Variant report

Variant	nsv825205
Chromosome Location	chr10:677475-804402
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:964)
CpG islands
(count:7579)
Chromatin interactive
region (count:59)
LncRNA
region (count:19)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:727897-728114	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:758256-758463	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:695549-696087	HepG2	liver:	n/a	n/a
4	ATF1	chr10:691655-691733	K562	blood:	n/a	n/a
5	ATF1	chr10:729319-729702	K562	blood:	n/a	n/a
6	BACH1	chr10:734911-735245	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:699656-699670	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:736069-736281	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:718041-718363	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr10:722079-722448	GM12878	blood:	n/a	n/a
11	BATF	chr10:722135-722417	GM12878	blood:	n/a	n/a
12	BATF	chr10:705986-706335	GM12878	blood:	n/a	n/a
13	BATF	chr10:723859-724161	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:705958-706431	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:722144-722453	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:723812-724184	GM12878	blood:	n/a	chr10:723831-723839 chr10:724070-724079 chr10:723932-723945
17	BCL11A	chr10:769301-769535	GM12878	blood:	n/a	n/a
18	BCL11A	chr10:743024-743363	GM12878	blood:	n/a	chr10:743188-743197
19	BCL3	chr10:745959-746729	GM12878	blood:	n/a	n/a
20	BCL3	chr10:746085-746825	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:769085-769382	K562	blood:	n/a	n/a
22	BHLHE40	chr10:711494-711760	K562	blood:	n/a	chr10:711672-711681 chr10:711670-711683 chr10:711666-711687 chr10:711558-711571 chr10:711673-711682 chr10:711671-711680 chr10:711672-711681
23	BHLHE40	chr10:695707-696007	HepG2	liver:	n/a	n/a
24	BHLHE40	chr10:769894-770344	K562	blood:	n/a	n/a
25	BHLHE40	chr10:695485-697003	HepG2	liver:	n/a	n/a
26	BHLHE40	chr10:743220-743294	GM12878	blood:	n/a	n/a
27	BHLHE40	chr10:679292-679487	HepG2	liver:	n/a	n/a
28	BHLHE40	chr10:764330-764448	K562	blood:	n/a	n/a
29	CBX3	chr10:769860-770105	K562	blood:	n/a	n/a
30	CEBPB	chr10:728114-728118	HepG2	liver:	n/a	n/a
31	CEBPB	chr10:758494-758788	HepG2	liver:	n/a	n/a
32	CEBPB	chr10:758153-758435	HepG2	liver:	n/a	chr10:758290-758301
33	CEBPB	chr10:776514-776865	HepG2	liver:	n/a	chr10:776667-776678
34	CEBPB	chr10:758539-758922	MCF-7	breast:	n/a	n/a
35	CEBPB	chr10:758216-758902	A549	lung:	n/a	chr10:758290-758301
36	CEBPB	chr10:695684-696164	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:695403-696085	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:711522-711790	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:732595-732615	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:776582-776736	Hela-S3	cervix:	n/a	chr10:776667-776678
41	CEBPB	chr10:776512-776828	A549	lung:	n/a	chr10:776667-776678
42	CEBPB	chr10:758593-758913	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr10:758529-758903	K562	blood:	n/a	n/a
44	CEBPB	chr10:758560-758911	A549	lung:	n/a	n/a
45	CEBPB	chr10:758111-758888	Hela-S3	cervix:	n/a	chr10:758290-758301
46	CEBPB	chr10:758035-758475	MCF-7	breast:	n/a	chr10:758290-758301
47	CEBPB	chr10:695464-696050	IMR90	lung:	n/a	n/a
48	CEBPB	chr10:735751-735902	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:758430-759010	A549	lung:	n/a	n/a
50	CEBPB	chr10:758054-758413	HepG2	liver:	n/a	chr10:758290-758301

(count:7579 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:686354-686404	Hela-S3	cervix:	n/a
2	chr10:729204-729254	PrEC	prostate:	n/a
3	chr10:743973-744023	A549	lung:	n/a
4	chr10:778123-778173	HL-60	blood:	n/a
5	chr10:778123-778173	MCF10A-Er-Src	breast:	n/a
6	chr10:729479-729529	NHDF-neo	bronchial:	n/a
7	chr10:686080-686130	NH-A	brain:	n/a
8	chr10:709564-709614	HEEpiC	esophagus:	n/a
9	chr10:725706-725756	AG09309	skin:	n/a
10	chr10:729570-729620	HEEpiC	esophagus:	n/a
11	chr10:729226-729276	HNPCEpiC	eye:	n/a
12	chr10:712032-712082	Hepatocyte	liver:	n/a
13	chr10:685091-685141	HepG2	liver:	n/a
14	chr10:686080-686130	HRCEpiC	kidney:	n/a
15	chr10:742727-742777	Hela-S3	cervix:	n/a
16	chr10:686354-686404	Hela-S3	cervix:	n/a
17	chr10:729204-729254	PrEC	prostate:	n/a
18	chr10:743973-744023	A549	lung:	n/a
19	chr10:778123-778173	HL-60	blood:	n/a
20	chr10:778123-778173	MCF10A-Er-Src	breast:	n/a
21	chr10:729479-729529	NHDF-neo	bronchial:	n/a
22	chr10:686080-686130	NH-A	brain:	n/a
23	chr10:709564-709614	HEEpiC	esophagus:	n/a
24	chr10:725706-725756	AG09309	skin:	n/a
25	chr10:729570-729620	HEEpiC	esophagus:	n/a
26	chr10:729226-729276	HNPCEpiC	eye:	n/a
