Variant report

Variant	esv2755529
Chromosome Location	chr1:165813862-165858354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1040)
CpG islands
(count:245)
Chromatin interactive
region (count:83)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:165825244-165825728	K562	blood:	n/a	n/a
2	ARID3A	chr1:165826411-165826816	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:165815456-165815907	K562	blood:	n/a	n/a
4	ARID3A	chr1:165856237-165856809	HepG2	liver:	n/a	n/a
5	ATF1	chr1:165820344-165820573	K562	blood:	n/a	n/a
6	ATF1	chr1:165840696-165840993	K562	blood:	n/a	n/a
7	ATF1	chr1:165837253-165837261	K562	blood:	n/a	n/a
8	ATF1	chr1:165828202-165828263	K562	blood:	n/a	n/a
9	ATF2	chr1:165846985-165847652	GM12878	blood:	n/a	n/a
10	ATF2	chr1:165844341-165844867	GM12878	blood:	n/a	n/a
11	ATF2	chr1:165840448-165841133	GM12878	blood:	n/a	n/a
12	ATF2	chr1:165840569-165841062	GM12878	blood:	n/a	n/a
13	ATF2	chr1:165844404-165844775	GM12878	blood:	n/a	n/a
14	ATF2	chr1:165847014-165847635	GM12878	blood:	n/a	n/a
15	BACH1	chr1:165815606-165815615	K562	blood:	n/a	n/a
16	BATF	chr1:165852301-165852617	GM12878	blood:	n/a	n/a
17	BATF	chr1:165847111-165847707	GM12878	blood:	n/a	n/a
18	BATF	chr1:165847191-165847618	GM12878	blood:	n/a	n/a
19	BATF	chr1:165840547-165840957	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:165840543-165840935	GM12878	blood:	n/a	chr1:165840757-165840766
21	BCL11A	chr1:165847154-165847586	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:165840599-165840935	GM12878	blood:	n/a	chr1:165840757-165840766
23	BCL11A	chr1:165847222-165847432	GM12878	blood:	n/a	n/a
24	BCL3	chr1:165847115-165847675	GM12878	blood:	n/a	n/a
25	BCLAF1	chr1:165847114-165847552	GM12878	blood:	n/a	n/a
26	BCLAF1	chr1:165840452-165841113	GM12878	blood:	n/a	chr1:165840757-165840766
27	BCLAF1	chr1:165840400-165841023	GM12878	blood:	n/a	chr1:165840757-165840766
28	BCLAF1	chr1:165847161-165847619	GM12878	blood:	n/a	n/a
29	BCLAF1	chr1:165844365-165844885	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:165851353-165851816	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:165840462-165841023	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:165820282-165820589	K562	blood:	n/a	n/a
33	BHLHE40	chr1:165823374-165823678	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:165847125-165847553	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:165820258-165820663	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:165815721-165815826	K562	blood:	n/a	n/a
37	BHLHE40	chr1:165826174-165826622	GM12878	blood:	n/a	n/a
38	BHLHE40	chr1:165844477-165844784	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:165854852-165854998	GM12878	blood:	n/a	n/a
40	BRCA1	chr1:165823472-165823613	GM12878	blood:	n/a	n/a
41	CBX3	chr1:165846615-165847020	K562	blood:	n/a	n/a
42	CBX3	chr1:165840507-165841327	K562	blood:	n/a	n/a
43	CBX3	chr1:165842767-165843147	K562	blood:	n/a	n/a
44	CCNT2	chr1:165815621-165815972	K562	blood:	n/a	n/a
45	CEBPB	chr1:165826462-165826837	MCF-7	breast:	n/a	n/a
46	CEBPB	chr1:165840624-165840890	GM12878	blood:	n/a	n/a
47	CEBPB	chr1:165826409-165826797	K562	blood:	n/a	n/a
48	CEBPB	chr1:165822825-165823223	K562	blood:	n/a	chr1:165823182-165823195
49	CEBPB	chr1:165827454-165827489	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:165857133-165857454	MCF-7	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:165853483-165853533	A549	lung:	n/a
2	chr1:165853483-165853533	A549	lung:	n/a
3	chr1:165843584-165843634	NHDF-neo	bronchial:	n/a
4	chr1:165843584-165843634	Hela-S3	cervix:	n/a
5	chr1:165843584-165843634	NH-A	brain:	n/a
6	chr1:165853483-165853533	Jurkat	blood:	n/a
7	chr1:165843584-165843634	AG04450	lung:	fetal
8	chr1:165823772-165823822	IMR90	lung:	fetal
9	chr1:165826270-165826320	GM12891	blood:	n/a
10	chr1:165823772-165823822	HEK293	kidney:	embryo
11	chr1:165826270-165826320	K562	blood:	n/a
12	chr1:165823772-165823822	HRE	kidney:	n/a
13	chr1:165843584-165843634	SK-N-SH	brain:	n/a
14	chr1:165823772-165823822	HCM	heart:	n/a
15	chr1:165853483-165853533	HCM	heart:	n/a
16	chr1:165843584-165843634	Hepatocyte	liver:	n/a
17	chr1:165823772-165823822	CMK	blood:	n/a
18	chr1:165826270-165826320	NHDF-neo	bronchial:	n/a
19	chr1:165826270-165826320	HCPEpiC	choroid plexus:	n/a
20	chr1:165826270-165826320	HRPEpiC	eye:	n/a
21	chr1:165853483-165853533	AG04449	skin:	fetal
22	chr1:165826270-165826320	ovcar-3	ovarian:	n/a
