Variant report

Variant	nsv966373
Chromosome Location	chr4:120373841-120375667
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:120375640-120376007	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:120375657-120375939	K562	blood:	n/a	n/a
3	ATF1	chr4:120375410-120376174	K562	blood:	n/a	n/a
4	ATF2	chr4:120375574-120376077	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
5	ATF2	chr4:120375555-120376037	GM12878	blood:	n/a	chr4:120375758-120375769
6	ATF2	chr4:120375554-120376118	H1-hESC	embryonic stem cell:	n/a	chr4:120375758-120375769
7	ATF2	chr4:120375508-120376132	GM12878	blood:	n/a	chr4:120375758-120375769
8	ATF3	chr4:120375585-120375981	A549	lung:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
9	ATF3	chr4:120375667-120376101	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
10	ATF3	chr4:120375591-120376108	K562	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
11	ATF3	chr4:120375534-120376115	HepG2	liver:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
12	ATF3	chr4:120375643-120376128	GM12878	blood:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
13	ATF3	chr4:120375570-120376147	H1-hESC	embryonic stem cell:	n/a	chr4:120375748-120375768 chr4:120375782-120375795 chr4:120375756-120375769 chr4:120375784-120375804
14	BATF	chr4:120375371-120376260	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:120375469-120376323	GM12878	blood:	n/a	n/a
16	BCL3	chr4:120375586-120376104	A549	lung:	n/a	n/a
17	BCLAF1	chr4:120375555-120376089	GM12878	blood:	n/a	n/a
18	BCLAF1	chr4:120375644-120376123	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:120375666-120376228	K562	blood:	n/a	n/a
20	BRCA1	chr4:120375591-120376075	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr4:120375657-120376065	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr4:120375579-120376037	K562	blood:	n/a	n/a
23	CBX3	chr4:120374867-120376298	K562	blood:	n/a	n/a
24	CEBPB	chr4:120375396-120375977	K562	blood:	n/a	n/a
25	CEBPB	chr4:120375417-120375936	A549	lung:	n/a	n/a
26	CEBPB	chr4:120375366-120375954	K562	blood:	n/a	n/a
27	CEBPB	chr4:120375413-120375995	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:120375439-120376084	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:120375413-120375949	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:120375400-120376070	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:120375455-120375925	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:120375425-120375563	HepG2	liver:	n/a	n/a
33	CEBPD	chr4:120375316-120375938	K562	blood:	n/a	n/a
34	CEBPD	chr4:120375633-120376140	HepG2	liver:	n/a	n/a
35	CHD2	chr4:120375606-120376150	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr4:120375631-120376139	GM12878	blood:	n/a	n/a
37	CHD2	chr4:120375644-120376161	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr4:120375371-120376117	HepG2	liver:	n/a	n/a
39	CREB1	chr4:120375581-120376083	ECC-1	luminal epithelium:	n/a	n/a
40	CREB1	chr4:120375487-120376118	GM12878	blood:	n/a	n/a
41	CREB1	chr4:120375651-120376225	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr4:120375572-120376066	A549	lung:	n/a	n/a
43	CREB1	chr4:120375641-120376081	ECC-1	luminal epithelium:	n/a	n/a
44	CREB1	chr4:120375622-120376239	K562	blood:	n/a	n/a
45	CREB1	chr4:120375370-120376141	K562	blood:	n/a	n/a
46	CREB1	chr4:120375358-120376212	A549	lung:	n/a	n/a
47	CREB1	chr4:120375382-120376154	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr4:120375493-120376109	GM12878	blood:	n/a	n/a
49	CREB1	chr4:120375605-120376099	HepG2	liver:	n/a	n/a
50	CTBP2	chr4:120375642-120376070	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120375409-120375459	ECC-1	luminal epithelium:	n/a
2	chr4:120375409-120375459	HRPEpiC	eye:	n/a
3	chr4:120375409-120375459	U87	brain:	n/a
4	chr4:120375409-120375459	GM12891	blood:	n/a
5	chr4:120375409-120375459	Hepatocyte	liver:	n/a
6	chr4:120375409-120375459	SAEC	small airway:	n/a
7	chr4:120375409-120375459	HMEC	breast:	n/a
8	chr4:120375409-120375459	GM06990	blood:	n/a
9	chr4:120375409-120375459	BE2_C	brain:	n/a
10	chr4:120375409-120375459	MCF10A-Er-Src	breast:	n/a
11	chr4:120375409-120375459	AG10803	skin:	n/a
12	chr4:120375409-120375459	NHDF-neo	bronchial:	n/a
13	chr4:120375409-120375459	HL-60	blood:	n/a
14	chr4:120375409-120375459	SK-N-MC	brain:	n/a
15	chr4:120375409-120375459	LNCaP	prostate:	n/a
16	chr4:120375409-120375459	NHBE	bronchial:	n/a
17	chr4:120375409-120375459	GM19239	blood:	n/a
18	chr4:120375409-120375459	K562	blood:	n/a
19	chr4:120375409-120375459	IMR90	lung:	fetal
20	chr4:120375409-120375459	HEK293	kidney:	embryo
21	chr4:120375409-120375459	SK-N-SH_RA	brain:	n/a
22	chr4:120375409-120375459	GM12892	blood:	n/a
23	chr4:120375409-120375459	ProgFib	skin:	n/a
24	chr4:120375409-120375459	ovcar-3	ovarian:	n/a
25	chr4:120375409-120375459	Caco-2	colon:	n/a
26	chr4:120375409-120375459	HRE	kidney:	n/a
27	chr4:120375409-120375459	A549	lung:	n/a
28	chr4:120375409-120375459	HAEpiC	amniotic membrane:	n/a
29	chr4:120375409-120375459	GM12878	blood:	n/a
