Variant report

Variant	nsv461632
Chromosome Location	chr4:120158734-120180790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:120158972-120159927	GM12878	blood:	n/a	n/a
2	ATF2	chr4:120159072-120159821	GM12878	blood:	n/a	n/a
3	BATF	chr4:120159096-120159862	GM12878	blood:	n/a	n/a
4	BATF	chr4:120159046-120159845	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	CEBPB	chr4:120158914-120159893	GM12878	blood:	n/a	n/a
12	CREB1	chr4:120159186-120159793	GM12878	blood:	n/a	n/a
13	CTCF	chr4:120176340-120176490	HEK293	kidney:	n/a	n/a
14	CTCF	chr4:120159320-120159470	HMF	breast:	n/a	n/a
15	CTCF	chr4:120176440-120176590	HFF-Myc	foreskin:	n/a	n/a
16	CTCF	chr4:120176460-120176610	K562	blood:	n/a	n/a
17	CTCF	chr4:120176340-120176490	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr4:120176480-120176630	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr4:120176440-120176590	BJ	skin:	n/a	n/a
20	CTCF	chr4:120176401-120176627	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr4:120176315-120176627	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr4:120176476-120176517	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:120176886-120176918	GM10248	blood:	n/a	n/a
24	CTCF	chr4:120176340-120176490	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr4:120176460-120176610	HCM	heart:	n/a	n/a
26	CTCF	chr4:120176460-120176610	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr4:120180317-120180377	Fibrobl	skin:	n/a	n/a
28	CTCF	chr4:120176420-120176570	HepG2	liver:	n/a	n/a
29	CTCF	chr4:120176320-120176470	WERI-Rb-1	eye:	n/a	n/a
30	EBF1	chr4:120159288-120159671	GM12878	blood:	n/a	n/a
31	EBF1	chr4:120159246-120159816	GM12878	blood:	n/a	n/a
32	EGR1	chr4:120159290-120159496	GM12878	blood:	n/a	n/a
33	ELF1	chr4:120159214-120159601	GM12878	blood:	n/a	n/a
34	ELK1	chr4:120159730-120159869	K562	blood:	n/a	n/a
35	EP300	chr4:120159220-120159752	GM12878	blood:	n/a	n/a
36	EP300	chr4:120159187-120159632	GM12878	blood:	n/a	n/a
37	EP300	chr4:120159230-120159644	GM12878	blood:	n/a	n/a
38	FOS	chr4:120159316-120159491	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:120159313-120159413	MCF10A-Er-Src	breast:	n/a	n/a
40	FOSL2	chr4:120158533-120158760	HepG2	liver:	n/a	n/a
41	FOXM1	chr4:120159037-120159740	GM12878	blood:	n/a	n/a
42	FOXM1	chr4:120159024-120159799	GM12878	blood:	n/a	n/a
43	GATA3	chr4:120161646-120161846	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr4:120163788-120163995	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr4:120159076-120159514	SH-SY5Y	brain:	n/a	n/a
46	IKZF1	chr4:120159042-120159765	GM12878	blood:	n/a	n/a
47	IRF4	chr4:120159075-120159763	GM12878	blood:	n/a	n/a
48	IRF4	chr4:120159052-120159853	GM12878	blood:	n/a	n/a
49	JUND	chr4:120159230-120159761	GM12878	blood:	n/a	n/a
50	MAFF	chr4:120158930-120159138	HepG2	liver:	n/a	chr4:120158977-120158995

