Variant report

Variant	nsv593691
Chromosome Location	chr4:10013173-10050141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1487)
CpG islands
(count:1101)
Chromatin interactive
region (count:36)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1487 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10048100-10048213	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:10023038-10023398	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:10027037-10027405	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10018550-10019341	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:10032742-10033066	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:10046913-10047474	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:10013565-10013836	K562	blood:	n/a	n/a
8	ARID3A	chr4:10020424-10020705	K562	blood:	n/a	n/a
9	ATF1	chr4:10025316-10025600	K562	blood:	n/a	n/a
10	ATF1	chr4:10013493-10013865	K562	blood:	n/a	n/a
11	ATF2	chr4:10020339-10020818	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:10020411-10021134	GM12878	blood:	n/a	n/a
13	ATF3	chr4:10020471-10020640	GM12878	blood:	n/a	n/a
14	ATF3	chr4:10020397-10020713	K562	blood:	n/a	n/a
15	ATF3	chr4:10034340-10034597	K562	blood:	n/a	chr4:10034394-10034408
16	ATF3	chr4:10020361-10020755	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr4:10013615-10013860	K562	blood:	n/a	n/a
18	BACH1	chr4:10034449-10034649	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:10028131-10028378	K562	blood:	n/a	n/a
20	BACH1	chr4:10020394-10020795	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr4:10020385-10020681	GM12878	blood:	n/a	n/a
22	BATF	chr4:10025493-10025778	GM12878	blood:	n/a	chr4:10025549-10025562 chr4:10025631-10025642
23	BCLAF1	chr4:10020375-10020821	GM12878	blood:	n/a	chr4:10020403-10020412
24	BCLAF1	chr4:10020322-10020853	GM12878	blood:	n/a	chr4:10020403-10020412
25	BCLAF1	chr4:10015371-10015740	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:10020385-10021139	K562	blood:	n/a	chr4:10020562-10020578
27	BHLHE40	chr4:10016817-10017109	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:10035036-10035063	HepG2	liver:	n/a	n/a
29	BHLHE40	chr4:10016839-10017001	K562	blood:	n/a	n/a
30	BHLHE40	chr4:10025784-10025918	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:10025337-10026056	K562	blood:	n/a	n/a
32	BHLHE40	chr4:10015445-10015605	K562	blood:	n/a	n/a
33	BHLHE40	chr4:10020426-10020935	GM12878	blood:	n/a	chr4:10020562-10020578
34	BHLHE40	chr4:10034385-10034876	K562	blood:	n/a	n/a
35	BHLHE40	chr4:10015418-10015621	GM12878	blood:	n/a	n/a
36	BRCA1	chr4:10015552-10015687	GM12878	blood:	n/a	n/a
37	BRCA1	chr4:10036771-10036891	HepG2	liver:	n/a	n/a
38	BRCA1	chr4:10020424-10020721	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr4:10046976-10047593	HCT-116	colon:	n/a	n/a
40	CBX3	chr4:10020385-10020680	K562	blood:	n/a	n/a
41	CBX3	chr4:10020317-10021175	K562	blood:	n/a	n/a
42	CBX3	chr4:10013617-10013966	K562	blood:	n/a	n/a
43	CBX3	chr4:10044228-10044589	K562	blood:	n/a	n/a
44	CBX3	chr4:10044299-10044537	K562	blood:	n/a	n/a
45	CBX3	chr4:10047117-10047557	HCT-116	colon:	n/a	n/a
46	CCNT2	chr4:10034938-10035359	K562	blood:	n/a	n/a
47	CCNT2	chr4:10020432-10020793	K562	blood:	n/a	n/a
48	CCNT2	chr4:10013714-10013988	K562	blood:	n/a	n/a
49	CEBPB	chr4:10034224-10034768	A549	lung:	n/a	n/a
50	CEBPB	chr4:10023017-10023301	IMR90	lung:	n/a	chr4:10023167-10023178

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10022984-10023034	HRCEpiC	kidney:	n/a
2	chr4:10024412-10024462	AG09319	gingival:	n/a
3	chr4:10042842-10042892	HCM	heart:	n/a
4	chr4:10022984-10023034	HRCEpiC	kidney:	n/a
5	chr4:10024412-10024462	AG09319	gingival:	n/a
6	chr4:10042842-10042892	HCM	heart:	n/a
7	chr4:10020634-10020684	PFSK-1	brain:	n/a
8	chr4:10023201-10023251	PFSK-1	brain:	n/a
9	chr4:10020882-10020932	HUVEC	blood vessel:	n/a
10	chr4:10042198-10042248	SKMC	muscle:	n/a
11	chr4:10020360-10020410	AoSMC	blood vessel:	n/a
12	chr4:10024412-10024462	AG10803	skin:	n/a
13	chr4:10042449-10042499	HNPCEpiC	eye:	n/a
14	chr4:10020360-10020410	GM12878	blood:	n/a
15	chr4:10042198-10042248	HL-60	blood:	n/a
16	chr4:10016908-10016958	HNPCEpiC	eye:	n/a
17	chr4:10042449-10042499	U87	brain:	n/a
