Variant report

Variant	nsv885808
Chromosome Location	chr6:36659932-36684518
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:244)
Chromatin interactive
region (count:55)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:36659948-36660288	K562	blood:	n/a	n/a
2	ATF1	chr6:36668625-36668845	K562	blood:	n/a	n/a
3	ATF1	chr6:36678052-36678253	K562	blood:	n/a	n/a
4	ATF2	chr6:36659508-36660457	GM12878	blood:	n/a	n/a
5	BATF	chr6:36663263-36663505	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:36666622-36666707	K562	blood:	n/a	n/a
7	BHLHE40	chr6:36667689-36667896	K562	blood:	n/a	n/a
8	CBX3	chr6:36669244-36669614	K562	blood:	n/a	n/a
9	CCNT2	chr6:36661025-36661080	K562	blood:	n/a	n/a
10	CEBPB	chr6:36679544-36679725	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:36674332-36674417	Hela-S3	cervix:	n/a	chr6:36674393-36674404
12	CEBPB	chr6:36679346-36679845	MCF-7	breast:	n/a	n/a
13	CEBPB	chr6:36679479-36679908	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:36677290-36677479	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:36665511-36665591	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:36679421-36679856	MCF-7	breast:	n/a	n/a
17	CEBPB	chr6:36674249-36674531	IMR90	lung:	n/a	chr6:36674393-36674404
18	CEBPB	chr6:36674255-36674512	A549	lung:	n/a	chr6:36674393-36674404
19	CEBPB	chr6:36674259-36674477	K562	blood:	n/a	chr6:36674393-36674404
20	CEBPB	chr6:36679449-36679811	K562	blood:	n/a	n/a
21	CEBPB	chr6:36679475-36679749	K562	blood:	n/a	n/a
22	CEBPB	chr6:36679450-36679900	A549	lung:	n/a	n/a
23	CEBPB	chr6:36679528-36679888	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:36670119-36670260	HepG2	liver:	n/a	chr6:36670157-36670168 chr6:36670157-36670170
25	CEBPB	chr6:36679480-36679800	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:36677285-36677410	K562	blood:	n/a	n/a
27	CEBPB	chr6:36674234-36674536	HepG2	liver:	n/a	chr6:36674393-36674404
28	CHD2	chr6:36660044-36660311	GM12878	blood:	n/a	n/a
29	CTCF	chr6:36669440-36669590	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:36669460-36669610	HEK293	kidney:	n/a	n/a
31	CTCF	chr6:36669400-36669550	K562	blood:	n/a	n/a
32	CTCF	chr6:36669427-36669576	LNCaP	prostate:	n/a	n/a
33	CTCF	chr6:36669460-36669610	HRE	kidney:	n/a	n/a
34	CTCF	chr6:36669374-36669638	GM12878	blood:	n/a	n/a
35	CTCF	chr6:36669454-36669574	GM19239	blood:	n/a	n/a
36	CTCF	chr6:36669440-36669590	GM12873	blood:	n/a	n/a
37	CTCF	chr6:36669552-36669558	Lung_OC	lung:	n/a	n/a
38	CTCF	chr6:36669300-36669450	NHEK	skin:	n/a	n/a
39	CTCF	chr6:36669432-36669612	GM10266	blood:	n/a	n/a
40	CTCF	chr6:36669329-36669686	GM12878	blood:	n/a	n/a
41	CTCF	chr6:36669460-36669610	HepG2	liver:	n/a	n/a
42	CTCF	chr6:36669420-36669570	NHEK	skin:	n/a	n/a
43	CTCF	chr6:36669375-36669613	HepG2	liver:	n/a	n/a
44	CTCF	chr6:36669400-36669602	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:36669354-36669698	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:36669440-36669590	GM12874	blood:	n/a	n/a
47	CTCF	chr6:36669420-36669570	BE2_C	brain:	n/a	n/a
48	CTCF	chr6:36669179-36669694	HepG2	liver:	n/a	n/a
49	CTCF	chr6:36669420-36669570	GM12866	blood:	n/a	n/a
50	CTCF	chr6:36669440-36669590	GM12867	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:36665554-36665604	PrEC	prostate:	n/a
2	chr6:36665554-36665604	AG09309	skin:	n/a
3	chr6:36665554-36665604	T-47D	breast:	n/a
4	chr6:36669758-36669808	HCM	heart:	n/a
5	chr6:36665611-36665661	HIPEpiC	eye:	n/a
6	chr6:36669758-36669808	HRE	kidney:	n/a
7	chr6:36665620-36665670	HRCEpiC	kidney:	n/a
8	chr6:36665620-36665670	ECC-1	luminal epithelium:	n/a
9	chr6:36665620-36665670	HL-60	blood:	n/a
10	chr6:36665554-36665604	SK-N-MC	brain:	n/a
11	chr6:36665620-36665670	AoSMC	blood vessel:	n/a
12	chr6:36669758-36669808	SK-N-SH_RA	brain:	n/a
13	chr6:36665611-36665661	GM19239	blood:	n/a
14	chr6:36665620-36665670	U87	brain:	n/a
15	chr6:36669758-36669808	NH-A	brain:	n/a
16	chr6:36665611-36665661	HUVEC	blood vessel:	n/a
17	chr6:36665611-36665661	GM12891	blood:	n/a
18	chr6:36669758-36669808	Caco-2	colon:	n/a
19	chr6:36669758-36669808	GM06990	blood:	n/a
20	chr6:36665620-36665670	PANC-1	pancreas:	n/a
21	chr6:36665620-36665670	Hela-S3	cervix:	n/a
22	chr6:36665554-36665604	RPTEC	kidney:	n/a
23	chr6:36665611-36665661	HCT-116	colon:	n/a
