Variant report

Variant	nsv518757
Chromosome Location	chr4:78637265-78695138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:319)
CpG islands
(count:122)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78656146-78656387	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:78656137-78656446	K562	blood:	n/a	n/a
3	ATF1	chr4:78639665-78639873	K562	blood:	n/a	n/a
4	ATF1	chr4:78656121-78656470	K562	blood:	n/a	n/a
5	ATF3	chr4:78639739-78639946	K562	blood:	n/a	n/a
6	BACH1	chr4:78656123-78656385	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:78656101-78656374	K562	blood:	n/a	n/a
8	BATF	chr4:78656180-78656486	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:78656112-78656557	K562	blood:	n/a	n/a
10	CBX3	chr4:78656046-78656514	K562	blood:	n/a	n/a
11	CBX3	chr4:78683755-78684087	K562	blood:	n/a	n/a
12	CCNT2	chr4:78656174-78656429	K562	blood:	n/a	n/a
13	CEBPB	chr4:78656014-78656541	K562	blood:	n/a	n/a
14	CEBPB	chr4:78693937-78694670	IMR90	lung:	n/a	chr4:78694460-78694473 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694473 chr4:78694460-78694473 chr4:78694460-78694471 chr4:78694462-78694471
15	CEBPB	chr4:78694313-78694611	K562	blood:	n/a	chr4:78694460-78694473 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694473 chr4:78694460-78694473 chr4:78694460-78694471 chr4:78694462-78694471
16	CEBPB	chr4:78639656-78639952	K562	blood:	n/a	n/a
17	CEBPB	chr4:78663134-78663475	HepG2	liver:	n/a	chr4:78663311-78663322 chr4:78663171-78663184
18	CEBPB	chr4:78656066-78656414	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:78639649-78639866	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:78694897-78695129	K562	blood:	n/a	chr4:78695010-78695021
21	CEBPB	chr4:78639559-78640038	K562	blood:	n/a	n/a
22	CEBPB	chr4:78694323-78694601	Hela-S3	cervix:	n/a	chr4:78694460-78694473 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694473 chr4:78694460-78694473 chr4:78694460-78694471 chr4:78694462-78694471
23	CEBPB	chr4:78686892-78687261	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:78694285-78694638	HepG2	liver:	n/a	chr4:78694460-78694473 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694473 chr4:78694460-78694473 chr4:78694460-78694471 chr4:78694462-78694471
25	CEBPB	chr4:78663079-78663495	IMR90	lung:	n/a	chr4:78663311-78663322 chr4:78663171-78663184
26	CEBPB	chr4:78656118-78656280	K562	blood:	n/a	n/a
27	CEBPB	chr4:78686910-78687263	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:78683894-78684169	HepG2	liver:	n/a	chr4:78684024-78684035
29	CEBPB	chr4:78694906-78695200	IMR90	lung:	n/a	chr4:78695010-78695021
30	CEBPB	chr4:78655957-78656512	K562	blood:	n/a	n/a
31	CEBPB	chr4:78656109-78656512	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:78694983-78695066	H1-hESC	embryonic stem cell:	n/a	chr4:78695010-78695021
33	CEBPB	chr4:78657032-78657238	K562	blood:	n/a	n/a
34	CEBPB	chr4:78663029-78663477	K562	blood:	n/a	chr4:78663311-78663322 chr4:78663171-78663184
35	CEBPB	chr4:78693937-78694114	A549	lung:	n/a	n/a
36	CEBPB	chr4:78686972-78687125	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:78640691-78640849	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:78694343-78694646	A549	lung:	n/a	chr4:78694460-78694473 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694471 chr4:78694462-78694473 chr4:78694460-78694473 chr4:78694460-78694471 chr4:78694462-78694471
39	CEBPB	chr4:78639643-78639857	K562	blood:	n/a	n/a
40	CEBPB	chr4:78663246-78663460	A549	lung:	n/a	chr4:78663311-78663322
41	CEBPB	chr4:78693943-78694124	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:78649467-78649902	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:78686865-78687261	HepG2	liver:	n/a	n/a
44	CTCF	chr4:78649500-78649650	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr4:78649718-78649828	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:78656140-78656370	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr4:78656200-78656350	AG09319	gingival:	n/a	n/a
48	CTCF	chr4:78656200-78656350	AG09309	skin:	n/a	n/a
49	CTCF	chr4:78649720-78649870	GM12873	blood:	n/a	n/a
50	CTCF	chr4:78649040-78649190	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78638815-78638865	HCT-116	colon:	n/a
2	chr4:78692537-78692587	HEK293	kidney:	embryo
