Variant report

Variant	nsv546820
Chromosome Location	chr1:92273644-92558583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3643)
CpG islands
(count:4279)
Chromatin interactive
region (count:87)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3643 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92296732-92297514	HepG2	liver:	n/a	chr1:92297485-92297501
2	ARID3A	chr1:92463047-92463494	K562	blood:	n/a	n/a
3	ARID3A	chr1:92283136-92283452	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:92392821-92393186	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:92392911-92393150	K562	blood:	n/a	n/a
6	ARID3A	chr1:92310527-92311162	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:92545717-92545724	K562	blood:	n/a	n/a
8	ARID3A	chr1:92317145-92317468	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:92348921-92349309	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:92463265-92463529	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:92282827-92282923	K562	blood:	n/a	n/a
12	ARID3A	chr1:92281548-92281943	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:92545681-92545684	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:92348918-92349315	K562	blood:	n/a	n/a
15	ARID3A	chr1:92344000-92344448	HepG2	liver:	n/a	n/a
16	ARID3A	chr1:92504254-92504757	HepG2	liver:	n/a	n/a
17	ARID3A	chr1:92300668-92300994	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:92292432-92293961	HepG2	liver:	n/a	n/a
19	ARID3A	chr1:92351242-92351293	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:92351519-92352531	HepG2	liver:	n/a	n/a
21	ARID3A	chr1:92424619-92424819	HepG2	liver:	n/a	n/a
22	ARID3A	chr1:92285078-92285270	HepG2	liver:	n/a	n/a
23	ARID3A	chr1:92295888-92296212	HepG2	liver:	n/a	n/a
24	ATF1	chr1:92360017-92360202	K562	blood:	n/a	n/a
25	ATF1	chr1:92530637-92530857	K562	blood:	n/a	n/a
26	ATF2	chr1:92338095-92338511	GM12878	blood:	n/a	n/a
27	ATF2	chr1:92341664-92342230	GM12878	blood:	n/a	n/a
28	ATF2	chr1:92343078-92343855	GM12878	blood:	n/a	n/a
29	ATF2	chr1:92343239-92343765	GM12878	blood:	n/a	n/a
30	ATF2	chr1:92338008-92338650	GM12878	blood:	n/a	n/a
31	ATF3	chr1:92351477-92351827	A549	lung:	n/a	n/a
32	ATF3	chr1:92414808-92414936	K562	blood:	n/a	chr1:92414878-92414887 chr1:92414867-92414887
33	BACH1	chr1:92458760-92458932	K562	blood:	n/a	n/a
34	BACH1	chr1:92494875-92495995	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr1:92352167-92352293	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr1:92331752-92331754	K562	blood:	n/a	n/a
37	BACH1	chr1:92283656-92284243	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr1:92351076-92351915	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr1:92290748-92290750	K562	blood:	n/a	n/a
40	BATF	chr1:92341701-92342110	GM12878	blood:	n/a	n/a
41	BATF	chr1:92343339-92343755	GM12878	blood:	n/a	chr1:92343581-92343591 chr1:92343580-92343591
42	BATF	chr1:92341639-92342169	GM12878	blood:	n/a	n/a
43	BATF	chr1:92338200-92338562	GM12878	blood:	n/a	n/a
44	BATF	chr1:92324984-92325220	GM12878	blood:	n/a	n/a
45	BATF	chr1:92343331-92343754	GM12878	blood:	n/a	chr1:92343581-92343591 chr1:92343580-92343591
46	BATF	chr1:92338142-92338596	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:92343351-92343764	GM12878	blood:	n/a	n/a
48	BCL11A	chr1:92338227-92338457	GM12878	blood:	n/a	n/a
49	BCL11A	chr1:92338171-92338574	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:92343450-92343624	GM12878	blood:	n/a	n/a

(count:4279 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92542467-92542517	HCM	heart:	n/a
2	chr1:92496160-92496210	NHDF-neo	bronchial:	n/a
3	chr1:92351216-92351266	SK-N-SH	brain:	n/a
4	chr1:92351641-92351691	HIPEpiC	eye:	n/a
5	chr1:92546040-92546090	AG10803	skin:	n/a
6	chr1:92494997-92495047	HRCEpiC	kidney:	n/a
7	chr1:92414910-92414960	MCF10A-Er-Src	breast:	n/a
8	chr1:92495342-92495392	HL-60	blood:	n/a
9	chr1:92295946-92295996	HL-60	blood:	n/a
10	chr1:92542467-92542517	HCM	heart:	n/a
11	chr1:92496160-92496210	NHDF-neo	bronchial:	n/a
12	chr1:92351216-92351266	SK-N-SH	brain:	n/a
13	chr1:92351641-92351691	HIPEpiC	eye:	n/a
14	chr1:92546040-92546090	AG10803	skin:	n/a
15	chr1:92494997-92495047	HRCEpiC	kidney:	n/a
16	chr1:92414910-92414960	MCF10A-Er-Src	breast:	n/a
17	chr1:92495342-92495392	HL-60	blood:	n/a
18	chr1:92295946-92295996	HL-60	blood:	n/a
19	chr1:92338262-92338312	BJ	skin:	n/a
20	chr1:92545898-92545948	CMK	blood:	n/a
21	chr1:92546470-92546520	T-47D	breast:	n/a
22	chr1:92542467-92542517	HIPEpiC	eye:	n/a
23	chr1:92415145-92415195	NH-A	brain:	n/a
24	chr1:92546135-92546185	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:92495720-92495770	BE2_C	brain:	n/a
26	chr1:92496160-92496210	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:92502933-92502983	K562	blood:	n/a
