Variant report

Variant	nsv600423
Chromosome Location	chr5:177860454-178010145
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1447)
CpG islands
(count:3848)
Chromatin interactive
region (count:90)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1447 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177875635-177876882	K562	blood:	n/a	n/a
2	ARID3A	chr5:177880009-177880448	K562	blood:	n/a	n/a
3	ARID3A	chr5:177888233-177888383	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:177877562-177878156	K562	blood:	n/a	n/a
5	ATF1	chr5:177876057-177876633	K562	blood:	n/a	n/a
6	ATF1	chr5:177993173-177993348	K562	blood:	n/a	n/a
7	ATF1	chr5:177914943-177915183	K562	blood:	n/a	n/a
8	ATF2	chr5:177982753-177983284	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:177982792-177983283	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:177886021-177886090	K562	blood:	n/a	n/a
11	BACH1	chr5:177888080-177888450	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:178003565-178003761	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:177869383-177869508	K562	blood:	n/a	n/a
14	BACH1	chr5:177982556-177983199	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:177956139-177956325	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:177920408-177920532	K562	blood:	n/a	n/a
17	BACH1	chr5:177984618-177984625	K562	blood:	n/a	n/a
18	BACH1	chr5:177872621-177872910	K562	blood:	n/a	n/a
19	BACH1	chr5:177934563-177934814	K562	blood:	n/a	n/a
20	BACH1	chr5:177986972-177987041	K562	blood:	n/a	n/a
21	BACH1	chr5:177969361-177969365	K562	blood:	n/a	n/a
22	BACH1	chr5:177876133-177876859	K562	blood:	n/a	n/a
23	BCLAF1	chr5:177876134-177876491	K562	blood:	n/a	n/a
24	BHLHE40	chr5:177918301-177918460	K562	blood:	n/a	chr5:177918370-177918383
25	BHLHE40	chr5:177876113-177877870	K562	blood:	n/a	n/a
26	BHLHE40	chr5:178007428-178007484	K562	blood:	n/a	n/a
27	BHLHE40	chr5:177930090-177930416	K562	blood:	n/a	n/a
28	BHLHE40	chr5:177956208-177956472	K562	blood:	n/a	n/a
29	BHLHE40	chr5:177980034-177980313	K562	blood:	n/a	n/a
30	BHLHE40	chr5:177934517-177934717	K562	blood:	n/a	n/a
31	BHLHE40	chr5:177974306-177974548	K562	blood:	n/a	n/a
32	BHLHE40	chr5:177984564-177984758	K562	blood:	n/a	n/a
33	BHLHE40	chr5:177880099-177880651	K562	blood:	n/a	n/a
34	BHLHE40	chr5:177929771-177930071	GM12878	blood:	n/a	n/a
35	BHLHE40	chr5:177910649-177910918	GM12878	blood:	n/a	n/a
36	BHLHE40	chr5:177962319-177962548	K562	blood:	n/a	n/a
37	BHLHE40	chr5:177921213-177921579	K562	blood:	n/a	n/a
38	BHLHE40	chr5:177888120-177888558	K562	blood:	n/a	n/a
39	BHLHE40	chr5:177956283-177956517	GM12878	blood:	n/a	n/a
40	BHLHE40	chr5:177910645-177910908	K562	blood:	n/a	n/a
41	BHLHE40	chr5:177981768-177982464	K562	blood:	n/a	n/a
42	BHLHE40	chr5:177895932-177896151	K562	blood:	n/a	n/a
43	BRCA1	chr5:177888202-177888501	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr5:177888215-177888415	HepG2	liver:	n/a	n/a
45	CBX3	chr5:177876066-177876600	K562	blood:	n/a	n/a
46	CBX3	chr5:177934424-177934912	K562	blood:	n/a	n/a
47	CBX3	chr5:177981899-177982378	K562	blood:	n/a	n/a
48	CBX3	chr5:177876014-177876642	K562	blood:	n/a	n/a
49	CBX3	chr5:177934495-177934851	K562	blood:	n/a	n/a
50	CCNT2	chr5:177876058-177876813	K562	blood:	n/a	chr5:177876543-177876552 chr5:177876671-177876680 chr5:177876666-177876675

(count:3848 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177981891-177981941	Caco-2	colon:	n/a
2	chr5:177913485-177913535	NH-A	brain:	n/a
3	chr5:178004204-178004254	ECC-1	luminal epithelium:	n/a
4	chr5:177991670-177991720	NT2-D1	testis:	n/a
5	chr5:177952737-177952787	AG04450	lung:	fetal
6	chr5:177981891-177981941	Caco-2	colon:	n/a
7	chr5:177913485-177913535	NH-A	brain:	n/a
8	chr5:178004204-178004254	ECC-1	luminal epithelium:	n/a
9	chr5:177991670-177991720	NT2-D1	testis:	n/a
10	chr5:177952737-177952787	AG04450	lung:	fetal
11	chr5:178000774-178000824	A549	lung:	n/a
12	chr5:178007671-178007721	ovcar-3	ovarian:	n/a
13	chr5:177941879-177941929	HCPEpiC	choroid plexus:	n/a
14	chr5:177882221-177882271	SK-N-MC	brain:	n/a
15	chr5:177986696-177986746	HEEpiC	esophagus:	n/a
16	chr5:177991670-177991720	PANC-1	pancreas:	n/a
17	chr5:177956199-177956249	HEK293	kidney:	embryo
18	chr5:177913468-177913518	HUVEC	blood vessel:	n/a
19	chr5:177952737-177952787	PrEC	prostate:	n/a
20	chr5:177942470-177942520	AG10803	skin:	n/a
21	chr5:177876830-177876880	SK-N-SH_RA	brain:	n/a
22	chr5:177987724-177987774	HRPEpiC	eye:	n/a
23	chr5:177980691-177980741	NT2-D1	testis:	n/a
24	chr5:178003633-178003683	NT2-D1	testis:	n/a