27	chr10:712032-712082	Hepatocyte	liver:	n/a
28	chr10:685091-685141	HepG2	liver:	n/a
29	chr10:686080-686130	HRCEpiC	kidney:	n/a
30	chr10:742727-742777	Hela-S3	cervix:	n/a
31	chr10:742727-742777	AoSMC	blood vessel:	n/a
32	chr10:743286-743336	HEK293	kidney:	embryo
33	chr10:729916-729966	PANC-1	pancreas:	n/a
34	chr10:737336-737386	SKMC	muscle:	n/a
35	chr10:729479-729529	HPAEpiC	pulmonary alveolar:	n/a
36	chr10:729711-729761	AG10803	skin:	n/a
37	chr10:708425-708475	NB4	blood:	n/a
38	chr10:726822-726872	NHDF-neo	bronchial:	n/a
39	chr10:693439-693489	PrEC	prostate:	n/a
40	chr10:736083-736133	AoSMC	blood vessel:	n/a
41	chr10:696332-696382	MCF10A-Er-Src	breast:	n/a
42	chr10:679322-679372	HRPEpiC	eye:	n/a
43	chr10:711897-711947	SKMC	muscle:	n/a
44	chr10:696321-696371	RPTEC	kidney:	n/a
45	chr10:729570-729620	GM12892	blood:	n/a
46	chr10:729479-729529	LNCaP	prostate:	n/a
47	chr10:743286-743336	HRE	kidney:	n/a
48	chr10:710082-710132	K562	blood:	n/a
49	chr10:766464-766514	Caco-2	colon:	n/a
50	chr10:698162-698212	HPAEpiC	pulmonary alveolar:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:717115..720273-chr10:724564..727281,3	MCF-7	breast:
2	chr10:733710..735507-chr10:754476..756731,2	MCF-7	breast:
3	chr10:676250..679405-chr10:680596..683070,3	MCF-7	breast:
4	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
5	chr10:736326..739216-chr10:743425..745379,3	K562	blood:
6	chr10:735546..737660-chr10:741311..743613,2	MCF-7	breast:
7	chr10:656339..658937-chr10:722531..724771,2	MCF-7	breast:
8	chr10:783561..786479-chr10:789093..790752,2	MCF-7	breast:
9	chr10:701409..702201-chr19:4341065..4341565,2	MCF-7	breast:
10	chr10:723887..725590-chr10:731403..733656,2	MCF-7	breast:
11	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
12	chr10:705629..708619-chr10:732652..734638,2	MCF-7	breast:
13	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
14	chr10:719611..721837-chr10:748749..751307,2	K562	blood:
15	chr10:739318..742202-chr10:834057..836421,2	MCF-7	breast:
16	chr10:731969..737087-chr10:747564..751327,5	MCF-7	breast:
17	chr10:668740..670601-chr10:679784..682752,2	K562	blood:
18	chr10:734436..736142-chr10:751742..753613,2	MCF-7	breast:
19	chr10:750983..753337-chr10:755498..757369,2	MCF-7	breast:
20	chr10:736326..739216-chr10:743425..745379,3	K562	blood:
21	chr10:687008..688714-chr10:699568..702258,2	MCF-7	breast:
22	chr10:756021..758273-chr10:765053..767183,2	MCF-7	breast:
23	chr10:734350..736432-chr10:761399..763324,2	MCF-7	breast:
24	chr10:735855..737615-chr10:818949..821134,2	MCF-7	breast:
25	chr10:692996..695820-chr10:700101..701896,2	MCF-7	breast:
26	chr10:778218..778758-chr10:824666..825446,2	MCF-7	breast:
27	chr10:757872..760729-chr10:776939..779568,2	MCF-7	breast:
28	chr10:705629..708619-chr10:732652..734638,2	MCF-7	breast:
29	chr10:732975..736358-chr10:737675..743965,7	MCF-7	breast:
30	chr10:670049..672648-chr10:675180..678695,4	MCF-7	breast:
31	chr10:698785..701781-chr10:833421..835495,2	MCF-7	breast:
32	chr10:778218..778962-chr10:824579..825446,5	MCF-7	breast:
33	chr10:674481..678808-chr10:734028..737251,4	MCF-7	breast:
34	chr10:583403..585208-chr10:714450..715956,2	K562	blood:
35	chr10:684852..686965-chr10:1094186..1096344,2	MCF-7	breast:
36	chr10:674481..678808-chr10:734028..737251,4	MCF-7	breast:
37	chr10:733710..735507-chr10:754476..756731,2	MCF-7	breast:
38	chr10:734188..737067-chr10:751931..753657,2	MCF-7	breast:
39	chr10:691751..694285-chr10:694356..695999,2	K562	blood:
40	chr10:678817..681667-chr10:734486..736272,2	MCF-7	breast:
41	chr10:721854..725155-chr10:733736..736400,3	MCF-7	breast:
42	chr10:676250..679405-chr10:680596..683070,3	MCF-7	breast:
43	chr10:719611..721837-chr10:748749..751307,2	K562	blood:
44	chr10:739447..741646-chr10:745969..747507,2	MCF-7	breast:
45	chr10:712816..715288-chr10:723469..725023,2	MCF-7	breast:
46	chr10:692009..694331-chr10:706518..708449,2	MCF-7	breast:
47	chr10:762176..765127-chr10:765238..767512,2	MCF-7	breast:
48	chr10:692996..695820-chr10:700101..701896,2	MCF-7	breast:
49	chr10:733954..737075-chr10:737496..740853,6	MCF-7	breast:
50	chr10:678262..679765-chr10:686218..688304,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-4	chr10:789932-789973	XLOC_008335
2	lnc-C10orf108-3	chr10:737256-737679	NONHSAT010870
3	lnc-C10orf108-1	chr10:696231-696382	NONHSAT010867
4	lnc-C10orf108-4	chr10:790517-790898	XLOC_008335
5	lnc-C10orf108-6	chr10:779932-779973	NONHSAT010872
6	lnc-C10orf108-6	chr10:780517-780898	NONHSAT010872
7	lnc-C10orf108-5	chr10:714400-715521	ENSG00000272992.1
8	lnc-C10orf108-3	chr10:736184-736265	XLOC_008334
9	lnc-C10orf108-1	chr10:695888-696118	NONHSAT010867
