Variant report

Variant	nsv465172
Chromosome Location	chr1:10757199-10796866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:471)
CpG islands
(count:1590)
Chromatin interactive
region (count:68)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10777365-10777652	K562	blood:	n/a	n/a
2	ARID3A	chr1:10791060-10791514	HepG2	liver:	n/a	n/a
3	ATF1	chr1:10777412-10777648	K562	blood:	n/a	n/a
4	ATF3	chr1:10795000-10795326	K562	blood:	n/a	n/a
5	BACH1	chr1:10788799-10788909	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:10764501-10765022	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:10793966-10794468	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:10764322-10764864	HepG2	liver:	n/a	n/a
9	BHLHE40	chr1:10764023-10764249	K562	blood:	n/a	n/a
10	BRCA1	chr1:10764695-10764882	H1-hESC	embryonic stem cell:	n/a	n/a
11	CCNT2	chr1:10777414-10777638	K562	blood:	n/a	n/a
12	CEBPB	chr1:10791105-10791630	HCT-116	colon:	n/a	n/a
13	CEBPB	chr1:10791043-10791528	A549	lung:	n/a	n/a
14	CEBPB	chr1:10791112-10791699	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:10769448-10769852	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:10772022-10772211	HepG2	liver:	n/a	chr1:10772060-10772071
17	CEBPB	chr1:10764723-10764853	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:10791074-10791523	A549	lung:	n/a	n/a
19	CEBPB	chr1:10795059-10795307	K562	blood:	n/a	n/a
20	CEBPB	chr1:10766412-10766548	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:10791073-10791663	A549	lung:	n/a	n/a
22	CEBPB	chr1:10784192-10784519	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:10795073-10795250	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:10771940-10772120	IMR90	lung:	n/a	chr1:10772060-10772071
25	CEBPB	chr1:10771974-10772124	A549	lung:	n/a	chr1:10772060-10772071
26	CEBPB	chr1:10784201-10784500	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:10791090-10791576	MCF-7	breast:	n/a	n/a
28	CEBPB	chr1:10791043-10791575	HCT-116	colon:	n/a	n/a
29	CEBPB	chr1:10791084-10791691	MCF-7	breast:	n/a	n/a
30	CEBPB	chr1:10791096-10791674	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:10791270-10791307	K562	blood:	n/a	n/a
32	CEBPB	chr1:10791053-10791492	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr1:10764493-10764847	H1-hESC	embryonic stem cell:	n/a	chr1:10764785-10764795
34	CHD2	chr1:10774925-10774933	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr1:10764768-10765002	HepG2	liver:	n/a	chr1:10764785-10764795
36	CREB1	chr1:10764270-10765046	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr1:10764313-10765226	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTBP2	chr1:10768559-10769716	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr1:10775669-10775729	GM20000	blood:	n/a	n/a
40	CTCF	chr1:10759540-10759690	SAEC	small airway:	n/a	chr1:10759656-10759665
41	CTCF	chr1:10793480-10793492	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:10782780-10782930	HMEC	breast:	n/a	n/a
43	CTCF	chr1:10765030-10765039	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:10790245-10790318	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr1:10767844-10767934	Lung_OC	lung:	n/a	n/a
46	CTCF	chr1:10793435-10793479	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr1:10795620-10795770	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr1:10782800-10782950	NHEK	skin:	n/a	n/a
49	CTCF	chr1:10764680-10764830	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:10765011-10765028	MCF-7	breast:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10769910-10769960	H1-hESC	embryonic stem cell:	embryo
2	chr1:10784363-10784413	PrEC	prostate:	n/a
3	chr1:10764273-10764323	HRCEpiC	kidney:	n/a
4	chr1:10781431-10781481	SAEC	small airway:	n/a
5	chr1:10769910-10769960	H1-hESC	embryonic stem cell:	embryo
6	chr1:10784363-10784413	PrEC	prostate:	n/a
7	chr1:10764273-10764323	HRCEpiC	kidney:	n/a
8	chr1:10781431-10781481	SAEC	small airway:	n/a
9	chr1:10788928-10788978	HRPEpiC	eye:	n/a
10	chr1:10764512-10764562	SK-N-MC	brain:	n/a
11	chr1:10788219-10788269	SAEC	small airway:	n/a
12	chr1:10795020-10795070	SK-N-SH_RA	brain:	n/a
13	chr1:10764512-10764562	HUVEC	blood vessel:	n/a
14	chr1:10764273-10764323	HCM	heart:	n/a
15	chr1:10761983-10762033	GM12892	blood:	n/a
16	chr1:10764886-10764936	Hepatocyte	liver:	n/a
17	chr1:10757436-10757486	RPTEC	kidney:	n/a
18	chr1:10781431-10781481	SK-N-SH	brain:	n/a
19	chr1:10757954-10758004	HAEpiC	amniotic membrane:	n/a
20	chr1:10757954-10758004	NB4	blood:	n/a
21	chr1:10788801-10788851	HCM	heart:	n/a