28	chr1:92414737-92414787	HRCEpiC	kidney:	n/a
29	chr1:92347850-92347900	AG09309	skin:	n/a
30	chr1:92415145-92415195	ProgFib	skin:	n/a
31	chr1:92351956-92352006	GM12892	blood:	n/a
32	chr1:92351641-92351691	T-47D	breast:	n/a
33	chr1:92351487-92351537	BJ	skin:	n/a
34	chr1:92542467-92542517	NT2-D1	testis:	n/a
35	chr1:92542467-92542517	HepG2	liver:	n/a
36	chr1:92351487-92351537	BE2_C	brain:	n/a
37	chr1:92414782-92414832	HNPCEpiC	eye:	n/a
38	chr1:92495342-92495392	PANC-1	pancreas:	n/a
39	chr1:92546135-92546185	ovcar-3	ovarian:	n/a
40	chr1:92545898-92545948	ProgFib	skin:	n/a
41	chr1:92282206-92282256	AG10803	skin:	n/a
42	chr1:92350133-92350183	HCPEpiC	choroid plexus:	n/a
43	chr1:92414520-92414570	AG09309	skin:	n/a
44	chr1:92351686-92351736	SK-N-MC	brain:	n/a
45	chr1:92351047-92351097	Jurkat	blood:	n/a
46	chr1:92347850-92347900	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:92494997-92495047	AG09319	gingival:	n/a
48	chr1:92414221-92414271	PrEC	prostate:	n/a
49	chr1:92351047-92351097	GM12892	blood:	n/a
50	chr1:92329399-92329449	Hepatocyte	liver:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:92351741..92353429-chr1:92365967..92368466,2	K562	blood:
2	chr1:92542913..92545844-chr1:92825979..92827706,2	K562	blood:
3	chr1:91966132..91968252-chr1:92404869..92406833,2	K562	blood:
4	chr1:92306378..92308491-chr1:92309526..92312029,2	K562	blood:
5	chr1:92329344..92331517-chr1:92335405..92337042,2	K562	blood:
6	chr1:92351002..92351971-chr1:117602866..117603496,2	Hela-S3	cervix:
7	chr1:92531679..92534472-chr1:92536505..92538325,2	K562	blood:
8	chr1:92545812..92549091-chr1:92549918..92553923,4	K562	blood:
9	chr1:92348748..92351822-chr1:92353645..92358232,4	K562	blood:
10	chr1:92316915..92318823-chr1:92321459..92323103,2	K562	blood:
11	chr1:92271912..92274176-chr1:92284969..92287951,2	K562	blood:
12	chr1:92294575..92296142-chr1:92299914..92302131,2	K562	blood:
13	chr1:92341690..92345444-chr1:92349151..92352209,5	K562	blood:
14	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
15	chr1:92529291..92531947-chr1:92544374..92546080,2	K562	blood:
16	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
17	chr1:92411395..92413821-chr1:92420439..92422796,2	K562	blood:
18	chr1:92343661..92345545-chr1:92351555..92353451,2	K562	blood:
19	chr1:91978918..91979433-chr1:92392533..92393092,2	K562	blood:
20	chr1:92309780..92313855-chr1:92314421..92317529,4	K562	blood:
21	chr1:92288953..92291560-chr1:92301020..92303109,2	K562	blood:
22	chr1:92306378..92308491-chr1:92309526..92312029,2	K562	blood:
23	chr1:92271912..92274176-chr1:92284969..92287951,2	K562	blood:
24	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
25	chr1:92259196..92261708-chr1:92278967..92281416,2	K562	blood:
26	chr1:92500741..92502488-chr1:92762793..92765174,2	MCF-7	breast:
27	chr1:92463193..92463783-chr1:92756674..92757244,2	MCF-7	breast:
28	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
29	chr1:92288953..92291560-chr1:92301020..92303109,3	K562	blood:
30	chr1:92544652..92546280-chr1:92558053..92559585,2	K562	blood:
31	chr1:92269279..92272009-chr1:92273334..92276001,3	K562	blood:
32	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
33	chr1:92359622..92362110-chr1:92365556..92367175,2	K562	blood:
34	chr1:92309780..92313855-chr1:92314421..92317529,4	K562	blood:
35	chr1:92097267..92098889-chr1:92337688..92339607,2	K562	blood:
36	chr1:92085074..92086910-chr1:92278209..92279900,2	K562	blood:
37	chr1:92359622..92362110-chr1:92365556..92367175,2	K562	blood:
38	chr1:91964010..91966765-chr1:92464590..92467417,2	K562	blood:
39	chr1:92082754..92083639-chr1:92392516..92393512,4	MCF-7	breast:
40	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
41	chr1:91995716..91996502-chr1:92392369..92393018,2	MCF-7	breast:
42	chr1:92418160..92421480-chr1:92423319..92426988,3	K562	blood:
43	chr1:92283210..92285190-chr1:92295185..92297126,2	K562	blood:
44	chr1:92490161..92492607-chr1:92493368..92497617,3	K562	blood:
45	chr1:92274046..92275550-chr1:92277677..92280459,2	K562	blood:
46	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
47	chr1:91994551..91996997-chr1:92385610..92388191,2	K562	blood:
48	chr1:92354436..92357349-chr1:92361835..92364580,4	K562	blood:
49	chr1:92415221..92417669-chr1:92420291..92422618,2	K562	blood:
50	chr1:92359348..92361445-chr1:92361640..92364597,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPHX4-2	chr1:92415457-92415856	NONHSAT004444
2	lnc-HFM1-3	chr1:92351587-92351708	NONHSAT004441
3	lnc-EPHX4-2	chr1:92415447-92415869	NONHSAT004446
4	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004444
5	lnc-HFM1-3	chr1:92329396-92329836	NONHSAT004441