10	lnc-C10orf108-1	chr10:696017-696382	NR_027152
11	lnc-C10orf108-1	chr10:707966-708058	NR_027152
12	lnc-C10orf108-1	chr10:708731-711109	NR_027152
13	lnc-C10orf108-3	chr10:737257-737679	XLOC_008334
14	lnc-LARP4B-3	chr10:724395-724591	NONHSAT010869
15	lnc-C10orf108-1	chr10:709498-709642	ENSG00000242357.1
16	lnc-C10orf108-3	chr10:736183-736265	NONHSAT010870
17	lnc-LARP4B-3	chr10:724715-724736	NONHSAT010869
18	lnc-C10orf108-1	chr10:712158-712562	ENSG00000242357.1
19	lnc-C10orf108-1	chr10:697051-698595	NONHSAT010867

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5699-3p	chr10:687639-687660	MIMAT0022492
hsa-miR-5699-5p	chr10:687688-687709	MIMAT0027103

No data

Variant related genes	Relation type
MIR5699	TF binding region
ENSG00000231601	TF binding region
PRR26	TF binding region
DIP2C	TF binding region
ENSG00000242357	TF binding region
ENSG00000272992	TF binding region
MIR5699	CpG island
ENSG00000231601	CpG island
PRR26	CpG island
DIP2C	CpG island
ENSG00000242357	CpG island
ENSG00000272992	CpG island
ENSG00000047056	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000225140	chromatin interactions
ENSG00000180525	chromatin interactions
ENSG00000272992	chromatin interactions
ENSG00000151240	chromatin interactions
ENSG00000263511	chromatin interactions
ENSG00000231601	chromatin interactions
PTGS2	miRNA target sites
PTK2	miRNA target sites
SEC23IP	miRNA target sites
SEC24A	miRNA target sites

Extended variants
information (count: 6243 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6243 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578030573	chr10:677503-677504	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs112770820	chr10:677516-677517	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374123901	chr10:677519-677520	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs151012690	chr10:677551-677552	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548119041	chr10:677554-677555	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564660678	chr10:677558-677559	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs533614339	chr10:677565-677566	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550227937	chr10:677573-677574	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570017767	chr10:677579-677580	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535965510	chr10:677708-677709	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117744038	chr10:677748-677749	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565745467	chr10:677749-677750	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533824561	chr10:677766-677767	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551665233	chr10:677767-677768	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs7073688	chr10:677855-677856	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs576604613	chr10:677862-677863	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7100832	chr10:677883-677884	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs556341376	chr10:677888-677889	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557165499	chr10:677913-677914	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567781255	chr10:677923-677924	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs74831617	chr10:677930-677931	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs191827511	chr10:677954-677955	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs561485326	chr10:677956-677957	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs7078091	chr10:677983-677984	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs7077311	chr10:678000-678001	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs564799596	chr10:678028-678029	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs370149507	chr10:678040-678041	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573290028	chr10:678095-678096	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533768256	chr10:678129-678130	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545275800	chr10:678159-678160	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372065468	chr10:678171-678172	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543624280	chr10:678175-678176	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563910180	chr10:678176-678177	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs529328528	chr10:678182-678183	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs144437219	chr10:678197-678198	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs565731460	chr10:678263-678264	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147819696	