chr1:113415281-113415647	K562	blood:	n/a	n/a
33	CCNT2	chr1:113431343-113431678	K562	blood:	n/a	n/a
34	CCNT2	chr1:113436504-113436740	K562	blood:	n/a	n/a
35	CCNT2	chr1:113446723-113447017	K562	blood:	n/a	n/a
36	CCNT2	chr1:113448691-113449002	K562	blood:	n/a	n/a
37	CCNT2	chr1:113447659-113448067	K562	blood:	n/a	n/a
38	CEBPB	chr1:113386774-113387098	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:113383834-113384109	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr1:113394312-113394617	K562	blood:	n/a	n/a
41	CEBPB	chr1:113420126-113420592	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:113397800-113398144	IMR90	lung:	n/a	chr1:113397958-113397969
43	CEBPB	chr1:113386872-113387013	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:113394293-113394634	K562	blood:	n/a	n/a
45	CEBPB	chr1:113394323-113394637	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:113386765-113387060	A549	lung:	n/a	n/a
47	CEBPB	chr1:113394309-113394671	IMR90	lung:	n/a	n/a
48	CEBPB	chr1:113397795-113398109	HepG2	liver:	n/a	chr1:113397958-113397969
49	CEBPB	chr1:113394315-113394515	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:113383814-113384195	MCF-7	breast:	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	chr1:113447460-113447510	GM06990	blood:	n/a
2	chr1:113392116-113392166	T-47D	breast:	n/a
3	chr1:113447460-113447510	GM06990	blood:	n/a
4	chr1:113392116-113392166	T-47D	breast:	n/a
5	chr1:113392388-113392438	CMK	blood:	n/a
6	chr1:113392388-113392438	HIPEpiC	eye:	n/a
7	chr1:113394877-113394927	HRPEpiC	eye:	n/a
8	chr1:113392116-113392166	HepG2	liver:	n/a
9	chr1:113447460-113447510	Caco-2	colon:	n/a
10	chr1:113392617-113392667	Hepatocyte	liver:	n/a
11	chr1:113393176-113393226	SAEC	small airway:	n/a
12	chr1:113425263-113425313	HIPEpiC	eye:	n/a
13	chr1:113425263-113425313	AG09319	gingival:	n/a
14	chr1:113394877-113394927	U87	brain:	n/a
15	chr1:113394877-113394927	ovcar-3	ovarian:	n/a
16	chr1:113393176-113393226	MCF10A-Er-Src	breast:	n/a
17	chr1:113425263-113425313	HRE	kidney:	n/a
18	chr1:113393179-113393229	ECC-1	luminal epithelium:	n/a
19	chr1:113393176-113393226	BE2_C	brain:	n/a
20	chr1:113421910-113421960	HNPCEpiC	eye:	n/a
21	chr1:113392116-113392166	HUVEC	blood vessel:	n/a
22	chr1:113390019-113390069	H1-hESC	embryonic stem cell:	embryo
23	chr1:113392388-113392438	IMR90	lung:	fetal
24	chr1:113393179-113393229	PrEC	prostate:	n/a
25	chr1:113392388-113392438	SK-N-SH_RA	brain:	n/a
26	chr1:113392116-113392166	HL-60	blood:	n/a
27	chr1:113394877-113394927	HL-60	blood:	n/a
28	chr1:113393176-113393226	T-47D	breast:	n/a
29	chr1:113392116-113392166	GM19239	blood:	n/a
30	chr1:113394877-113394927	GM06990	blood:	n/a
31	chr1:113392116-113392166	AG10803	skin:	n/a
32	chr1:113421910-113421960	H1-hESC	embryonic stem cell:	embryo
33	chr1:113425263-113425313	AoSMC	blood vessel:	n/a
34	chr1:113392388-113392438	HRPEpiC	eye:	n/a
35	chr1:113393179-113393229	RPTEC	kidney:	n/a
36	chr1:113392781-113392831	H1-hESC	embryonic stem cell:	embryo
37	chr1:113392617-113392667	A549	lung:	n/a
38	chr1:113392162-113392212	HepG2	liver:	n/a
39	chr1:113393179-113393229	HEEpiC	esophagus:	n/a
40	chr1:113421910-113421960	AG09309	skin:	n/a
41	chr1:113393176-113393226	BJ	skin:	n/a
42	chr1:113392388-113392438	HepG2	liver:	n/a
43	chr1:113393176-113393226	ECC-1	luminal epithelium:	n/a
44	chr1:113425263-113425313	H1-hESC	embryonic stem cell:	embryo
45	chr1:113421910-113421960	ECC-1	luminal epithelium:	n/a
46	chr1:113392781-113392831	ovcar-3	ovarian:	n/a
47	chr1:113447460-113447510	NHBE	bronchial:	n/a
48	chr1:113392617-113392667	MCF10A-Er-Src	breast:	n/a
49	chr1:113392162-113392212	HL-60	blood:	n/a
50	chr1:113392162-113392212	SK-N-SH	brain:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:113441801..113445545-chr1:113447072..113449494,3	K562	blood:
2	chr1:113448232..113450362-chr1:113454684..113457292,4	K562	blood:
3	chr1:113415018..113417156-chr1:113420570..113423546,3	K562	blood:
4	chr1:113441801..113445545-chr1:113447072..113449494,3	K562	blood:
5	chr1:113420602..113421810-chr1:113584981..113585927,5	K562	blood:
6	chr1:113442871..113445131-chr1:113497859..113500702,2	K562	blood:
7	chr1:113421355..113423469-chr1:113497371..113499587,2	MCF-7	breast:
8	chr1:113421698..113424521-chr1:113497162..113501677,6	K562	blood:
9	chr1:113424350..113426244-chr1:113426854..113428692,2	MCF-7	breast:
10	chr1:113424435..113426998-chr1:113430244..113432680,3	K562	blood:
11	chr1:113429664..113431749-chr1:113436515..113438078,2	K562	blood:
12	chr1:113432563..113435506-chr1:113438129..113441050,2	K562	blood:
13	chr1:113445849..113448733-chr1:113470984..113473265,2	K562	blood:
14	chr1:113423643..113425440-chr1:113613953..113616307,2	K562	blood:
15	chr1:113423151..113424795-chr1:113615741..113617336,2	MCF-7	breast:
16	chr1:113442578..113444928-chr1:113615994..113617542,2	K562	blood:
17	chr1:113414731..113417256-chr1:113497022..113499484,2	K562	blood:
18	chr1:113423539..113425457-chr1:113613953..113617483,4	K562	blood:
19	chr1:113392230..113394904-chr1:113422287..113425247,2	MCF-7	breast:
20	chr1:113424350..113426244-chr1:113426854..113428692,2	MCF-7	breast:
21	chr1:113351576..113352442-chr1:113423249..113424028,4	MCF-7	breast:
22	chr1:113420012..113422020-chr1:113615413..113617603,2	K562	blood:
23	chr1:113423348..113424191-chr1:113615233..113616019,3	MCF-7	breast:
24	chr1:113379016..113381976-chr1:113384140..113386902,2	MCF-7	breast:
25	chr1:113447709..113449566-chr1:113450371..113452210,2	K562	blood:
26	chr1:113423245..113423835-chr1:113585324..113585888,3	MCF-7	breast:
27	chr1:113423471..113424047-chr1:113496482..113497380,2	MCF-7	breast:
28	chr1:113342047..113343911-chr1:113444698..113447399,2	K562	blood:
29	chr1:113446003..113448854-chr1:113463781..113465733,2	MCF-7	breast:
30	chr1:113424435..113426998-chr1:113430244..113432680,3	K562	blood:
31	chr1:113425134..113427690-chr1:113436011..113438422,2	K562	blood:
32	chr1:113411911..113414258-chr1:113419696..113422107,2	MCF-7	breast:
33	chr1:113448893..113450506-chr1:113473671..113476266,2	K562	blood:
34	chr1:113430436..113432167-chr1:113476191..113478962,2	K562	blood:
35	chr1:113423306..113424369-chr1:113584838..113585867,15	MCF-7	breast:
36	chr1:113422315..113424969-chr1:113580165..113583110,2	K562	blood:
37	chr1:113445363..113447698-chr1:113464880..113466505,2	K562	blood:
38	chr1:113413526..113415499-chr1:113588812..113591393,2	MCF-7	breast:
39	chr1:113379016..113381976-chr1:113384140..113386902,2	MCF-7	breast:
40	chr1:113448862..113452902-chr1:113455376..113458880,4	K562	blood:
41	chr1:113445118..113448523-chr1:113453652..113455842,3	MCF-7	breast:
42	chr1:113415018..113417156-chr1:113420570..113423546,3	K562	blood:
43	chr1:113255487..113258161-chr1:113420887..113423423,3	K562	blood:
44	chr1:113421587..113424736-chr1:113583992..113587746,3	K562	blood:
45	chr1:113346242..113347922-chr1:113394008..113395856,2	MCF-7	breast:
46	chr1:113445368..113447569-chr1:113467662..113470258,2	K562	blood:
47	chr1:113448950..113451242-chr1:113537407..113540142,2	MCF-7	breast:
48	chr1:113422181..113424521-chr1:113435432..113438293,2	K562	blood:
49	chr1:113444785..113447653-chr1:113457108..113462049,4	K562	blood:
50	chr1:113423347..113424253-chr1:113498007..113499021,4	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM19A3-2	chr1:113419562-113419606	XLOC_000348
2	lnc-FAM19A3-6	chr1:113390931-113391200	NONHSAT005281
3	lnc-FAM19A3-7	chr1:113400131-113400686	NONHSAT005292
4	lnc-SLC16A1-1	chr1:113391576-113391672	NONHSAT005284
5	lnc-FAM19A3-2	chr1:113420352-113420493	XLOC_000348
6	lnc-FAM19A3-6	chr1:113390931-113391200	NONHSAT005288
7	lnc-SLC16A1-1	chr1:113392568-113392706	ucscGeneNc_uc001ede_1
8	lnc-FAM19A3-6	chr1:113377818-113377983	NONHSAT005288
9	lnc-FAM19A3-7	chr1:113400759-113400763	NONHSAT005292
10	lnc-FAM19A3-2	chr1:113420352-113420489	XLOC_000348
11	lnc-FAM19A3-2	chr1:113392698-113393049	XLOC_000348
12	lnc-SLC16A1-1	chr1:113383110-113383202	NONHSAT005284
13	lnc-FAM19A3-7	chr1:113399850-113401156	NONHSAT005291
14	lnc-SLC16A1-1	chr1:113392302-113392399	ENSG00000215866.3
15	lnc-SLC16A1-1	chr1:113391576-113391672	XLOC_000966
16	lnc-SLC16A1-1	chr1:113383110-113383202	XLOC_000966
17	lnc-SLC16A1-1	chr1:113417084-113417247	ucscGeneNc_uc001ede_1
18	lnc-SLC16A1-1	chr1:113392302-113392437	XLOC_000966
19	lnc-SLC16A1-1	chr1:113383110-113383202	XLOC_000966
20	lnc-FAM19A3-2	chr1:113392392-113393049	NONHSAT005289
21	lnc-SLC16A1-1	chr1:113392302-113393265	NONHSAT005284
22	lnc-FAM19A3-2	chr1:113420352-113420459	NONHSAT005289
23	lnc-SLC16A1-1	chr1:113392302-113392401	XLOC_000966
24	lnc-SLC16A1-1	chr1:113392302-113393265	XLOC_000966
25	lnc-SLC16A1-1	chr1:113383110-113383202	ENSG00000215866.3
26	lnc-FAM19A3-2	chr1:113392650-113393049	XLOC_000348

No data

Variant related genes	Relation type
ENSG00000224167	TF binding region
ENSG00000215866	TF binding region
