Variant report

Variant	nsv1004239
Chromosome Location	chr2:51226169-51606258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:908)
CpG islands
(count:1587)
Chromatin interactive
region (count:18)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr2:51259057-51259636	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:51524637-51524938	GM12878	blood:	n/a	n/a
4	ATF2	chr2:51259020-51259511	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:51330505-51330576	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:51439527-51439799	GM12878	blood:	n/a	chr2:51439631-51439642
9	BHLHE40	chr2:51439638-51439779	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:51524627-51524983	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:51330297-51330702	HepG2	liver:	n/a	n/a
12	BRCA1	chr2:51330435-51330474	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
15	CCNT2	chr2:51398751-51398851	K562	blood:	n/a	n/a
16	CEBPB	chr2:51328029-51328351	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:51547032-51547286	HepG2	liver:	n/a	chr2:51547159-51547170
18	CEBPB	chr2:51573328-51573689	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:51496429-51496495	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:51335991-51336268	Hela-S3	cervix:	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
21	CEBPB	chr2:51485456-51485732	ECC-1	luminal epithelium:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
22	CEBPB	chr2:51325442-51325765	IMR90	lung:	n/a	chr2:51325594-51325607
23	CEBPB	chr2:51491236-51491509	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:51255984-51256364	HepG2	liver:	n/a	chr2:51256172-51256183
25	CEBPB	chr2:51255896-51256399	A549	lung:	n/a	chr2:51256172-51256183
26	CEBPB	chr2:51515920-51516087	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:51547030-51547286	IMR90	lung:	n/a	chr2:51547159-51547170
28	CEBPB	chr2:51324687-51324910	HepG2	liver:	n/a	chr2:51324819-51324830
29	CEBPB	chr2:51330496-51330704	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:51499694-51499837	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:51556715-51557086	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:51485458-51485815	A549	lung:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
33	CEBPB	chr2:51240147-51240542	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:51461631-51461892	HepG2	liver:	n/a	chr2:51461726-51461737
35	CEBPB	chr2:51461597-51461861	A549	lung:	n/a	chr2:51461726-51461737
36	CEBPB	chr2:51259207-51259533	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
38	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
39	CEBPB	chr2:51272267-51272564	A549	lung:	n/a	chr2:51272397-51272408 chr2:51272396-51272409
40	CEBPB	chr2:51335946-51336321	K562	blood:	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
41	CEBPB	chr2:51485456-51485813	K562	blood:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
42	CEBPB	chr2:51485448-51485831	IMR90	lung:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
43	CEBPB	chr2:51314497-51314768	A549	lung:	n/a	chr2:51314679-51314692 chr2:51314681-51314692 chr2:51314679-51314692 chr2:51314681-51314692
44	CEBPB	chr2:51282778-51283040	IMR90	lung:	n/a	chr2:51282886-51282897
45	CEBPB	chr2:51229679-51229969	HepG2	liver:	n/a	chr2:51229820-51229831
46	CEBPB	chr2:51255989-51256366	IMR90	lung:	n/a	chr2:51256172-51256183
47	CEBPB	chr2:51461638-51461868	IMR90	lung:	n/a	chr2:51461726-51461737
48	CEBPB	chr2:51605097-51605135	HepG2	liver:	n/a	chr2:51605108-51605119
49	CEBPB	chr2:51515830-51516103	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr2:51565289-51565476	HepG2	liver:	n/a	chr2:51565342-51565353

