Variant report

Variant	nsv1029589
Chromosome Location	chr8:11392880-11429147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1916)
CpG islands
(count:979)
Chromatin interactive
region (count:33)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1916 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:11402856-11404232	GM12878	blood:	n/a	n/a
2	ATF2	chr8:11396380-11397039	GM12878	blood:	n/a	n/a
3	ATF2	chr8:11411191-11411587	GM12878	blood:	n/a	n/a
4	ATF2	chr8:11395042-11395933	GM12878	blood:	n/a	n/a
5	ATF2	chr8:11396080-11397110	GM12878	blood:	n/a	n/a
6	ATF2	chr8:11416020-11416567	GM12878	blood:	n/a	n/a
7	ATF2	chr8:11402957-11404256	GM12878	blood:	n/a	n/a
8	ATF2	chr8:11421987-11422609	GM12878	blood:	n/a	n/a
9	ATF2	chr8:11411156-11411616	GM12878	blood:	n/a	n/a
10	ATF2	chr8:11418701-11418997	GM12878	blood:	n/a	n/a
11	ATF2	chr8:11416028-11417072	GM12878	blood:	n/a	n/a
12	ATF2	chr8:11394202-11396059	GM12878	blood:	n/a	n/a
13	ATF2	chr8:11421419-11423115	GM12878	blood:	n/a	n/a
14	BACH1	chr8:11411316-11411548	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:11422005-11422013	K562	blood:	n/a	n/a
16	BACH1	chr8:11421479-11422408	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr8:11403808-11404213	GM12878	blood:	n/a	n/a
18	BATF	chr8:11403094-11403686	GM12878	blood:	n/a	n/a
19	BATF	chr8:11403782-11404243	GM12878	blood:	n/a	n/a
20	BATF	chr8:11403194-11403693	GM12878	blood:	n/a	n/a
21	BATF	chr8:11416168-11416454	GM12878	blood:	n/a	n/a
22	BATF	chr8:11395253-11395756	GM12878	blood:	n/a	n/a
23	BATF	chr8:11396541-11396828	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:11403188-11403628	GM12878	blood:	n/a	chr8:11403287-11403296
25	BCL11A	chr8:11403087-11403748	GM12878	blood:	n/a	chr8:11403287-11403296
26	BCL11A	chr8:11395105-11395737	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:11403843-11404135	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:11416159-11416609	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:11403784-11404237	GM12878	blood:	n/a	n/a
30	BCL3	chr8:11395141-11395868	GM12878	blood:	n/a	chr8:11395756-11395769
31	BCL3	chr8:11416115-11417171	GM12878	blood:	n/a	n/a
32	BCL3	chr8:11396535-11396917	GM12878	blood:	n/a	n/a
33	BCL3	chr8:11403089-11403697	GM12878	blood:	n/a	chr8:11403287-11403296
34	BCL3	chr8:11421891-11422340	A549	lung:	n/a	chr8:11422235-11422243
35	BCL3	chr8:11395245-11395778	GM12878	blood:	n/a	chr8:11395756-11395769
36	BCL3	chr8:11418521-11418953	GM12878	blood:	n/a	chr8:11418702-11418710
37	BCL3	chr8:11421867-11422432	GM12878	blood:	n/a	chr8:11422235-11422243
38	BCL3	chr8:11422664-11423817	GM12878	blood:	n/a	n/a
39	BCL3	chr8:11403124-11403747	GM12878	blood:	n/a	chr8:11403287-11403296
40	BCL3	chr8:11403839-11404194	GM12878	blood:	n/a	n/a
41	BCL3	chr8:11423267-11423719	GM12878	blood:	n/a	n/a
42	BCL3	chr8:11421305-11422586	GM12878	blood:	n/a	chr8:11422235-11422243
43	BCLAF1	chr8:11402954-11403779	GM12878	blood:	n/a	chr8:11403287-11403296
44	BCLAF1	chr8:11394904-11396045	GM12878	blood:	n/a	chr8:11395756-11395769
45	BCLAF1	chr8:11421273-11422842	GM12878	blood:	n/a	chr8:11422235-11422243
46	BCLAF1	chr8:11416069-11416680	GM12878	blood:	n/a	n/a
47	BCLAF1	chr8:11403056-11404256	GM12878	blood:	n/a	chr8:11403287-11403296
48	BCLAF1	chr8:11416733-11417157	GM12878	blood:	n/a	n/a
49	BCLAF1	chr8:11411229-11411661	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:11424543-11425004	GM12878	blood:	n/a	chr8:11424896-11424905

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11413234-11413284	IMR90	lung:	fetal
2	chr8:11422167-11422217	NHDF-neo	bronchial:	n/a
3	chr8:11413043-11413093	HCM	heart:	n/a
4	chr8:11413234-11413284	IMR90	lung:	fetal
5	chr8:11422167-11422217	NHDF-neo	bronchial:	n/a
6	chr8:11413043-11413093	HCM	heart:	n/a
7	chr8:11418058-11418108	RPTEC	kidney:	n/a
8	chr8:11413186-11413236	T-47D	breast:	n/a
9	chr8:11422167-11422217	BE2_C	brain:	n/a
10	chr8:11422167-11422217	CMK	blood:	n/a
11	chr8:11413186-11413236	BE2_C	brain:	n/a
12	chr8:11402219-11402269	AG09309	skin:	n/a
13	chr8:11421594-11421644	Jurkat	blood:	n/a
14	chr8:11416365-11416415	HCPEpiC	choroid plexus:	n/a
15	chr8:11413043-11413093	GM12891	blood:	n/a
16	chr8:11413234-11413284	SK-N-SH_RA	brain:	n/a
17	chr8:11422433-11422483	HL-60	blood:	n/a
18	chr8:11422167-11422217	HRPEpiC	eye:	n/a