chr10:678266-678267	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141269107	chr10:678293-678294	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs183697414	chr10:678302-678303	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558899843	chr10:678327-678328	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539745123	chr10:678342-678343	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs556041341	chr10:678344-678345	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs200457760	chr10:678369-678370	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs569844687	chr10:678373-678374	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs146955807	chr10:678374-678375	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs555548866	chr10:678398-678399	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs572050929	chr10:678400-678401	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs1251166	chr10:678410-678411	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs541063617	chr10:678411-678412	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112238837	chr10:678425-678426	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:2688 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:667600-679200	Weak transcription	Gastric	stomach
2	chr10:669200-680000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr10:670600-679400	Weak transcription	Aorta	Aorta
4	chr10:671400-679400	Weak transcription	Fetal Lung	lung
5	chr10:671600-679200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr10:672000-680200	Strong transcription	Fetal Intestine Small	intestine
7	chr10:672000-700000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr10:672200-677600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr10:672200-679400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr10:672200-679400	Weak transcription	NH-A	brain
11	chr10:672200-679800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr10:672200-681200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr10:672200-683800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr10:672200-690600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:672400-679400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr10:672400-680000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr10:672600-679200	Weak transcription	Fetal Brain Male	brain
18	chr10:672600-681200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr10:672600-681400	Weak transcription	Placenta	Placenta
20	chr10:672600-682600	Weak transcription	Esophagus	oesophagus
21	chr10:672600-695800	Weak transcription	NHLF	lung
22	chr10:672800-679200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr10:672800-680000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr10:672800-683400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr10:673000-680000	Weak transcription	HSMMtube	muscle
26	chr10:673200-679400	Weak transcription	Right Atrium	heart
27	chr10:673600-687400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr10:674000-679400	Weak transcription	Fetal Heart	heart
29	chr10:674600-678800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr10:674600-682000	Weak transcription	Adipose Nuclei	Adipose
31	chr10:675600-678800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr10:675600-681400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:675800-678800	Weak transcription	Stomach Smooth Muscle	stomach
34	chr10:675800-679200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr10:676000-678800	Weak transcription	Ovary	ovary
36	chr10:676000-679200	Weak transcription	Pancreas	Pancrea
37	chr10:676000-679200	Weak transcription	Spleen	Spleen
38	chr10:676000-680400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr10:676400-677600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr10:676400-677600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr10:676800-678000	Weak transcription	Fetal Intestine Large	intestine
42	chr10:676800-678200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr10:676800-679400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr10:676800-680200	Weak transcription	Fetal Kidney	kidney
45	chr10:677000-678200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr10:677000-678200	Enhancers	Brain Anterior Caudate	brain
47	chr10:677000-678200	Enhancers	Brain Hippocampus Middle	brain
48	chr10:677000-678800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr10:677000-678800	Weak transcription	Brain Angular Gyrus	brain
50	chr10:677000-678800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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