Variant report

Variant	nsv470012
Chromosome Location	chr4:8171401-8233341
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2679)
CpG islands
(count:2014)
Chromatin interactive
region (count:86)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2679 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8202213-8202581	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:8193241-8193530	K562	blood:	n/a	n/a
3	ARID3A	chr4:8227773-8228124	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:8200832-8201080	HepG2	liver:	n/a	n/a
5	ATF1	chr4:8193132-8193494	K562	blood:	n/a	n/a
6	ATF1	chr4:8220182-8220394	K562	blood:	n/a	n/a
7	ATF1	chr4:8202225-8202706	K562	blood:	n/a	n/a
8	ATF1	chr4:8223428-8223513	K562	blood:	n/a	n/a
9	ATF2	chr4:8230227-8230995	GM12878	blood:	n/a	n/a
10	ATF2	chr4:8200545-8201122	GM12878	blood:	n/a	n/a
11	ATF2	chr4:8230182-8231087	GM12878	blood:	n/a	n/a
12	ATF2	chr4:8203157-8203703	GM12878	blood:	n/a	n/a
13	ATF2	chr4:8194497-8194842	GM12878	blood:	n/a	n/a
14	ATF2	chr4:8200447-8201221	GM12878	blood:	n/a	n/a
15	ATF2	chr4:8173906-8174284	GM12878	blood:	n/a	n/a
16	ATF2	chr4:8203146-8203570	GM12878	blood:	n/a	n/a
17	ATF3	chr4:8202500-8202669	K562	blood:	n/a	n/a
18	ATF3	chr4:8193135-8193450	K562	blood:	n/a	n/a
19	BACH1	chr4:8230123-8230900	H1-hESC	embryonic stem cell:	n/a	chr4:8230476-8230490
20	BACH1	chr4:8178248-8178365	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr4:8227896-8228237	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr4:8230293-8230668	K562	blood:	n/a	chr4:8230476-8230490
23	BATF	chr4:8194508-8194766	GM12878	blood:	n/a	n/a
24	BATF	chr4:8223336-8223630	GM12878	blood:	n/a	n/a
25	BATF	chr4:8193128-8193453	GM12878	blood:	n/a	chr4:8193312-8193323 chr4:8193313-8193323
26	BATF	chr4:8230281-8230848	GM12878	blood:	n/a	chr4:8230476-8230486
27	BATF	chr4:8230352-8230584	GM12878	blood:	n/a	chr4:8230476-8230486
28	BATF	chr4:8223277-8223584	GM12878	blood:	n/a	n/a
29	BCL11A	chr4:8230278-8230620	GM12878	blood:	n/a	n/a
30	BCL11A	chr4:8230171-8231050	GM12878	blood:	n/a	n/a
31	BCL11A	chr4:8203102-8203453	GM12878	blood:	n/a	chr4:8203444-8203453
32	BCL11A	chr4:8203313-8203587	GM12878	blood:	n/a	chr4:8203444-8203453
33	BCL11A	chr4:8173954-8174336	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:8200750-8201203	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
35	BCL11A	chr4:8194519-8194733	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:8200742-8201148	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
37	BCL3	chr4:8230261-8231421	GM12878	blood:	n/a	n/a
38	BCL3	chr4:8182619-8183005	GM12878	blood:	n/a	n/a
39	BCL3	chr4:8173697-8173995	GM12878	blood:	n/a	n/a
40	BCL3	chr4:8182148-8182928	GM12878	blood:	n/a	n/a
41	BCL3	chr4:8174044-8174444	GM12878	blood:	n/a	n/a
42	BCLAF1	chr4:8230183-8231019	GM12878	blood:	n/a	n/a
43	BCLAF1	chr4:8194359-8194806	GM12878	blood:	n/a	n/a
44	BCLAF1	chr4:8200397-8201149	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
45	BCLAF1	chr4:8173866-8174279	GM12878	blood:	n/a	n/a
46	BCLAF1	chr4:8200346-8201218	GM12878	blood:	n/a	chr4:8200963-8200972 chr4:8200816-8200829 chr4:8200751-8200760
47	BCLAF1	chr4:8203140-8203628	GM12878	blood:	n/a	chr4:8203444-8203453
48	BHLHE40	chr4:8228103-8228124	HepG2	liver:	n/a	n/a
49	BHLHE40	chr4:8207826-8208041	GM12878	blood:	n/a	n/a
50	BHLHE40	chr4:8203297-8203306	K562	blood:	n/a	n/a

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8230053-8230103	HEEpiC	esophagus:	n/a
2	chr4:8230053-8230103	HEEpiC	esophagus:	n/a
3	chr4:8200774-8200824	Jurkat	blood:	n/a
4	chr4:8185163-8185213	HRE	kidney:	n/a
5	chr4:8174148-8174198	H1-hESC	embryonic stem cell:	embryo
6	chr4:8230829-8230879	AG10803	skin:	n/a
7	chr4:8230829-8230879	HIPEpiC	eye:	n/a
8	chr4:8193353-8193403	Jurkat	blood:	n/a
9	chr4:8200549-8200599	HCPEpiC	choroid plexus:	n/a
10	chr4:8229159-8229209	U87	brain:	n/a
11	chr4:8193310-8193360	K562	blood:	n/a
12	chr4:8207058-8207108	HEK293	kidney:	embryo
13	chr4:8185163-8185213	NT2-D1	testis:	n/a
14	chr4:8230847-8230897	A549	lung:	n/a
15	chr4:8233264-8233314	T-47D	breast:	n/a
16	chr4:8233126-8233176	PANC-1	pancreas:	n/a
17	chr4:8216813-8216863	SK-N-MC	brain:	n/a
18	chr4:8200549-8200599	Jurkat	blood:	n/a
19	chr4:8201128-8201178	HCPEpiC	choroid plexus:	n/a
20	chr4:8202491-8202541	Caco-2	colon:	n/a
21	chr4:8174148-8174198	U87	brain:	n/a