24	chr6:36665620-36665670	SKMC	muscle:	n/a
25	chr6:36669758-36669808	A549	lung:	n/a
26	chr6:36665620-36665670	HCPEpiC	choroid plexus:	n/a
27	chr6:36665611-36665661	AG04450	lung:	fetal
28	chr6:36665620-36665670	HMEC	breast:	n/a
29	chr6:36669758-36669808	PANC-1	pancreas:	n/a
30	chr6:36665611-36665661	SK-N-MC	brain:	n/a
31	chr6:36669758-36669808	PFSK-1	brain:	n/a
32	chr6:36665611-36665661	NHBE	bronchial:	n/a
33	chr6:36665620-36665670	GM12878	blood:	n/a
34	chr6:36665611-36665661	HRPEpiC	eye:	n/a
35	chr6:36665554-36665604	GM19239	blood:	n/a
36	chr6:36669758-36669808	ovcar-3	ovarian:	n/a
37	chr6:36665554-36665604	AG09319	gingival:	n/a
38	chr6:36665554-36665604	HIPEpiC	eye:	n/a
39	chr6:36665554-36665604	NHBE	bronchial:	n/a
40	chr6:36665611-36665661	AoSMC	blood vessel:	n/a
41	chr6:36665554-36665604	PFSK-1	brain:	n/a
42	chr6:36669758-36669808	HRCEpiC	kidney:	n/a
43	chr6:36669758-36669808	H1-hESC	embryonic stem cell:	embryo
44	chr6:36665620-36665670	ovcar-3	ovarian:	n/a
45	chr6:36669758-36669808	NHDF-neo	bronchial:	n/a
46	chr6:36669758-36669808	Jurkat	blood:	n/a
47	chr6:36665554-36665604	AG10803	skin:	n/a
48	chr6:36665611-36665661	HRE	kidney:	n/a
49	chr6:36665611-36665661	IMR90	lung:	fetal
50	chr6:36665611-36665661	HL-60	blood:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:36658383..36660114-chr6:36663933..36665549,2	MCF-7	breast:
2	chr6:36561573..36563528-chr6:36666285..36668118,2	K562	blood:
3	chr6:36577490..36580113-chr6:36675769..36678702,3	K562	blood:
4	chr6:36560786..36563528-chr6:36659372..36662028,2	K562	blood:
5	chr6:36647044..36648855-chr6:36663270..36664993,2	MCF-7	breast:
6	chr6:36668981..36671610-chr6:36673989..36676606,2	K562	blood:
7	chr6:36658841..36660500-chr6:36665313..36667930,3	MCF-7	breast:
8	chr6:36590882..36591428-chr6:36669194..36670304,3	MCF-7	breast:
9	chr6:36658841..36660500-chr6:36665313..36667930,3	MCF-7	breast:
10	chr6:36650057..36652668-chr6:36663338..36666266,2	K562	blood:
11	chr6:36560848..36563528-chr6:36666618..36669519,2	K562	blood:
12	chr6:36562026..36564404-chr6:36670618..36673536,2	K562	blood:
13	chr6:36665939..36668161-chr6:36669239..36671316,2	MCF-7	breast:
14	chr6:36680840..36682367-chr6:36685860..36687656,2	K562	blood:
15	chr6:36650062..36652279-chr6:36667260..36670117,2	MCF-7	breast:
16	chr6:36659068..36661515-chr6:36679186..36681005,2	MCF-7	breast:
17	chr6:36644113..36646429-chr6:36664735..36667230,2	K562	blood:
18	chr6:36658383..36660114-chr6:36663933..36665549,2	MCF-7	breast:
19	chr6:36659288..36661808-chr6:36668728..36671591,2	MCF-7	breast:
20	chr6:36560978..36562524-chr6:36680718..36682396,2	K562	blood:
21	chr6:36662298..36665035-chr6:36665168..36667578,2	MCF-7	breast:
22	chr6:36675406..36676950-chr6:36681349..36683776,2	K562	blood:
23	chr6:36562412..36564652-chr6:36674547..36676281,2	K562	blood:
24	chr6:36572659..36575634-chr6:36662126..36664637,2	K562	blood:
25	chr6:36670687..36673370-chr6:36685914..36688268,2	K562	blood:
26	chr6:36658059..36660618-chr6:36709664..36711830,2	MCF-7	breast:
27	chr6:36664831..36667181-chr6:36668098..36669647,2	MCF-7	breast:
28	chr6:36646049..36647874-chr6:36669736..36673163,4	MCF-7	breast:
29	chr6:36662298..36665035-chr6:36665168..36667578,2	MCF-7	breast:
30	chr6:36560786..36563777-chr6:36658792..36660872,2	K562	blood:
31	chr6:36659068..36661515-chr6:36679186..36681005,2	MCF-7	breast:
32	chr6:36659288..36661808-chr6:36668728..36671591,2	MCF-7	breast:
33	chr6:36646383..36648847-chr6:36677115..36679652,2	MCF-7	breast:
34	chr6:36576769..36579207-chr6:36667077..36668814,2	K562	blood:
35	chr6:36591348..36591899-chr6:36668578..36669604,3	K562	blood:
36	chr6:36650715..36656032-chr6:36664945..36667924,5	MCF-7	breast:
37	chr6:36645391..36647920-chr6:36680659..36684331,3	MCF-7	breast:
38	chr6:36650316..36652178-chr6:36659155..36660681,2	MCF-7	breast:
39	chr6:36659558..36662002-chr6:36724611..36726643,2	MCF-7	breast:
40	chr6:36670725..36674166-chr6:36726971..36730200,3	MCF-7	breast:
41	chr6:36684189..36687540-chr6:36688167..36692245,5	MCF-7	breast:
42	chr6:36674085..36676921-chr6:36682929..36685200,2	K562	blood:
43	chr6:36644981..36649007-chr6:36657170..36660306,4	K562	blood:
44	chr6:36665939..36668161-chr6:36669239..36671316,2	MCF-7	breast:
45	chr6:36664831..36667181-chr6:36668098..36669647,2	MCF-7	breast:
46	chr6:36648865..36650746-chr6:36679299..36682231,2	K562	blood:
47	chr6:36560048..36562524-chr6:36680718..36683853,3	K562	blood:
48	chr6:36646719..36650011-chr6:36657952..36660291,4	MCF-7	breast:
49	chr6:36671517..36673727-chr6:36709746..36712131,2	K562	blood:
50	chr6:36668981..36671610-chr6:36673989..36676606,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPNE5-2	chr6:36675495-36676067	uc_189_-

No data

Variant related genes	Relation type
RAB44	TF binding region
RAB44	CpG island
ENSG00000112081	chromatin interactions
ENSG00000255587	chromatin interactions
ENSG00000124762	chromatin interactions
ENSG00000124772	chromatin interactions

Extended variants
information (count: 984 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6937605	chr6:36659932-36659933	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187248892	chr6:36659938-36659939	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs150481808	chr6:36659964-36659965	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs528362816	chr6:36659997-36659998	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs138301087	chr6:36660028-36660029	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs567867979	chr6:36660092-36660093	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs78488736	chr6:36660105-36660106	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs35328363	chr6:36660109-36660110	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs568595586	chr6:36660136-36660137	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs553179172	chr6:36660152-36660153	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs539076201	chr6:36660224-36660225	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs201566475	chr6:36660234-36660235	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs11759823	chr6:36660298-36660299	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557466258	chr6:36660355-36660356	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs377025837	chr6:36660379-36660380	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs571164905	chr6:36660424-36660425	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs6457938	chr6:36660453-36660454	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
18	rs553537670	chr6:36660457-36660458	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs35427489	chr6:36660480-36660481	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs34126793	chr6:36660499-36660500	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189318654	chr6:36660536-36660537	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs542360500	chr6:36660538-36660539	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs557526518	chr6:36660585-36660586	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs575803409	chr6:36660594-36660595	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546217860	chr6:36660638-36660639	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs377554532	chr6:36660654-36660655	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149196004	chr6:36660666-36660667	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs180873094	chr6:36660716-36660717	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs553560139	chr6:36660720-36660721	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs145094606	chr6:36660785-36660786	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs80114708	chr6:36660799-36660800	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529086473	chr6:36660862-36660863	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142441773	chr6:36660907-36660908	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145952165	chr6:36660959-36660960	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374469893	chr6:36661007-36661008	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532877789	chr6:36661040-36661041	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs148193628	chr6:36661236-36661237	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553844697	chr6:36661245-36661246	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77930044	chr6:36661250-36661251	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs535351845	chr6:36661251-36661252	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs185625246	chr6:36661341-36661342	