25	chr5:177915909-177915959	HCPEpiC	choroid plexus:	n/a
26	chr5:178004204-178004254	RPTEC	kidney:	n/a
27	chr5:177895047-177895097	GM12878	blood:	n/a
28	chr5:178002446-178002496	BE2_C	brain:	n/a
29	chr5:177980944-177980994	Hepatocyte	liver:	n/a
30	chr5:177875140-177875190	HUVEC	blood vessel:	n/a
31	chr5:177870233-177870283	NT2-D1	testis:	n/a
32	chr5:177946120-177946170	HAEpiC	amniotic membrane:	n/a
33	chr5:177892911-177892961	GM12892	blood:	n/a
34	chr5:177942470-177942520	LNCaP	prostate:	n/a
35	chr5:177870233-177870283	T-47D	breast:	n/a
36	chr5:177991670-177991720	AG04450	lung:	fetal
37	chr5:177913468-177913518	HMEC	breast:	n/a
38	chr5:177876930-177876980	HCPEpiC	choroid plexus:	n/a
39	chr5:177951909-177951959	BE2_C	brain:	n/a
40	chr5:177891221-177891271	NH-A	brain:	n/a
41	chr5:177875140-177875190	MCF10A-Er-Src	breast:	n/a
42	chr5:177980755-177980805	BE2_C	brain:	n/a
43	chr5:177942470-177942520	Caco-2	colon:	n/a
44	chr5:178003633-178003683	HEK293	kidney:	embryo
45	chr5:178004685-178004735	NB4	blood:	n/a
46	chr5:177949147-177949197	PANC-1	pancreas:	n/a
47	chr5:177949147-177949197	SKMC	muscle:	n/a
48	chr5:177952737-177952787	AG09309	skin:	n/a
49	chr5:177987648-177987698	ECC-1	luminal epithelium:	n/a
50	chr5:177870233-177870283	NB4	blood:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:177861655..177863245-chr5:177875652..177877153,2	K562	blood:
2	chr5:177864722..177866446-chr5:177868114..177869710,2	K562	blood:
3	chr5:177940111..177942825-chr5:177947320..177948869,2	MCF-7	breast:
4	chr5:177933177..177935280-chr5:177937428..177940309,2	MCF-7	breast:
5	chr5:177997965..178000895-chr5:178002250..178003802,2	MCF-7	breast:
6	chr5:177861712..177865085-chr5:177866946..177869684,3	K562	blood:
7	chr5:177876265..177878231-chr5:177880241..177881910,2	K562	blood:
8	chr5:177861063..177863215-chr5:177895852..177898464,2	K562	blood:
9	chr5:177633748..177635466-chr5:177877015..177878524,2	K562	blood:
10	chr5:177846034..177846976-chr5:177861076..177861723,3	MCF-7	breast:
11	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
12	chr12:66043001..66043501-chr5:177956345..177956885,2	Hela-S3	cervix:
13	chr5:177933177..177935280-chr5:177937428..177940309,2	MCF-7	breast:
14	chr5:177844557..177846538-chr5:177860811..177863618,2	K562	blood:
15	chr5:177974829..177978775-chr5:177979610..177982986,3	MCF-7	breast:
16	chr5:177995855..177997941-chr5:178001993..178004774,2	K562	blood:
17	chr5:177871515..177874034-chr5:177875821..177877688,2	MCF-7	breast:
18	chr5:178001407..178003756-chr5:178005377..178007780,2	K562	blood:
19	chr5:177894292..177896063-chr5:177897258..177899224,2	K562	blood:
20	chr5:178001407..178003756-chr5:178005377..178007780,2	K562	blood:
21	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:
22	chr5:177888252..177888759-chr5:177978244..177978784,2	K562	blood:
23	chr5:177630692..177632975-chr5:177978768..177981207,2	MCF-7	breast:
24	chr5:177893036..177895122-chr5:177964444..177967291,2	K562	blood:
25	chr5:177977818..177978619-chr5:178017535..178018077,2	MCF-7	breast:
26	chr5:177881991..177885625-chr5:177886030..177888202,3	MCF-7	breast:
27	chr5:177879886..177881970-chr5:177890471..177892015,2	K562	blood:
28	chr5:177873433..177876156-chr5:177880110..177882555,2	K562	blood:
29	chr5:177888015..177888839-chr5:177977833..177978735,3	MCF-7	breast:
30	chr5:177865902..177866648-chr5:177887888..177888885,2	K562	blood:
31	chr5:177879886..177881970-chr5:177890471..177892015,2	K562	blood:
32	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:
33	chr5:177887719..177888721-chr5:177977307..177978270,3	MCF-7	breast:
34	chr5:177876786..177879529-chr5:177883377..177886367,2	K562	blood:
35	chr5:177974829..177978775-chr5:177979610..177982986,3	MCF-7	breast:
36	chr5:177706698..177707593-chr5:177977751..177978699,5	MCF-7	breast:
37	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
38	chr1:31203803..31206340-chr5:177974675..177976195,2	K562	blood:
39	chr5:177887805..177889193-chr5:178016576..178017370,3	MCF-7	breast:
40	chr5:177997965..178000895-chr5:178002250..178003802,2	MCF-7	breast:
41	chr5:177879706..177881386-chr5:177883345..177884930,2	K562	blood:
42	chr5:177863976..177865906-chr5:177865925..177867596,2	MCF-7	breast:
43	chr5:177912045..177914389-chr5:177919098..177921696,2	MCF-7	breast:
44	chr5:177879706..177881386-chr5:177883345..177884930,2	K562	blood:
45	chr5:177841800..177844284-chr5:177969427..177971380,2	K562	blood:
46	chr5:177861712..177865085-chr5:177866946..177869684,3	K562	blood:
47	chr5:177882178..177883994-chr5:177886180..177888676,2	K562	blood:
48	chr5:177639899..177641495-chr5:177970061..177972011,2	K562	blood:
49	chr5:177865902..177866648-chr5:177887888..177888885,2	K562	blood:
50	chr5:177912045..177914389-chr5:177919098..177921696,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLK4-1	chr5:177865682-177866970	ENSG00000245688.1
2	lnc-CLK4-2	chr5:177950506-177950714	NONHSAT105537
3	lnc-CLK4-2	chr5:177989599-177989727	NONHSAT105537
4	lnc-CLK4-2	chr5:177988845-177989007	NONHSAT105537
5	lnc-CLK4-2	chr5:177987683-177987749	NONHSAT105537
6	lnc-CLK4-1	chr5:177869927-177870095	ENSG00000245688.1

No data

Variant related genes	Relation type
COL23A1	TF binding region
ENSG00000245688	TF binding region
COL23A1	CpG island
ENSG00000245688	CpG island
ENSG00000197451	chromatin interactions
ENSG00000050767	chromatin interactions
ENSG00000245688	chromatin interactions

Extended variants
information (count: 6307 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:6307 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4357054	chr5:177860454-177860455	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112215942	chr5:177860461-177860462	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376064062	chr5:177860462-177860463	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370215373	chr5:177860493-177860494	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540651989	chr5:177860494-177860495	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570615060	chr5:177860497-177860498	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537994721	chr5:177860513-177860514	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs202222189	chr5:177860576-177860577	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187564341	chr5:177860601-177860602	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373949805	chr5:177860602-177860603	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368136581	chr5:177860629-177860630	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568474496	chr5:177860632-177860633	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141889854	chr5:177860640-177860641	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113011523	chr5:177860670-177860671	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138506063	chr5:177860684-177860685	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10065268	chr5:177860713-177860714	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs558438987	chr5:177860761-177860762	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576703057	chr5:177860779-177860780	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76340491	chr5:177860798-177860799	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561271983	chr5:177860807-177860808	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557413251	chr5:177860815-177860816	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34076387	chr5:177860821-177860822	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540378691	chr5:177860847-177860848	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142547226	chr5:177860850-177860851	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561606471	chr5:177860875-177860876	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573602772	chr5:177860878-177860879	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192500167	chr5:177860891-177860892	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182779649	chr5:177860937-177860938	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533030344	chr5:177861031-177861032	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188714262	chr5:177861054-177861055	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34513211	chr5:177861073-177861074	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563182946	chr5:177861083-177861084	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111244972	chr5:177861087-177861088	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7356757	chr5:177861145-177861146	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs137993647	chr5:177861195-177861196	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568430810	chr5:177861203-177861204	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535856477	chr5:177861279-177861280	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1109115	chr5:177861310-177861311	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7356761	chr5:177861328-177861329	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566064295	