Variant report

Variant	esv1811736
Chromosome Location	chr4:10454409-10467939
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:646)
CpG islands
(count:1771)
Chromatin interactive
region (count:19)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10459741-10459919	K562	blood:	n/a	n/a
2	ARID3A	chr4:10460913-10461399	K562	blood:	n/a	n/a
3	ATF3	chr4:10462880-10463147	K562	blood:	n/a	n/a
4	BACH1	chr4:10462826-10463788	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:10462736-10463370	K562	blood:	n/a	n/a
6	BACH1	chr4:10458630-10459108	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:10461300-10461416	K562	blood:	n/a	n/a
8	BATF	chr4:10461948-10462177	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:10462844-10463255	K562	blood:	n/a	chr4:10462953-10462969 chr4:10462950-10462966 chr4:10462947-10462963 chr4:10462949-10462965 chr4:10463133-10463149
10	BHLHE40	chr4:10458017-10458645	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:10462903-10463146	GM12878	blood:	n/a	chr4:10462953-10462969 chr4:10462950-10462966 chr4:10462947-10462963 chr4:10462949-10462965
12	BHLHE40	chr4:10458951-10459247	GM12878	blood:	n/a	chr4:10459125-10459141
13	BHLHE40	chr4:10459217-10460106	K562	blood:	n/a	n/a
14	BHLHE40	chr4:10460967-10461712	K562	blood:	n/a	n/a
15	BRCA1	chr4:10462928-10463022	GM12878	blood:	n/a	n/a
16	BRCA1	chr4:10463085-10463106	HepG2	liver:	n/a	n/a
17	CBX3	chr4:10458207-10458558	K562	blood:	n/a	n/a
18	CBX3	chr4:10459827-10460193	K562	blood:	n/a	n/a
19	CBX3	chr4:10462293-10463603	K562	blood:	n/a	n/a
20	CBX3	chr4:10462629-10463372	K562	blood:	n/a	n/a
21	CCNT2	chr4:10462773-10463268	K562	blood:	n/a	n/a
22	CCNT2	chr4:10458055-10459262	K562	blood:	n/a	chr4:10458645-10458654 chr4:10458501-10458510 chr4:10458704-10458713
23	CCNT2	chr4:10459488-10460006	K562	blood:	n/a	chr4:10459969-10459978
24	CEBPB	chr4:10462027-10462167	K562	blood:	n/a	n/a
25	CEBPB	chr4:10462820-10463261	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:10456451-10456636	K562	blood:	n/a	n/a
27	CHD1	chr4:10458182-10458487	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr4:10458305-10458582	GM12878	blood:	n/a	chr4:10458502-10458512
29	CHD2	chr4:10458042-10458733	GM12878	blood:	n/a	chr4:10458502-10458512 chr4:10458125-10458135
30	CHD2	chr4:10458313-10458518	H1-hESC	embryonic stem cell:	n/a	chr4:10458502-10458512
31	CHD2	chr4:10461170-10461366	K562	blood:	n/a	n/a
32	CHD2	chr4:10462900-10463412	H1-hESC	embryonic stem cell:	n/a	chr4:10463287-10463297 chr4:10463178-10463188
33	CHD2	chr4:10458975-10459466	GM12878	blood:	n/a	n/a
34	CHD2	chr4:10463573-10463605	HepG2	liver:	n/a	n/a
35	CHD2	chr4:10459845-10459931	K562	blood:	n/a	n/a
36	CHD2	chr4:10462965-10463149	GM12878	blood:	n/a	n/a
37	CHD2	chr4:10458270-10458572	K562	blood:	n/a	chr4:10458502-10458512
38	CHD2	chr4:10462689-10463317	K562	blood:	n/a	chr4:10463287-10463297 chr4:10463178-10463188
39	CREB1	chr4:10462856-10463323	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr4:10458194-10458641	A549	lung:	n/a	n/a
41	CREB1	chr4:10458845-10459076	A549	lung:	n/a	n/a
42	CREB1	chr4:10458116-10458662	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr4:10458065-10458644	GM12878	blood:	n/a	n/a
44	CTCF	chr4:10462966-10463187	Medullo	brain:	n/a	n/a
45	CTCF	chr4:10463000-10463150	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr4:10463000-10463150	GM12873	blood:	n/a	n/a
47	CTCF	chr4:10463000-10463150	GM12870	blood:	n/a	n/a
48	CTCF	chr4:10462980-10463130	HCM	heart:	n/a	n/a
49	CTCF	chr4:10462873-10463435	K562	blood:	n/a	n/a
50	CTCF	chr4:10463000-10463150	HUVEC	blood vessel:	n/a	n/a