6	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004446
7	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004443
8	lnc-BRDT-1	chr1:92404826-92405131	NONHSAT004442
9	lnc-EPHX4-2	chr1:92414960-92415076	NONHSAT004446
10	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004445
11	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004445
12	lnc-EPHX4-2	chr1:92415447-92415889	NONHSAT004445
13	lnc-EPHX4-2	chr1:92415457-92415859	NONHSAT004443
14	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004443
15	lnc-GLMN-2	chr1:92295333-92295631	NONHSAT004440
16	lnc-EPHX4-2	chr1:92414955-92415076	NONHSAT004444

No data

Variant related genes	Relation type
LPCAT2BP	TF binding region
RN7SL653P	TF binding region
TGFBR3	TF binding region
BTBD8	TF binding region
SETSIP	TF binding region
BRDT	TF binding region
EPHX4	TF binding region
RN7SL235P	TF binding region
LPCAT2BP	CpG island
RN7SL653P	CpG island
TGFBR3	CpG island
BTBD8	CpG island
SETSIP	CpG island
BRDT	CpG island
EPHX4	CpG island
RN7SL235P	CpG island
ENSG00000233228	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000172031	chromatin interactions
ENSG00000239794	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000162669	chromatin interactions
ENSG00000189195	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000116830	chromatin interactions
ENSG00000069702	chromatin interactions

Extended variants
information (count: 8124 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:8124 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10493859	chr1:92273644-92273645	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374173380	chr1:92273667-92273668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200284327	chr1:92273672-92273673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570794701	chr1:92273673-92273674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs202233678	chr1:92273684-92273685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535001585	chr1:92273685-92273686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145881560	chr1:92273728-92273729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs137897129	chr1:92273765-92273766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs284154	chr1:92273778-92273779	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs570356535	chr1:92273782-92273783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184543445	chr1:92273809-92273810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575000466	chr1:92273828-92273829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188218039	chr1:92273829-92273830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557825459	chr1:92273835-92273836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34150519	chr1:92273896-92273897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572787854	chr1:92273899-92273900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191864869	chr1:92273911-92273912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540206505	chr1:92274038-92274039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538842970	chr1:92274076-92274077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573848258	chr1:92274083-92274084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544420956	chr1:92274101-92274102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562718149	chr1:92274107-92274108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs61781098	chr1:92274109-92274110	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs552736052	chr1:92274121-92274122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566278981	chr1:92274168-92274169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149456517	chr1:92274214-92274215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376822333	chr1:92274237-92274238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114871074	chr1:92274259-92274260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546938559	chr1:92274295-92274296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2492090	chr1:92274297-92274298	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs4658273	chr1:92274308-92274309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs558790039	chr1:92274316-92274317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148627291	chr1:92274348-92274349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113656357	chr1:92274349-92274350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569149426	chr1:92274398-92274399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539631228	chr1:92274412-92274413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs284153	chr1:92274420-92274421	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs141260442	