22	chr1:10757436-10757486	HMEC	breast:	n/a
23	chr1:10769910-10769960	T-47D	breast:	n/a
24	chr1:10788928-10788978	AG09319	gingival:	n/a
25	chr1:10757892-10757942	BJ	skin:	n/a
26	chr1:10761983-10762033	HRCEpiC	kidney:	n/a
27	chr1:10757954-10758004	BE2_C	brain:	n/a
28	chr1:10795020-10795070	MCF-7	breast:	n/a
29	chr1:10758995-10759045	HCPEpiC	choroid plexus:	n/a
30	chr1:10757892-10757942	HUVEC	blood vessel:	n/a
31	chr1:10769910-10769960	AG09319	gingival:	n/a
32	chr1:10796411-10796461	MCF-7	breast:	n/a
33	chr1:10781431-10781481	CMK	blood:	n/a
34	chr1:10788219-10788269	HEEpiC	esophagus:	n/a
35	chr1:10764896-10764946	NT2-D1	testis:	n/a
36	chr1:10757436-10757486	PFSK-1	brain:	n/a
37	chr1:10788928-10788978	GM19239	blood:	n/a
38	chr1:10795394-10795444	NH-A	brain:	n/a
39	chr1:10794229-10794279	HepG2	liver:	n/a
40	chr1:10789713-10789763	GM06990	blood:	n/a
41	chr1:10757954-10758004	SKMC	muscle:	n/a
42	chr1:10772782-10772832	Hela-S3	cervix:	n/a
43	chr1:10757902-10757952	HCF	heart:	n/a
44	chr1:10757892-10757942	T-47D	breast:	n/a
45	chr1:10764273-10764323	HRE	kidney:	n/a
46	chr1:10772782-10772832	RPTEC	kidney:	n/a
47	chr1:10757902-10757952	T-47D	breast:	n/a
48	chr1:10764512-10764562	PANC-1	pancreas:	n/a
49	chr1:10772782-10772832	GM19239	blood:	n/a
50	chr1:10764273-10764323	HPAEpiC	pulmonary alveolar:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:10770352..10771145-chr1:10784796..10785695,2	MCF-7	breast:
2	chr1:10785675..10789087-chr1:10792936..10797329,5	K562	blood:
3	chr1:10766508..10770411-chr1:10778762..10780630,3	MCF-7	breast:
4	chr1:10755720..10757634-chr1:10782788..10785288,3	K562	blood:
5	chr1:10774888..10776718-chr1:10783178..10785593,2	MCF-7	breast:
6	chr1:10755955..10758112-chr1:10760865..10764378,3	K562	blood:
7	chr1:10767210..10770062-chr1:10773957..10776729,2	K562	blood:
8	chr1:10784744..10785323-chr1:10795558..10796339,2	MCF-7	breast:
9	chr1:10788243..10790152-chr1:11118737..11121718,2	MCF-7	breast:
10	chr1:10778524..10780309-chr1:10784096..10785836,2	MCF-7	breast:
11	chr1:10785941..10789087-chr1:10792936..10795105,3	K562	blood:
12	chr1:10756914..10759117-chr1:10783394..10785219,2	MCF-7	breast:
13	chr1:10781321..10784166-chr1:10789319..10791144,2	K562	blood:
14	chr1:10755720..10757634-chr1:10782788..10785288,3	K562	blood:
15	chr1:10774888..10776718-chr1:10783178..10785593,2	MCF-7	breast:
16	chr1:10762949..10764545-chr1:10839417..10840947,2	MCF-7	breast:
17	chr1:10739997..10741906-chr1:10786836..10789661,2	MCF-7	breast:
18	chr1:10772697..10775308-chr1:10780608..10782302,2	MCF-7	breast:
19	chr1:10757865..10759730-chr1:10835841..10837432,3	MCF-7	breast:
20	chr1:10715834..10717814-chr1:10789112..10791954,2	K562	blood:
21	chr1:10752976..10755910-chr1:10763152..10766470,3	MCF-7	breast:
22	chr1:10756914..10759117-chr1:10783394..10785219,2	MCF-7	breast:
23	chr1:10754753..10757262-chr1:10761899..10764106,2	MCF-7	breast:
24	chr1:10753473..10759637-chr1:10760137..10763540,7	K562	blood:
25	chr1:10758262..10760519-chr1:10763379..10765606,2	MCF-7	breast:
26	chr1:10767210..10770062-chr1:10773957..10776729,2	K562	blood:
27	chr1:10770692..10771316-chr1:10810904..10811625,4	MCF-7	breast:
28	chr1:10777259..10780263-chr1:10782530..10785488,3	K562	blood:
29	chr1:10769186..10770686-chr1:10780232..10782829,2	K562	blood:
30	chr1:10781321..10784166-chr1:10789319..10791144,2	K562	blood:
31	chr1:10795633..10796463-chr1:10810945..10811751,3	MCF-7	breast:
32	chr1:10753350..10756890-chr1:10792534..10795103,3	K562	blood:
33	chr1:10770352..10771145-chr1:10784796..10785695,2	MCF-7	breast:
34	chr1:10769186..10770686-chr1:10780232..10782829,2	K562	blood:
35	chr1:10793053..10795572-chr1:10798812..10801250,2	K562	blood:
36	chr1:10777007..10778883-chr1:10781713..10785066,3	K562	blood:
37	chr1:10772697..10775308-chr1:10780608..10782302,2	MCF-7	breast:
38	chr1:10758262..10760519-chr1:10763379..10765606,2	MCF-7	breast:
39	chr1:10759222..10762054-chr13:20579251..20582130,2	MCF-7	breast:
40	chr1:10777259..10780263-chr1:10782530..10785488,3	K562	blood:
41	chr1:10756523..10758997-chr1:10766760..10768325,2	K562	blood:
42	chr1:10770350..10771237-chr1:10795718..10796246,2	MCF-7	breast:
43	chr1:10782189..10784150-chr1:10795398..10797015,2	K562	blood:
44	chr1:10770350..10771237-chr1:10795718..10796246,2	MCF-7	breast:
45	chr1:10765025..10766775-chr1:10767958..10770170,2	MCF-7	breast:
46	chr1:10762987..10765112-chr1:10783613..10786344,2	MCF-7	breast:
47	chr1:10782189..10784150-chr1:10795398..10797015,2	K562	blood:
48	chr1:10784744..10785323-chr1:10795558..10796339,2	MCF-7	breast:
49	chr1:10752709..10754408-chr1:10782360..10784898,3	MCF-7	breast:
50	chr1:10766508..10770411-chr1:10778762..10780630,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1orf127-2	chr1:10774405-10774620	uc_8_-
2	lnc-PEX14-8	chr1:10774405-10774620	uc_8_+
3	lnc-PEX14-7	chr1:10758720-10758975	uc_7_+
4	lnc-DFFA-9	chr1:10765549-10765632	NONHSAT000868
5	lnc-DFFA-9	chr1:10764253-10764619	NONHSAT000868
6	lnc-DFFA-8	chr1:10758720-10758975	uc_7_-

No data

Variant related genes	Relation type
CASZ1	TF binding region
CASZ1	CpG island
ENSG00000251503	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000175279	chromatin interactions
ENSG00000130940	chromatin interactions
ENSG00000121741	chromatin interactions
ENSG00000116649	chromatin interactions

Extended variants
information (count: 1601 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1601 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4845948	chr1:10757199-10757200	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537692605	chr1:10757228-10757229	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs556028117	chr1:10757230-10757231	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs577891096	chr1:10757233-10757234	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs145398174	chr1:10757234-10757235	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs551235847	chr1:10757242-10757243	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs572021615	chr1:10757289-10757290	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs542702634	chr1:10757298-10757299	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs560968887	chr1:10757423-10757424	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs529507756	chr1:10757445-10757446	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs537825958	chr1:10757562-10757563	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs56996870	chr1:10757604-10757605	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs563181803	chr1:10757633-10757634	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs559860907	chr1:10757647-10757648	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs4845842	chr1:10757651-10757652	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs566722567	chr1:10757653-10757654	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs496795	chr1:10757656-10757657	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs549022161	chr1:10757675-10757676	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs567471341	chr1:10757688-10757689	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs537629942	chr1:10757716-10757717	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs188632995	chr1:10757729-10757730	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs75799176	chr1:10757797-10757798	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs538530105	chr1:10757820-10757821	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs147695662	chr1:10757853-10757854	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs74466822	chr1:10757858-10757859	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs542685879	chr1:10757861-10757862	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs527293957	chr1:10757871-10757872	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs150198718	chr1:10757887-10757888	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs576232962	chr1:10757892-10757893	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs544803888	chr1:10757893-10757894	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs710132	chr1:10757902-10757903	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs138736546	chr1:10757916-10757917	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs545327944	chr1:10757934-10757935	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs560846886	chr1:10757941-10757942	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs527678995	chr1:10757954-10757955	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs191900369	chr1:10757983-10757984	Bivalent Enhancer Weak transcription Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs567408687	chr1:10758010-10758011	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs531660793	chr1:10758025-10758026	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs550271054	chr1:10758027-10758028	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs368258029	chr1:10758053-10758054	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs611877	