19	chr8:11421934-11421984	BJ	skin:	n/a
20	chr8:11413186-11413236	HRCEpiC	kidney:	n/a
21	chr8:11411487-11411537	HCT-116	colon:	n/a
22	chr8:11417517-11417567	ProgFib	skin:	n/a
23	chr8:11421594-11421644	NHBE	bronchial:	n/a
24	chr8:11413186-11413236	HCPEpiC	choroid plexus:	n/a
25	chr8:11422433-11422483	MCF-7	breast:	n/a
26	chr8:11402219-11402269	H1-hESC	embryonic stem cell:	embryo
27	chr8:11413043-11413093	NB4	blood:	n/a
28	chr8:11419707-11419757	ECC-1	luminal epithelium:	n/a
29	chr8:11424789-11424839	GM19239	blood:	n/a
30	chr8:11421934-11421984	T-47D	breast:	n/a
31	chr8:11413234-11413284	NB4	blood:	n/a
32	chr8:11422433-11422483	NB4	blood:	n/a
33	chr8:11413043-11413093	HMEC	breast:	n/a
34	chr8:11413234-11413284	NHDF-neo	bronchial:	n/a
35	chr8:11422167-11422217	A549	lung:	n/a
36	chr8:11424789-11424839	ProgFib	skin:	n/a
37	chr8:11413186-11413236	NHDF-neo	bronchial:	n/a
38	chr8:11417517-11417567	AG09309	skin:	n/a
39	chr8:11419707-11419757	HCF	heart:	n/a
40	chr8:11417517-11417567	PFSK-1	brain:	n/a
41	chr8:11421934-11421984	NHBE	bronchial:	n/a
42	chr8:11413043-11413093	HNPCEpiC	eye:	n/a
43	chr8:11413043-11413093	RPTEC	kidney:	n/a
44	chr8:11418058-11418108	BE2_C	brain:	n/a
45	chr8:11413043-11413093	HRPEpiC	eye:	n/a
46	chr8:11422730-11422780	SK-N-SH_RA	brain:	n/a
47	chr8:11421934-11421984	NHDF-neo	bronchial:	n/a
48	chr8:11402219-11402269	PANC-1	pancreas:	n/a
49	chr8:11421934-11421984	HAEpiC	amniotic membrane:	n/a
50	chr8:11411487-11411537	HCPEpiC	choroid plexus:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
2	chr8:11271149..11271854-chr8:11412541..11413131,2	MCF-7	breast:
3	chr8:11379820..11382247-chr8:11420170..11422972,2	MCF-7	breast:
4	chr8:11421719..11422643-chr8:11446645..11447610,4	K562	blood:
5	chr8:11389216..11391992-chr8:11394333..11396573,2	MCF-7	breast:
6	chr8:11421707..11422824-chr8:11816126..11817083,9	K562	blood:
7	chr8:11331911..11334130-chr8:11408479..11410507,2	MCF-7	breast:
8	chr8:11422187..11423813-chr8:11429710..11432078,2	MCF-7	breast:
9	chr8:11418474..11420140-chr8:11572245..11574135,2	K562	blood:
10	chr8:11426984..11428613-chr8:11595138..11596810,2	K562	blood:
11	chr8:11270794..11271511-chr8:11421638..11422402,4	MCF-7	breast:
12	chr8:11411028..11411558-chr8:11446874..11447601,2	K562	blood:
13	chr8:11421781..11422781-chr8:11603539..11604516,9	K562	blood:
14	chr8:11399538..11402795-chr8:11403672..11407842,3	K562	blood:
15	chr8:11424667..11425261-chr8:11603180..11604185,3	MCF-7	breast:
16	chr8:11428917..11429796-chr8:11587902..11588451,3	MCF-7	breast:
17	chr8:11409226..11411204-chr8:11413317..11416179,2	K562	blood:
18	chr8:11421842..11422772-chr8:11603355..11604431,7	MCF-7	breast:
19	chr8:11390853..11393388-chr8:11395895..11397560,2	K562	blood:
20	chr8:11410226..11416148-chr8:11417699..11422629,5	K562	blood:
21	chr8:11410226..11416148-chr8:11417699..11422629,5	K562	blood:
22	chr8:11421778..11422656-chr8:11816114..11817045,3	MCF-7	breast:
23	chr8:11390853..11393388-chr8:11395895..11397560,2	K562	blood:
24	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
25	chr8:11286965..11287640-chr8:11410754..11411417,2	MCF-7	breast:
26	chr8:11394487..11397060-chr8:11401001..11403258,2	K562	blood:
27	chr8:11422237..11424811-chr8:11602615..11604781,2	MCF-7	breast:
28	chr8:11266732..11267234-chr8:11421696..11422273,2	K562	blood:
29	chr8:11420542..11422083-chr8:11608840..11610442,2	MCF-7	breast:
30	chr8:11422289..11424857-chr8:11598109..11600598,2	MCF-7	breast:
31	chr8:11421685..11422256-chr8:11800840..11801381,2	K562	blood:
32	chr8:11409226..11411204-chr8:11413317..11416179,2	K562	blood:
33	chr8:11424324..11425489-chr8:11573800..11574792,3	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-148O21.2.1-2	chr8:11415399-11415531	ENSG00000255518.1
2	lnc-RP11-148O21.2.1-1	chr8:11416421-11416495	ENSG00000255354.1
3	lnc-RP11-148O21.2.1-1	chr8:11417293-11417529	ENSG00000255354.1
4	lnc-RP11-148O21.3.1-1	chr8:11410733-11411089	ENSG00000254774.1
5	lnc-RP11-148O21.3.1-2	chr8:11409997-11410500	ENSG00000269954.1
6	lnc-RP11-148O21.2.1-1	chr8:11415975-11416256	ENSG00000255354.1
7	lnc-RP11-148O21.3.1-1	chr8:11411639-11411716	ENSG00000254774.1
8	lnc-RP11-148O21.2.1-2	chr8:11413760-11414170	ENSG00000255518.1

No data

Variant related genes	Relation type