ENSG00000228040	TF binding region
ENSG00000224167	CpG island
ENSG00000215866	CpG island
ENSG00000228040	CpG island
ENSG00000238198	chromatin interactions
ENSG00000261595	chromatin interactions
ENSG00000155367	chromatin interactions
ENSG00000228040	chromatin interactions
ENSG00000198799	chromatin interactions
ENSG00000215866	chromatin interactions
ENSG00000229020	chromatin interactions
ENSG00000224167	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000226419	chromatin interactions
CREB5	miRNA target sites
HAUS6	miRNA target sites
CTDSPL	miRNA target sites
NCOR2	miRNA target sites
PPIF	miRNA target sites
CDH12	miRNA target sites

Extended variants
information (count: 2954 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2954 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376618777	chr1:113376629-113376630	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs567803567	chr1:113376632-113376633	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs535210387	chr1:113376633-113376634	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs181662687	chr1:113376679-113376680	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs115126303	chr1:113376704-113376705	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs553324631	chr1:113376738-113376739	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs187357881	chr1:113376793-113376794	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs564754392	chr1:113376798-113376799	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs538620742	chr1:113376825-113376826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532045597	chr1:113376831-113376832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189244878	chr1:113376852-113376853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181013546	chr1:113376858-113376859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551957883	chr1:113376956-113376957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537585364	chr1:113377002-113377003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557489280	chr1:113377027-113377028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561724610	chr1:113377049-113377050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79587905	chr1:113377055-113377056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542888740	chr1:113377078-113377079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150238672	chr1:113377085-113377086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200350744	chr1:113377093-113377094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559638595	chr1:113377099-113377100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201362635	chr1:113377107-113377108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201270078	chr1:113377124-113377125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573237261	chr1:113377128-113377129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs56796488	chr1:113377131-113377132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565172736	chr1:113377145-113377146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12082642	chr1:113377146-113377147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144611272	chr1:113377178-113377179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547077653	chr1:113377308-113377309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71513998	chr1:113377311-113377312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111227282	chr1:113377327-113377328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185035021	chr1:113377352-113377353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71513999	chr1:113377425-113377426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546850368	chr1:113377428-113377429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568585763	chr1:113377431-113377432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566750427	chr1:113377531-113377532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149853517	chr1:113377536-113377537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538980380	chr1:113377588-113377589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539236605	chr1:113377671-113377672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140203142	chr1:113377674-113377675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568769623	chr1:113377691-113377692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150336573	