Variant report

Variant	nsv876600
Chromosome Location	chr3:20273130-20674832
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1698)
CpG islands
(count:551)
Chromatin interactive
region (count:83)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1698 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20366598-20367214	K562	blood:	n/a	n/a
2	ARID3A	chr3:20362800-20363279	K562	blood:	n/a	n/a
3	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:20361861-20362463	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:20553373-20553610	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:20630843-20631125	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:20368591-20368761	K562	blood:	n/a	n/a
8	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
9	ARID3A	chr3:20371522-20371864	K562	blood:	n/a	n/a
10	ARID3A	chr3:20364750-20365312	K562	blood:	n/a	n/a
11	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
12	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
13	ARID3A	chr3:20363620-20364094	K562	blood:	n/a	chr3:20363734-20363750
14	ATF1	chr3:20346503-20346616	K562	blood:	n/a	n/a
15	ATF1	chr3:20521702-20521870	K562	blood:	n/a	n/a
16	ATF1	chr3:20364790-20365451	K562	blood:	n/a	n/a
17	ATF1	chr3:20366606-20366910	K562	blood:	n/a	n/a
18	ATF2	chr3:20288131-20288515	GM12878	blood:	n/a	n/a
19	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr3:20288074-20288600	GM12878	blood:	n/a	n/a
21	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
22	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
23	BACH1	chr3:20363669-20363903	K562	blood:	n/a	n/a
24	BACH1	chr3:20616608-20616882	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr3:20535546-20535645	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:20578833-20579051	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr3:20492139-20492474	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr3:20536253-20536368	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr3:20492146-20492486	K562	blood:	n/a	n/a
30	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr3:20366536-20366578	K562	blood:	n/a	n/a
32	BACH1	chr3:20649604-20649855	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr3:20394371-20394578	K562	blood:	n/a	n/a
34	BATF	chr3:20277379-20277647	GM12878	blood:	n/a	n/a
35	BATF	chr3:20277377-20277645	GM12878	blood:	n/a	n/a
36	BATF	chr3:20288158-20288422	GM12878	blood:	n/a	chr3:20288290-20288301
37	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
38	BATF	chr3:20288183-20288438	GM12878	blood:	n/a	chr3:20288290-20288301
39	BCL11A	chr3:20288232-20288418	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:20288193-20288461	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:20371437-20371693	H1-hESC	embryonic stem cell:	n/a	n/a
42	BHLHE40	chr3:20361903-20362390	HepG2	liver:	n/a	n/a
43	BHLHE40	chr3:20381816-20382255	K562	blood:	n/a	n/a
44	BHLHE40	chr3:20371536-20371904	K562	blood:	n/a	n/a
45	BHLHE40	chr3:20355407-20355580	A549	lung:	n/a	n/a
46	BHLHE40	chr3:20366210-20366396	K562	blood:	n/a	n/a
47	BHLHE40	chr3:20364697-20365365	K562	blood:	n/a	n/a
48	BHLHE40	chr3:20394266-20394730	K562	blood:	n/a	n/a
49	BHLHE40	chr3:20306641-20306956	K562	blood:	n/a	n/a
50	BRCA1	chr3:20381852-20382113	Hela-S3	cervix:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20589671-20589721	ECC-1	luminal epithelium:	n/a
2	chr3:20418856-20418906	AG09309	skin:	n/a
3	chr3:20589671-20589721	ECC-1	luminal epithelium:	n/a
4	chr3:20418856-20418906	AG09309	skin:	n/a
5	chr3:20371290-20371340	Hepatocyte	liver:	n/a
6	chr3:20371290-20371340	HCPEpiC	choroid plexus:	n/a
7	chr3:20418856-20418906	MCF10A-Er-Src	breast:	n/a
8	chr3:20589671-20589721	HEEpiC	esophagus:	n/a
9	chr3:20321584-20321634	CMK	blood:	n/a
10	chr3:20575513-20575563	AG10803	skin:	n/a
11	chr3:20589671-20589721	SK-N-SH	brain:	n/a
12	chr3:20412342-20412392	GM12891	blood:	n/a
13	chr3:20575513-20575563	HRPEpiC	eye:	n/a
14	chr3:20448283-20448333	NT2-D1	testis:	n/a
15	chr3:20321584-20321634	Hela-S3	cervix:	n/a
16	chr3:20589760-20589810	MCF10A-Er-Src	breast:	n/a
17	chr3:20522301-20522351	SAEC	small airway:	n/a
18	chr3:20589760-20589810	HAEpiC	amniotic membrane:	n/a
19	chr3:20589760-20589810	GM12878	blood:	n/a
20	chr3:20448283-20448333	HMEC	breast:	n/a
21	chr3:20522301-20522351	HAEpiC	amniotic membrane:	n/a
22	chr3:20448283-20448333	HCPEpiC	choroid plexus:	n/a
23	chr3:20522301-20522351	SK-N-MC	brain:	n/a
24	chr3:20321584-20321634	HepG2	liver:	n/a
25	chr3:20448283-20448333	AG04450	lung:	fetal
26	chr3:20418856-20418906	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:20371290-20371340	Jurkat	blood:	n/a
28	chr3:20589671-20589721	HRPEpiC	eye:	n/a
29	chr3:20589760-20589810	SK-N-SH_RA	brain:	n/a
30	chr3:20448283-20448333	HEEpiC	esophagus:	n/a
31	chr3:20412342-20412392	Hepatocyte	liver:	n/a
32	chr3:20371290-20371340	SK-N-MC	brain:	n/a
33	chr3:20321584-20321634	NT2-D1	testis:	n/a
34	chr3:20412342-20412392	PrEC	prostate:	n/a
35	chr3:20575513-20575563	U87	brain:	n/a
36	chr3:20412342-20412392	IMR90	lung:	fetal
37	chr3:20321584-20321634	HCF	heart:	n/a
38	chr3:20522301-20522351	HRPEpiC	eye:	n/a
39	chr3:20418856-20418906	PrEC	prostate:	n/a
40	chr3:20412342-20412392	AG04450	lung:	fetal
41	chr3:20448283-20448333	NHDF-neo	bronchial:	n/a
42	chr3:20321584-20321634	AG09319	gingival:	n/a
43	chr3:20371290-20371340	AG10803	skin:	n/a
44	chr3:20589760-20589810	BJ	skin:	n/a
45	chr3:20418856-20418906	LNCaP	prostate:	n/a
46	chr3:20589760-20589810	SK-N-SH	brain:	n/a
47	chr3:20371290-20371340	HIPEpiC	eye:	n/a
48	chr3:20522301-20522351	HUVEC	blood vessel:	n/a
49	chr3:20522301-20522351	HCT-116	colon:	n/a
50	chr3:20575513-20575563	CMK	blood:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
2	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
3	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