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs568756436	chr6:36661353-36661354	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190129156	chr6:36661367-36661368	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs557577321	chr6:36661431-36661432	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575815505	chr6:36661510-36661511	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs182366458	chr6:36661541-36661542	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs80310768	chr6:36661637-36661638	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs547612599	chr6:36661645-36661646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185948733	chr6:36661659-36661660	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs141127499	chr6:36661666-36661667	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36651200-36660000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr6:36654800-36660200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr6:36655000-36660000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr6:36655000-36660000	Weak transcription	Pancreas	Pancrea
5	chr6:36655000-36660200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:36655000-36660200	Weak transcription	Thymus	Thymus
7	chr6:36655000-36660400	Weak transcription	Stomach Mucosa	stomach
8	chr6:36655000-36672000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:36655200-36660000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr6:36655200-36660200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:36655200-36660400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:36655200-36660400	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:36655200-36660800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr6:36655200-36661200	Weak transcription	Aorta	Aorta
15	chr6:36655200-36669400	Weak transcription	Gastric	stomach
16	chr6:36655400-36660000	Weak transcription	Dnd41	blood
17	chr6:36655400-36660400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr6:36655600-36660000	Weak transcription	Colonic Mucosa	Colon
19	chr6:36655600-36660200	Weak transcription	Adipose Nuclei	Adipose
20	chr6:36655600-36660200	Weak transcription	Fetal Muscle Leg	muscle
21	chr6:36655600-36660200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr6:36655600-36660800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:36655600-36660800	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr6:36655600-36661000	Weak transcription	HSMM	muscle
25	chr6:36655600-36663400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:36655800-36660200	Weak transcription	NHDF-Ad	bronchial
27	chr6:36655800-36660600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:36655800-36660800	Weak transcription	Lung	lung
29	chr6:36656000-36660600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:36656000-36661000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr6:36656200-36665200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:36657400-36660200	Enhancers	Primary B cells from cord blood	blood
33	chr6:36657400-36663600	Enhancers	Primary B cells from peripheral blood	blood
34	chr6:36657800-36661200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:36658200-36661200	Enhancers	HMEC	breast
36	chr6:36658400-36661200	Enhancers	NHEK	skin
37	chr6:36658800-36661200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:36658800-36661400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:36658800-36663200	Enhancers	Fetal Heart	heart
40	chr6:36659000-36661000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr6:36659000-36661000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:36659200-36660800	Enhancers	Primary hematopoietic stem cells	blood
43	chr6:36659200-36661000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr6:36659200-36661000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr6:36659200-36661000	Enhancers	GM12878-XiMat	blood
46	chr6:36659200-36661200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr6:36659200-36661400	Enhancers	Spleen	Spleen
48	chr6:36659400-36660200	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr6:36659400-36660400	Enhancers	Fetal Intestine Large	intestine
50	chr6:36659400-36660400	Enhancers	Placenta	Placenta

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