18	chr4:10020555-10020605	HCPEpiC	choroid plexus:	n/a
19	chr4:10041776-10041826	HIPEpiC	eye:	n/a
20	chr4:10034580-10034630	HRE	kidney:	n/a
21	chr4:10041776-10041826	MCF-7	breast:	n/a
22	chr4:10016908-10016958	Hepatocyte	liver:	n/a
23	chr4:10034580-10034630	Jurkat	blood:	n/a
24	chr4:10020634-10020684	GM12892	blood:	n/a
25	chr4:10034580-10034630	AG04450	lung:	fetal
26	chr4:10024412-10024462	AG09309	skin:	n/a
27	chr4:10042198-10042248	HepG2	liver:	n/a
28	chr4:10020882-10020932	AoSMC	blood vessel:	n/a
29	chr4:10020360-10020410	AG09309	skin:	n/a
30	chr4:10041776-10041826	A549	lung:	n/a
31	chr4:10042449-10042499	T-47D	breast:	n/a
32	chr4:10023201-10023251	HEK293	kidney:	embryo
33	chr4:10024412-10024462	Hela-S3	cervix:	n/a
34	chr4:10020555-10020605	SK-N-SH_RA	brain:	n/a
35	chr4:10019009-10019059	ovcar-3	ovarian:	n/a
36	chr4:10042198-10042248	NT2-D1	testis:	n/a
37	chr4:10019009-10019059	NT2-D1	testis:	n/a
38	chr4:10024412-10024462	SK-N-SH_RA	brain:	n/a
39	chr4:10023201-10023251	SAEC	small airway:	n/a
40	chr4:10020882-10020932	PFSK-1	brain:	n/a
41	chr4:10021355-10021405	NHDF-neo	bronchial:	n/a
42	chr4:10020555-10020605	GM12878	blood:	n/a
43	chr4:10042842-10042892	CMK	blood:	n/a
44	chr4:10042842-10042892	PrEC	prostate:	n/a
45	chr4:10042842-10042892	PFSK-1	brain:	n/a
46	chr4:10021025-10021075	HRCEpiC	kidney:	n/a
47	chr4:10019009-10019059	T-47D	breast:	n/a
48	chr4:10042842-10042892	AG04450	lung:	fetal
49	chr4:10024364-10024414	HMEC	breast:	n/a
50	chr4:10034580-10034630	ovcar-3	ovarian:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10043237..10045316-chr4:10079369..10081759,2	K562	blood:
2	chr4:10031896..10034212-chr4:10409451..10411616,2	K562	blood:
3	chr4:10020627..10022375-chr4:10032476..10035233,2	K562	blood:
4	chr4:10013756..10016342-chr4:10019504..10023873,3	K562	blood:
5	chr4:9704779..9705714-chr4:10015117..10016069,5	MCF-7	breast:
6	chr4:10019661..10022849-chr4:10023062..10025452,3	K562	blood:
7	chr4:10014545..10016342-chr4:10019504..10022397,2	K562	blood:
8	chr4:10014497..10017156-chr4:10035550..10037272,2	K562	blood:
9	chr4:10032509..10034533-chr4:10096806..10099727,2	K562	blood:
10	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
11	chr4:10015413..10017936-chr4:10018958..10020655,2	MCF-7	breast:
12	chr4:9764428..9765300-chr4:10016550..10017565,3	K562	blood:
13	chr4:10031202..10033907-chr4:10037747..10039900,2	K562	blood:
14	chr4:9704873..9705750-chr4:10016280..10017221,3	K562	blood:
15	chr4:10028896..10030894-chr4:10122706..10125313,2	K562	blood:
16	chr4:10031202..10033907-chr4:10037747..10039900,2	K562	blood:
17	chr4:9764370..9765339-chr4:10015197..10016013,4	MCF-7	breast:
18	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
19	chr4:10033030..10034868-chr4:10118461..10119964,2	MCF-7	breast:
20	chr4:10019661..10022849-chr4:10023062..10025452,3	K562	blood:
21	chr4:10020622..10022306-chr4:10022841..10025006,2	MCF-7	breast:
22	chr4:10020691..10022205-chr4:10031735..10034033,2	K562	blood:
23	chr4:10043077..10045943-chr4:10118148..10121673,3	K562	blood:
24	chr4:10015413..10017936-chr4:10018958..10020655,2	MCF-7	breast:
25	chr4:10020536..10023325-chr4:10025799..10029050,4	K562	blood:
26	chr4:10008851..10011783-chr4:10012924..10016004,5	MCF-7	breast:
27	chr4:10014497..10017156-chr4:10035550..10037272,2	K562	blood:
28	chr4:10020622..10022306-chr4:10022841..10025006,2	MCF-7	breast:
29	chr4:10019361..10022054-chr4:10108000..10110178,2	K562	blood:
30	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
31	chr4:9764793..9765717-chr4:10015113..10016017,3	MCF-7	breast:
32	chr4:9764417..9765133-chr4:10016121..10017439,5	MCF-7	breast:
33	chr4:9763456..9766236-chr4:10014004..10016919,3	K562	blood:
34	chr4:9766485..9767197-chr4:10016698..10017481,2	MCF-7	breast:
35	chr4:9770192..9773137-chr4:10024212..10026749,2	K562	blood:
36	chr4:10008415..10010213-chr4:10011796..10014245,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-3	chr4:10041754-10042012	NONHSAT095153
2	lnc-WDR1-3	chr4:10036546-10037004	NONHSAT095155
3	lnc-WDR1-5	chr4:10030642-10030924	NONHSAT095152
4	lnc-WDR1-3	chr4:10035858-10036380	NONHSAT095155
5	lnc-WDR1-5	chr4:10027348-10027630	NONHSAT095152
6	lnc-WDR1-3	chr4:10036546-10037004	NONHSAT095154
