Variant report

Variant	nsv465283
Chromosome Location	chr1:10767902-10815421
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:507)
CpG islands
(count:1223)
Chromatin interactive
region (count:81)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	BHLHE40	chr1:10806161-10806358	K562	blood:	n/a	n/a
7	BHLHE40	chr1:10793966-10794468	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:10797447-10797691	K562	blood:	n/a	n/a
9	CCNT2	chr1:10777414-10777638	K562	blood:	n/a	n/a
10	CEBPB	chr1:10772022-10772211	HepG2	liver:	n/a	chr1:10772060-10772071
11	CEBPB	chr1:10769448-10769852	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr1:10791090-10791576	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:10791096-10791674	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:10805611-10805660	IMR90	lung:	n/a	chr1:10805635-10805646
15	CEBPB	chr1:10791270-10791307	K562	blood:	n/a	n/a
16	CEBPB	chr1:10795073-10795250	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:10784192-10784519	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:10795059-10795307	K562	blood:	n/a	n/a
19	CEBPB	chr1:10798817-10798820	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:10806053-10806159	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:10791073-10791663	A549	lung:	n/a	n/a
22	CEBPB	chr1:10805528-10805782	Hela-S3	cervix:	n/a	chr1:10805635-10805646
23	CEBPB	chr1:10805452-10805807	HepG2	liver:	n/a	chr1:10805635-10805646
24	CEBPB	chr1:10791043-10791575	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:10771974-10772124	A549	lung:	n/a	chr1:10772060-10772071
26	CEBPB	chr1:10791112-10791699	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:10791043-10791528	A549	lung:	n/a	n/a
28	CEBPB	chr1:10784201-10784500	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:10791074-10791523	A549	lung:	n/a	n/a
30	CEBPB	chr1:10791053-10791492	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:10771940-10772120	IMR90	lung:	n/a	chr1:10772060-10772071
32	CEBPB	chr1:10791084-10791691	MCF-7	breast:	n/a	n/a
33	CEBPB	chr1:10805566-10805687	HepG2	liver:	n/a	chr1:10805635-10805646
34	CEBPB	chr1:10791105-10791630	HCT-116	colon:	n/a	n/a
35	CHD2	chr1:10774925-10774933	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr1:10768559-10769716	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr1:10798509-10798556	Pancreas_OC	pancreas:	n/a	chr1:10798523-10798536
38	CTCF	chr1:10813380-10813530	HMEC	breast:	n/a	n/a
39	CTCF	chr1:10813480-10813630	GM12874	blood:	n/a	n/a
40	CTCF	chr1:10813380-10813530	HEK293	kidney:	n/a	n/a
41	CTCF	chr1:10813460-10813610	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:10813460-10813610	GM12864	blood:	n/a	n/a
43	CTCF	chr1:10813320-10813470	HCT-116	colon:	n/a	n/a
44	CTCF	chr1:10811340-10811490	HepG2	liver:	n/a	n/a
45	CTCF	chr1:10811400-10811550	K562	blood:	n/a	n/a
46	CTCF	chr1:10782800-10782950	NHEK	skin:	n/a	n/a
47	CTCF	chr1:10813440-10813590	GM12873	blood:	n/a	n/a
48	CTCF	chr1:10813400-10813550	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr1:10775669-10775729	GM20000	blood:	n/a	n/a
50	CTCF	chr1:10786667-10786740	NHEK	skin:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10768738-10768788	BJ	skin:	n/a
2	chr1:10796411-10796461	LNCaP	prostate:	n/a
3	chr1:10802080-10802130	Jurkat	blood:	n/a
4	chr1:10768738-10768788	BJ	skin:	n/a
5	chr1:10796411-10796461	LNCaP	prostate:	n/a
6	chr1:10802080-10802130	Jurkat	blood:	n/a
7	chr1:10796411-10796461	HNPCEpiC	eye:	n/a
8	chr1:10781431-10781481	K562	blood:	n/a
9	chr1:10795394-10795444	PFSK-1	brain:	n/a
10	chr1:10795394-10795444	HIPEpiC	eye:	n/a
11	chr1:10794229-10794279	AG10803	skin:	n/a
12	chr1:10804939-10804989	SK-N-MC	brain:	n/a
13	chr1:10788801-10788851	Hela-S3	cervix:	n/a
14	chr1:10799025-10799075	MCF10A-Er-Src	breast:	n/a
15	chr1:10795020-10795070	ovcar-3	ovarian:	n/a
16	chr1:10784363-10784413	HCM	heart:	n/a
17	chr1:10796823-10796873	GM12892	blood:	n/a
18	chr1:10795394-10795444	A549	lung:	n/a
19	chr1:10768738-10768788	AoSMC	blood vessel:	n/a
20	chr1:10799738-10799788	SAEC	small airway:	n/a
21	chr1:10768738-10768788	AG09309	skin:	n/a
22	chr1:10796823-10796873	SK-N-SH	brain:	n/a
23	chr1:10796411-10796461	ProgFib	skin:	n/a
24	chr1:10802080-10802130	AG09319	gingival:	n/a
25	chr1:10794229-10794279	MCF-7	breast:	n/a
26	chr1:10802080-10802130	LNCaP	prostate:	n/a
27	chr1:10795394-10795444	NH-A	brain:	n/a