30	chr4:120375409-120375459	NH-A	brain:	n/a
31	chr4:120375409-120375459	PrEC	prostate:	n/a
32	chr4:120375409-120375459	AG04449	skin:	fetal
33	chr4:120375409-120375459	PANC-1	pancreas:	n/a
34	chr4:120375409-120375459	H1-hESC	embryonic stem cell:	embryo
35	chr4:120375409-120375459	HCT-116	colon:	n/a
36	chr4:120375409-120375459	HIPEpiC	eye:	n/a
37	chr4:120375409-120375459	HCPEpiC	choroid plexus:	n/a
38	chr4:120375409-120375459	HRCEpiC	kidney:	n/a
39	chr4:120375409-120375459	HEEpiC	esophagus:	n/a
40	chr4:120375409-120375459	Jurkat	blood:	n/a
41	chr4:120375409-120375459	HCM	heart:	n/a
42	chr4:120375409-120375459	AG04450	lung:	fetal
43	chr4:120375409-120375459	RPTEC	kidney:	n/a
44	chr4:120375409-120375459	HUVEC	blood vessel:	n/a
45	chr4:120375409-120375459	T-47D	breast:	n/a
46	chr4:120375409-120375459	Hela-S3	cervix:	n/a
47	chr4:120375409-120375459	AG09319	gingival:	n/a
48	chr4:120375409-120375459	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:120375409-120375459	AoSMC	blood vessel:	n/a
50	chr4:120375409-120375459	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:120132920..120134685-chr4:120374052..120375829,2	K562	blood:
2	chr4:120372429..120374699-chr4:120400382..120402462,2	K562	blood:
3	chr4:119679216..119681142-chr4:120375525..120377542,2	MCF-7	breast:
4	chr4:120132920..120134685-chr4:120374052..120375829,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE5A-3	chr4:120375401-120375783	NONHSAT098065

No data

Variant related genes	Relation type
ENSG00000250950	TF binding region
ENSG00000248280	TF binding region
ENSG00000245958	TF binding region
ENSG00000250950	CpG island
ENSG00000248280	CpG island
ENSG00000245958	CpG island
ENSG00000150961	chromatin interactions
ENSG00000178636	chromatin interactions
ENSG00000145390	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554365086	chr4:120373844-120373845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574274541	chr4:120373879-120373880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145687471	chr4:120373911-120373912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375729484	chr4:120373924-120373925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576418253	chr4:120373952-120373953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192054906	chr4:120373961-120373962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558521193	chr4:120373963-120373964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572454239	chr4:120373992-120373993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565401172	chr4:120374072-120374073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs545679112	chr4:120374096-120374097	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371700388	chr4:120374104-120374105	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs527734739	chr4:120374120-120374121	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546400595	chr4:120374171-120374172	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184983305	chr4:120374274-120374275	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs529054425	chr4:120374369-120374370	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs138723720	chr4:120374370-120374371	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs189201222	chr4:120374376-120374377	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs115113519	chr4:120374378-120374379	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs551041025	chr4:120374383-120374384	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs376870420	chr4:120374387-120374388	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs571328370	chr4:120374408-120374409	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs56372521	chr4:120374431-120374432	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs553881185	chr4:120374435-120374436	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs147093170	chr4:120374439-120374440	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs574953401	chr4:120374451-120374452	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs543969889	chr4:120374464-120374465	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs57917963	chr4:120374466-120374467	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
28	rs202241120	chr4:120374488-120374489	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs375018492	chr4:120374489-120374490	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs58620507	chr4:120374491-120374492	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs193061739	chr4:120374496-120374497	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs574331652	chr4:120374502-120374503	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs59483034	chr4:120374514-120374515	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
