Variant report

Variant	nsv524994
Chromosome Location	chr4:8373832-8380857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:916)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr4:8374921-8375373	GM12878	blood:	n/a	n/a
2	BCL3	chr4:8374852-8375403	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:8376765-8376915	K562	blood:	n/a	n/a
4	CHD2	chr4:8377263-8377280	K562	blood:	n/a	n/a
5	CTCF	chr4:8377126-8377354	H1-hESC	embryonic stem cell:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
6	CTCF	chr4:8377176-8377269	H1-hESC	embryonic stem cell:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
7	CTCF	chr4:8377140-8377290	SK-N-SH_RA	brain:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
8	CTCF	chr4:8377200-8377350	GM06990	blood:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
9	CTCF	chr4:8377220-8377370	WERI-Rb-1	eye:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
10	CTCF	chr4:8378360-8378510	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr4:8377160-8377310	HBMEC	blood vessel:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
12	EP300	chr4:8377949-8378656	ECC-1	luminal epithelium:	n/a	n/a
13	GATA3	chr4:8377757-8378060	SH-SY5Y	brain:	n/a	n/a
14	HMGN3	chr4:8379130-8379293	K562	blood:	n/a	n/a
15	MAX	chr4:8378249-8378624	ECC-1	luminal epithelium:	n/a	n/a
16	MAX	chr4:8378052-8378569	ECC-1	luminal epithelium:	n/a	n/a
17	NFATC1	chr4:8374912-8375422	GM12878	blood:	n/a	n/a
18	NFATC1	chr4:8374869-8375319	GM12878	blood:	n/a	n/a
19	NFIC	chr4:8377960-8378735	ECC-1	luminal epithelium:	n/a	n/a
20	NFIC	chr4:8378083-8378689	ECC-1	luminal epithelium:	n/a	n/a
21	PBX3	chr4:8374946-8375156	GM12878	blood:	n/a	n/a
22	POLR2A	chr4:8375005-8375014	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr4:8377475-8377493	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr4:8375051-8375250	ECC-1	luminal epithelium:	n/a	n/a
25	POLR2A	chr4:8377765-8377790	GM12878	blood:	n/a	n/a
26	POLR2A	chr4:8374650-8374678	K562	blood:	n/a	n/a
27	POLR2A	chr4:8375405-8375611	ECC-1	luminal epithelium:	n/a	n/a
28	POLR2A	chr4:8374525-8374568	K562	blood:	n/a	n/a
29	POLR2A	chr4:8376839-8376853	K562	blood:	n/a	n/a
30	POLR2A	chr4:8375922-8376041	K562	blood:	n/a	n/a
31	POLR2A	chr4:8374917-8375386	K562	blood:	n/a	n/a
32	POLR2A	chr4:8376298-8376499	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr4:8378403-8379364	K562	blood:	n/a	n/a
34	POLR2A	chr4:8374887-8375357	GM12892	blood:	n/a	n/a
35	POLR2A	chr4:8378712-8378879	GM12878	blood:	n/a	n/a
36	RAD21	chr4:8377011-8377387	H1-hESC	embryonic stem cell:	n/a	n/a
37	STAT5A	chr4:8374908-8375333	GM12878	blood:	n/a	n/a
38	TCF12	chr4:8378025-8378741	ECC-1	luminal epithelium:	n/a	chr4:8378703-8378710 chr4:8378325-8378333
39	TCF12	chr4:8377983-8378715	ECC-1	luminal epithelium:	n/a	chr4:8378703-8378710 chr4:8378325-8378333
40	TCF3	chr4:8374945-8375200	GM12878	blood:	n/a	n/a
41	TCF3	chr4:8374930-8375397	GM12878	blood:	n/a	n/a
42	TEAD4	chr4:8378076-8378626	ECC-1	luminal epithelium:	n/a	n/a
43	ZNF143	chr4:8378598-8378776	H1-hESC	embryonic stem cell:	n/a	n/a
44	ZNF384	chr4:8380761-8381037	K562	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8376254-8376304	GM06990	blood:	n/a
2	chr4:8376254-8376304	GM06990	blood:	n/a
3	chr4:8378176-8378226	NHBE	bronchial:	n/a
4	chr4:8374429-8374479	Hela-S3	cervix:	n/a
5	chr4:8376908-8376958	NH-A	brain:	n/a
6	chr4:8375240-8375290	SAEC	small airway:	n/a
7	chr4:8375268-8375318	SAEC	small airway:	n/a
8	chr4:8378176-8378226	T-47D	breast:	n/a
9	chr4:8376254-8376304	GM12892	blood:	n/a
10	chr4:8375240-8375290	MCF10A-Er-Src	breast:	n/a
11	chr4:8379573-8379623	AG04450	lung:	fetal
12	chr4:8376908-8376958	SK-N-MC	brain:	n/a
13	chr4:8375268-8375318	SK-N-MC	brain:	n/a
14	chr4:8379238-8379288	NHBE	bronchial:	n/a
15	chr4:8375240-8375290	A549	lung:	n/a
16	chr4:8376835-8376885	GM12892	blood:	n/a
17	chr4:8379238-8379288	GM06990	blood:	n/a
18	chr4:8378947-8378997	CMK	blood:	n/a
19	chr4:8374429-8374479	Hepatocyte	liver:	n/a
20	chr4:8374697-8374747	GM19239	blood:	n/a
21	chr4:8376835-8376885	ECC-1	luminal epithelium:	n/a
22	chr4:8379238-8379288	IMR90	lung:	fetal
23	chr4:8374561-8374611	Jurkat	blood:	n/a
24	chr4:8376835-8376885	MCF-7	breast:	n/a
25	chr4:8378947-8378997	AG04450	lung:	fetal
26	chr4:8376764-8376814	HCPEpiC	choroid plexus:	n/a
27	chr4:8374561-8374611	PrEC	prostate:	n/a
28	chr4:8379238-8379288	Caco-2	colon:	n/a
29	chr4:8379573-8379623	T-47D	breast:	n/a
30	chr4:8378947-8378997	SKMC	muscle:	n/a
31	chr4:8379238-8379288	LNCaP	prostate:	n/a
32	chr4:8375268-8375318	HNPCEpiC	eye:	n/a
33	chr4:8374182-8374232	AG10803	skin:	n/a