22	chr4:8207119-8207169	HCF	heart:	n/a
23	chr4:8230847-8230897	HRPEpiC	eye:	n/a
24	chr4:8207119-8207169	BJ	skin:	n/a
25	chr4:8221101-8221151	Caco-2	colon:	n/a
26	chr4:8228048-8228098	H1-hESC	embryonic stem cell:	embryo
27	chr4:8185163-8185213	GM12891	blood:	n/a
28	chr4:8185163-8185213	HRCEpiC	kidney:	n/a
29	chr4:8233264-8233314	AG10803	skin:	n/a
30	chr4:8207058-8207108	HRCEpiC	kidney:	n/a
31	chr4:8201128-8201178	AoSMC	blood vessel:	n/a
32	chr4:8207250-8207300	AG04449	skin:	fetal
33	chr4:8231787-8231837	CMK	blood:	n/a
34	chr4:8193310-8193360	H1-hESC	embryonic stem cell:	embryo
35	chr4:8207058-8207108	U87	brain:	n/a
36	chr4:8207325-8207375	NH-A	brain:	n/a
37	chr4:8207058-8207108	AG09309	skin:	n/a
38	chr4:8230847-8230897	HRCEpiC	kidney:	n/a
39	chr4:8202491-8202541	HAEpiC	amniotic membrane:	n/a
40	chr4:8201560-8201610	SAEC	small airway:	n/a
41	chr4:8221101-8221151	HAEpiC	amniotic membrane:	n/a
42	chr4:8200852-8200902	HepG2	liver:	n/a
43	chr4:8201128-8201178	NT2-D1	testis:	n/a
44	chr4:8233264-8233314	A549	lung:	n/a
45	chr4:8229159-8229209	Hepatocyte	liver:	n/a
46	chr4:8200974-8201024	AG09319	gingival:	n/a
47	chr4:8229159-8229209	Hela-S3	cervix:	n/a
48	chr4:8206575-8206625	HRPEpiC	eye:	n/a
49	chr4:8229159-8229209	MCF-7	breast:	n/a
50	chr4:8206575-8206625	HCM	heart:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8193914..8196178-chr4:8208983..8211317,3	MCF-7	breast:
2	chr4:8210808..8214935-chr4:8218365..8221781,3	K562	blood:
3	chr4:8178683..8179355-chr4:8239861..8240827,2	K562	blood:
4	chr17:58130754..58132699-chr4:8184311..8186643,2	MCF-7	breast:
5	chr4:8018368..8020892-chr4:8193998..8196693,2	MCF-7	breast:
6	chr17:41464192..41465862-chr4:8218786..8220286,2	K562	blood:
7	chr4:8196365..8198460-chr4:8203921..8207190,4	K562	blood:
8	chr4:8158932..8160891-chr4:8178387..8181198,2	MCF-7	breast:
9	chr4:8202798..8206403-chr4:8207013..8209683,3	K562	blood:
10	chr4:8181018..8183687-chr4:8185277..8188138,2	MCF-7	breast:
11	chr4:8178129..8181116-chr4:8187357..8190314,2	K562	blood:
12	chr4:8202937..8205415-chr4:8232393..8234006,2	K562	blood:
13	chr11:62608635..62609624-chr4:8218786..8219306,3	MCF-7	breast:
14	chr4:8189772..8192369-chr4:8193436..8194981,2	K562	blood:
15	chr17:41465548..41466152-chr4:8218286..8218806,2	MCF-7	breast:
16	chr4:8211892..8215889-chr4:8218251..8222766,5	MCF-7	breast:
17	chr4:8012081..8014539-chr4:8181803..8184689,2	MCF-7	breast:
18	chr4:8169433..8172146-chr4:8180743..8183455,2	MCF-7	breast:
19	chr4:8199393..8202510-chr4:8203198..8206188,4	MCF-7	breast:
20	chr4:8179921..8181904-chr4:8189631..8192248,3	MCF-7	breast:
21	chr4:8178129..8181116-chr4:8187357..8190314,2	K562	blood:
22	chr4:8199821..8202591-chr4:8203028..8206014,3	K562	blood:
23	chr17:41398862..41401693-chr4:8218786..8220306,3	K562	blood:
24	chr4:8206620..8209251-chr4:8213740..8215490,2	MCF-7	breast:
25	chr4:8159731..8162461-chr4:8191940..8193551,2	MCF-7	breast:
26	chr4:8178298..8179365-chr4:8239616..8240695,4	MCF-7	breast:
27	chr4:8209569..8211422-chr4:8212311..8214321,2	K562	blood:
28	chr4:8177372..8179736-chr4:8243215..8245049,2	K562	blood:
29	chr4:8195725..8198126-chr4:8238876..8240631,2	MCF-7	breast:
30	chr4:8203500..8205646-chr4:8217325..8220224,2	MCF-7	breast:
31	chr4:8219379..8221157-chr4:8375226..8376743,2	MCF-7	breast:
32	chr3:73158604..73161603-chr4:8218786..8220306,4	K562	blood:
33	chr4:8184952..8186912-chr4:8408862..8412072,3	MCF-7	breast:
34	chr17:41464192..41467813-chr4:8218786..8220306,6	K562	blood:
35	chr4:8193914..8196178-chr4:8208983..8211317,3	MCF-7	breast:
36	chr2:241500035..241500801-chr4:8192986..8193759,2	HCT-116	colon:
37	chr4:8178210..8179173-chr4:8194105..8195549,8	MCF-7	breast:
38	chr4:8179293..8181973-chr4:8183474..8185384,4	MCF-7	breast:
39	chr4:8178210..8179173-chr4:8194105..8195549,8	MCF-7	breast:
40	chr4:8178126..8179213-chr4:8194505..8195435,5	MCF-7	breast:
41	chr1:160082463..160083986-chr4:8218786..8220306,2	K562	blood:
42	chr4:8211892..8215889-chr4:8218251..8222766,5	MCF-7	breast:
43	chr4:8199821..8202591-chr4:8203028..8206014,3	K562	blood:
44	chr11:62609146..62609723-chr4:8218786..8219286,2	HCT-116	colon:
45	chr4:8189772..8192369-chr4:8193436..8194981,2	K562	blood:
46	chr4:8181697..8186152-chr4:8199354..8203571,7	MCF-7	breast:
47	chr4:8196058..8199736-chr4:8201784..8203810,3	K562	blood:
48	chr4:8020965..8023057-chr4:8187753..8190682,2	MCF-7	breast:
49	chr17:41466254..41467859-chr4:8218786..8220306,2	MCF-7	breast:
50	chr4:8202937..8205415-chr4:8232393..8234006,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HTRA3-5	chr4:8203113-8203274	NONHSAT095079
2	lnc-HTRA3-5	chr4:8206894-8206990	NONHSAT095079
3	lnc-HTRA3-5	chr4:8201025-8201132	NONHSAT095078
4	lnc-HTRA3-5	chr4:8206894-8207339	NONHSAT095078

No data

Variant related genes	Relation type
SH3TC1	TF binding region
GMPSP1	TF binding region
SH3TC1	CpG island
GMPSP1	CpG island
ENSG00000151790	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000188542	chromatin interactions
ENSG00000144504	chromatin interactions
ENSG00000155275	chromatin interactions
ENSG00000163995	chromatin interactions
ENSG00000125089	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 3347 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:3347 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10938694	chr4:8171401-8171402	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550485240	chr4:8171402-8171403	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147603607	chr4:8171420-8171421	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111348976	chr4:8171421-8171422	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs73077947	chr4:8171447-8171448	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533882078	chr4:8171482-8171483	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs16841858	chr4:8171483-8171484	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566628378	chr4:8171485-8171486	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78949535	chr4:8171507-8171508	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115462751	chr4:8171521-8171522	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192925928	chr4:8171531-8171532	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148117052	chr4:8171537-8171538	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563836587	chr4:8171566-8171567	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141833749	chr4:8171603-8171604	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs377053149	chr4:8171604-8171605	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554180503	chr4:8171630-8171631	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7676828	chr4:8171705-8171706	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542176324	chr4:8171713-8171714	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183991025	chr4:8171714-8171715	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150200921	chr4:8171735-8171736	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs573517105	chr4:8171771-8171772	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs544037127	chr4:8171798-8171799	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs562636189	chr4:8171819-8171820	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs372637253	chr4:8171839-8171840	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs188676618	chr4:8171845-8171846	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs560095839	chr4:8171852-8171853	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs181407849	chr4:8171854-8171855	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs555360137	chr4:8171886-8171887	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs549113332	chr4:8171905-8171906	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs567400146	chr4:8171906-8171907	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs183727440	chr4:8171923-8171924	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs76366438	chr4:8171933-8171934	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs571840376	chr4:8171977-8171978	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs539330615	chr4:8172022-8172023	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs138943312	chr4:8172037-8172038	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs373013924	chr4:8172038-8172039	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs572427571	chr4:8172090-8172091	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532553590	chr4:8172104-8172105	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs79763862	chr4:8172109-8172110	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs146396485	