Variant report

Variant	esv2763386
Chromosome Location	chr4:120143861-120186968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:123)
Chromatin interactive
region (count:40)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:120159072-120159821	GM12878	blood:	n/a	n/a
2	ATF2	chr4:120158972-120159927	GM12878	blood:	n/a	n/a
3	BATF	chr4:120159046-120159845	GM12878	blood:	n/a	n/a
4	BATF	chr4:120159096-120159862	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:120159220-120159604	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:120159152-120159850	GM12878	blood:	n/a	n/a
7	BCL3	chr4:120159006-120159597	GM12878	blood:	n/a	n/a
8	BCLAF1	chr4:120159158-120159822	GM12878	blood:	n/a	n/a
9	BCLAF1	chr4:120159068-120159759	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:120159260-120159796	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:120149582-120149677	K562	blood:	n/a	n/a
12	BHLHE40	chr4:120155016-120155266	K562	blood:	n/a	n/a
13	CCNT2	chr4:120186967-120187139	K562	blood:	n/a	n/a
14	CEBPB	chr4:120146818-120146905	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:120158914-120159893	GM12878	blood:	n/a	n/a
16	CEBPB	chr4:120146737-120146902	A549	lung:	n/a	n/a
17	CEBPB	chr4:120148912-120149221	IMR90	lung:	n/a	n/a
18	CREB1	chr4:120159186-120159793	GM12878	blood:	n/a	n/a
19	CTCF	chr4:120149400-120149550	AG10803	skin:	n/a	n/a
20	CTCF	chr4:120176340-120176490	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr4:120176340-120176490	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr4:120176340-120176490	HEK293	kidney:	n/a	n/a
23	CTCF	chr4:120176460-120176610	HCM	heart:	n/a	n/a
24	CTCF	chr4:120176420-120176570	HepG2	liver:	n/a	n/a
25	CTCF	chr4:120176460-120176610	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr4:120176315-120176627	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:120181710-120181715	K562	blood:	n/a	n/a
28	CTCF	chr4:120176320-120176470	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr4:120176480-120176630	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr4:120159320-120159470	HMF	breast:	n/a	n/a
31	CTCF	chr4:120151607-120151677	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr4:120176440-120176590	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr4:120180317-120180377	Fibrobl	skin:	n/a	n/a
34	CTCF	chr4:120176886-120176918	GM10248	blood:	n/a	n/a
35	CTCF	chr4:120176401-120176627	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:120176476-120176517	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:120157968-120158009	GM13976	blood:	n/a	n/a
38	CTCF	chr4:120176460-120176610	K562	blood:	n/a	n/a
39	CTCF	chr4:120176440-120176590	BJ	skin:	n/a	n/a
40	CUX1	chr4:120155450-120155463	K562	blood:	n/a	n/a
41	CUX1	chr4:120154916-120155020	GM12878	blood:	n/a	n/a
42	E2F4	chr4:120158316-120158327	MCF10A-Er-Src	breast:	n/a	n/a
43	EBF1	chr4:120159246-120159816	GM12878	blood:	n/a	n/a
44	EBF1	chr4:120159288-120159671	GM12878	blood:	n/a	n/a
45	EGR1	chr4:120154930-120155210	K562	blood:	n/a	n/a
46	EGR1	chr4:120154909-120155214	K562	blood:	n/a	n/a
47	EGR1	chr4:120159290-120159496	GM12878	blood:	n/a	n/a
48	ELF1	chr4:120159214-120159601	GM12878	blood:	n/a	n/a
49	ELF1	chr4:120154942-120155231	K562	blood:	n/a	chr4:120155116-120155129
50	ELK1	chr4:120159730-120159869	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120155096-120155146	HNPCEpiC	eye:	n/a
2	chr4:120155096-120155146	HNPCEpiC	eye:	n/a
3	chr4:120162316-120162366	SK-N-SH_RA	brain:	n/a
4	chr4:120162316-120162366	SAEC	small airway:	n/a
5	chr4:120155096-120155146	GM12892	blood:	n/a
6	chr4:120155096-120155146	AG09319	gingival:	n/a
7	chr4:120162316-120162366	HNPCEpiC	eye:	n/a
8	chr4:120155096-120155146	RPTEC	kidney:	n/a
9	chr4:120162316-120162366	GM12892	blood:	n/a
10	chr4:120155096-120155146	AoSMC	blood vessel:	n/a
11	chr4:120155096-120155146	HUVEC	blood vessel:	n/a
12	chr4:120155096-120155146	GM06990	blood:	n/a
13	chr4:120155096-120155146	ECC-1	luminal epithelium:	n/a
14	chr4:120155096-120155146	NT2-D1	testis:	n/a
15	chr4:120155096-120155146	CMK	blood:	n/a
16	chr4:120155096-120155146	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:120155096-120155146	HCM	heart:	n/a
18	chr4:120155096-120155146	Caco-2	colon:	n/a
19	chr4:120155096-120155146	AG09309	skin:	n/a
20	chr4:120155096-120155146	ProgFib	skin:	n/a
21	chr4:120162316-120162366	ECC-1	luminal epithelium:	n/a