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120162316-120162366	SK-N-SH	brain:	n/a
2	chr4:120162316-120162366	NHBE	bronchial:	n/a
3	chr4:120162316-120162366	Jurkat	blood:	n/a
4	chr4:120162316-120162366	NT2-D1	testis:	n/a
5	chr4:120162316-120162366	GM06990	blood:	n/a
6	chr4:120162316-120162366	PFSK-1	brain:	n/a
7	chr4:120162316-120162366	PANC-1	pancreas:	n/a
8	chr4:120162316-120162366	MCF-7	breast:	n/a
9	chr4:120162316-120162366	GM12878	blood:	n/a
10	chr4:120162316-120162366	H1-hESC	embryonic stem cell:	embryo
11	chr4:120162316-120162366	HCM	heart:	n/a
12	chr4:120162316-120162366	Caco-2	colon:	n/a
13	chr4:120162316-120162366	U87	brain:	n/a
14	chr4:120162316-120162366	SK-N-SH_RA	brain:	n/a
15	chr4:120162316-120162366	Hepatocyte	liver:	n/a
16	chr4:120162316-120162366	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:120162316-120162366	IMR90	lung:	fetal
18	chr4:120162316-120162366	PrEC	prostate:	n/a
19	chr4:120162316-120162366	HRE	kidney:	n/a
20	chr4:120162316-120162366	GM19239	blood:	n/a
21	chr4:120162316-120162366	ovcar-3	ovarian:	n/a
22	chr4:120162316-120162366	NH-A	brain:	n/a
23	chr4:120162316-120162366	HNPCEpiC	eye:	n/a
24	chr4:120162316-120162366	HCT-116	colon:	n/a
25	chr4:120162316-120162366	HepG2	liver:	n/a
26	chr4:120162316-120162366	ECC-1	luminal epithelium:	n/a
27	chr4:120162316-120162366	HRPEpiC	eye:	n/a
28	chr4:120162316-120162366	HCF	heart:	n/a
29	chr4:120162316-120162366	CMK	blood:	n/a
30	chr4:120162316-120162366	HL-60	blood:	n/a
31	chr4:120162316-120162366	MCF10A-Er-Src	breast:	n/a
32	chr4:120162316-120162366	AG09319	gingival:	n/a
33	chr4:120162316-120162366	AG04450	lung:	fetal
34	chr4:120162316-120162366	HEEpiC	esophagus:	n/a
35	chr4:120162316-120162366	SKMC	muscle:	n/a
36	chr4:120162316-120162366	HMEC	breast:	n/a
37	chr4:120162316-120162366	HAEpiC	amniotic membrane:	n/a
38	chr4:120162316-120162366	AG10803	skin:	n/a
39	chr4:120162316-120162366	LNCaP	prostate:	n/a
40	chr4:120162316-120162366	HUVEC	blood vessel:	n/a
41	chr4:120162316-120162366	SK-N-MC	brain:	n/a
42	chr4:120162316-120162366	AoSMC	blood vessel:	n/a
43	chr4:120162316-120162366	ProgFib	skin:	n/a
44	chr4:120162316-120162366	AG04449	skin:	fetal
45	chr4:120162316-120162366	HCPEpiC	choroid plexus:	n/a
46	chr4:120162316-120162366	HRCEpiC	kidney:	n/a
47	chr4:120162316-120162366	GM12891	blood:	n/a
48	chr4:120162316-120162366	A549	lung:	n/a
49	chr4:120162316-120162366	BE2_C	brain:	n/a
50	chr4:120162316-120162366	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:120158506..120160403-chr4:120160643..120163574,2	MCF-7	breast:
2	chr4:120135683..120138360-chr4:120179744..120182686,3	K562	blood:
3	chr4:120132950..120135145-chr4:120157017..120160702,4	MCF-7	breast:
4	chr4:120131927..120134724-chr4:120165743..120168558,4	K562	blood:
5	chr4:120176059..120178836-chr4:120180893..120184210,4	K562	blood:
6	chr4:120131912..120135684-chr4:120163783..120168921,6	MCF-7	breast:
7	chr4:120158506..120160403-chr4:120160643..120163574,2	MCF-7	breast:
8	chr4:120132009..120134724-chr4:120165743..120167609,3	K562	blood:
9	chr4:119991797..119993940-chr4:120168867..120171491,2	MCF-7	breast:
10	chr4:120133904..120136281-chr4:120160209..120162488,2	K562	blood:
11	chr4:120162306..120165092-chr4:120183039..120184970,2	K562	blood:

(count:2 , 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

No data

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

Extended variants
information (count: 756 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:756 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10024967	chr4:120158734-120158735	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557520167	chr4:120158765-120158766	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs547748391	chr4:120158834-120158835	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs75525778	chr4:120158874-120158875	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs149980454	chr4:120158931-120158932	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs550449320	chr4:120159012-120159013	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs147705332	chr4:120159016-120159017	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs539603469	chr4:120159017-120159018	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs11931312	chr4:120159023-120159024	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs575211802	chr4:120159055-120159056	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs567139972	chr4:120159105-120159106	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs553094859	chr4:120159112-120159113	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs142418489	chr4:120159121-120159122	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs188682562	chr4:120159159-120159160	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs575598632	chr4:120159185-120159186	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs538251930	chr4:120159215-120159216	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs544687009	chr4:120159271-120159272	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs11944880	chr4:120159334-120159335	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs578052231	chr4:120159346-120159347	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs116117181	chr4:120159504-120159505	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs62328370	chr4:120159522-120159523	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs146988362	chr4:120159591-120159592	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs147608224	chr4:120159598-120159599	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs542173954	chr4:120159611-120159612	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs541748944	chr4:120159656-120159657	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs149113468	chr4:120159677-120159678	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs143163443	chr4:120159681-120159682	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs544396857	chr4:120159714-120159715	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs550556625	chr4:120159746-120159747	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs112559673	chr4:120159842-120159843	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs148270682	chr4:120159910-120159911	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs17049968	chr4:120159916-120159917	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs141176071	chr4:120159928-120159929	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs74516697	chr4:120160124-120160125	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536153838	chr4:120160159-120160160	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs549453037	chr4:120160236-120160237	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569545938	chr4:120160238-120160239	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs116050803	chr4:120160272-120160273	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528685477	chr4:120160312-120160313	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556313626	chr4:120160340-120160341	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs199550094	chr4:120160367-120160368	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs578009937	chr4:120160451-120160452	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs140456747	chr4:120160456-120160457	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs398107913	chr4:120160463-120160464	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs534060236	chr4:120160505-120160506	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs141430476	chr4:120160530-120160531	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs572746521	chr4:120160614-120160615	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs191638520	chr4:120160659-120160660	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs541709862	chr4:120160672-120160673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559109762	chr4:120160673-120160674	Weak transcription Strong transcription Genic enhancers	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:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120134800-120170000	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:120135000-120170400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:120135000-120195800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:120135200-120163600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr4:120135200-120176200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr4:120135200-120176200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:120135400-120159000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr4:120135400-120194600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr4:120135600-120173800	Weak transcription	Brain Anterior Caudate	brain
10	chr4:120136200-120219200	Weak transcription	Brain Angular Gyrus	brain
11	chr4:120139400-120165800	Weak transcription	Fetal Kidney	kidney
12	chr4:120140600-120167400	Weak transcription	Colonic Mucosa	Colon
13	chr4:120140800-120158800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr4:120141000-120158800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr4:120141000-120192400	Weak transcription	Hela-S3	cervix
16	chr4:120143000-120167200	Weak transcription	Placenta	Placenta
17	chr4:120143000-120176200	Weak transcription	Esophagus	oesophagus
18	chr4:120143800-120167000	Weak transcription	Fetal Intestine Large	intestine
19	chr4:120146000-120178600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr4:120146400-120158800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:120148200-120213600	Weak transcription	Fetal Muscle Leg	muscle
22	chr4:120152200-120159000	Weak transcription	Gastric	stomach
23	chr4:120152200-120167200	Weak transcription	Pancreas	Pancrea
24	chr4:120153600-120158800	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr4:120153800-120160600	Weak transcription	HSMM	muscle
26	chr4:120154800-120161800	Weak transcription	A549	lung
27	chr4:120155000-120166200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr4:120155200-120161000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:120155200-120163400	Weak transcription	Brain Hippocampus Middle	brain
30	chr4:120155200-120167000	Weak transcription	NH-A	brain
31	chr4:120155400-120159000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr4:120155400-120159000	Weak transcription	Stomach Mucosa	stomach
33	chr4:120155400-120159000	Weak transcription	K562	blood
34	chr4:120155400-120159400	Strong transcription	Left Ventricle	heart
35	chr4:120155400-120160600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr4:120155400-120160600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr4:120155400-120165200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:120155400-120165800	Weak transcription	Primary B cells from peripheral blood	blood
39	chr4:120155400-120166400	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr4:120155400-120167200	Weak transcription	Aorta	Aorta
41	chr4:120155400-120167200	Weak transcription	Fetal Thymus	thymus
42	chr4:120155400-120167400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr4:120155400-120169800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr4:120155400-120169800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr4:120155400-120169800	Weak transcription	Ovary	ovary
46	chr4:120155400-120176200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:120155400-120176400	Weak transcription	Right Ventricle	heart
48	chr4:120155600-120158800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:120155600-120158800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr4:120155600-120158800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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