Variant report

Variant	nsv535702
Chromosome Location	chr2:51046996-51358191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:51330523-51330544	HepG2	liver:	n/a	n/a
2	ATF2	chr2:51259020-51259511	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:51259057-51259636	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:51083034-51083154	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:51330505-51330576	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr2:51330297-51330702	HepG2	liver:	n/a	n/a
10	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr2:51330435-51330474	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr2:51185262-51185455	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
16	CEBPB	chr2:51163450-51163794	HepG2	liver:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
17	CEBPB	chr2:51080893-51081164	Hela-S3	cervix:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
18	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
19	CEBPB	chr2:51179763-51180618	IMR90	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
20	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
21	CEBPB	chr2:51328029-51328351	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:51185077-51185269	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185201-51185210 chr2:51185201-51185210
23	CEBPB	chr2:51185072-51185406	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
24	CEBPB	chr2:51229696-51229991	IMR90	lung:	n/a	chr2:51229820-51229831
25	CEBPB	chr2:51185063-51185361	K562	blood:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
26	CEBPB	chr2:51178589-51178949	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
28	CEBPB	chr2:51330496-51330704	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:51172595-51172790	HepG2	liver:	n/a	chr2:51172679-51172690
30	CEBPB	chr2:51282778-51283040	IMR90	lung:	n/a	chr2:51282886-51282897
31	CEBPB	chr2:51259207-51259533	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:51084914-51085194	A549	lung:	n/a	chr2:51085060-51085071
33	CEBPB	chr2:51179698-51180729	Hela-S3	cervix:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
34	CEBPB	chr2:51196168-51196459	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:51080924-51081178	H1-hESC	embryonic stem cell:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
36	CEBPB	chr2:51196131-51196377	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:51185008-51185377	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
38	CEBPB	chr2:51080873-51081218	IMR90	lung:	n/a	chr2:51081037-51081050 chr2:51081039-51081048
39	CEBPB	chr2:51185023-51185436	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
40	CEBPB	chr2:51240147-51240542	MCF-7	breast:	n/a	n/a
41	CEBPB	chr2:51084918-51085221	HepG2	liver:	n/a	chr2:51085060-51085071
42	CEBPB	chr2:51325442-51325765	IMR90	lung:	n/a	chr2:51325594-51325607
43	CEBPB	chr2:51255998-51256347	A549	lung:	n/a	chr2:51256172-51256183
44	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
45	CEBPB	chr2:51335948-51336305	HepG2	liver:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
46	CEBPB	chr2:51335993-51336283	H1-hESC	embryonic stem cell:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
47	CEBPB	chr2:51255984-51256364	HepG2	liver:	n/a	chr2:51256172-51256183
48	CEBPB	chr2:51255964-51256336	MCF-7	breast:	n/a	chr2:51256172-51256183
49	CEBPB	chr2:51256004-51256330	K562	blood:	n/a	chr2:51256172-51256183
50	CEBPB	chr2:51272267-51272564	A549	lung:	n/a	chr2:51272397-51272408 chr2:51272396-51272409

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51056884-51056934	HIPEpiC	eye:	n/a
2	chr2:51254132-51254182	HL-60	blood:	n/a
3	chr2:51252301-51252351	SK-N-SH_RA	brain:	n/a
4	chr2:51255627-51255677	HEK293	kidney:	embryo
5	chr2:51231649-51231699	AG09309	skin:	n/a
6	chr2:51260003-51260053	ovcar-3	ovarian:	n/a
7	chr2:51254170-51254220	ECC-1	luminal epithelium:	n/a
8	chr2:51057548-51057598	HRE	kidney:	n/a
9	chr2:51254170-51254220	HUVEC	blood vessel:	n/a
10	chr2:51259697-51259747	SAEC	small airway:	n/a
11	chr2:51056884-51056934	HIPEpiC	eye:	n/a
12	chr2:51254132-51254182	HL-60	blood:	n/a
13	chr2:51252301-51252351	SK-N-SH_RA	brain:	n/a
14	chr2:51255627-51255677	HEK293	kidney:	embryo
15	chr2:51231649-51231699	AG09309	skin:	n/a
16	chr2:51260003-51260053	ovcar-3	ovarian:	n/a
17	chr2:51254170-51254220	ECC-1	luminal epithelium:	n/a
18	chr2:51057548-51057598	HRE	kidney:	n/a
19	chr2:51254170-51254220	HUVEC	blood vessel:	n/a
20	chr2:51259697-51259747	SAEC	small airway:	n/a
21	chr2:51255627-51255677	GM12878	blood:	n/a
22	chr2:51057218-51057268	HepG2	liver:	n/a
23	chr2:51260739-51260789	HEEpiC	esophagus:	n/a
24	chr2:51254981-51255031	HL-60	blood:	n/a
25	chr2:51259807-51259857	CMK	blood:	n/a
26	chr2:51252301-51252351	NHBE	bronchial:	n/a
27	chr2:51254170-51254220	HCT-116	colon:	n/a
28	chr2:51255324-51255374	Hepatocyte	liver:	n/a
29	chr2:51259786-51259836	HRCEpiC	kidney:	n/a
30	chr2:51254102-51254152	GM12892	blood:	n/a
31	chr2:51260399-51260449	RPTEC	kidney:	n/a
32	chr2:51254981-51255031	GM06990	blood:	n/a
33	chr2:51056884-51056934	AoSMC	blood vessel:	n/a
34	chr2:51252301-51252351	PrEC	prostate:	n/a
35	chr2:51259786-51259836	Caco-2	colon:	n/a
36	chr2:51259703-51259753	IMR90	lung:	fetal
37	chr2:51259703-51259753	HL-60	blood:	n/a
38	chr2:51254170-51254220	U87	brain:	n/a
39	chr2:51255324-51255374	BJ	skin:	n/a
