Variant report

Variant	nsv878608
Chromosome Location	chr4:8349738-8386720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:2136)
Chromatin interactive
region (count:30)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:8359490-8359857	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:8359436-8359516	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:8385904-8386155	GM12878	blood:	n/a	n/a
4	BATF	chr4:8385984-8386148	GM12878	blood:	n/a	n/a
5	BCL3	chr4:8374852-8375403	GM12878	blood:	n/a	n/a
6	BCL3	chr4:8383586-8383809	GM12878	blood:	n/a	n/a
7	BCL3	chr4:8374921-8375373	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:8373374-8373615	K562	blood:	n/a	n/a
9	BHLHE40	chr4:8349911-8350172	GM12878	blood:	n/a	chr4:8350024-8350033
10	BHLHE40	chr4:8372628-8373087	K562	blood:	n/a	chr4:8372836-8372845 chr4:8372836-8372845
11	BHLHE40	chr4:8385991-8386223	GM12878	blood:	n/a	chr4:8386188-8386204
12	BHLHE40	chr4:8369879-8369917	K562	blood:	n/a	n/a
13	BHLHE40	chr4:8349739-8350219	K562	blood:	n/a	chr4:8350024-8350033
14	BHLHE40	chr4:8376765-8376915	K562	blood:	n/a	n/a
15	BHLHE40	chr4:8351624-8351692	K562	blood:	n/a	n/a
16	BHLHE40	chr4:8354399-8354611	K562	blood:	n/a	chr4:8354498-8354507 chr4:8354496-8354512
17	BHLHE40	chr4:8349894-8350191	HepG2	liver:	n/a	chr4:8350024-8350033
18	CEBPB	chr4:8353775-8353986	HepG2	liver:	n/a	n/a
19	CHD1	chr4:8359330-8359337	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:8377263-8377280	K562	blood:	n/a	n/a
21	CHD2	chr4:8359488-8360184	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr4:8383735-8383929	HepG2	liver:	n/a	n/a
23	CTCF	chr4:8353880-8354030	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr4:8368600-8368750	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr4:8366700-8366850	GM12878	blood:	n/a	chr4:8366793-8366811 chr4:8366799-8366808
26	CTCF	chr4:8377200-8377350	GM06990	blood:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
27	CTCF	chr4:8377126-8377354	H1-hESC	embryonic stem cell:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
28	CTCF	chr4:8383700-8383850	AG04449	skin:	n/a	n/a
29	CTCF	chr4:8377220-8377370	WERI-Rb-1	eye:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
30	CTCF	chr4:8383700-8383795	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:8385640-8385790	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr4:8371880-8372030	Caco-2	colon:	n/a	n/a
33	CTCF	chr4:8383682-8383812	NHEK	skin:	n/a	n/a
34	CTCF	chr4:8377160-8377310	HBMEC	blood vessel:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
35	CTCF	chr4:8377176-8377269	H1-hESC	embryonic stem cell:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
36	CTCF	chr4:8378360-8378510	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr4:8385780-8385930	AG10803	skin:	n/a	n/a
38	CTCF	chr4:8377140-8377290	SK-N-SH_RA	brain:	n/a	chr4:8377223-8377241 chr4:8377226-8377239 chr4:8377226-8377235
39	CUX1	chr4:8356940-8357223	GM12878	blood:	n/a	n/a
40	E2F4	chr4:8361892-8362092	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F6	chr4:8369784-8369902	K562	blood:	n/a	n/a
42	EBF1	chr4:8356980-8357278	GM12878	blood:	n/a	n/a
43	EBF1	chr4:8386041-8386211	GM12878	blood:	n/a	n/a
44	EBF1	chr4:8372303-8372546	GM12878	blood:	n/a	n/a
45	EGR1	chr4:8353562-8353985	MCF-7	breast:	n/a	chr4:8353735-8353757
46	EGR1	chr4:8359889-8360235	H1-hESC	embryonic stem cell:	n/a	n/a
47	EP300	chr4:8357063-8357427	Hela-S3	cervix:	n/a	n/a
48	EP300	chr4:8386036-8386214	GM12878	blood:	n/a	chr4:8386086-8386093 chr4:8386056-8386066 chr4:8386104-8386118
49	EP300	chr4:8357104-8357304	GM12878	blood:	n/a	n/a
50	EP300	chr4:8377949-8378656	ECC-1	luminal epithelium:	n/a	n/a