chr1:113377707-113377708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs137978431	chr1:113377708-113377709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189547022	chr1:113377714-113377715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569823845	chr1:113377749-113377750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77689292	chr1:113377762-113377763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200641310	chr1:113377770-113377771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573071615	chr1:113377829-113377830	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs530225550	chr1:113377849-113377850	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs6671379	chr1:113377884-113377885	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1519 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113364200-113392000	Weak transcription	Right Atrium	heart
2	chr1:113365200-113382600	Weak transcription	HUVEC	blood vessel
3	chr1:113369200-113392000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:113369600-113383600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr1:113370000-113379400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:113370000-113383400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:113370600-113383400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:113370600-113383400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:113374600-113383200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:113375600-113379400	Weak transcription	Placenta	Placenta
11	chr1:113376200-113376800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:113376400-113376800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:113376400-113376800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr1:113376400-113376800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:113376400-113376800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:113376400-113377000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:113376600-113376800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr1:113376800-113378000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:113376800-113379400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr1:113376800-113379400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:113376800-113383400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr1:113378200-113378400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:113378200-113378400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr1:113378200-113378400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:113378200-113378600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:113378200-113379400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:113378200-113379800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:113378200-113379800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr1:113378400-113379400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:113378400-113379600	Enhancers	NHDF-Ad	bronchial
31	chr1:113378400-113379800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:113378400-113379800	Enhancers	Osteobl	bone
33	chr1:113378400-113380000	Enhancers	NHEK	skin
34	chr1:113378600-113378800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:113378600-113379600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:113378600-113379600	Enhancers	HMEC	breast
37	chr1:113378600-113380600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr1:113378800-113383000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:113379400-113379600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:113379400-113379600	Enhancers	Right Ventricle	heart
41	chr1:113379400-113379600	Enhancers	Hela-S3	cervix
42	chr1:113379400-113379800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr1:113379400-113380000	Enhancers	Placenta	Placenta
44	chr1:113379400-113380200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr1:113379400-113380200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr1:113379400-113381000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:113379400-113381000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:113379600-113380600	Weak transcription	Hela-S3	cervix
49	chr1:113379600-113382800	Weak transcription	HMEC	breast
50	chr1:113379800-113383200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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