40	chr2:51254102-51254152	H1-hESC	embryonic stem cell:	embryo
41	chr2:51057218-51057268	HCF	heart:	n/a
42	chr2:51254981-51255031	AG10803	skin:	n/a
43	chr2:51255324-51255374	BE2_C	brain:	n/a
44	chr2:51056822-51056872	HCPEpiC	choroid plexus:	n/a
45	chr2:51074881-51074931	PANC-1	pancreas:	n/a
46	chr2:51218880-51218930	AG09309	skin:	n/a
47	chr2:51260399-51260449	HAEpiC	amniotic membrane:	n/a
48	chr2:51259552-51259602	HMEC	breast:	n/a
49	chr2:51259552-51259602	GM12892	blood:	n/a
50	chr2:51231649-51231699	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
2	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
3	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
4	chr2:51135133..51137954-chr2:51139685..51141436,2	MCF-7	breast:
5	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
6	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
7	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
8	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
9	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
10	chr2:51084150..51086897-chr2:51088805..51090362,2	K562	blood:
11	chr2:51113708..51115897-chr2:51117205..51120148,2	K562	blood:
12	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
13	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
14	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
15	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
16	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
17	chr2:51288072..51290967-chr2:232569534..232571521,2	MCF-7	breast:
18	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
19	chr2:51144781..51146893-chr2:51147491..51149076,2	K562	blood:
20	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652
2	lnc-NRXN1-3	chr2:51282723-51282956	NONHSAT070652
3	lnc-NRXN1-3	chr2:51283579-51283793	l_1833_chr2:51283578-51306188_testes
4	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
5	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
6	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
7	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1
8	lnc-CHAC2-4	chr2:51279495-51279592	ENSG00000231918.1
9	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648
10	lnc-NRXN1-3	chr2:51283633-51283791	NONHSAT070652

Variant related genes	Relation type
ENSG00000238165	TF binding region
NRXN1	TF binding region
ENSG00000216011	TF binding region
ENSG00000272385	TF binding region
ENSG00000231918	TF binding region
ENSG00000238165	CpG island
NRXN1	CpG island
ENSG00000216011	CpG island
ENSG00000272385	CpG island
ENSG00000231918	CpG island

Extended variants
information (count: 10451 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:10451 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549693234	chr2:51047008-51047009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189443984	chr2:51047020-51047021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75128891	chr2:51047049-51047050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556226117	chr2:51047076-51047077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577733674	chr2:51047082-51047083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75886274	chr2:51047083-51047084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185788992	chr2:51047131-51047132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572261434	chr2:51047136-51047137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191478227	chr2:51047189-51047190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561280222	chr2:51047236-51047237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576083013	chr2:51047262-51047263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148836913	chr2:51047269-51047270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149137650	chr2:51047277-51047278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543476721	chr2:51047299-51047300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11125326	chr2:51047313-51047314	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs532264916	chr2:51047324-51047325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9309203	chr2:51047358-51047359	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs560512653	chr2:51047377-51047378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181173433	chr2:51047378-51047379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72889455	chr2:51047422-51047423	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs369348082	chr2:51047485-51047486	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs373163250	chr2:51047507-51047508	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs567655571	chr2:51047556-51047557	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs537816717	chr2:51047577-51047578	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs142390306	chr2:51047586-51047587	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs185385399	chr2:51047601-51047602	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs538764062	chr2:51047619-51047620	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs151327684	chr2:51047692-51047693	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs535519434	chr2:51047727-51047728	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs140641105	chr2:51047748-51047749	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs4140858	chr2:51047765-51047766	