ENSG00000255518	TF binding region
LINC00208	TF binding region
ENSG00000269954	TF binding region
BLK	TF binding region
ENSG00000255354	TF binding region
ENSG00000254774	TF binding region
ENSG00000255518	CpG island
LINC00208	CpG island
ENSG00000269954	CpG island
BLK	CpG island
ENSG00000255354	CpG island
ENSG00000254774	CpG island
ENSG00000255518	chromatin interactions
ENSG00000269954	chromatin interactions
ENSG00000154319	chromatin interactions
ENSG00000254774	chromatin interactions
ENSG00000136573	chromatin interactions

Extended variants
information (count: 2307 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:2307 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9329246	chr8:11392880-11392881	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568751940	chr8:11392920-11392921	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536191379	chr8:11392956-11392957	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2248791	chr8:11393025-11393026	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs190158727	chr8:11393058-11393059	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs181780907	chr8:11393087-11393088	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs185822133	chr8:11393111-11393112	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs371251826	chr8:11393121-11393122	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs576906101	chr8:11393138-11393139	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs190294691	chr8:11393157-11393158	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs182521104	chr8:11393158-11393159	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs577818923	chr8:11393181-11393182	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs78161669	chr8:11393200-11393201	Genic enhancers Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142248471	chr8:11393253-11393254	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563095363	chr8:11393256-11393257	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575104733	chr8:11393286-11393287	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558371656	chr8:11393287-11393288	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533748979	chr8:11393299-11393300	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553761725	chr8:11393309-11393310	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573840246	chr8:11393325-11393326	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62489135	chr8:11393329-11393330	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs528603419	chr8:11393355-11393356	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546959220	chr8:11393386-11393387	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562083202	chr8:11393392-11393393	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113402001	chr8:11393416-11393417	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs76927874	chr8:11393450-11393451	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs569435177	chr8:11393462-11393463	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs141690324	chr8:11393477-11393478	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555196376	chr8:11393504-11393505	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs551734479	chr8:11393508-11393509	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs570511450	chr8:11393509-11393510	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs534434530	chr8:11393560-11393561	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs147058976	chr8:11393592-11393593	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs117291495	chr8:11393598-11393599	Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs116448234	chr8:11393610-11393611	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs62489136	chr8:11393617-11393618	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560895657	chr8:11393689-11393690	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545954692	chr8:11393701-11393702	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557704885	chr8:11393728-11393729	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2248700	chr8:11393745-11393746	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs540395068	chr8:11393748-11393749	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2248699	