3	chr4:78638815-78638865	A549	lung:	n/a
4	chr4:78638815-78638865	BJ	skin:	n/a
5	chr4:78692537-78692587	MCF10A-Er-Src	breast:	n/a
6	chr4:78638815-78638865	NHDF-neo	bronchial:	n/a
7	chr4:78692537-78692587	HL-60	blood:	n/a
8	chr4:78638815-78638865	RPTEC	kidney:	n/a
9	chr4:78692537-78692587	IMR90	lung:	fetal
10	chr4:78692537-78692587	HCPEpiC	choroid plexus:	n/a
11	chr4:78692537-78692587	AG09319	gingival:	n/a
12	chr4:78692537-78692587	A549	lung:	n/a
13	chr4:78638815-78638865	HRCEpiC	kidney:	n/a
14	chr4:78692537-78692587	AG09309	skin:	n/a
15	chr4:78692537-78692587	HMEC	breast:	n/a
16	chr4:78692537-78692587	U87	brain:	n/a
17	chr4:78692537-78692587	HCM	heart:	n/a
18	chr4:78638815-78638865	U87	brain:	n/a
19	chr4:78692537-78692587	HRE	kidney:	n/a
20	chr4:78692537-78692587	LNCaP	prostate:	n/a
21	chr4:78638815-78638865	NHBE	bronchial:	n/a
22	chr4:78692537-78692587	K562	blood:	n/a
23	chr4:78692537-78692587	HAEpiC	amniotic membrane:	n/a
24	chr4:78638815-78638865	HCM	heart:	n/a
25	chr4:78692537-78692587	AG04450	lung:	fetal
26	chr4:78692537-78692587	Jurkat	blood:	n/a
27	chr4:78638815-78638865	NH-A	brain:	n/a
28	chr4:78638815-78638865	NT2-D1	testis:	n/a
29	chr4:78692537-78692587	MCF-7	breast:	n/a
30	chr4:78692537-78692587	HEEpiC	esophagus:	n/a
31	chr4:78692537-78692587	GM12892	blood:	n/a
32	chr4:78692537-78692587	HNPCEpiC	eye:	n/a
33	chr4:78638815-78638865	SAEC	small airway:	n/a
34	chr4:78692537-78692587	AoSMC	blood vessel:	n/a
35	chr4:78692537-78692587	GM12878	blood:	n/a
36	chr4:78638815-78638865	LNCaP	prostate:	n/a
37	chr4:78692537-78692587	ovcar-3	ovarian:	n/a
38	chr4:78638815-78638865	BE2_C	brain:	n/a
39	chr4:78638815-78638865	IMR90	lung:	fetal
40	chr4:78692537-78692587	T-47D	breast:	n/a
41	chr4:78692537-78692587	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:78638815-78638865	HCF	heart:	n/a
43	chr4:78692537-78692587	H1-hESC	embryonic stem cell:	embryo
44	chr4:78638815-78638865	HepG2	liver:	n/a
45	chr4:78638815-78638865	HCPEpiC	choroid plexus:	n/a
46	chr4:78692537-78692587	SKMC	muscle:	n/a
47	chr4:78638815-78638865	GM19239	blood:	n/a
48	chr4:78638815-78638865	AG04450	lung:	fetal
49	chr4:78638815-78638865	GM12891	blood:	n/a
50	chr4:78692537-78692587	HIPEpiC	eye:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78648017..78651931-chr4:78652126..78656070,5	K562	blood:
2	chr4:78665271..78668242-chr4:78674089..78675600,2	MCF-7	breast:
3	chr4:78635590..78638425-chr4:78740544..78742482,2	K562	blood:
4	chr4:78682864..78685032-chr4:78685330..78687891,2	K562	blood:
5	chr4:78649825..78652816-chr4:78654825..78657424,2	K562	blood:
6	chr4:78664695..78666373-chr4:78741463..78744231,2	K562	blood:
7	chr4:78676527..78678706-chr4:78694641..78697046,2	K562	blood:
8	chr4:78660857..78662460-chr4:78663917..78665509,2	K562	blood:
9	chr4:78660857..78662460-chr4:78663917..78665509,2	K562	blood:
10	chr4:78655466..78657702-chr4:78779436..78782397,2	K562	blood:
11	chr4:78658089..78660891-chr4:78661211..78663779,2	K562	blood:
12	chr4:78642397..78643983-chr4:78651007..78652865,2	K562	blood:
13	chr4:78641368..78643849-chr4:78739049..78741787,2	MCF-7	breast:
14	chr4:78642397..78643983-chr4:78651007..78652865,2	K562	blood:
15	chr4:78642128..78644545-chr4:78649464..78651620,2	MCF-7	breast:
16	chr4:78642128..78644545-chr4:78649464..78651620,2	MCF-7	breast:
17	chr4:78647944..78650924-chr4:78655794..78657335,2	MCF-7	breast:
18	chr4:78657605..78659562-chr4:78738158..78740699,2	K562	blood:
19	chr4:78682864..78685032-chr4:78685330..78687891,2	K562	blood:
20	chr4:78676799..78679930-chr4:78739858..78742459,3	K562	blood:
21	chr4:78691071..78693777-chr4:78741289..78743098,2	K562	blood:
22	chr4:78676527..78678706-chr4:78694641..78697046,2	K562	blood:
23	chr4:78649825..78652816-chr4:78654825..78657424,2	K562	blood:
24	chr4:78647944..78650924-chr4:78655794..78657335,2	MCF-7	breast:
25	chr4:78684761..78686865-chr4:78691156..78693434,2	K562	blood:
26	chr4:78665271..78668242-chr4:78674089..78675600,2	MCF-7	breast:
27	chr4:78684761..78686865-chr4:78691156..78693434,2	K562	blood:
28	chr4:78635743..78638907-chr4:78739780..78742951,3	K562	blood:

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CNOT6L	hsa-miR-186-5p	chr4:78663305-78663326
2	CNOT6L	hsa-miR-186-5p	chr4:78647205-78647226
3	CNOT6L	hsa-miR-186-5p	chr4:78640213-78640207