7	lnc-WDR1-3	chr4:10035858-10036286	NONHSAT095154
8	lnc-WDR1-3	chr4:10035849-10037764	NONHSAT095153

No data

Variant related genes	Relation type
SLC2A9	TF binding region
SLC2A9	CpG island
ENSG00000109667	chromatin interactions
ENSG00000264931	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 1619 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1619 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6845554	chr4:10013173-10013174	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3756238	chr4:10013202-10013203	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs368322097	chr4:10013223-10013224	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569329211	chr4:10013263-10013264	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533220951	chr4:10013270-10013271	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs3834235	chr4:10013292-10013293	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71936526	chr4:10013298-10013299	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182874881	chr4:10013300-10013301	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78511292	chr4:10013321-10013322	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535572048	chr4:10013341-10013342	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10939654	chr4:10013344-10013345	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs533961923	chr4:10013345-10013346	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377550768	chr4:10013354-10013355	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs3756237	chr4:10013378-10013379	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs537300804	chr4:10013451-10013452	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3756236	chr4:10013463-10013464	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs577510477	chr4:10013465-10013466	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149457985	chr4:10013474-10013475	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143903193	chr4:10013481-10013482	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74594181	chr4:10013485-10013486	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs578131943	chr4:10013526-10013527	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544743888	chr4:10013572-10013573	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553854067	chr4:10013577-10013578	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572048979	chr4:10013581-10013582	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542678090	chr4:10013682-10013683	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542164586	chr4:10013705-10013706	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553361978	chr4:10013736-10013737	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78698809	chr4:10013759-10013760	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73805486	chr4:10013762-10013763	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543701529	chr4:10013857-10013858	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs4280729	chr4:10013861-10013862	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs553583051	chr4:10013865-10013866	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563442235	chr4:10013871-10013872	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs180756992	chr4:10013893-10013894	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368538025	chr4:10013906-10013907	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560249756	chr4:10013922-10013923	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs527672751	chr4:10013947-10013948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549013984	chr4:10013969-10013970	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567327193	chr4:10014014-10014015	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79040444	chr4:10014021-10014022	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185988642	chr4:10014025-10014026	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs571720792	chr4:10014053-10014054	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539248625	chr4:10014082-10014083	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73805487	chr4:10014098-10014099	