Variant report

Variant	nsv948354
Chromosome Location	chr2:51188566-51521625
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	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:51330505-51330576	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:51439527-51439799	GM12878	blood:	n/a	chr2:51439631-51439642
8	BHLHE40	chr2:51330297-51330702	HepG2	liver:	n/a	n/a
9	BHLHE40	chr2:51439638-51439779	GM12878	blood:	n/a	n/a
10	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr2:51330435-51330474	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
14	CCNT2	chr2:51398751-51398851	K562	blood:	n/a	n/a
15	CEBPB	chr2:51485499-51485822	A549	lung:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
16	CEBPB	chr2:51259207-51259533	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:51485456-51485732	ECC-1	luminal epithelium:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
18	CEBPB	chr2:51461631-51461892	HepG2	liver:	n/a	chr2:51461726-51461737
19	CEBPB	chr2:51485458-51485831	H1-hESC	embryonic stem cell:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
20	CEBPB	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
21	CEBPB	chr2:51496291-51496595	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:51335946-51336285	A549	lung:	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
23	CEBPB	chr2:51255980-51256366	H1-hESC	embryonic stem cell:	n/a	chr2:51256172-51256183
24	CEBPB	chr2:51335948-51336306	IMR90	lung:	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
25	CEBPB	chr2:51196305-51196335	K562	blood:	n/a	n/a
26	CEBPB	chr2:51255984-51256364	HepG2	liver:	n/a	chr2:51256172-51256183
27	CEBPB	chr2:51272267-51272564	A549	lung:	n/a	chr2:51272397-51272408 chr2:51272396-51272409
28	CEBPB	chr2:51324687-51324910	HepG2	liver:	n/a	chr2:51324819-51324830
29	CEBPB	chr2:51491236-51491509	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:51282778-51283040	IMR90	lung:	n/a	chr2:51282886-51282897
31	CEBPB	chr2:51196130-51196480	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:51485548-51485789	ECC-1	luminal epithelium:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
33	CEBPB	chr2:51461597-51461861	A549	lung:	n/a	chr2:51461726-51461737
34	CEBPB	chr2:51461638-51461868	IMR90	lung:	n/a	chr2:51461726-51461737
35	CEBPB	chr2:51445290-51445497	H1-hESC	embryonic stem cell:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
36	CEBPB	chr2:51229696-51229991	IMR90	lung:	n/a	chr2:51229820-51229831
37	CEBPB	chr2:51392842-51393189	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:51485449-51485821	Hela-S3	cervix:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
39	CEBPB	chr2:51256004-51256330	K562	blood:	n/a	chr2:51256172-51256183
40	CEBPB	chr2:51445259-51445582	HepG2	liver:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
41	CEBPB	chr2:51485456-51485813	K562	blood:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
42	CEBPB	chr2:51392868-51393388	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:51255998-51256347	A549	lung:	n/a	chr2:51256172-51256183
44	CEBPB	chr2:51499694-51499837	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:51330315-51330732	IMR90	lung:	n/a	n/a
46	CEBPB	chr2:51229679-51229969	HepG2	liver:	n/a	chr2:51229820-51229831
47	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
48	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
49	CEBPB	chr2:51236313-51236416	A549	lung:	n/a	n/a
50	CEBPB	chr2:51314497-51314768	A549	lung:	n/a	chr2:51314679-51314692 chr2:51314681-51314692 chr2:51314679-51314692 chr2:51314681-51314692