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51254170-51254220	SAEC	small airway:	n/a
2	chr2:51254170-51254220	SAEC	small airway:	n/a
3	chr2:51255324-51255374	AG04449	skin:	fetal
4	chr2:51228125-51228175	PFSK-1	brain:	n/a
5	chr2:51260003-51260053	NT2-D1	testis:	n/a
6	chr2:51260003-51260053	SK-N-SH_RA	brain:	n/a
7	chr2:51260003-51260053	PANC-1	pancreas:	n/a
8	chr2:51254132-51254182	AG10803	skin:	n/a
9	chr2:51260003-51260053	GM12891	blood:	n/a
10	chr2:51260739-51260789	Jurkat	blood:	n/a
11	chr2:51259697-51259747	HAEpiC	amniotic membrane:	n/a
12	chr2:51254170-51254220	NH-A	brain:	n/a
13	chr2:51259703-51259753	H1-hESC	embryonic stem cell:	embryo
14	chr2:51254132-51254182	BJ	skin:	n/a
15	chr2:51260399-51260449	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:51259807-51259857	NHBE	bronchial:	n/a
17	chr2:51259693-51259743	A549	lung:	n/a
18	chr2:51254170-51254220	Jurkat	blood:	n/a
19	chr2:51260739-51260789	NT2-D1	testis:	n/a
20	chr2:51254981-51255031	HUVEC	blood vessel:	n/a
21	chr2:51259703-51259753	HRPEpiC	eye:	n/a
22	chr2:51254823-51254873	ovcar-3	ovarian:	n/a
23	chr2:51240310-51240360	Hepatocyte	liver:	n/a
24	chr2:51254102-51254152	ECC-1	luminal epithelium:	n/a
25	chr2:51259697-51259747	SK-N-MC	brain:	n/a
26	chr2:51379080-51379130	ECC-1	luminal epithelium:	n/a
27	chr2:51378948-51378998	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:51254132-51254182	HCF	heart:	n/a
29	chr2:51254981-51255031	U87	brain:	n/a
30	chr2:51259786-51259836	GM19239	blood:	n/a
31	chr2:51231649-51231699	A549	lung:	n/a
32	chr2:51255627-51255677	T-47D	breast:	n/a
33	chr2:51379080-51379130	ProgFib	skin:	n/a
34	chr2:51260003-51260053	HCM	heart:	n/a
35	chr2:51231649-51231699	U87	brain:	n/a
36	chr2:51378948-51378998	HCM	heart:	n/a
37	chr2:51254021-51254071	T-47D	breast:	n/a
38	chr2:51260003-51260053	HUVEC	blood vessel:	n/a
39	chr2:51240310-51240360	HIPEpiC	eye:	n/a
40	chr2:51255306-51255356	Hela-S3	cervix:	n/a
41	chr2:51228125-51228175	A549	lung:	n/a
42	chr2:51231649-51231699	HUVEC	blood vessel:	n/a
43	chr2:51231649-51231699	HEEpiC	esophagus:	n/a
44	chr2:51240310-51240360	GM19239	blood:	n/a
45	chr2:51259697-51259747	Jurkat	blood:	n/a
46	chr2:51259786-51259836	SAEC	small airway:	n/a
47	chr2:51259807-51259857	RPTEC	kidney:	n/a
48	chr2:51260003-51260053	A549	lung:	n/a
49	chr2:51259807-51259857	AoSMC	blood vessel:	n/a
50	chr2:51259697-51259747	AoSMC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:51288072..51290967-chr2:232569534..232571521,2	MCF-7	breast:
2	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
3	chr2:51566884..51569185-chr2:51570886..51573371,2	K562	blood:
4	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
5	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
6	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
7	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
8	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
9	chr2:51554002..51556424-chr2:51560919..51562851,2	K562	blood:
10	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
11	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
12	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
13	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
14	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
15	chr2:51566884..51569185-chr2:51570886..51573371,2	K562	blood:
16	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
17	chr2:51107834..51110098-chr2:51577616..51579275,2	K562	blood:
18	chr2:51554002..51556424-chr2:51560919..51562851,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
2	lnc-NRXN1-4	chr2:51423222-51423493	l_1834_chr2:51413303-51423493_76bGuttman_hLF
3	lnc-NRXN1-2	chr2:51569718-51569990	XLOC_002094
4	lnc-NRXN1-1	chr2:51430129-51430299	ENSG00000237374
5	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
6	lnc-CHAC2-4	chr2:51279495-51279592	ENSG00000231918.1
7	lnc-CHAC2-4	chr2:51605233-51605311	ENSG00000231918.1
8	lnc-NRXN1-2	chr2:51559800-51560035	XLOC_002094
9	lnc-NRXN1-3	chr2:51283579-51283793	l_1833_chr2:51283578-51306188_testes
10	lnc-NRXN1-2	chr2:51571329-51571385	XLOC_002094
11	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1
12	lnc-NRXN1-2	chr2:51560653-51560787	XLOC_002094
13	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
14	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
15	lnc-NRXN1-4	chr2:51414157-51414291	l_1834_chr2:51413303-51423493_76bGuttman_hLF
16	lnc-NRXN1-2	chr2:51560653-51560787	XLOC_002094
17	lnc-NRXN1-2	chr2:51559800-51560035	XLOC_002094
18	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
19	lnc-CHAC2-4	chr2:51555527-51555627	ENSG00000231918.1
20	lnc-NRXN1-2	chr2:51560653-51560803	XLOC_002094
21	lnc-NRXN1-3	chr2:51283633-51283791	NONHSAT070652
22	lnc-NRXN1-2	chr2:51569718-51569990	XLOC_002094
23	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
24	lnc-NRXN1-4	chr2:51413304-51413539	l_1834_chr2:51413303-51423493_76bGuttman_hLF
25	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
26	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
27	lnc-NRXN1-2	chr2:51569718-51569850	XLOC_002094
28	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652
29	lnc-NRXN1-3	chr2:51282723-51282956	NONHSAT070652