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10458454-10458504	AG10803	skin:	n/a
2	chr4:10459132-10459182	HCF	heart:	n/a
3	chr4:10458454-10458504	AG10803	skin:	n/a
4	chr4:10459132-10459182	HCF	heart:	n/a
5	chr4:10459128-10459178	GM06990	blood:	n/a
6	chr4:10463620-10463670	GM06990	blood:	n/a
7	chr4:10459132-10459182	HEK293	kidney:	embryo
8	chr4:10459929-10459979	A549	lung:	n/a
9	chr4:10459929-10459979	Hela-S3	cervix:	n/a
10	chr4:10458531-10458581	NHBE	bronchial:	n/a
11	chr4:10459435-10459485	NH-A	brain:	n/a
12	chr4:10461465-10461515	H1-hESC	embryonic stem cell:	embryo
13	chr4:10467319-10467369	NT2-D1	testis:	n/a
14	chr4:10463350-10463400	HCM	heart:	n/a
15	chr4:10461465-10461515	HMEC	breast:	n/a
16	chr4:10462903-10462953	AG04450	lung:	fetal
17	chr4:10463590-10463640	HNPCEpiC	eye:	n/a
18	chr4:10458454-10458504	Caco-2	colon:	n/a
19	chr4:10461465-10461515	GM06990	blood:	n/a
20	chr4:10463350-10463400	HL-60	blood:	n/a
21	chr4:10458454-10458504	IMR90	lung:	fetal
22	chr4:10459183-10459233	H1-hESC	embryonic stem cell:	embryo
23	chr4:10462849-10462899	AG04449	skin:	fetal
24	chr4:10458531-10458581	GM12891	blood:	n/a
25	chr4:10458049-10458099	LNCaP	prostate:	n/a
26	chr4:10462903-10462953	AG09309	skin:	n/a
27	chr4:10458454-10458504	ovcar-3	ovarian:	n/a
28	chr4:10459929-10459979	Jurkat	blood:	n/a
29	chr4:10459435-10459485	AG09309	skin:	n/a
30	chr4:10463749-10463799	A549	lung:	n/a
31	chr4:10463620-10463670	ovcar-3	ovarian:	n/a
32	chr4:10467319-10467369	AG09309	skin:	n/a
33	chr4:10458531-10458581	NT2-D1	testis:	n/a
34	chr4:10463749-10463799	SK-N-SH_RA	brain:	n/a
35	chr4:10459352-10459402	HL-60	blood:	n/a
36	chr4:10458531-10458581	HepG2	liver:	n/a
37	chr4:10462849-10462899	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:10467319-10467369	HEK293	kidney:	embryo
39	chr4:10459228-10459278	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:10456597-10456647	HRE	kidney:	n/a
41	chr4:10459836-10459886	PrEC	prostate:	n/a
42	chr4:10459163-10459213	NB4	blood:	n/a
43	chr4:10461465-10461515	AG04450	lung:	fetal
44	chr4:10458165-10458215	GM19239	blood:	n/a
45	chr4:10461465-10461515	HEEpiC	esophagus:	n/a
46	chr4:10463620-10463670	SKMC	muscle:	n/a
47	chr4:10459435-10459485	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:10460009-10460059	BJ	skin:	n/a
49	chr4:10458531-10458581	SAEC	small airway:	n/a
50	chr4:10463620-10463670	K562	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10436820..10442109-chr4:10453962..10457876,6	K562	blood:
2	chr4:10182377..10185038-chr4:10453503..10456156,2	K562	blood:
3	chr4:10186685..10189037-chr4:10459555..10461188,2	K562	blood:
4	chr4:10114078..10122203-chr4:10455501..10461954,12	K562	blood:
5	chr4:10117123..10120331-chr4:10451418..10454682,4	K562	blood:
6	chr4:10111136..10113091-chr4:10453721..10455357,2	K562	blood:
7	chr4:10104180..10106384-chr4:10453224..10455811,2	K562	blood:
8	chr4:10177971..10181867-chr4:10459708..10464611,4	K562	blood:
9	chr4:10439495..10442453-chr4:10454853..10458527,4	K562	blood:
10	chr4:10168181..10169847-chr4:10460956..10462626,2	K562	blood:
11	chr4:10142152..10144542-chr4:10456013..10458159,2	K562	blood:
12	chr4:10462498..10464981-chr4:10471870..10474447,2	K562	blood:
13	chr4:10116897..10119989-chr4:10451461..10454968,3	K562	blood:
14	chr4:10117460..10124392-chr4:10456675..10465032,17	K562	blood:
15	chr17:34890127..34891028-chr4:10458093..10458597,2	HCT-116	colon:
16	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
17	chr4:10285232..10288182-chr4:10462590..10465325,2	K562	blood:
18	chr4:10122860..10124582-chr4:10454402..10456296,2	K562	blood:
19	chr4:10463521..10466499-chr4:10467971..10469908,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLNK-2	chr4:10458941-10459034	NONHSAT095502
2	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095503
3	lnc-CLNK-2	chr4:10458758-10458800	NONHSAT095503
4	lnc-CLNK-2	chr4:10452511-10454646	NONHSAT095501
5	lnc-CLNK-2	chr4:10458941-10459032	NONHSAT095501
6	lnc-CLNK-2	chr4:10456218-10456612	NONHSAT095501
7	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095502