(count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8376254-8376304	A549	lung:	n/a
2	chr4:8376254-8376304	A549	lung:	n/a
3	chr4:8378176-8378226	Hela-S3	cervix:	n/a
4	chr4:8368601-8368651	RPTEC	kidney:	n/a
5	chr4:8376835-8376885	HEK293	kidney:	embryo
6	chr4:8351738-8351788	GM12892	blood:	n/a
7	chr4:8359458-8359508	NB4	blood:	n/a
8	chr4:8374697-8374747	RPTEC	kidney:	n/a
9	chr4:8378947-8378997	LNCaP	prostate:	n/a
10	chr4:8375268-8375318	PFSK-1	brain:	n/a
11	chr4:8376254-8376304	HRCEpiC	kidney:	n/a
12	chr4:8386198-8386248	AG09309	skin:	n/a
13	chr4:8386266-8386316	ovcar-3	ovarian:	n/a
14	chr4:8378947-8378997	AG10803	skin:	n/a
15	chr4:8386188-8386238	AG04449	skin:	fetal
16	chr4:8351738-8351788	NT2-D1	testis:	n/a
17	chr4:8386266-8386316	HCF	heart:	n/a
18	chr4:8376254-8376304	HUVEC	blood vessel:	n/a
19	chr4:8354138-8354188	SAEC	small airway:	n/a
20	chr4:8386198-8386248	HAEpiC	amniotic membrane:	n/a
21	chr4:8368486-8368536	SAEC	small airway:	n/a
22	chr4:8359247-8359297	HIPEpiC	eye:	n/a
23	chr4:8376835-8376885	HMEC	breast:	n/a
24	chr4:8368601-8368651	PrEC	prostate:	n/a
25	chr4:8372758-8372808	K562	blood:	n/a
26	chr4:8376908-8376958	HCT-116	colon:	n/a
27	chr4:8376908-8376958	HepG2	liver:	n/a
28	chr4:8373438-8373488	SAEC	small airway:	n/a
29	chr4:8378176-8378226	GM19239	blood:	n/a
30	chr4:8355043-8355093	NT2-D1	testis:	n/a
31	chr4:8386188-8386238	CMK	blood:	n/a
32	chr4:8375268-8375318	GM12878	blood:	n/a
33	chr4:8386266-8386316	GM12891	blood:	n/a
34	chr4:8375240-8375290	HRPEpiC	eye:	n/a
35	chr4:8376254-8376304	MCF10A-Er-Src	breast:	n/a
36	chr4:8359269-8359319	T-47D	breast:	n/a
37	chr4:8376764-8376814	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:8359269-8359319	GM06990	blood:	n/a
39	chr4:8373516-8373566	NHDF-neo	bronchial:	n/a
40	chr4:8375240-8375290	AoSMC	blood vessel:	n/a
41	chr4:8374182-8374232	Hepatocyte	liver:	n/a
42	chr4:8351738-8351788	GM12878	blood:	n/a
43	chr4:8379238-8379288	GM06990	blood:	n/a
44	chr4:8374429-8374479	RPTEC	kidney:	n/a
45	chr4:8359458-8359508	AG04450	lung:	fetal
46	chr4:8379238-8379288	GM19239	blood:	n/a
47	chr4:8373438-8373488	IMR90	lung:	fetal
48	chr4:8376835-8376885	Hela-S3	cervix:	n/a
49	chr4:8376908-8376958	NHDF-neo	bronchial:	n/a
50	chr4:8375240-8375290	AG10803	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
2	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
3	chr4:8358055..8360875-chr4:8366726..8369353,3	K562	blood:
4	chr4:8380860..8383722-chr4:8386573..8388850,2	K562	blood:
5	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
6	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
7	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
8	chr4:8385149..8387717-chr4:8393140..8395716,2	K562	blood:
9	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
10	chr4:8380856..8382490-chr4:8382492..8384875,2	MCF-7	breast:
11	chr4:8383597..8386239-chr4:8397040..8399494,2	K562	blood:
12	chr4:8380860..8383722-chr4:8386573..8388850,2	K562	blood:
13	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
14	chr4:8380856..8382490-chr4:8382492..8384875,2	MCF-7	breast:
15	chr4:8308134..8310233-chr4:8366379..8367956,2	K562	blood:
16	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
17	chr4:8370118..8372500-chr4:8374648..8377546,2	K562	blood:
18	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
19	chr4:8372807..8374828-chr4:8375470..8377502,2	K562	blood:
20	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
21	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
22	chr4:8372002..8373720-chr4:8374604..8376742,2	MCF-7	breast:
23	chr4:8359754..8361327-chr4:8385821..8388152,2	MCF-7	breast:
24	chr4:8346988..8348504-chr4:8352358..8355226,2	K562	blood:
25	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
26	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
27	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
28	chr4:8385368..8387475-chr4:8389606..8391227,2	MCF-7	breast:
29	chr4:8338499..8340014-chr4:8350078..8351770,2	K562	blood:
30	chr4:8385799..8388766-chr4:8429513..8431932,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HTRA3-4	chr4:8358049-8358702	NONHSAT095089
2	lnc-METTL19-5	chr4:8376346-8376594	l_2595_chr4:8372786-8374779_heart
3	lnc-ACOX3-5	chr4:8367183-8367485	NONHSAT095091
4	lnc-METTL19-5	chr4:8374584-8374779	l_2595_chr4:8372786-8374779_heart
5	lnc-ACOX3-1	chr4:8357038-8359103	ENSG00000251615
6	lnc-HTRA3-4	chr4:8358805-8360149	NONHSAT095089
7	lnc-ACOX3-5	chr4:8365860-8366475	NONHSAT095091
8	lnc-METTL19-5	chr4:8372787-8373149	l_2595_chr4:8372786-8374779_heart
9	lnc-ACOX3-1	chr4:8356817-8359103	NONHSAT095088
10	lnc-ACOX3-1	chr4:8356817-8360065	ENSG00000251615.3