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51259693-51259743	HEEpiC	esophagus:	n/a
2	chr2:51218880-51218930	GM12878	blood:	n/a
3	chr2:51259693-51259743	HEEpiC	esophagus:	n/a
4	chr2:51218880-51218930	GM12878	blood:	n/a
5	chr2:51254823-51254873	Hela-S3	cervix:	n/a
6	chr2:51254981-51255031	HAEpiC	amniotic membrane:	n/a
7	chr2:51255306-51255356	SK-N-SH_RA	brain:	n/a
8	chr2:51254132-51254182	PANC-1	pancreas:	n/a
9	chr2:51255306-51255356	HCF	heart:	n/a
10	chr2:51259552-51259602	HAEpiC	amniotic membrane:	n/a
11	chr2:51259703-51259753	NHDF-neo	bronchial:	n/a
12	chr2:51259693-51259743	SK-N-MC	brain:	n/a
13	chr2:51259703-51259753	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:51260739-51260789	Hepatocyte	liver:	n/a
15	chr2:51260739-51260789	IMR90	lung:	fetal
16	chr2:51260739-51260789	HCPEpiC	choroid plexus:	n/a
17	chr2:51254021-51254071	HCM	heart:	n/a
18	chr2:51259493-51259543	SK-N-MC	brain:	n/a
19	chr2:51259693-51259743	SKMC	muscle:	n/a
20	chr2:51260739-51260789	Caco-2	colon:	n/a
21	chr2:51254132-51254182	LNCaP	prostate:	n/a
22	chr2:51255324-51255374	Hepatocyte	liver:	n/a
23	chr2:51240310-51240360	NB4	blood:	n/a
24	chr2:51255306-51255356	K562	blood:	n/a
25	chr2:51240310-51240360	AG04449	skin:	fetal
26	chr2:51260399-51260449	NT2-D1	testis:	n/a
27	chr2:51231649-51231699	HL-60	blood:	n/a
28	chr2:51254170-51254220	K562	blood:	n/a
29	chr2:51379080-51379130	H1-hESC	embryonic stem cell:	embryo
30	chr2:51255306-51255356	CMK	blood:	n/a
31	chr2:51218880-51218930	HEEpiC	esophagus:	n/a
32	chr2:51240310-51240360	MCF-7	breast:	n/a
33	chr2:51259786-51259836	HCPEpiC	choroid plexus:	n/a
34	chr2:51259693-51259743	HEK293	kidney:	embryo
35	chr2:51259697-51259747	NHDF-neo	bronchial:	n/a
36	chr2:51259552-51259602	RPTEC	kidney:	n/a
37	chr2:51446925-51446975	RPTEC	kidney:	n/a
38	chr2:51379080-51379130	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:51259786-51259836	MCF10A-Er-Src	breast:	n/a
40	chr2:51254102-51254152	GM19239	blood:	n/a
41	chr2:51254170-51254220	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:51254132-51254182	NB4	blood:	n/a
43	chr2:51379080-51379130	AG09309	skin:	n/a
44	chr2:51254170-51254220	RPTEC	kidney:	n/a
45	chr2:51259493-51259543	Hepatocyte	liver:	n/a
46	chr2:51379080-51379130	ProgFib	skin:	n/a
47	chr2:51259693-51259743	LNCaP	prostate:	n/a
48	chr2:51259693-51259743	PFSK-1	brain:	n/a
49	chr2:51254823-51254873	GM12878	blood:	n/a
50	chr2:51254981-51255031	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
2	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
3	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
4	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
5	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
6	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
7	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
8	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
9	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
10	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
11	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
12	chr2:51288072..51290967-chr2:232569534..232571521,2	MCF-7	breast:
13	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
14	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
2	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1
3	lnc-NRXN1-4	chr2:51423222-51423493	l_1834_chr2:51413303-51423493_76bGuttman_hLF
4	lnc-NRXN1-3	chr2:51283633-51283791	NONHSAT070652
5	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
6	lnc-NRXN1-4	chr2:51414157-51414291	l_1834_chr2:51413303-51423493_76bGuttman_hLF
7	lnc-NRXN1-3	chr2:51282723-51282956	NONHSAT070652
8	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
9	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652
10	lnc-NRXN1-1	chr2:51430129-51430299	ENSG00000237374
11	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
12	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
13	lnc-CHAC2-4	chr2:51279495-51279592	ENSG00000231918.1
14	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
15	lnc-NRXN1-4	chr2:51413304-51413539	l_1834_chr2:51413303-51423493_76bGuttman_hLF
16	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
17	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
18	lnc-NRXN1-3	chr2:51283579-51283793	l_1833_chr2:51283578-51306188_testes

