Variant report

Variant	nsv966480
Chromosome Location	chr4:120144708-120160847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

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	chr4:120155016-120155266	K562	blood:	n/a	n/a
11	BHLHE40	chr4:120159260-120159796	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:120149582-120149677	K562	blood:	n/a	n/a
13	CEBPB	chr4:120158914-120159893	GM12878	blood:	n/a	n/a
14	CEBPB	chr4:120146818-120146905	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:120148912-120149221	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:120146737-120146902	A549	lung:	n/a	n/a
17	CREB1	chr4:120159186-120159793	GM12878	blood:	n/a	n/a
18	CTCF	chr4:120157968-120158009	GM13976	blood:	n/a	n/a
19	CTCF	chr4:120149400-120149550	AG10803	skin:	n/a	n/a
20	CTCF	chr4:120159320-120159470	HMF	breast:	n/a	n/a
21	CTCF	chr4:120151607-120151677	Pancreas_OC	pancreas:	n/a	n/a
22	CUX1	chr4:120154916-120155020	GM12878	blood:	n/a	n/a
23	CUX1	chr4:120155450-120155463	K562	blood:	n/a	n/a
24	E2F4	chr4:120158316-120158327	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr4:120159246-120159816	GM12878	blood:	n/a	n/a
26	EBF1	chr4:120159288-120159671	GM12878	blood:	n/a	n/a
27	EGR1	chr4:120154909-120155214	K562	blood:	n/a	n/a
28	EGR1	chr4:120154930-120155210	K562	blood:	n/a	n/a
29	EGR1	chr4:120159290-120159496	GM12878	blood:	n/a	n/a
30	ELF1	chr4:120159214-120159601	GM12878	blood:	n/a	n/a
31	ELF1	chr4:120154942-120155231	K562	blood:	n/a	chr4:120155116-120155129
32	ELK1	chr4:120159730-120159869	K562	blood:	n/a	n/a
33	EP300	chr4:120158584-120158710	GM12878	blood:	n/a	n/a
34	EP300	chr4:120159187-120159632	GM12878	blood:	n/a	n/a
35	EP300	chr4:120154879-120155297	K562	blood:	n/a	chr4:120155118-120155127 chr4:120155273-120155281
36	EP300	chr4:120159220-120159752	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	chr4:120158502-120158730	HepG2	liver:	n/a	n/a
41	FOSL2	chr4:120158533-120158760	HepG2	liver:	n/a	n/a
42	FOXM1	chr4:120159037-120159740	GM12878	blood:	n/a	n/a
43	FOXM1	chr4:120159024-120159799	GM12878	blood:	n/a	n/a
44	GABPA	chr4:120158599-120158689	Hela-S3	cervix:	n/a	n/a
45	GATA3	chr4:120148785-120149332	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr4:120159076-120159514	SH-SY5Y	brain:	n/a	n/a
47	GTF2F1	chr4:120152826-120152876	H1-hESC	embryonic stem cell:	n/a	n/a
48	HEY1	chr4:120151959-120152392	K562	blood:	n/a	n/a
49	IKZF1	chr4:120159042-120159765	GM12878	blood:	n/a	n/a
50	IRF4	chr4:120159052-120159853	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120155096-120155146	H1-hESC	embryonic stem cell:	embryo
2	chr4:120155096-120155146	AoSMC	blood vessel:	n/a
3	chr4:120155096-120155146	AG04450	lung:	fetal
4	chr4:120155096-120155146	GM12892	blood:	n/a
5	chr4:120155096-120155146	NHDF-neo	bronchial:	n/a
6	chr4:120155096-120155146	NHBE	bronchial:	n/a
7	chr4:120155096-120155146	GM06990	blood:	n/a
8	chr4:120155096-120155146	Caco-2	colon:	n/a
9	chr4:120155096-120155146	AG09319	gingival:	n/a
10	chr4:120155096-120155146	SK-N-SH	brain:	n/a
11	chr4:120155096-120155146	GM12891	blood:	n/a
12	chr4:120155096-120155146	HAEpiC	amniotic membrane:	n/a
13	chr4:120155096-120155146	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:120155096-120155146	ECC-1	luminal epithelium:	n/a
15	chr4:120155096-120155146	RPTEC	kidney:	n/a
16	chr4:120155096-120155146	HCPEpiC	choroid plexus:	n/a
17	chr4:120155096-120155146	HRPEpiC	eye:	n/a
18	chr4:120155096-120155146	T-47D	breast:	n/a
19	chr4:120155096-120155146	HepG2	liver:	n/a
20	chr4:120155096-120155146	HRCEpiC	kidney:	n/a
21	chr4:120155096-120155146	MCF-7	breast:	n/a
22	chr4:120155096-120155146	HCM	heart:	n/a
23	chr4:120155096-120155146	BJ	skin:	n/a
24	chr4:120155096-120155146	Hela-S3	cervix:	n/a
25	chr4:120155096-120155146	PANC-1	pancreas:	n/a
26	chr4:120155096-120155146	HMEC	breast:	n/a
27	chr4:120155096-120155146	ProgFib	skin:	n/a
28	chr4:120155096-120155146	IMR90	lung:	fetal
29	chr4:120155096-120155146	AG09309	skin:	n/a
30	chr4:120155096-120155146	Jurkat	blood:	n/a
31	chr4:120155096-120155146	PFSK-1	brain:	n/a
32	chr4:120155096-120155146	Hepatocyte	liver:	n/a
33	chr4:120155096-120155146	HRE	kidney:	n/a
34	chr4:120155096-120155146	GM12878	blood:	n/a
35	chr4:120155096-120155146	HCF	heart:	n/a
36	chr4:120155096-120155146	SK-N-SH_RA	brain:	n/a
37	chr4:120155096-120155146	HIPEpiC	eye:	n/a
38	chr4:120155096-120155146	K562	blood:	n/a
39	chr4:120155096-120155146	NB4	blood:	n/a
40	chr4:120155096-120155146	A549	lung:	n/a
41	chr4:120155096-120155146	NH-A	brain:	n/a
42	chr4:120155096-120155146	AG10803	skin:	n/a
43	chr4:120155096-120155146	SKMC	muscle:	n/a
44	chr4:120155096-120155146	HEK293	kidney:	embryo
45	chr4:120155096-120155146	HCT-116	colon:	n/a
46	chr4:120155096-120155146	HL-60	blood:	n/a
47	chr4:120155096-120155146	SAEC	small airway:	n/a
48	chr4:120155096-120155146	CMK	blood:	n/a
49	chr4:120155096-120155146	GM19239	blood:	n/a