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs4140859	chr2:51047777-51047778	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs576420299	chr2:51047778-51047779	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs543412386	chr2:51047779-51047780	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs190638348	chr2:51047863-51047864	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs576954878	chr2:51047907-51047908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs570784815	chr2:51047933-51047934	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs577312408	chr2:51047946-51047947	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs540768070	chr2:51047952-51047953	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs559426623	chr2:51047953-51047954	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs527866944	chr2:51048023-51048024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543223672	chr2:51048027-51048028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561219662	chr2:51048089-51048090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531888712	chr2:51048148-51048149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546190717	chr2:51048184-51048185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539748652	chr2:51048190-51048191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549726607	chr2:51048197-51048198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571296180	chr2:51048332-51048333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374426069	chr2:51048354-51048355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145892829	chr2:51048356-51048357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	17989066	CNVD
Autism	19404257	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51041400-51051800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:51046600-51047400	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr2:51047400-51048000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr2:51047600-51048800	Enhancers	Brain Germinal Matrix	brain
5	chr2:51048000-51048800	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr2:51048800-51050000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:51048800-51056800	Weak transcription	Brain Germinal Matrix	brain
8	chr2:51050000-51051000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr2:51050200-51050400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:51050400-51051600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:51051600-51052800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:51051800-51052000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:51052000-51052400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:51052400-51054200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:51053000-51058600	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:51054000-51054400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:51054400-51057400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr2:51056800-51057600	Enhancers	Fetal Brain Male	brain
19	chr2:51056800-51057800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr2:51056800-51057800	Enhancers	Fetal Brain Female	brain
21	chr2:51056800-51059800	Enhancers	Brain Germinal Matrix	brain
22	chr2:51056800-51060000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr2:51057200-51057400	Enhancers	Brain Anterior Caudate	brain
24	chr2:51057200-51058800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr2:51057400-51057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:51057400-51058400	Weak transcription	Brain Anterior Caudate	brain
27	chr2:51057600-51058000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:51057600-51058800	Weak transcription	Fetal Brain Male	brain
29	chr2:51057800-51058200	Weak transcription	Fetal Brain Female	brain
30	chr2:51058000-51059600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:51058200-51059800	Enhancers	Fetal Brain Female	brain
32	chr2:51058400-51058800	Enhancers	Brain Anterior Caudate	brain
33	chr2:51058400-51059800	Enhancers	Brain Cingulate Gyrus	brain
34	chr2:51058600-51058800	Enhancers	Brain Hippocampus Middle	brain
35	chr2:51058600-51059400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:51058600-51059600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:51058600-51059800	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr2:51058800-51059000	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr2:51058800-51059400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:51058800-51059400	Active TSS	Brain Anterior Caudate	brain
41	chr2:51058800-51060000	Enhancers	Fetal Brain Male	brain
42	chr2:51059000-51059200	Enhancers	Brain Hippocampus Middle	brain
43	chr2:51059200-51059400	Active TSS	Brain Hippocampus Middle	brain
44	chr2:51059400-51059800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:51059600-51065200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:51059800-51074200	Weak transcription	Brain Germinal Matrix	brain
47	chr2:51062000-51062200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr2:51062200-51063600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:51062200-51064400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr2:51063200-51063400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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