22	chr4:120155096-120155146	AG04450	lung:	fetal
23	chr4:120155096-120155146	HEEpiC	esophagus:	n/a
24	chr4:120155096-120155146	AG04449	skin:	fetal
25	chr4:120162316-120162366	PrEC	prostate:	n/a
26	chr4:120155096-120155146	IMR90	lung:	fetal
27	chr4:120162316-120162366	IMR90	lung:	fetal
28	chr4:120162316-120162366	AG04449	skin:	fetal
29	chr4:120162316-120162366	HRE	kidney:	n/a
30	chr4:120162316-120162366	A549	lung:	n/a
31	chr4:120162316-120162366	NH-A	brain:	n/a
32	chr4:120155096-120155146	NHBE	bronchial:	n/a
33	chr4:120162316-120162366	GM12878	blood:	n/a
34	chr4:120162316-120162366	HCT-116	colon:	n/a
35	chr4:120155096-120155146	SAEC	small airway:	n/a
36	chr4:120155096-120155146	SK-N-SH	brain:	n/a
37	chr4:120155096-120155146	SKMC	muscle:	n/a
38	chr4:120155096-120155146	BE2_C	brain:	n/a
39	chr4:120155096-120155146	T-47D	breast:	n/a
40	chr4:120162316-120162366	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:120162316-120162366	HAEpiC	amniotic membrane:	n/a
42	chr4:120162316-120162366	CMK	blood:	n/a
43	chr4:120155096-120155146	SK-N-MC	brain:	n/a
44	chr4:120162316-120162366	HepG2	liver:	n/a
45	chr4:120155096-120155146	HRPEpiC	eye:	n/a
46	chr4:120162316-120162366	Hepatocyte	liver:	n/a
47	chr4:120162316-120162366	PFSK-1	brain:	n/a
48	chr4:120162316-120162366	AG10803	skin:	n/a
49	chr4:120155096-120155146	Hepatocyte	liver:	n/a
50	chr4:120155096-120155146	HCF	heart:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120183641..120184141-chr8:43096068..43096724,2	MCF-7	breast:
2	chr4:120183641..120184141-chr8:43094991..43095897,2	MCF-7	breast:
3	chr4:120133844..120135886-chr4:120156323..120158493,2	MCF-7	breast:
4	chr4:120154917..120156794-chr4:120375661..120377548,2	K562	blood:
5	chr4:120151295..120153749-chr4:120154352..120157062,2	K562	blood:
6	chr21:28250452..28251450-chr4:120183161..120184161,2	MCF-7	breast:
7	chr4:120183141..120184141-chr8:43096226..43096751,3	MCF-7	breast:
8	chr4:120158506..120160403-chr4:120160643..120163574,2	MCF-7	breast:
9	chr4:120131912..120135684-chr4:120163783..120168921,6	MCF-7	breast:
10	chr4:120132067..120136254-chr4:120151434..120157051,7	K562	blood:
11	chr4:120132950..120135145-chr4:120157017..120160702,4	MCF-7	breast:
12	chr4:120151994..120154554-chr4:120157115..120160600,3	K562	blood:
13	chr4:120184028..120185733-chr4:120187407..120189044,3	K562	blood:
14	chr4:120132915..120135599-chr4:120147447..120150353,2	MCF-7	breast:
15	chr4:120146321..120148170-chr4:120150599..120152803,2	K562	blood:
16	chr4:120162306..120165092-chr4:120183039..120184970,2	K562	blood:
17	chr4:120176059..120178836-chr4:120180893..120184210,4	K562	blood:
18	chr4:120158506..120160403-chr4:120160643..120163574,2	MCF-7	breast:
19	chr4:120134215..120136562-chr4:120145620..120147384,3	MCF-7	breast:
20	chr4:120183161..120184141-chr8:43095223..43095920,2	MCF-7	breast:
21	chr4:120162306..120165092-chr4:120183039..120184970,2	K562	blood:
22	chr4:120135683..120138360-chr4:120179744..120182686,3	K562	blood:
23	chr4:120132760..120135331-chr4:120151065..120152751,2	MCF-7	breast:
24	chr4:120151295..120153749-chr4:120154352..120157062,2	K562	blood:
25	chr4:120136237..120140737-chr4:120147652..120152174,4	MCF-7	breast:
26	chr4:120132009..120134724-chr4:120165743..120167609,3	K562	blood:
27	chr4:120132621..120134518-chr4:120147698..120150178,2	K562	blood:
28	chr4:120131927..120134724-chr4:120165743..120168558,4	K562	blood:
29	chr4:120155653..120158497-chr4:120158665..120160752,2	K562	blood:
30	chr4:120132397..120137812-chr4:120151434..120157051,7	K562	blood:
31	chr4:119960403..119963318-chr4:120145478..120148032,2	MCF-7	breast:
32	chr4:120153288..120155840-chr4:120986022..120987789,2	K562	blood:
33	chr4:120146321..120148170-chr4:120150599..120152803,2	K562	blood:
34	chr4:119991797..119993940-chr4:120168867..120171491,2	MCF-7	breast:
35	chr4:120136312..120137869-chr4:120152346..120153933,2	K562	blood:
36	chr4:120133051..120135487-chr4:120141278..120144342,3	MCF-7	breast:
37	chr4:120133904..120136281-chr4:120160209..120162488,2	K562	blood:
38	chr4:120132754..120134825-chr4:120185311..120187985,2	MCF-7	breast:
39	chr4:120182924..120185910-chr4:120187445..120191655,4	K562	blood:
40	chr4:120133408..120135615-chr4:120143734..120145837,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP53-1	chr4:120160373-120160467	NONHSAT098039