No data

Variant related genes	Relation type
ZNF518B	TF binding region
ZNF518B	CpG island
ENSG00000141140	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000251296	chromatin interactions
ENSG00000184886	chromatin interactions
ENSG00000250505	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 409 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:409 , 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	rs527453363	chr4:10454491-10454492	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs545637889	chr4:10454497-10454498	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs560731722	chr4:10454505-10454506	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs527998913	chr4:10454508-10454509	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs60445736	chr4:10454511-10454512	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs111413536	chr4:10454518-10454519	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs375280504	chr4:10454519-10454520	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs138281322	chr4:10454526-10454527	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs79437705	chr4:10454593-10454594	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs187064369	chr4:10454605-10454606	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs571088621	chr4:10454633-10454634	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs538418830	chr4:10454691-10454692	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs530366870	chr4:10454717-10454718	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs149211485	chr4:10454722-10454723	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs549348854	chr4:10454779-10454780	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs192334547	chr4:10454823-10454824	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs143384007	chr4:10454826-10454827	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs139036143	chr4:10454838-10454839	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs377199192	chr4:10454851-10454852	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs184286963	chr4:10454920-10454921	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs111420973	chr4:10454952-10454953	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs146315772	chr4:10454968-10454969	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs577026928	chr4:10454991-10454992	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs12019277	chr4:10454994-10454995	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs560670127	chr4:10455023-10455024	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs541971146	chr4:10455045-10455046	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
27	rs114535981	chr4:10455057-10455058	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
28	rs561320612	chr4:10455060-10455061	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs531636392	chr4:10455140-10455141	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs550172600	chr4:10455179-10455180	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
31	rs201003762	chr4:10455187-10455188	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
32	rs11482052	chr4:10455188-10455189	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
33	rs398106981	chr4:10455197-10455198	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
34	rs565005869	chr4:10455209-10455210	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
35	rs532481827	chr4:10455217-10455218	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
36	rs576866862	chr4:10455219-10455220	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
37	rs6836073	chr4:10455241-10455242	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
38	rs557795114	chr4:10455268-10455269	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
39	rs565588388	chr4:10455285-10455286	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
40	rs190553926	chr4:10455313-10455314	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
41	rs182379718	chr4:10455314-10455315	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
42	rs548212236	chr4:10455344-10455345	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
43	rs566743766	chr4:10455345-10455346	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
44	rs569953211	chr4:10455369-10455370	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
45	rs371454268	chr4:10455380-10455381	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
46	rs146571028	chr4:10455390-10455391	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
47	rs184431025	chr4:10455410-10455411	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
48	rs76009914	chr4:10455499-10455500	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
49	rs370456155	chr4:10455547-10455548	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs560640225	chr4:10455557-10455558	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
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
Wilms tumour	21544195	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
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
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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD

Chromatin state (count:1116 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10443200-10457000	ZNF genes & repeats	Brain Germinal Matrix	brain
2	chr4:10443400-10457000	ZNF genes & repeats	Fetal Brain Female	brain
3	chr4:10443800-10456400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:10443800-10456800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:10444600-10456600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:10444800-10457000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:10445200-10454600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:10445400-10454600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
9	chr4:10446000-10456600	Strong transcription	HSMM	muscle
10	chr4:10447200-10456800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:10447800-10455600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr4:10448000-10455600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:10448000-10455600	Weak transcription	Right Ventricle	heart
14	chr4:10448000-10455800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr4:10448000-10456200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr4:10448000-10458000	Weak transcription	Brain Angular Gyrus	brain
17	chr4:10448200-10455800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:10448400-10456200	Strong transcription	K562	blood
19	chr4:10448400-10457400	Strong transcription	NHEK	skin
20	chr4:10449000-10456600	Strong transcription	Primary B cells from cord blood	blood
21	chr4:10449200-10455600	Weak transcription	HSMMtube	muscle
22	chr4:10449200-10455800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr4:10449200-10456400	Weak transcription	Fetal Heart	heart
24	chr4:10449200-10457600	Weak transcription	Rectal Smooth Muscle	rectum
25	chr4:10449600-10456800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr4:10449600-10456800	Strong transcription	Fetal Muscle Trunk	muscle
27	chr4:10450000-10456400	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr4:10450000-10457000	Strong transcription	Placenta	Placenta
29	chr4:10450000-10457400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr4:10450200-10455600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr4:10450200-10457400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:10450400-10456600	Strong transcription	Fetal Thymus	thymus
33	chr4:10450600-10457800	Weak transcription	Psoas Muscle	Psoas
34	chr4:10450600-10458000	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr4:10450800-10457200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:10451000-10455800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:10451000-10457200	Strong transcription	Fetal Intestine Large	intestine
38	chr4:10451200-10457000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:10451200-10457200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
40	chr4:10451400-10454600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
41	chr4:10451400-10456600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:10451400-10456800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:10451400-10456800	Strong transcription	Primary B cells from peripheral blood	blood
44	chr4:10451600-10456400	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:10451600-10456800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:10451600-10457000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:10451800-10456000	Weak transcription	Colon Smooth Muscle	Colon
48	chr4:10451800-10456600	Strong transcription	A549	lung
49	chr4:10451800-10456800	Strong transcription	HUVEC	blood vessel
50	chr4:10451800-10457000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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