28	chr1:10769910-10769960	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:10795020-10795070	PANC-1	pancreas:	n/a
30	chr1:10799738-10799788	GM19239	blood:	n/a
31	chr1:10781431-10781481	GM12878	blood:	n/a
32	chr1:10795394-10795444	Caco-2	colon:	n/a
33	chr1:10799025-10799075	IMR90	lung:	fetal
34	chr1:10804939-10804989	BJ	skin:	n/a
35	chr1:10788219-10788269	PANC-1	pancreas:	n/a
36	chr1:10804939-10804989	T-47D	breast:	n/a
37	chr1:10769910-10769960	ovcar-3	ovarian:	n/a
38	chr1:10795020-10795070	GM06990	blood:	n/a
39	chr1:10772782-10772832	PFSK-1	brain:	n/a
40	chr1:10788219-10788269	K562	blood:	n/a
41	chr1:10796823-10796873	BE2_C	brain:	n/a
42	chr1:10799738-10799788	NB4	blood:	n/a
43	chr1:10807676-10807726	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:10769910-10769960	Jurkat	blood:	n/a
45	chr1:10796411-10796461	SK-N-SH	brain:	n/a
46	chr1:10807676-10807726	PANC-1	pancreas:	n/a
47	chr1:10795394-10795444	GM12891	blood:	n/a
48	chr1:10794229-10794279	HCT-116	colon:	n/a
49	chr1:10802038-10802088	NH-A	brain:	n/a
50	chr1:10795020-10795070	NH-A	brain:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:10769186..10770686-chr1:10780232..10782829,2	K562	blood:
2	chr1:10774888..10776718-chr1:10783178..10785593,2	MCF-7	breast:
3	chr1:10772697..10775308-chr1:10780608..10782302,2	MCF-7	breast:
4	chr1:10770352..10771145-chr1:10784796..10785695,2	MCF-7	breast:
5	chr1:10795633..10796463-chr1:10810945..10811751,3	MCF-7	breast:
6	chr1:10774888..10776718-chr1:10783178..10785593,2	MCF-7	breast:
7	chr1:10781321..10784166-chr1:10789319..10791144,2	K562	blood:
8	chr1:10781321..10784166-chr1:10789319..10791144,2	K562	blood:
9	chr1:10797814..10799876-chr1:10804060..10805794,2	K562	blood:
10	chr1:10797814..10799876-chr1:10804060..10805794,2	K562	blood:
11	chr1:10770692..10771316-chr1:10810904..10811625,4	MCF-7	breast:
12	chr1:10804412..10806275-chr1:10818371..10819913,2	MCF-7	breast:
13	chr1:10770692..10771316-chr1:10810904..10811625,4	MCF-7	breast:
14	chr1:10777007..10778883-chr1:10781713..10785066,3	K562	blood:
15	chr1:10812217..10813950-chr1:10854150..10856771,2	MCF-7	breast:
16	chr1:10772697..10775308-chr1:10780608..10782302,2	MCF-7	breast:
17	chr1:10795746..10798099-chr1:10799422..10802020,2	K562	blood:
18	chr1:10777259..10780263-chr1:10782530..10785488,3	K562	blood:
19	chr1:10770350..10771237-chr1:10795718..10796246,2	MCF-7	breast:
20	chr1:10807075..10808739-chr1:10811624..10813204,2	MCF-7	breast:
21	chr1:10787544..10788371-chr1:10810895..10811410,2	MCF-7	breast:
22	chr1:10710685..10713213-chr1:10801542..10803296,2	K562	blood:
23	chr1:10778524..10780309-chr1:10784096..10785836,2	MCF-7	breast:
24	chr1:10784744..10785323-chr1:10795558..10796339,2	MCF-7	breast:
25	chr1:10753350..10756890-chr1:10792534..10795103,3	K562	blood:
26	chr1:10777007..10778883-chr1:10781713..10785066,3	K562	blood:
27	chr1:10810911..10812812-chr1:10814536..10816677,2	MCF-7	breast:
28	chr1:10795633..10796463-chr1:10810924..10811751,4	MCF-7	breast:
29	chr1:10770350..10771237-chr1:10795718..10796246,2	MCF-7	breast:
30	chr1:10795633..10796463-chr1:10810924..10811751,4	MCF-7	breast:
31	chr1:10785675..10789087-chr1:10792936..10797329,5	K562	blood:
32	chr1:10752709..10754408-chr1:10782360..10784898,3	MCF-7	breast:
33	chr1:10795633..10796463-chr1:10810945..10811751,3	MCF-7	breast:
34	chr1:10795746..10798099-chr1:10799422..10802020,2	K562	blood:
35	chr1:10756914..10759117-chr1:10783394..10785219,2	MCF-7	breast:
36	chr1:10807075..10808739-chr1:10811624..10813204,2	MCF-7	breast:
37	chr1:10778524..10780309-chr1:10784096..10785836,2	MCF-7	breast:
38	chr1:10789630..10791683-chr1:10843060..10845092,2	MCF-7	breast:
39	chr1:10806063..10809176-chr1:10811831..10815536,3	K562	blood:
40	chr1:10762987..10765112-chr1:10783613..10786344,2	MCF-7	breast:
41	chr1:10782189..10784150-chr1:10795398..10797015,2	K562	blood:
42	chr1:10765025..10766775-chr1:10767958..10770170,2	MCF-7	breast:
43	chr1:10801419..10805496-chr1:10805680..10808575,3	K562	blood:
44	chr1:10813375..10816020-chr1:10863170..10865862,2	MCF-7	breast:
45	chr1:10798503..10801151-chr1:10807014..10809995,2	K562	blood:
46	chr1:10785941..10789087-chr1:10792936..10795105,3	K562	blood:
47	chr1:10793053..10795572-chr1:10798812..10801250,2	K562	blood:
48	chr1:10767210..10770062-chr1:10773957..10776729,2	K562	blood:
49	chr1:10801419..10805496-chr1:10805680..10808575,3	K562	blood:
50	chr1:10814415..10817304-chr1:10845859..10848548,2	K562	blood:

(count:2 , 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_+

No data

Variant related genes	Relation type
CASZ1	TF binding region
CASZ1	CpG island
ENSG00000130940	chromatin interactions
ENSG00000156011	chromatin interactions
ENSG00000116649	chromatin interactions

Extended variants
information (count: 1950 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1950 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs488834	chr1:10767902-10767903	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs284293	chr1:10767930-10767931	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs570283599	chr1:10767931-10767932	Enhancers Weak transcription Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs145186780	chr1:10767965-10767966	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs574239207	chr1:10767982-10767983	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs570943133	chr1:10767987-10767988	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs616519	chr1:10768002-10768003	Enhancers Bivalent Enhancer Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs151300150	chr1:10768074-10768075	Enhancers Bivalent Enhancer Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs140553745	chr1:10768096-10768097	Enhancers Bivalent Enhancer Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs72641476	chr1:10768104-10768105	Enhancers Bivalent Enhancer Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527471722	chr1:10768136-10768137	Enhancers Bivalent Enhancer Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549192836	chr1:10768197-10768198	Enhancers Bivalent Enhancer Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189444758	chr1:10768220-10768221	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538097837	chr1:10768293-10768294	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs556682566	chr1:10768296-10768297	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs74896427	chr1:10768307-10768308	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs79031475	chr1:10768360-10768361	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538687461	chr1:10768367-10768368	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553883272	chr1:10768371-10768372	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572141804	chr1:10768436-10768437	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs137991550	chr1:10768437-10768438	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555898955	chr1:10768451-10768452	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536306375	chr1:10768464-10768465	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116460167	chr1:10768473-10768474	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377163021	chr1:10768525-10768526	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562881664	chr1:10768571-10768572	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs577611796	chr1:10768572-10768573	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs545028333	chr1:10768582-10768583	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs560196953	chr1:10768604-10768605	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527750347	chr1:10768609-10768610	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs549214533	chr1:10768665-10768666	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs368046633	chr1:10768730-10768731	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs572968022	chr1:10768738-10768739	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs180954244	chr1:10768801-10768802	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550097377	chr1:10768910-10768911	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571597240	chr1:10768919-10768920	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538624767	chr1:10768933-10768934	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540173442	chr1:10768970-10768971	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs143390494	chr1:10768988-10768989	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs116663793	chr1:10768989-10768990	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs150448352	chr1:10769024-10769025	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs542839721	chr1:10769028-10769029	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs56961164	