34	chr4:8378947-8378997	A549	lung:	n/a
35	chr4:8376254-8376304	SKMC	muscle:	n/a
36	chr4:8376764-8376814	ovcar-3	ovarian:	n/a
37	chr4:8375268-8375318	HUVEC	blood vessel:	n/a
38	chr4:8375240-8375290	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:8375268-8375318	IMR90	lung:	fetal
40	chr4:8377208-8377258	HCPEpiC	choroid plexus:	n/a
41	chr4:8374561-8374611	SK-N-SH_RA	brain:	n/a
42	chr4:8376835-8376885	SAEC	small airway:	n/a
43	chr4:8376764-8376814	RPTEC	kidney:	n/a
44	chr4:8374697-8374747	NH-A	brain:	n/a
45	chr4:8376764-8376814	A549	lung:	n/a
46	chr4:8376764-8376814	NB4	blood:	n/a
47	chr4:8376254-8376304	AG09309	skin:	n/a
48	chr4:8376908-8376958	SKMC	muscle:	n/a
49	chr4:8378176-8378226	A549	lung:	n/a
50	chr4:8376254-8376304	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:8372807..8374828-chr4:8375470..8377502,2	K562	blood:
2	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
3	chr4:8380856..8382490-chr4:8382492..8384875,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL19-5	chr4:8374584-8374779	l_2595_chr4:8372786-8374779_heart
2	lnc-METTL19-5	chr4:8376346-8376594	l_2595_chr4:8372786-8374779_heart

No data

Variant related genes	Relation type
ACOX3	TF binding region
ACOX3	CpG island
ENSG00000087008	chromatin interactions

Extended variants
information (count: 416 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs747582	chr4:8373832-8373833	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368624024	chr4:8373847-8373848	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563407998	chr4:8373848-8373849	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181040197	chr4:8373862-8373863	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543166612	chr4:8373891-8373892	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs747581	chr4:8373893-8373894	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs532477054	chr4:8373900-8373901	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370641581	chr4:8373941-8373942	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs565697312	chr4:8373964-8373965	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529627766	chr4:8373997-8373998	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548318361	chr4:8374047-8374048	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548385266	chr4:8374053-8374054	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569725174	chr4:8374115-8374116	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374136723	chr4:8374122-8374123	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs115920673	chr4:8374123-8374124	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559237324	chr4:8374150-8374151	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10023885	chr4:8374183-8374184	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs535358919	chr4:8374190-8374191	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553363435	chr4:8374244-8374245	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569841631	chr4:8374247-8374248	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111619339	chr4:8374271-8374272	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541781805	chr4:8374300-8374301	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557039898	chr4:8374310-8374311	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs575380160	chr4:8374317-8374318	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73085876	chr4:8374331-8374332	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556580604	chr4:8374334-8374335	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564772073	chr4:8374342-8374343	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532186344	chr4:8374349-8374350	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs368017587	chr4:8374353-8374354	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs827011	chr4:8374359-8374360	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs114532701	chr4:8374360-8374361	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552125478	chr4:8374365-8374366	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143259608	chr4:8374371-8374372	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563266455	chr4:8374421-8374422	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10024067	chr4:8374430-8374431	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs555660999	chr4:8374475-8374476	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552283095	chr4:8374476-8374477	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571048708	chr4:8374486-8374487	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs73085877	