50	chr4:120155096-120155146	HEEpiC	esophagus:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120132760..120135331-chr4:120151065..120152751,2	MCF-7	breast:
2	chr4:120154917..120156794-chr4:120375661..120377548,2	K562	blood:
3	chr4:120151295..120153749-chr4:120154352..120157062,2	K562	blood:
4	chr4:120132915..120135599-chr4:120147447..120150353,2	MCF-7	breast:
5	chr4:120151994..120154554-chr4:120157115..120160600,3	K562	blood:
6	chr4:120153288..120155840-chr4:120986022..120987789,2	K562	blood:
7	chr4:120133408..120135615-chr4:120143734..120145837,2	MCF-7	breast:
8	chr4:120146321..120148170-chr4:120150599..120152803,2	K562	blood:
9	chr4:120151295..120153749-chr4:120154352..120157062,2	K562	blood:
10	chr4:120132621..120134518-chr4:120147698..120150178,2	K562	blood:
11	chr4:120132397..120137812-chr4:120151434..120157051,7	K562	blood:
12	chr4:120132950..120135145-chr4:120157017..120160702,4	MCF-7	breast:
13	chr4:120155653..120158497-chr4:120158665..120160752,2	K562	blood:
14	chr4:120158506..120160403-chr4:120160643..120163574,2	MCF-7	breast:
15	chr4:120146321..120148170-chr4:120150599..120152803,2	K562	blood:
16	chr4:120133904..120136281-chr4:120160209..120162488,2	K562	blood:
17	chr4:119960403..119963318-chr4:120145478..120148032,2	MCF-7	breast:
18	chr4:120136312..120137869-chr4:120152346..120153933,2	K562	blood:
19	chr4:120133844..120135886-chr4:120156323..120158493,2	MCF-7	breast:
20	chr4:120134215..120136562-chr4:120145620..120147384,3	MCF-7	breast:
21	chr4:120132067..120136254-chr4:120151434..120157051,7	K562	blood:
22	chr4:120158506..120160403-chr4:120160643..120163574,2	MCF-7	breast:
23	chr4:120136237..120140737-chr4:120147652..120152174,4	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 497 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555886746	chr4:120144740-120144741	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs113012442	chr4:120144744-120144745	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs547759243	chr4:120144784-120144785	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs116627094	chr4:120144807-120144808	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558515913	chr4:120144823-120144824	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142828916	chr4:120144854-120144855	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540580274	chr4:120144884-120144885	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560288875	chr4:120144919-120144920	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs539982222	chr4:120144956-120144957	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536953926	chr4:120145009-120145010	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534289416	chr4:120145016-120145017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs377281190	chr4:120145065-120145066	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs116137079	chr4:120145080-120145081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs570276357	chr4:120145101-120145102	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs186581937	chr4:120145122-120145123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs115584700	chr4:120145135-120145136	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550454469	chr4:120145222-120145223	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs539217374	chr4:120145307-120145308	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs564077890	chr4:120145310-120145311	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs533082792	chr4:120145315-120145316	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs148443415	chr4:120145316-120145317	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566362261	chr4:120145317-120145318	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs564599621	chr4:120145343-120145344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111979690	chr4:120145392-120145393	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549127951	chr4:120145405-120145406	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368757674	chr4:120145432-120145433	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190610599	chr4:120145433-120145434	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs557918262	chr4:120145435-120145436	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs538481218	chr4:120145511-120145512	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs558392817	chr4:120145518-120145519	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs578161417	chr4:120145588-120145589	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs80075151	chr4:120145641-120145642	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577812706	chr4:120145679-120145680	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs554100751	chr4:120145687-120145688	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs141792619	chr4:120145729-120145730	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543083701	chr4:120145757-120145758	