23	chr1:165826270-165826320	GM12878	blood:	n/a
24	chr1:165853483-165853533	HRCEpiC	kidney:	n/a
25	chr1:165853483-165853533	HCT-116	colon:	n/a
26	chr1:165843584-165843634	BJ	skin:	n/a
27	chr1:165853483-165853533	PANC-1	pancreas:	n/a
28	chr1:165853483-165853533	HCPEpiC	choroid plexus:	n/a
29	chr1:165826270-165826320	Hela-S3	cervix:	n/a
30	chr1:165823772-165823822	ovcar-3	ovarian:	n/a
31	chr1:165843584-165843634	HCPEpiC	choroid plexus:	n/a
32	chr1:165823772-165823822	GM12878	blood:	n/a
33	chr1:165843584-165843634	K562	blood:	n/a
34	chr1:165843584-165843634	RPTEC	kidney:	n/a
35	chr1:165826270-165826320	BE2_C	brain:	n/a
36	chr1:165853483-165853533	HepG2	liver:	n/a
37	chr1:165853483-165853533	GM06990	blood:	n/a
38	chr1:165843584-165843634	AG09319	gingival:	n/a
39	chr1:165853483-165853533	SKMC	muscle:	n/a
40	chr1:165826270-165826320	A549	lung:	n/a
41	chr1:165823772-165823822	HepG2	liver:	n/a
42	chr1:165843584-165843634	HAEpiC	amniotic membrane:	n/a
43	chr1:165826270-165826320	CMK	blood:	n/a
44	chr1:165823772-165823822	SAEC	small airway:	n/a
45	chr1:165823772-165823822	HRPEpiC	eye:	n/a
46	chr1:165843584-165843634	SK-N-SH_RA	brain:	n/a
47	chr1:165843584-165843634	HCM	heart:	n/a
48	chr1:165843584-165843634	HRPEpiC	eye:	n/a
49	chr1:165853483-165853533	AG10803	skin:	n/a
50	chr1:165823772-165823822	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr1:165796694..165798989-chr1:165846477..165848096,2	MCF-7	breast:
2	chr1:165795539..165799937-chr1:165823038..165829386,11	MCF-7	breast:
3	chr1:165737521..165739447-chr1:165830879..165832839,2	K562	blood:
4	chr1:165828614..165831006-chr1:165847927..165850420,2	K562	blood:
5	chr1:165737074..165739760-chr1:165826771..165828478,2	K562	blood:
6	chr1:165796218..165798368-chr1:165845682..165848225,4	K562	blood:
7	chr1:165847598..165850540-chr1:165853656..165856352,3	K562	blood:
8	chr1:165847454..165850029-chr1:165851841..165853502,3	K562	blood:
9	chr1:165825199..165827895-chr1:165834221..165836941,2	K562	blood:
10	chr1:165840547..165841314-chr1:165883188..165884015,2	MCF-7	breast:
11	chr1:165847598..165850540-chr1:165853656..165856352,3	K562	blood:
12	chr1:165830166..165831693-chr1:165839207..165841395,2	MCF-7	breast:
13	chr1:165847454..165850029-chr1:165851841..165853502,3	K562	blood:
14	chr1:165840374..165842176-chr1:165842789..165845400,2	K562	blood:
15	chr1:165819266..165822080-chr1:165829077..165831771,2	MCF-7	breast:
16	chr1:165654373..165656083-chr1:165811609..165814179,2	K562	blood:
17	chr1:165819266..165822080-chr1:165829077..165831771,2	MCF-7	breast:
18	chr1:165826478..165828837-chr1:165829538..165831433,3	K562	blood:
19	chr1:165844323..165845929-chr1:165851824..165854208,2	MCF-7	breast:
20	chr1:165806407..165808791-chr1:165825833..165828310,2	MCF-7	breast:
21	chr1:165850733..165853515-chr1:165853523..165855444,2	MCF-7	breast:
22	chr1:165804707..165809840-chr1:165822123..165825220,4	K562	blood:
23	chr1:165797192..165797753-chr1:165840469..165841268,2	MCF-7	breast:
24	chr1:165812134..165815476-chr1:165816977..165818639,3	K562	blood:
25	chr1:165796641..165797306-chr1:165840359..165840882,2	K562	blood:
26	chr1:165851226..165853172-chr1:165855728..165858145,2	K562	blood:
27	chr1:165840374..165842176-chr1:165842789..165845400,2	K562	blood:
28	chr1:165840370..165840880-chr1:165883101..165884091,2	MCF-7	breast:
29	chr1:165822136..165824706-chr1:165825180..165827276,2	K562	blood:
30	chr1:165845971..165849103-chr1:165855397..165857265,3	MCF-7	breast:
31	chr1:165686871..165688066-chr1:165840434..165841110,4	MCF-7	breast:
32	chr1:165843122..165847161-chr1:165847770..165853662,6	K562	blood:
33	chr1:165795249..165797750-chr1:165827004..165828550,2	MCF-7	breast:
34	chr1:165687274..165687987-chr1:165840515..165841104,2	MCF-7	breast:
35	chr1:165815197..165817590-chr1:165830111..165832857,2	K562	blood:
36	chr1:165794990..165798842-chr1:165853370..165857191,6	K562	blood:
37	chr1:165825199..165827895-chr1:165834221..165836941,2	K562	blood:
38	chr1:165738310..165740092-chr1:165841486..165844202,2	K562	blood:
39	chr1:165851226..165853172-chr1:165855728..165858145,2	K562	blood:
40	chr1:165822075..165824045-chr1:165844384..165846604,2	K562	blood:
41	chr1:165818712..165822734-chr1:165823086..165826851,4	MCF-7	breast:
42	chr1:165796518..165799137-chr1:165848481..165850965,3	K562	blood:
43	chr1:165795506..165799769-chr1:165854711..165859131,6	MCF-7	breast:
44	chr1:165822075..165824045-chr1:165844384..165846604,2	K562	blood:
45	chr1:165812134..165815476-chr1:165816977..165818639,3	K562	blood:
46	chr1:165804707..165808619-chr1:165822123..165824856,3	K562	blood:
47	chr1:165826478..165828837-chr1:165829538..165831433,3	K562	blood:
48	chr1:165796425..165798673-chr1:165831080..165836072,5	K562	blood:
49	chr1:165857325..165860085-chr1:170499980..170501599,2	MCF-7	breast:
50	chr1:165828614..165831006-chr1:165847927..165850420,2	K562	blood:

No data

Variant related genes	Relation type
UCK2	TF binding region
UCK2	CpG island
ENSG00000224358	chromatin interactions
ENSG00000231407	chromatin interactions
ENSG00000120370	chromatin interactions
ENSG00000143179	chromatin interactions
ENSG00000143183	chromatin interactions

Extended variants
information (count: 1746 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1746 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11590711	chr1:165813862-165813863	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531235125	chr1:165813864-165813865	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537182374	chr1:165813871-165813872	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189970644	chr1:165813872-165813873	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561375601	chr1:165813927-165813928	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557403160	chr1:165813944-165813945	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373144416	chr1:165813987-165813988	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542599285	chr1:165814017-165814018	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138943244	chr1:165814021-165814022	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530029371	chr1:165814081-165814082	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547101318	chr1:165814086-165814087	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73029460	chr1:165814101-165814102	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs180844495	chr1:165814103-165814104	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs80076014	chr1:165814123-165814124	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537787996	chr1:165814124-165814125	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141022785	chr1:165814202-165814203	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371673391	chr1:165814234-165814235	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375938595	chr1:165814249-165814250	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574401368	chr1:165814278-165814279	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187395816	chr1:165814386-165814387	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs553694498	chr1:165814387-165814388	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs28480651	chr1:165814390-165814391	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs545868563	chr1:165814403-165814404	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs567598148	chr1:165814406-165814407	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs565526441	chr1:165814468-165814469	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs192089853	chr1:165814479-165814480	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs145131314	chr1:165814481-165814482	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs536235375	chr1:165814482-165814483	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs146877866	chr1:165814498-165814499	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201997088	chr1:165814506-165814507	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs74118913	chr1:165814569-165814570	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs140733673	chr1:165814570-165814571	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs560448763	chr1:165814579-165814580	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs532514194	chr1:165814580-165814581	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552241458	chr1:165814608-165814609	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552908647	chr1:165814662-165814663	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs567220376	chr1:165814696-165814697	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75019377	chr1:165814705-165814706	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs371304159	chr1:165814712-165814713	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs568279547	chr1:165814720-165814721	