chr5:177861339-177861340	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540178509	chr5:177861349-177861350	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558477760	chr5:177861394-177861395	Weak transcription Enhancers Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576741498	chr5:177861435-177861436	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537614738	chr5:177861439-177861440	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555456201	chr5:177861445-177861446	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573616175	chr5:177861602-177861603	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs200894067	chr5:177861621-177861622	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs541025405	chr5:177861711-177861712	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs559131446	chr5:177861741-177861742	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112106469	chr5:177861818-177861819	Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:1609 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177856000-177861400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:177856400-177861600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr5:177856600-177861000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr5:177856800-177861200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr5:177856800-177861600	Weak transcription	Brain Angular Gyrus	brain
6	chr5:177856800-177861600	Weak transcription	Fetal Heart	heart
7	chr5:177856800-177861800	Weak transcription	Left Ventricle	heart
8	chr5:177856800-177887200	Weak transcription	Right Atrium	heart
9	chr5:177857000-177861600	Weak transcription	Psoas Muscle	Psoas
10	chr5:177857000-177862600	Weak transcription	Gastric	stomach
11	chr5:177857000-177863800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr5:177857200-177862000	Weak transcription	Fetal Kidney	kidney
13	chr5:177859200-177861400	Enhancers	NHDF-Ad	bronchial
14	chr5:177859200-177862400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr5:177859200-177862600	Enhancers	Fetal Lung	lung
16	chr5:177859200-177866000	Genic enhancers	Fetal Thymus	thymus
17	chr5:177859400-177860600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr5:177859400-177860800	Enhancers	Dnd41	blood
19	chr5:177859400-177866600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr5:177859800-177860600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:177859800-177865000	Genic enhancers	Thymus	Thymus
22	chr5:177860000-177861200	Weak transcription	Adipose Nuclei	Adipose
23	chr5:177860000-177861600	Weak transcription	Spleen	Spleen
24	chr5:177860000-177864600	Weak transcription	Lung	lung
25	chr5:177860200-177861200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:177860200-177861200	Weak transcription	Right Ventricle	heart
27	chr5:177860200-177861800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr5:177860200-177862200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:177860600-177861800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:177860800-177863000	Weak transcription	Dnd41	blood
31	chr5:177861000-177861600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
32	chr5:177861000-177862600	Enhancers	Brain Cingulate Gyrus	brain
33	chr5:177861200-177861600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:177861200-177861600	Enhancers	Adipose Nuclei	Adipose
35	chr5:177861200-177861600	Enhancers	Placenta	Placenta
36	chr5:177861200-177861600	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr5:177861200-177862600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:177861200-177863000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr5:177861200-177863000	Enhancers	Right Ventricle	heart
40	chr5:177861400-177862800	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr5:177861400-177863000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:177861600-177861800	Bivalent Enhancer	Adipose Nuclei	Adipose
43	chr5:177861600-177861800	Enhancers	Spleen	Spleen
44	chr5:177861600-177862000	Enhancers	Brain Anterior Caudate	brain
45	chr5:177861600-177862000	Enhancers	Psoas Muscle	Psoas
46	chr5:177861600-177862200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr5:177861600-177862600	Enhancers	Brain Angular Gyrus	brain
48	chr5:177861600-177862600	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr5:177861600-177862600	Enhancers	Fetal Heart	heart
50	chr5:177861600-177862600	Enhancers	Skeletal Muscle Female	skeletal muscle

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