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs556283306	chr4:120145761-120145762	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs150599198	chr4:120145779-120145780	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs111356964	chr4:120145815-120145816	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs79602840	chr4:120145819-120145820	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs377648443	chr4:120145875-120145876	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533222359	chr4:120145922-120145923	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs56274942	chr4:120145953-120145954	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs114415672	chr4:120146005-120146006	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560073827	chr4:120146021-120146022	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs531987624	chr4:120146031-120146032	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528929527	chr4:120146041-120146042	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139619665	chr4:120146047-120146048	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568932160	chr4:120146108-120146109	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531437373	chr4:120146224-120146225	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120134800-120147000	Weak transcription	Fetal Brain Male	brain
2	chr4:120134800-120170000	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:120135000-120154800	Weak transcription	Primary B cells from cord blood	blood
4	chr4:120135000-120170400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:120135000-120195800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr4:120135200-120155000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:120135200-120155000	Weak transcription	Small Intestine	intestine
8	chr4:120135200-120163600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr4:120135200-120176200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr4:120135200-120176200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr4:120135400-120159000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:120135400-120194600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr4:120135600-120155000	Weak transcription	K562	blood
14	chr4:120135600-120173800	Weak transcription	Brain Anterior Caudate	brain
15	chr4:120136000-120145600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr4:120136200-120147400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr4:120136200-120148000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr4:120136200-120154400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr4:120136200-120219200	Weak transcription	Brain Angular Gyrus	brain
20	chr4:120136400-120151600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr4:120136400-120155000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr4:120136400-120155000	Weak transcription	Stomach Mucosa	stomach
23	chr4:120136400-120156400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:120137000-120151000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr4:120137400-120155000	Weak transcription	Right Atrium	heart
26	chr4:120137600-120154600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr4:120138400-120144800	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr4:120138600-120148000	Weak transcription	Pancreas	Pancrea
29	chr4:120138800-120155000	Weak transcription	Fetal Thymus	thymus
30	chr4:120139000-120148400	Weak transcription	Gastric	stomach
31	chr4:120139400-120149200	Weak transcription	Fetal Heart	heart
32	chr4:120139400-120151400	Weak transcription	HepG2	liver
33	chr4:120139400-120151600	Weak transcription	Psoas Muscle	Psoas
34	chr4:120139400-120165800	Weak transcription	Fetal Kidney	kidney
35	chr4:120139600-120145800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr4:120139600-120151200	Weak transcription	Primary T cells from cord blood	blood
37	chr4:120139600-120151600	Weak transcription	Aorta	Aorta
38	chr4:120139600-120153600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:120140000-120155000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:120140200-120154800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr4:120140200-120154800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr4:120140600-120151400	Weak transcription	Left Ventricle	heart
43	chr4:120140600-120151600	Weak transcription	Right Ventricle	heart
44	chr4:120140600-120167400	Weak transcription	Colonic Mucosa	Colon
45	chr4:120140800-120152800	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr4:120140800-120154600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr4:120140800-120154800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:120140800-120158800	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr4:120141000-120149200	Weak transcription	NHLF	lung
50	chr4:120141000-120151200	Weak transcription	Liver	Liver

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