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

Extended variants
information (count: 8421 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:8421 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10490165	chr2:51188566-51188567	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529599663	chr2:51188592-51188593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547830992	chr2:51188598-51188599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569405007	chr2:51188601-51188602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536786587	chr2:51188619-51188620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76359844	chr2:51188648-51188649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533691348	chr2:51188650-51188651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140033437	chr2:51188667-51188668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547705336	chr2:51188683-51188684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551987820	chr2:51188703-51188704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554126552	chr2:51188720-51188721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540896184	chr2:51188820-51188821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571828612	chr2:51188843-51188844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35746798	chr2:51188875-51188876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543039815	chr2:51188886-51188887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376562738	chr2:51188925-51188926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180856953	chr2:51188946-51188947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576594139	chr2:51188951-51188952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369562427	chr2:51188952-51188953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565395474	chr2:51188978-51188979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185044214	chr2:51189001-51189002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79850282	chr2:51189047-51189048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559222427	chr2:51189057-51189058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560754092	chr2:51189102-51189103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34227089	chr2:51189103-51189104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72533915	chr2:51189111-51189112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs397873368	chr2:51189112-51189113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529979659	chr2:51189124-51189125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11886723	chr2:51189125-51189126	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548156466	chr2:51189191-51189192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139255861	chr2:51189234-51189235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs70958634	chr2:51189236-51189237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62142993	chr2:51189312-51189313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114935278	chr2:51189323-51189324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112625636	chr2:51189324-51189325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189505782	chr2:51189330-51189331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376534069	chr2:51189357-51189358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538809525	chr2:51189366-51189367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554391224	chr2:51189385-51189386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372306396	chr2:51189432-51189433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182086185	chr2:51189452-51189453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186847902	chr2:51189470-51189471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576472007	chr2:51189476-51189477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116657517	chr2:51189519-51189520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558735625	chr2:51189520-51189521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577317510	chr2:51189563-51189564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540862241	chr2:51189575-51189576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200145354	chr2:51189656-51189657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77064406	chr2:51189659-51189660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4031417	chr2:51189681-51189682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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	18451855	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:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51176400-51190600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:51180400-51189400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:51183200-51190000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:51185400-51189000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:51185600-51190200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:51188000-51189400	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr2:51188800-51189800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:51189000-51189800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr2:51189200-51189800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:51189400-51190200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:51189400-51190200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr2:51189400-51190400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr2:51189800-51191000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr2:51190000-51190400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr2:51190200-51190800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr2:51190200-51192000	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr2:51190400-51221600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr2:51190600-51190800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr2:51191000-51191200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr2:51191200-51199000	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr2:51192000-51200400	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr2:51198000-51205600	Weak transcription	Fetal Brain Male	brain
23	chr2:51199000-51200800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:51199400-51200000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr2:51199800-51200200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr2:51200000-51200600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr2:51200200-51203800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr2:51200400-51200600	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr2:51200400-51201600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr2:51200600-51201000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr2:51200600-51202800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr2:51200800-51201200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr2:51201000-51201200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr2:51201200-51204200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:51201200-51205800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr2:51201400-51202000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr2:51201600-51202800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr2:51202000-51202400	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:51202000-51203800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:51202400-51203200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr2:51202400-51203400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:51202600-51203000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr2:51202800-51203000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr2:51202800-51203200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr2:51202800-51203200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:51203800-51204000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr2:51205000-51205400	Enhancers	Fetal Brain Female	brain
48	chr2:51205400-51205800	Weak transcription	Fetal Brain Female	brain
49	chr2:51205600-51205800	Enhancers	Fetal Brain Male	brain
50	chr2:51205600-51207400	Enhancers	Brain Germinal Matrix	brain

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