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs534053540	chr1:165814747-165814748	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs183461431	chr1:165814798-165814799	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570460732	chr1:165814808-165814809	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs145631544	chr1:165814836-165814837	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs531653796	chr1:165814907-165814908	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556279758	chr1:165815043-165815044	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs575940706	chr1:165815052-165815053	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs544504479	chr1:165815117-165815118	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs572010798	chr1:165815156-165815157	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs376278078	chr1:165815163-165815164	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165798800-165814200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:165799000-165818200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:165799200-165815800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr1:165808200-165814200	Enhancers	Duodenum Mucosa	Duodenum
5	chr1:165810800-165814000	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr1:165810800-165814000	Enhancers	Small Intestine	intestine
7	chr1:165810800-165814400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:165810800-165817000	Enhancers	Fetal Thymus	thymus
9	chr1:165811000-165814000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:165811200-165817000	Enhancers	Thymus	Thymus
11	chr1:165812000-165814200	Weak transcription	Fetal Brain Female	brain
12	chr1:165812000-165816600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:165812200-165820200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:165812200-165820200	Weak transcription	Spleen	Spleen
15	chr1:165812200-165823200	Weak transcription	Aorta	Aorta
16	chr1:165812200-165823200	Weak transcription	Fetal Stomach	stomach
17	chr1:165812200-165823400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:165812400-165814400	Enhancers	Dnd41	blood
19	chr1:165812400-165815000	Weak transcription	HepG2	liver
20	chr1:165812400-165815600	Enhancers	K562	blood
21	chr1:165812400-165818400	Weak transcription	Right Atrium	heart
22	chr1:165812400-165820200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr1:165812400-165820200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:165812400-165820200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:165812400-165820200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr1:165812400-165820200	Weak transcription	HSMMtube	muscle
27	chr1:165812400-165820400	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr1:165812400-165820400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:165812400-165821800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr1:165812400-165822200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr1:165812400-165823200	Weak transcription	Left Ventricle	heart
32	chr1:165812400-165823200	Weak transcription	Right Ventricle	heart
33	chr1:165812400-165823200	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:165812600-165814400	Enhancers	A549	lung
35	chr1:165812600-165820200	Weak transcription	Fetal Intestine Small	intestine
36	chr1:165812600-165820400	Weak transcription	Fetal Heart	heart
37	chr1:165812600-165821800	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr1:165812800-165814800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:165812800-165815600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr1:165812800-165818400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:165812800-165818400	Weak transcription	HMEC	breast
42	chr1:165812800-165820200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:165812800-165820200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr1:165812800-165820200	Weak transcription	NHEK	skin
45	chr1:165812800-165820200	Weak transcription	Osteobl	bone
46	chr1:165813000-165814200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:165813000-165814800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:165813000-165814800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:165813000-165815000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr1:165813000-165815000	Weak transcription	Lung	lung

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