4	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
5	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
6	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
7	chr3:20248922..20251335-chr3:20323167..20325698,2	K562	blood:
8	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
9	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
10	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
11	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
12	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
13	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
14	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
15	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
16	chr3:20381763..20382471-chr3:21525223..21526354,4	MCF-7	breast:
17	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
18	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
19	chr3:20558136..20559640-chr3:20560230..20563085,2	K562	blood:
20	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
21	chr3:20225982..20227551-chr3:20349845..20352725,2	K562	blood:
22	chr17:57920861..57923845-chr3:20581102..20583235,2	MCF-7	breast:
23	chr3:20381636..20382451-chr3:20971371..20972187,4	MCF-7	breast:
24	chr3:20576686..20578791-chr3:20582822..20585429,2	MCF-7	breast:
25	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
26	chr3:20514130..20516158-chr3:20517415..20519398,2	K562	blood:
27	chr3:20269133..20272394-chr3:20272728..20275710,3	K562	blood:
28	chr1:121485224..121485931-chr3:20620646..20621369,2	MCF-7	breast:
29	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
30	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
31	chr3:20553254..20553852-chr3:21257816..21258713,2	MCF-7	breast:
32	chr3:20514130..20516158-chr3:20517415..20519398,2	K562	blood:
33	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
34	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
35	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
36	chr3:20545213..20547317-chr3:20547570..20549760,2	K562	blood:
37	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
38	chr3:20553366..20553898-chr3:21257700..21258348,2	MCF-7	breast:
39	chr3:20618172..20620795-chr3:20622169..20624863,2	MCF-7	breast:
40	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:
41	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
42	chr3:20577616..20580422-chr3:20581225..20583967,3	K562	blood:
43	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
44	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:
45	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
46	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
47	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
48	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
49	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
50	chr3:20558136..20559640-chr3:20560230..20563085,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
2	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622
3	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1
4	lnc-KAT2B-6	chr3:20286533-20287951	NONHSAT088619
5	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
6	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595
7	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595
8	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
9	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
10	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
11	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595

No data

Variant related genes	Relation type
ENSG00000261734	TF binding region
RNU6-815P	TF binding region
RNU6-822P	TF binding region
ENSG00000231304	TF binding region
ENSG00000261734	CpG island
RNU6-815P	CpG island
RNU6-822P	CpG island
ENSG00000231304	CpG island
ENSG00000206807	chromatin interactions

Extended variants
information (count: 10489 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10489 , 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	rs9310615	chr3:20273130-20273131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563703340	chr3:20273154-20273155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559014197	chr3:20273283-20273284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148614746	chr3:20273321-20273322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181795362	chr3:20273352-20273353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553901684	chr3:20273365-20273366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533077892	chr3:20273451-20273452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572124826	chr3:20273461-20273462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142043634	chr3:20273477-20273478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79893431	chr3:20273491-20273492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78412090	chr3:20273493-20273494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560908174	chr3:20273500-20273501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531232312	chr3:20273506-20273507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11713069	chr3:20273528-20273529	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs11713070	chr3:20273531-20273532	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs532170719	chr3:20273640-20273641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547140851	chr3:20273825-20273826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565545606	chr3:20273844-20273845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375661023	chr3:20273870-20273871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184923157	chr3:20273875-20273876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188266674	chr3:20273877-20273878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs58534771	chr3:20273898-20273899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570011120	