No data

Variant related genes	Relation type
ENSG00000251615	TF binding region
ACOX3	TF binding region
ENSG00000251615	CpG island
ACOX3	CpG island
ENSG00000202054	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000251615	chromatin interactions

Extended variants
information (count: 1935 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1935 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1678305	chr4:8349738-8349739	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147916151	chr4:8349792-8349793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73799139	chr4:8349793-8349794	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs77453519	chr4:8349799-8349800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375740275	chr4:8349838-8349839	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs531948663	chr4:8349844-8349845	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs563159490	chr4:8349864-8349865	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs540647882	chr4:8349901-8349902	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs562466265	chr4:8349909-8349910	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs559004121	chr4:8349950-8349951	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs532929455	chr4:8349967-8349968	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs551172082	chr4:8349975-8349976	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs35668769	chr4:8349985-8349986	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs367888494	chr4:8349994-8349995	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs114334823	chr4:8350022-8350023	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs192875644	chr4:8350027-8350028	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs528625247	chr4:8350028-8350029	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs2015471	chr4:8350081-8350082	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs568390269	chr4:8350082-8350083	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs185406244	chr4:8350122-8350123	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs568445078	chr4:8350136-8350137	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs535871851	chr4:8350140-8350141	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs189426197	chr4:8350237-8350238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554463664	chr4:8350263-8350264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141650346	chr4:8350266-8350267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543268167	chr4:8350278-8350279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181227483	chr4:8350283-8350284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569579323	chr4:8350297-8350298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576757230	chr4:8350303-8350304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568804458	chr4:8350327-8350328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540607668	chr4:8350383-8350384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145328470	chr4:8350406-8350407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529747105	chr4:8350438-8350439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184880654	chr4:8350445-8350446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151041471	chr4:8350479-8350480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs60783208	chr4:8350526-8350527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs71175479	chr4:8350528-8350529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77242236	chr4:8350529-8350530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79853908	chr4:8350530-8350531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76269449	chr4:8350538-8350539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79810248	chr4:8350539-8350540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543588863	chr4:8350541-8350542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552828021	chr4:8350556-8350557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368507120	chr4:8350677-8350678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528830661	chr4:8350727-8350728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547008160	chr4:8350732-8350733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372769922	chr4:8350736-8350737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141084510	chr4:8350758-8350759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188131844	chr4:8350762-8350763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180999286	chr4:8350770-8350771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8342800-8352800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:8344600-8352800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:8344600-8354000	Weak transcription	Left Ventricle	heart
4	chr4:8345800-8353000	Weak transcription	Right Atrium	heart
5	chr4:8346400-8349800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:8346400-8351600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr4:8346800-8352800	Weak transcription	HSMMtube	muscle
8	chr4:8348800-8349800	Enhancers	Spleen	Spleen
9	chr4:8348800-8351400	Weak transcription	Fetal Muscle Leg	muscle
10	chr4:8349000-8350000	Enhancers	Ovary	ovary
11	chr4:8349000-8351600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:8349000-8353400	Weak transcription	Brain Anterior Caudate	brain
13	chr4:8349000-8353600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr4:8349000-8353600	Weak transcription	Brain Substantia Nigra	brain
15	chr4:8349000-8357600	Weak transcription	Fetal Heart	heart
16	chr4:8349200-8353000	Weak transcription	Brain Hippocampus Middle	brain
17	chr4:8349200-8353400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr4:8349400-8350200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr4:8349400-8350800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr4:8349400-8350800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:8349400-8353800	Weak transcription	Brain Angular Gyrus	brain
22	chr4:8349600-8350200	Enhancers	Fetal Thymus	thymus
23	chr4:8349600-8350400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:8349600-8352800	Weak transcription	Brain Cingulate Gyrus	brain
25	chr4:8349600-8353800	Weak transcription	Right Ventricle	heart
26	chr4:8349800-8350000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:8349800-8350000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr4:8349800-8350200	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr4:8349800-8350200	Bivalent Enhancer	Placenta	Placenta
30	chr4:8349800-8350200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr4:8349800-8350800	Enhancers	Primary hematopoietic stem cells	blood
32	chr4:8349800-8351600	Weak transcription	Spleen	Spleen
33	chr4:8350000-8350200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr4:8350000-8350400	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr4:8350000-8351400	Weak transcription	Ovary	ovary
36	chr4:8350000-8353000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:8350200-8352400	Weak transcription	Fetal Thymus	thymus
38	chr4:8351400-8355400	Enhancers	Fetal Muscle Leg	muscle
39	chr4:8351400-8356400	Enhancers	Ovary	ovary
40	chr4:8351600-8351800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:8351600-8351800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr4:8351600-8351800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:8351600-8351800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:8351600-8351800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:8351600-8351800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr4:8351600-8351800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:8351600-8351800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
48	chr4:8351600-8354600	Enhancers	Spleen	Spleen
49	chr4:8351600-8355400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr4:8351600-8356000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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