4	CNOT6L	hsa-miR-186-5p	chr4:78647245-78647266
5	CNOT6L	hsa-miR-106b-5p	chr4:78640144-78640165
6	CNOT6L	hsa-miR-106b-5p	chr4:78640150-78640143

Variant related genes	Relation type
CNOT6L	TF binding region
CNOT6L	CpG island
ENSG00000138767	chromatin interactions

Extended variants
information (count: 1840 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1840 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2866690	chr4:78637265-78637266	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78224989	chr4:78637297-78637298	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201136912	chr4:78637301-78637302	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77036073	chr4:78637302-78637303	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs116012360	chr4:78637403-78637404	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188592997	chr4:78637418-78637419	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554827705	chr4:78637421-78637422	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs74854414	chr4:78637481-78637482	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368240807	chr4:78637500-78637501	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534125028	chr4:78637640-78637641	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564691726	chr4:78637651-78637652	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530542061	chr4:78637688-78637689	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554025648	chr4:78637712-78637713	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572902436	chr4:78637720-78637721	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544743804	chr4:78637775-78637776	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148144859	chr4:78637804-78637805	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575287954	chr4:78637831-78637832	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544548821	chr4:78637862-78637863	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561154860	chr4:78637920-78637921	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550288495	chr4:78637977-78637978	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs367706819	chr4:78637996-78637997	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529960613	chr4:78638001-78638002	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs560632609	chr4:78638016-78638017	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181384859	chr4:78638108-78638109	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560057558	chr4:78638109-78638110	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs17448633	chr4:78638153-78638154	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552371434	chr4:78638270-78638271	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141879094	chr4:78638351-78638352	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs3205281	chr4:78638491-78638492	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs186063240	chr4:78638528-78638529	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs150641275	chr4:78638550-78638551	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573930963	chr4:78638593-78638594	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138990568	chr4:78638700-78638701	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537970844	chr4:78638707-78638708	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375316770	chr4:78638711-78638712	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554358469	chr4:78638729-78638730	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2134048	chr4:78638730-78638731	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs192079338	chr4:78638732-78638733	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7667418	chr4:78638741-78638742	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs142967513	chr4:78638747-78638748	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143041681	chr4:78638816-78638817	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs147217481	chr4:78638988-78638989	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538523751	chr4:78639051-78639052	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554567098	chr4:78639104-78639105	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150633183	chr4:78639134-78639135	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139699350	chr4:78639135-78639136	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199734421	chr4:78639189-78639190	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11377990	chr4:78639190-78639191	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs397732805	chr4:78639199-78639200	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149903318	chr4:78639200-78639201	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