chr4:8172157-8172158	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs576158003	chr4:8172164-8172165	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs544870367	chr4:8172166-8172167	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369116382	chr4:8172178-8172179	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs543992795	chr4:8172230-8172231	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs556610946	chr4:8172234-8172235	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs376585443	chr4:8172257-8172258	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs577813139	chr4:8172272-8172273	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs371121305	chr4:8172273-8172274	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs139653811	chr4:8172296-8172297	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs527260378	chr4:8172297-8172298	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8168000-8172200	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr4:8168400-8172200	Weak transcription	Gastric	stomach
3	chr4:8169800-8171800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:8170000-8171800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
5	chr4:8170400-8172600	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr4:8170600-8171600	Weak transcription	Esophagus	oesophagus
7	chr4:8170600-8171600	Weak transcription	Psoas Muscle	Psoas
8	chr4:8170600-8183200	Weak transcription	Right Atrium	heart
9	chr4:8170800-8173000	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr4:8170800-8175600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:8171000-8172800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr4:8171000-8173200	Weak transcription	Spleen	Spleen
13	chr4:8171200-8171600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:8171200-8171600	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:8171400-8172400	Enhancers	Placenta	Placenta
16	chr4:8171600-8171800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:8171600-8172400	Enhancers	Esophagus	oesophagus
18	chr4:8171600-8172400	Enhancers	Fetal Muscle Leg	muscle
19	chr4:8171600-8172400	Enhancers	Psoas Muscle	Psoas
20	chr4:8171800-8173000	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr4:8171800-8174000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:8172200-8172400	Active TSS	Gastric	stomach
23	chr4:8172200-8173400	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr4:8172400-8174400	Bivalent Enhancer	Placenta	Placenta
25	chr4:8172400-8175600	Weak transcription	Psoas Muscle	Psoas
26	chr4:8172400-8181600	Weak transcription	Esophagus	oesophagus
27	chr4:8172600-8175400	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr4:8173000-8173400	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr4:8173000-8173800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr4:8173000-8174400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:8173000-8174600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr4:8173200-8173400	Enhancers	Spleen	Spleen
33	chr4:8173200-8173600	Enhancers	GM12878-XiMat	blood
34	chr4:8173200-8174000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr4:8173200-8174400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr4:8173400-8173800	Enhancers	Primary B cells from peripheral blood	blood
37	chr4:8173400-8173800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr4:8173400-8173800	Weak transcription	Spleen	Spleen
39	chr4:8173400-8174000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
40	chr4:8173400-8174200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:8173400-8174400	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr4:8173400-8175800	Enhancers	Primary B cells from cord blood	blood
43	chr4:8173600-8174200	Enhancers	HSMMtube	muscle
44	chr4:8173600-8174400	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr4:8173600-8174600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr4:8173600-8174600	Flanking Active TSS	GM12878-XiMat	blood
47	chr4:8173800-8174000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:8173800-8174000	Bivalent Enhancer	Osteobl	bone
49	chr4:8173800-8174200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:8173800-8174400	Flanking Active TSS	Primary B cells from peripheral blood	blood

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