2	lnc-USP53-1	chr4:120160373-120160496	NONHSAT098037
3	lnc-USP53-1	chr4:120156445-120156566	NONHSAT098039
4	lnc-USP53-1	chr4:120156445-120156566	NONHSAT098037

No data

Variant related genes	Relation type
USP53	TF binding region
USP53	CpG island
ENSG00000178636	chromatin interactions
ENSG00000245958	chromatin interactions
ENSG00000145390	chromatin interactions
ENSG00000250950	chromatin interactions

Extended variants
information (count: 1405 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562347278	chr4:120143873-120143874	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs186623419	chr4:120143927-120143928	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560669804	chr4:120143951-120143952	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191073414	chr4:120144015-120144016	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs199848605	chr4:120144033-120144034	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs200499027	chr4:120144035-120144036	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369977979	chr4:120144036-120144037	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs200152715	chr4:120144037-120144038	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562830748	chr4:120144051-120144052	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs529385489	chr4:120144058-120144059	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376333648	chr4:120144171-120144172	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576442417	chr4:120144289-120144290	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541962852	chr4:120144302-120144303	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs9991222	chr4:120144363-120144364	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs530678425	chr4:120144418-120144419	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs565016174	chr4:120144438-120144439	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs34624042	chr4:120144466-120144467	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs181934138	chr4:120144491-120144492	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs373162584	chr4:120144502-120144503	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572695279	chr4:120144554-120144555	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs374059594	chr4:120144555-120144556	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564403609	chr4:120144611-120144612	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs566530823	chr4:120144647-120144648	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs9991582	chr4:120144690-120144691	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555886746	chr4:120144740-120144741	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs113012442	chr4:120144744-120144745	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547759243	chr4:120144784-120144785	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs116627094	chr4:120144807-120144808	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558515913	chr4:120144823-120144824	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs142828916	chr4:120144854-120144855	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540580274	chr4:120144884-120144885	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs560288875	chr4:120144919-120144920	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539982222	chr4:120144956-120144957	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536953926	chr4:120145009-120145010	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534289416	chr4:120145016-120145017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377281190	chr4:120145065-120145066	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs116137079	chr4:120145080-120145081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs570276357	chr4:120145101-120145102	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs186581937	chr4:120145122-120145123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs115584700	chr4:120145135-120145136	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs550454469	chr4:120145222-120145223	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs539217374	chr4:120145307-120145308	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564077890	chr4:120145310-120145311	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533082792	