No data

Variant related genes	Relation type
NRXN1	TF binding region
ENSG00000231918	TF binding region
ENSG00000237374	TF binding region
NRXN1	CpG island
ENSG00000231918	CpG island
ENSG00000237374	CpG island
PDCD10	miRNA target sites
PDCD4	miRNA target sites

Extended variants
information (count: 8358 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:8358 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17041178	chr2:51226248-51226249	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536942135	chr2:51226289-51226290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555008540	chr2:51226338-51226339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576006298	chr2:51226359-51226360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370299834	chr2:51226410-51226411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543444391	chr2:51226412-51226413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558542570	chr2:51226436-51226437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576896880	chr2:51226437-51226438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs937783	chr2:51226527-51226528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574056706	chr2:51226561-51226562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559455201	chr2:51226573-51226574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72874554	chr2:51226574-51226575	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs542088579	chr2:51226601-51226602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563612025	chr2:51226605-51226606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530844513	chr2:51226624-51226625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185699093	chr2:51226643-51226644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62143013	chr2:51226691-51226692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528149206	chr2:51226694-51226695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546418127	chr2:51226695-51226696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566261407	chr2:51226702-51226703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7599370	chr2:51226707-51226708	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181995909	chr2:51226717-51226718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569978752	chr2:51226772-51226773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537368769	chr2:51226777-51226778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558474811	chr2:51226787-51226788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547331011	chr2:51226793-51226794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184526182	chr2:51226797-51226798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6545189	chr2:51226801-51226802	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553221817	chr2:51226829-51226830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576490797	chr2:51226833-51226834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1995583	chr2:51226834-51226835	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs563497908	chr2:51226837-51226838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138612665	chr2:51226886-51226887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188117033	chr2:51226899-51226900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142754250	chr2:51226903-51226904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528122908	chr2:51226954-51226955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181282157	chr2:51226972-51226973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546651622	chr2:51226974-51226975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2216308	chr2:51227012-51227013	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs147371666	chr2:51227062-51227063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77267092	chr2:51227190-51227191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569916203	chr2:51227233-51227234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2193410	chr2:51227254-51227255	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs538827736	chr2:51227280-51227281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185683330	chr2:51227341-51227342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570820091	chr2:51227382-51227383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534744314	chr2:51227391-51227392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541277845	chr2:51227397-51227398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190791335	chr2:51227443-51227444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139683799	chr2:51227474-51227475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
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
Schizophrenia	17989066	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51207400-51237600	Weak transcription	Brain Germinal Matrix	brain
2	chr2:51218800-51226400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr2:51219400-51227200	Weak transcription	Brain Substantia Nigra	brain
4	chr2:51220200-51227200	Weak transcription	Fetal Brain Female	brain
5	chr2:51222600-51227200	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:51222800-51228000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:51225400-51226400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr2:51225600-51227800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr2:51226000-51231200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr2:51226200-51231400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:51226200-51232200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:51226400-51227800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:51226400-51228400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:51226400-51229200	Enhancers	Brain Cingulate Gyrus	brain
15	chr2:51226400-51229600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr2:51226600-51229000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:51226800-51229800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr2:51226800-51231200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr2:51227000-51227600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr2:51227000-51227600	Enhancers	Fetal Brain Male	brain
21	chr2:51227000-51229200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:51227200-51227400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:51227200-51227400	Enhancers	Brain Hippocampus Middle	brain
24	chr2:51227200-51227600	Enhancers	Brain Substantia Nigra	brain
25	chr2:51227200-51228200	Enhancers	Fetal Brain Female	brain
26	chr2:51227200-51229600	Enhancers	Brain Anterior Caudate	brain
27	chr2:51227400-51228000	Weak transcription	Brain Hippocampus Middle	brain
28	chr2:51227400-51229400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr2:51227400-51239800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr2:51227600-51228000	Weak transcription	Fetal Brain Male	brain
31	chr2:51227600-51228800	Weak transcription	Brain Substantia Nigra	brain
32	chr2:51227600-51230600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr2:51227800-51228200	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr2:51227800-51228200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:51228000-51228200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr2:51228000-51228200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr2:51228000-51228200	Enhancers	Fetal Brain Male	brain
38	chr2:51228000-51228400	Enhancers	Brain Angular Gyrus	brain
39	chr2:51228000-51229200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr2:51228000-51229600	Enhancers	Brain Hippocampus Middle	brain
41	chr2:51228200-51228600	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr2:51228200-51230600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr2:51228200-51230600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:51228200-51238400	Weak transcription	Fetal Brain Male	brain
45	chr2:51228200-51238800	Weak transcription	Fetal Brain Female	brain
46	chr2:51228400-51228600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr2:51228400-51228800	Weak transcription	Brain Angular Gyrus	brain
48	chr2:51228600-51229200	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr2:51228600-51234400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr2:51228800-51229000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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