chr1:92274450-92274451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369794119	chr1:92274466-92274467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555295252	chr1:92274476-92274477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147130221	chr1:92274504-92274505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201214467	chr1:92274505-92274506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373660453	chr1:92274535-92274536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs17878299	chr1:92274601-92274602	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376641489	chr1:92274657-92274658	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188529659	chr1:92274663-92274664	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545194172	chr1:92274690-92274691	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564439166	chr1:92274700-92274701	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528545063	chr1:92274737-92274738	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556957687	chr1:92274748-92274749	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4464 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92257600-92279400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:92262800-92277000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:92264800-92284200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr1:92266800-92277400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:92268200-92274600	Enhancers	Placenta	Placenta
6	chr1:92268600-92275200	Enhancers	NHDF-Ad	bronchial
7	chr1:92268600-92275800	Enhancers	Pancreas	Pancrea
8	chr1:92269400-92275600	Enhancers	Fetal Heart	heart
9	chr1:92269600-92275800	Enhancers	Left Ventricle	heart
10	chr1:92270000-92278000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:92270200-92274800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:92270200-92276800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr1:92270400-92274800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr1:92270400-92274800	Weak transcription	HSMM	muscle
15	chr1:92270400-92275600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:92270400-92277600	Weak transcription	Brain Anterior Caudate	brain
17	chr1:92270600-92274800	Weak transcription	Esophagus	oesophagus
18	chr1:92271000-92274000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr1:92271200-92274600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr1:92271200-92276200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr1:92271400-92274600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr1:92271400-92274800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr1:92271400-92274800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr1:92271400-92275000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr1:92271400-92276000	Weak transcription	Primary T cells from cord blood	blood
26	chr1:92271600-92274000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr1:92271600-92274600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr1:92271600-92274600	Weak transcription	GM12878-XiMat	blood
29	chr1:92271600-92274800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr1:92271600-92274800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr1:92271800-92275600	Enhancers	HUVEC	blood vessel
32	chr1:92272000-92274200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:92272000-92274600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr1:92272000-92279200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr1:92272200-92282600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr1:92272400-92285400	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr1:92272600-92274600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:92273000-92274800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr1:92273000-92277400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr1:92273000-92277400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:92273200-92275400	Weak transcription	Fetal Stomach	stomach
42	chr1:92273200-92277400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr1:92273400-92274400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:92273400-92274400	Weak transcription	Colon Smooth Muscle	Colon
45	chr1:92273400-92274600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:92273400-92274600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr1:92273400-92274600	Weak transcription	HepG2	liver
48	chr1:92273400-92274600	Weak transcription	Osteobl	bone
49	chr1:92273400-92274800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:92273400-92274800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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