lymphocytic leukemia	21291569	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
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
primary effusion lymphomas	17116491	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1385 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78621400-78645800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr4:78621600-78643800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:78622000-78638800	Weak transcription	NHEK	skin
4	chr4:78625000-78638800	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:78626400-78644400	Weak transcription	Placenta	Placenta
6	chr4:78626400-78645200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr4:78628400-78638200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:78628400-78638800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:78628400-78648400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:78628600-78641400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:78629000-78649400	Weak transcription	HMEC	breast
12	chr4:78629200-78676600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:78629400-78638200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr4:78629400-78649400	Weak transcription	Spleen	Spleen
15	chr4:78629400-78656200	Weak transcription	Small Intestine	intestine
16	chr4:78630000-78643600	Weak transcription	Duodenum Mucosa	Duodenum
17	chr4:78630200-78660000	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr4:78631200-78656000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr4:78631400-78639000	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr4:78631400-78643400	Weak transcription	Gastric	stomach
21	chr4:78631600-78638400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:78631600-78649400	Weak transcription	Brain Hippocampus Middle	brain
23	chr4:78631600-78652600	Weak transcription	Esophagus	oesophagus
24	chr4:78631800-78638000	Weak transcription	Fetal Intestine Large	intestine
25	chr4:78631800-78638800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr4:78631800-78640800	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr4:78631800-78649400	Weak transcription	Aorta	Aorta
28	chr4:78632000-78651800	Weak transcription	HepG2	liver
29	chr4:78632400-78640600	Weak transcription	Adipose Nuclei	Adipose
30	chr4:78632400-78642800	Weak transcription	Fetal Intestine Small	intestine
31	chr4:78632600-78697800	Weak transcription	Colonic Mucosa	Colon
32	chr4:78633000-78637400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr4:78633200-78639400	Strong transcription	Fetal Thymus	thymus
34	chr4:78633400-78641400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:78633600-78641400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:78633600-78642800	Weak transcription	Fetal Stomach	stomach
37	chr4:78633600-78645200	Weak transcription	Pancreas	Pancrea
38	chr4:78633800-78639200	Strong transcription	Dnd41	blood
39	chr4:78634000-78647600	Weak transcription	HSMM	muscle
40	chr4:78634200-78643400	Weak transcription	Lung	lung
41	chr4:78634400-78638200	Weak transcription	Left Ventricle	heart
42	chr4:78634400-78640600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr4:78634400-78643400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr4:78634600-78642400	Weak transcription	HSMMtube	muscle
45	chr4:78634800-78638000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr4:78634800-78638200	Weak transcription	Thymus	Thymus
47	chr4:78634800-78643000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr4:78634800-78643000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr4:78635000-78638800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr4:78635000-78646000	Weak transcription	Fetal Lung	lung

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