chr8:11393764-11393765	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs2248696	chr8:11393803-11393804	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs544659094	chr8:11393820-11393821	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs202095593	chr8:11393846-11393847	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79142660	chr8:11393863-11393864	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533485425	chr8:11393959-11393960	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs35772338	chr8:11393965-11393966	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7002570	chr8:11393975-11393976	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141027743	chr8:11393984-11393985	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Gastric cancer	22315472	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11383000-11407000	Weak transcription	Dnd41	blood
2	chr8:11391400-11395400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:11391800-11394800	Genic enhancers	Primary B cells from cord blood	blood
4	chr8:11392200-11393000	Enhancers	GM12878-XiMat	blood
5	chr8:11392200-11395600	Genic enhancers	Primary B cells from peripheral blood	blood
6	chr8:11392200-11397200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr8:11392400-11394800	Weak transcription	Fetal Thymus	thymus
8	chr8:11392400-11396800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:11392400-11397200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr8:11392400-11403400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr8:11393000-11393200	Flanking Active TSS	GM12878-XiMat	blood
12	chr8:11393200-11393400	Enhancers	GM12878-XiMat	blood
13	chr8:11393400-11393600	Flanking Active TSS	GM12878-XiMat	blood
14	chr8:11393600-11394200	Enhancers	GM12878-XiMat	blood
15	chr8:11394200-11395200	Flanking Active TSS	GM12878-XiMat	blood
16	chr8:11394800-11395200	Enhancers	Primary B cells from cord blood	blood
17	chr8:11394800-11396000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr8:11394800-11396400	Enhancers	Fetal Thymus	thymus
19	chr8:11395000-11395600	Enhancers	Liver	Liver
20	chr8:11395000-11395800	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr8:11395000-11396400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:11395200-11395400	Enhancers	Fetal Kidney	kidney
23	chr8:11395200-11395600	Enhancers	GM12878-XiMat	blood
24	chr8:11395200-11395800	Bivalent Enhancer	Fetal Lung	lung
25	chr8:11395200-11397600	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr8:11395400-11395600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr8:11395400-11395800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr8:11395400-11395800	Enhancers	Lung	lung
29	chr8:11395600-11395800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr8:11395600-11395800	Active TSS	Spleen	Spleen
31	chr8:11395600-11396400	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
32	chr8:11395600-11398000	Flanking Active TSS	GM12878-XiMat	blood
33	chr8:11395800-11396000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr8:11395800-11396200	Weak transcription	Spleen	Spleen
35	chr8:11396200-11396400	Enhancers	Spleen	Spleen
36	chr8:11396400-11396800	Genic enhancers	Primary B cells from peripheral blood	blood
37	chr8:11396400-11400000	Weak transcription	Spleen	Spleen
38	chr8:11396600-11397600	Enhancers	Fetal Lung	lung
39	chr8:11396800-11397000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr8:11396800-11397400	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr8:11396800-11398800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:11397200-11397400	Enhancers	Primary hematopoietic stem cells	blood
43	chr8:11397200-11397800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:11397400-11398200	Genic enhancers	Primary B cells from peripheral blood	blood
45	chr8:11397600-11398000	Enhancers	Primary B cells from cord blood	blood
46	chr8:11397600-11401000	Weak transcription	Fetal Lung	lung
47	chr8:11398000-11398200	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr8:11398000-11399200	Enhancers	GM12878-XiMat	blood
49	chr8:11398200-11398600	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr8:11398200-11400400	Enhancers	Primary B cells from cord blood	blood

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