chr1:10769037-10769038	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554373883	chr1:10769038-10769039	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs7539524	chr1:10769052-10769053	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538097034	chr1:10769079-10769080	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556416855	chr1:10769096-10769097	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7541920	chr1:10769170-10769171	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs185129130	chr1:10769179-10769180	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs553704437	chr1:10769201-10769202	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	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:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10756600-10776400	Enhancers	Fetal Heart	heart
2	chr1:10759600-10774200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr1:10760400-10768400	Strong transcription	Fetal Intestine Small	intestine
4	chr1:10760600-10769600	Weak transcription	Colon Smooth Muscle	Colon
5	chr1:10760600-10781600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:10764400-10769400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:10765200-10769200	Weak transcription	Lung	lung
8	chr1:10765400-10768000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:10765400-10768600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:10765400-10769200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:10765400-10773000	Weak transcription	Pancreas	Pancrea
12	chr1:10765600-10773000	Weak transcription	Colonic Mucosa	Colon
13	chr1:10765600-10781600	Weak transcription	Esophagus	oesophagus
14	chr1:10765800-10770400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr1:10766000-10768400	Weak transcription	Stomach Mucosa	stomach
16	chr1:10766000-10769000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr1:10766000-10769200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr1:10766000-10770400	Weak transcription	Gastric	stomach
19	chr1:10766000-10776800	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr1:10766000-10777200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr1:10766200-10768200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr1:10767000-10768000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:10767000-10770000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:10767200-10770600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:10767400-10768600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
26	chr1:10767400-10768800	Weak transcription	Left Ventricle	heart
27	chr1:10767400-10769200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr1:10767400-10769200	Weak transcription	Right Ventricle	heart
29	chr1:10767600-10768000	Bivalent Enhancer	Fetal Brain Male	brain
30	chr1:10767600-10768200	Strong transcription	Duodenum Mucosa	Duodenum
31	chr1:10767600-10768400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr1:10767600-10770600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:10767600-10771200	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr1:10767800-10768000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr1:10767800-10768000	Enhancers	Right Atrium	heart
36	chr1:10767800-10768200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr1:10768000-10768200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr1:10768000-10768800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:10768000-10769200	Weak transcription	Right Atrium	heart
40	chr1:10768200-10768400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr1:10768200-10768400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr1:10768200-10768400	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr1:10768200-10770000	Bivalent Enhancer	Fetal Brain Male	brain
44	chr1:10768200-10775000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr1:10768400-10768600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:10768400-10768600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
47	chr1:10768400-10768800	Enhancers	Stomach Mucosa	stomach
48	chr1:10768400-10769600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:10768400-10770200	Enhancers	Brain Germinal Matrix	brain
50	chr1:10768400-10770400	Enhancers	H1 Cell Line	embryonic stem cell

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