chr3:20273953-20273954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537085129	chr3:20274004-20274005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181030124	chr3:20274013-20274014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186435289	chr3:20274032-20274033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191287329	chr3:20274051-20274052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558399044	chr3:20274089-20274090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553565470	chr3:20274091-20274092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575104146	chr3:20274104-20274105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542682785	chr3:20274146-20274147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576467164	chr3:20274197-20274198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181493327	chr3:20274252-20274253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150698868	chr3:20274273-20274274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578256018	chr3:20274290-20274291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185742429	chr3:20274304-20274305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190543767	chr3:20274342-20274343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532231161	chr3:20274350-20274351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569262971	chr3:20274365-20274366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145964593	chr3:20274400-20274401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183076226	chr3:20274435-20274436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143835396	chr3:20274513-20274514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548647710	chr3:20274563-20274564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187946700	chr3:20274577-20274578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562477811	chr3:20274659-20274660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552242911	chr3:20274707-20274708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570869193	chr3:20274737-20274738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189680049	chr3:20274744-20274745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553725870	chr3:20274833-20274834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4857927	chr3:20274846-20274847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20272600-20276000	Enhancers	Liver	Liver
2	chr3:20273400-20273800	Enhancers	Fetal Intestine Large	intestine
3	chr3:20273600-20274600	Enhancers	Fetal Intestine Small	intestine
4	chr3:20273800-20275200	Weak transcription	Fetal Intestine Large	intestine
5	chr3:20274400-20277200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:20274600-20275000	Weak transcription	Fetal Intestine Small	intestine
7	chr3:20274600-20275400	Enhancers	Fetal Kidney	kidney
8	chr3:20274600-20275400	Enhancers	Fetal Lung	lung
9	chr3:20275000-20275600	Enhancers	Fetal Intestine Small	intestine
10	chr3:20275200-20275600	Enhancers	Fetal Intestine Large	intestine
11	chr3:20275600-20278000	Weak transcription	Fetal Intestine Large	intestine
12	chr3:20275600-20278000	Weak transcription	Fetal Intestine Small	intestine
13	chr3:20276000-20276600	Weak transcription	Liver	Liver
14	chr3:20276600-20278600	Enhancers	Liver	Liver
15	chr3:20276800-20277400	Enhancers	GM12878-XiMat	blood
16	chr3:20277200-20277400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr3:20278000-20278400	Enhancers	Fetal Intestine Small	intestine
18	chr3:20278000-20278600	Enhancers	Fetal Intestine Large	intestine
19	chr3:20278000-20278600	Enhancers	Stomach Mucosa	stomach
20	chr3:20278400-20282200	Weak transcription	Fetal Intestine Small	intestine
21	chr3:20278600-20282000	Weak transcription	Liver	Liver
22	chr3:20281200-20282400	Enhancers	Ovary	ovary
23	chr3:20281400-20282800	Enhancers	Aorta	Aorta
24	chr3:20281600-20282000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:20281600-20282000	Enhancers	Spleen	Spleen
26	chr3:20281600-20282600	Enhancers	Esophagus	oesophagus
27	chr3:20282800-20284000	Weak transcription	Aorta	Aorta
28	chr3:20284000-20284200	Enhancers	Aorta	Aorta
29	chr3:20287200-20289000	Enhancers	GM12878-XiMat	blood
30	chr3:20291800-20292200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr3:20291800-20292400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:20291800-20292400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:20291800-20293400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr3:20291800-20293400	Enhancers	H9 Cell Line	embryonic stem cell
35	chr3:20291800-20293600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr3:20292000-20292200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr3:20292000-20293200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr3:20292000-20293200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr3:20292000-20293200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr3:20292000-20293200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:20292200-20292400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr3:20292200-20292400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr3:20292200-20292800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr3:20292200-20293400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr3:20292200-20293400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr3:20292400-20292600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr3:20292400-20292800	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr3:20292400-20293200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:20292400-20296000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr3:20292600-20292800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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