chr1:10758057-10758058	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs184086469	chr1:10758058-10758059	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs493009	chr1:10758063-10758064	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs536298302	chr1:10758070-10758071	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs566025991	chr1:10758165-10758166	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536232059	chr1:10758171-10758172	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188574444	chr1:10758179-10758180	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576121728	chr1:10758183-10758184	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543121503	chr1:10758197-10758198	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554714271	chr1:10758232-10758233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	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
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	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
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10754600-10759800	Weak transcription	Fetal Kidney	kidney
2	chr1:10754600-10760200	Weak transcription	HSMMtube	muscle
3	chr1:10755200-10760600	Enhancers	Stomach Mucosa	stomach
4	chr1:10755400-10757200	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr1:10755400-10757400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr1:10755400-10759000	Weak transcription	Small Intestine	intestine
7	chr1:10755400-10759800	Weak transcription	Hela-S3	cervix
8	chr1:10755600-10757200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:10755600-10757400	Enhancers	Left Ventricle	heart
10	chr1:10755600-10757800	Enhancers	Pancreas	Pancrea
11	chr1:10755600-10758000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr1:10755600-10758400	Enhancers	Fetal Intestine Large	intestine
13	chr1:10755600-10759000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:10755600-10759200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr1:10755600-10759400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:10755600-10759800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr1:10755600-10760000	Weak transcription	HMEC	breast
18	chr1:10755600-10764200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:10755800-10759200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:10755800-10759400	Enhancers	Right Ventricle	heart
21	chr1:10755800-10760600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:10756000-10757200	Enhancers	Rectal Smooth Muscle	rectum
23	chr1:10756000-10757800	Weak transcription	Colonic Mucosa	Colon
24	chr1:10756000-10757800	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr1:10756000-10758800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:10756000-10758800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr1:10756000-10758800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:10756000-10759000	Weak transcription	Spleen	Spleen
29	chr1:10756000-10763200	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr1:10756200-10758600	Weak transcription	Lung	lung
31	chr1:10756200-10759000	Weak transcription	Ovary	ovary
32	chr1:10756400-10757400	Weak transcription	Esophagus	oesophagus
33	chr1:10756600-10757800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:10756600-10758000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr1:10756600-10758800	Weak transcription	Right Atrium	heart
36	chr1:10756600-10759000	Weak transcription	Fetal Lung	lung
37	chr1:10756600-10776400	Enhancers	Fetal Heart	heart
38	chr1:10756800-10757200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:10756800-10757600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr1:10756800-10759200	Weak transcription	Colon Smooth Muscle	Colon
41	chr1:10757000-10757200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:10757000-10757200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr1:10757000-10757600	Weak transcription	Gastric	stomach
44	chr1:10757000-10757600	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr1:10757000-10758000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr1:10757000-10758200	Genic enhancers	Fetal Intestine Small	intestine
47	chr1:10757000-10759200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr1:10757200-10757600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:10757200-10759800	Weak transcription	Rectal Smooth Muscle	rectum
50	chr1:10757400-10759000	Enhancers	Esophagus	oesophagus

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