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs192065413	chr4:10014121-10014122	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs536249948	chr4:10014130-10014131	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs115847025	chr4:10014140-10014141	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183193127	chr4:10014158-10014159	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs377313976	chr4:10014164-10014165	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565204387	chr4:10014191-10014192	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Sezary syndrome	18413736	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Schizophrenia	23813976	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1118 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9998400-10020400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr4:10007600-10013200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr4:10008600-10013400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:10008600-10013400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:10008600-10019600	Weak transcription	Right Ventricle	heart
6	chr4:10008600-10020200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr4:10008800-10020200	Weak transcription	Aorta	Aorta
8	chr4:10008800-10020400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr4:10009000-10019800	Weak transcription	Left Ventricle	heart
10	chr4:10009000-10020400	Weak transcription	Lung	lung
11	chr4:10009400-10020000	Weak transcription	Colonic Mucosa	Colon
12	chr4:10009600-10013800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr4:10009600-10015200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:10009800-10019600	Weak transcription	Placenta	Placenta
15	chr4:10010000-10019800	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr4:10010000-10020200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr4:10010000-10020400	Weak transcription	Esophagus	oesophagus
18	chr4:10010000-10021200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr4:10010400-10016000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr4:10010400-10018000	Genic enhancers	HepG2	liver
21	chr4:10010400-10019600	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr4:10010400-10019600	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr4:10010600-10019600	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr4:10010800-10016800	Weak transcription	Pancreas	Pancrea
25	chr4:10011000-10013400	Enhancers	GM12878-XiMat	blood
26	chr4:10011000-10015400	Weak transcription	Fetal Muscle Trunk	muscle
27	chr4:10011000-10019600	Weak transcription	Brain Anterior Caudate	brain
28	chr4:10011000-10019800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr4:10011000-10020000	Weak transcription	Stomach Mucosa	stomach
30	chr4:10011000-10020200	Weak transcription	Right Atrium	heart
31	chr4:10011600-10013600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:10011800-10017200	Weak transcription	HSMMtube	muscle
33	chr4:10011800-10019800	Weak transcription	Brain Substantia Nigra	brain
34	chr4:10011800-10020400	Weak transcription	Gastric	stomach
35	chr4:10012000-10015600	Weak transcription	Fetal Muscle Leg	muscle
36	chr4:10012200-10016200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr4:10012200-10020200	Weak transcription	Brain Hippocampus Middle	brain
38	chr4:10012400-10013800	Weak transcription	Fetal Intestine Large	intestine
39	chr4:10012400-10015200	Strong transcription	HMEC	breast
40	chr4:10012600-10014200	Enhancers	Fetal Brain Male	brain
41	chr4:10012800-10014000	Enhancers	Duodenum Mucosa	Duodenum
42	chr4:10012800-10015200	Strong transcription	NHEK	skin
43	chr4:10012800-10017000	Weak transcription	Fetal Stomach	stomach
44	chr4:10012800-10019000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:10013000-10013400	Weak transcription	Fetal Intestine Small	intestine
46	chr4:10013000-10013600	Enhancers	Liver	Liver
47	chr4:10013000-10015400	Enhancers	K562	blood
48	chr4:10013000-10019600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:10013200-10014200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr4:10013400-10014000	Enhancers	Brain Germinal Matrix	brain

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