chr4:8374520-8374521	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs185484123	chr4:8374534-8374535	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190738734	chr4:8374544-8374545	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553791967	chr4:8374601-8374602	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs556974880	chr4:8374627-8374628	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs377150751	chr4:8374634-8374635	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs375232405	chr4:8374690-8374691	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs150878710	chr4:8374695-8374696	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs576981150	chr4:8374698-8374699	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs181507841	chr4:8374732-8374733	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs559599790	chr4:8374733-8374734	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs862345	chr4:8374760-8374761	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:53)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8354600-8381000	Weak transcription	Right Atrium	heart
2	chr4:8355800-8384800	Weak transcription	Fetal Lung	lung
3	chr4:8360400-8394000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:8360400-8395600	Weak transcription	NHEK	skin
5	chr4:8362000-8395400	Weak transcription	Fetal Brain Male	brain
6	chr4:8362800-8380200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:8364000-8383400	Weak transcription	Colonic Mucosa	Colon
8	chr4:8364000-8388600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:8364200-8387000	Weak transcription	Dnd41	blood
10	chr4:8364600-8376800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:8364600-8378200	Weak transcription	NH-A	brain
12	chr4:8364800-8387000	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr4:8364800-8392400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:8365000-8382800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr4:8365000-8385000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr4:8365200-8385000	Weak transcription	NHLF	lung
17	chr4:8365400-8376400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr4:8365400-8383600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:8365600-8382200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr4:8365600-8388800	Weak transcription	Primary B cells from peripheral blood	blood
21	chr4:8365800-8383600	Strong transcription	Fetal Stomach	stomach
22	chr4:8366000-8382800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr4:8366400-8376000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr4:8366400-8378200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:8366400-8378200	Weak transcription	Small Intestine	intestine
26	chr4:8366400-8378600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr4:8366400-8380600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:8366400-8411600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr4:8366600-8375000	Weak transcription	Brain Substantia Nigra	brain
30	chr4:8366800-8386000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:8366800-8390000	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr4:8367000-8375400	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr4:8367400-8379200	Weak transcription	HSMMtube	muscle
34	chr4:8367400-8384800	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr4:8367400-8386800	Weak transcription	Primary B cells from cord blood	blood
36	chr4:8367800-8384800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:8368000-8378800	Weak transcription	Colon Smooth Muscle	Colon
38	chr4:8368000-8380600	Weak transcription	Thymus	Thymus
39	chr4:8368400-8374600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr4:8368400-8379200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr4:8368400-8388400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:8368600-8375000	Weak transcription	Fetal Brain Female	brain
43	chr4:8368600-8376200	Weak transcription	Brain Angular Gyrus	brain
44	chr4:8368600-8380600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:8368800-8374200	Weak transcription	Aorta	Aorta
46	chr4:8368800-8375400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:8368800-8375800	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr4:8368800-8379600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:8368800-8382600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr4:8368800-8384200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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