34	rs184674093	chr4:120374521-120374522	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs58416902	chr4:120374639-120374640	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs56153715	chr4:120374644-120374645	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs576611414	chr4:120374654-120374655	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs370759008	chr4:120374692-120374693	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs189137224	chr4:120374696-120374697	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs565098346	chr4:120374699-120374700	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs572090052	chr4:120374744-120374745	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs541152974	chr4:120374750-120374751	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs561040273	chr4:120374751-120374752	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs115560350	chr4:120374757-120374758	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs200461376	chr4:120374774-120374775	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs59182778	chr4:120374798-120374799	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs562825832	chr4:120374842-120374843	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs531472870	chr4:120374845-120374846	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs181233686	chr4:120374932-120374933	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs183811634	chr4:120374937-120374938	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120328800-120375200	Weak transcription	Ovary	ovary
2	chr4:120345400-120375200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr4:120349400-120375400	Weak transcription	Lung	lung
4	chr4:120353200-120375000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:120353200-120375200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:120353200-120375200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr4:120353400-120375200	Weak transcription	Pancreas	Pancrea
8	chr4:120354000-120375000	Weak transcription	Placenta	Placenta
9	chr4:120354400-120375200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr4:120354600-120375200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr4:120354800-120375600	Weak transcription	Spleen	Spleen
12	chr4:120355000-120375200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr4:120355200-120375000	Weak transcription	Fetal Muscle Leg	muscle
14	chr4:120355800-120375000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr4:120357800-120375000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr4:120358400-120374800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr4:120358600-120375200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:120358800-120375200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr4:120359000-120375400	Weak transcription	Left Ventricle	heart
20	chr4:120360000-120375200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr4:120360000-120375400	Weak transcription	Brain Substantia Nigra	brain
22	chr4:120360000-120375400	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr4:120360200-120375400	Weak transcription	Esophagus	oesophagus
24	chr4:120360400-120375200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr4:120361400-120375200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr4:120361400-120375400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr4:120361800-120375200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr4:120362400-120375200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr4:120362600-120375200	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr4:120363400-120375000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:120364000-120375200	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr4:120364000-120375400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr4:120364000-120375400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr4:120364400-120375200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:120364400-120375200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr4:120364400-120375400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:120365000-120375200	Weak transcription	Brain Angular Gyrus	brain
38	chr4:120365200-120375200	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr4:120366600-120375200	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr4:120367000-120375000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:120367600-120375400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:120368400-120375400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:120368800-120375200	Weak transcription	Primary T cells from cord blood	blood
44	chr4:120370000-120374600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:120370000-120374600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:120370000-120375200	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr4:120370000-120375200	Weak transcription	Brain Anterior Caudate	brain
48	chr4:120370000-120375200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr4:120370000-120375200	Weak transcription	Fetal Stomach	stomach
50	chr4:120370200-120375200	Weak transcription	Adipose Nuclei	Adipose

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