chr4:120145315-120145316	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs148443415	chr4:120145316-120145317	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs566362261	chr4:120145317-120145318	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs564599621	chr4:120145343-120145344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111979690	chr4:120145392-120145393	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs549127951	chr4:120145405-120145406	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs368757674	chr4:120145432-120145433	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1158 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120134600-120144600	Weak transcription	Spleen	Spleen
2	chr4:120134800-120147000	Weak transcription	Fetal Brain Male	brain
3	chr4:120134800-120170000	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:120135000-120154800	Weak transcription	Primary B cells from cord blood	blood
5	chr4:120135000-120170400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:120135000-120195800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr4:120135200-120155000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:120135200-120155000	Weak transcription	Small Intestine	intestine
9	chr4:120135200-120163600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr4:120135200-120176200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr4:120135200-120176200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr4:120135400-120159000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr4:120135400-120194600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr4:120135600-120155000	Weak transcription	K562	blood
15	chr4:120135600-120173800	Weak transcription	Brain Anterior Caudate	brain
16	chr4:120136000-120145600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr4:120136200-120147400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr4:120136200-120148000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr4:120136200-120154400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr4:120136200-120219200	Weak transcription	Brain Angular Gyrus	brain
21	chr4:120136400-120151600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr4:120136400-120155000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr4:120136400-120155000	Weak transcription	Stomach Mucosa	stomach
24	chr4:120136400-120156400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr4:120137000-120151000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr4:120137400-120155000	Weak transcription	Right Atrium	heart
27	chr4:120137600-120154600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr4:120138400-120144400	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr4:120138400-120144600	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr4:120138400-120144800	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr4:120138600-120148000	Weak transcription	Pancreas	Pancrea
32	chr4:120138800-120155000	Weak transcription	Fetal Thymus	thymus
33	chr4:120139000-120148400	Weak transcription	Gastric	stomach
34	chr4:120139400-120149200	Weak transcription	Fetal Heart	heart
35	chr4:120139400-120151400	Weak transcription	HepG2	liver
36	chr4:120139400-120151600	Weak transcription	Psoas Muscle	Psoas
37	chr4:120139400-120165800	Weak transcription	Fetal Kidney	kidney
38	chr4:120139600-120145800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:120139600-120151200	Weak transcription	Primary T cells from cord blood	blood
40	chr4:120139600-120151600	Weak transcription	Aorta	Aorta
41	chr4:120139600-120153600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:120140000-120155000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:120140200-120154800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr4:120140200-120154800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr4:120140600-120151400	Weak transcription	Left Ventricle	heart
46	chr4:120140600-120151600	Weak transcription	Right Ventricle	heart
47	chr4:120140600-120167400	Weak transcription	Colonic Mucosa	Colon
48	chr4:120140800-120152800	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr4:120140800-120154600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr4:120140800-120154800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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